@article {3083, title = {Realization of portable room temperature nanodiamond 13C hyperpolarizer}, year = {Submitted}, author = {A. Ajoy and R. Nazaryan and E. Druga and K. Liu and B. Han and J.T. Oon and M. Gierth and R. Tsang and J.H. Walton and C.A. Meriles and J.A. Reimer and D. Suter and A. Pines} } @article {3531, title = {Rotaxane probes for the detection of hydrogen peroxide by 129Xe hyperCEST NMR}, journal = {Angewandte Chemie International Edition}, year = {2019}, doi = {10.1002/anie.201903045}, url = {https://onlinelibrary.wiley.com/doi/full/10.1002/anie.201903045}, author = {Klass, Sarah H and Truxal, Ashley E and Fiala, T A and Kelly, Joseph and Nguyen, Dang and Finbloom, Joel A and Wemmer, David E and Pines, Alexander and Francis, Matthew B} } @article {3193, title = {Zero-Field Nuclear Magnetic Resonance of Chemically Exchanging Systems}, journal = {Nature Communications}, volume = {10}, year = {2019}, month = {07/2019}, abstract = {

Zero- to ultralow-field (ZULF) nuclear magnetic resonance (NMR) is an emerging tool for precision chemical analysis. In this work, we study dynamic processes and investigate the influence of chemical exchange on ZULF NMR J-spectra. We develop a computational approach that allows quantitative calculation of J-spectra in the presence of chemical exchange and apply it to study aqueous solutions of [15N]ammonium (15N) as a model system. We show that pH-dependent chemical exchange substantially affects the J-spectra and, in some cases, can lead to degradation and complete disappearance of the spectral features. To demonstrate potential applications of ZULF NMR for chemistry and biomedicine, we show a ZULF NMR spectrum of [2-13C]pyruvic acid hyperpolarized via dissolution dynamic nuclear polarization (dDNP). We foresee applications of affordable and scalable ZULF NMR coupled with hyperpolarization to study chemical exchange phenomena in vivo and in situations where high-field NMR detection is not possible to implement.

}, doi = {https://doi.org/10.1038/s41467-019-10787-9}, url = {https://www.nature.com/articles/s41467-019-10787-9?fbclid=IwAR1MB5nAamCMGynKRk0sjD6V8rTlZ329IvrVKrCwIO8QjrEH4wD23BV5gak}, author = {Danila Barskiy and Michael Tayler and Irene Marco-Rius and John Kurhanewicz and Daniel Vigneron and Sevil Cikrikci and Ayca Aydogdu and Moritz Reh and Andrey Pravdivtsev and Jan-Bernd H{\"o}vener and John Blanchard and Teng Wu and Dmitry Budker and Alexander Pines} } @article {2979, title = {Orientation independent room-temperature optical 13C hyperpolarization in powdered diamond}, journal = {Science Advances}, volume = {4}, year = {2018}, month = {05/2018}, abstract = {

Dynamic nuclear polarization via contact with electronic spins has emerged as an attractive route to enhance the sensitivity of nuclear magnetic resonance beyond the traditional limits imposed by magnetic field strength and temperature. Among the various alternative implementations, the use of nitrogen vacancy (NV) centers in diamond\—a paramagnetic point defect whose spin can be optically polarized at room temperature\—has attracted widespread attention, but applications have been hampered by the need to align the NV axis with the external magnetic field. We overcome this hurdle through the combined use of continuous optical illumination and a microwave sweep over a broad frequency range. As a proof of principle, we demonstrate our approach using powdered diamond with which we attain bulk 13C spin polarization in excess of 0.25\% under ambient conditions. Remarkably, our technique acts efficiently on diamond crystals of all orientations and polarizes nuclear spins with a sign that depends exclusively on the direction of the microwave sweep. Our work paves the way toward the use of hyperpolarized diamond particles as imaging contrast agents for biosensing and, ultimately, for the hyperpolarization
of nuclear spins in arbitrary liquids brought in contact with their surface.

}, doi = {10.1126/sciadv.aar5492 }, url = {http://advances.sciencemag.org/content/4/5/eaar5492}, author = {Ashok Ajoy and Kristina Liu and Raff Nazaryan and Xudong Lv and Pablo R. Zangara and Benjamin Safvati and Guoqing Wang and Daniel Arnold and Grace Li and Arthur Lin and Priyanka Raghavan and Emanuel Druga and Siddharth Dhomkar and Daniela Pagliero and Jeffrey A. Reimer and Dieter Suter and Carlos A. Meriles and Alexander Pines} } @article {2963, title = {Rapid Catalyst Capture Enables Metal-Free para-Hydrogen-Based Hyperpolarized Contrast Agents}, journal = {The Journal of Physical Chemistry Letters}, volume = {9}, year = {2018}, month = {05/2018}, pages = {2721{\textendash}2724}, abstract = {

Hyperpolarization techniques based on the use of\ para-hydrogen provide orders of magnitude signal enhancement for magnetic resonance spectroscopy and imaging. The main drawback limiting widespread applicability of\ para-hydrogen-based techniques in biomedicine is the presence of organometallic compounds (the polarization transfer catalysts) in solution with hyperpolarized contrast agents. These catalysts are typically complexes of platinum-group metals, and their administration in vivo should be avoided. Herein, we show how extraction of a hyperpolarized compound from an organic phase to an aqueous phase combined with a rapid (less than 10 s) Ir-based catalyst capture by metal scavenging agents can produce pure\ para-hydrogen-based hyperpolarized contrast agents, as demonstrated by high-resolution nuclear magnetic resonance (NMR) spectroscopy and inductively coupled plasma atomic emission spectroscopy (ICP-AES). The presented methodology enables fast and efficient means of producing pure hyperpolarized aqueous solutions for biomedical and other uses.

}, doi = {10.1021/acs.jpclett.8b01007}, url = {https://pubs.acs.org/doi/abs/10.1021/acs.jpclett.8b01007}, author = {Danila A Barskiy and Lucia A Ke and Xingyang Li and Vincent Stevenson and Nevin Widarman and Hao Zhang and Ashley Truxal and Alexander Pines} } @article {1867, title = {129Xe NMR Relaxation-Based Macromolecular Sensing}, journal = {JACS Communication}, volume = {138}, year = {2016}, month = {07/2016}, chapter = {9747}, author = {Muller Gomes and Phuong Dao and Keunghong Jeong and Clancy Slack and Christophoros Vassiliou and Matthew B. Francis and David Wemmer and Alexander Pines} } @article {1955, title = {Nondisruptive Dissolution of Hyperpolarized 129Xe into Viscous Aqueous and Organic Liquid Crystalline Environments}, journal = {Angewandte Chemie }, year = {2016}, type = {Communication}, author = {AE Truxal and CC Slack and MD Gomes and CC Vassiliou and DE Wemmer and A Pines} } @article {2297, title = {Rotaxane probes for protease detection by 129Xe hyperCEST NMR}, journal = {Chemical Communications}, year = {2016}, month = {12/2016}, doi = {10.1039/C6CC09302G}, author = {Slack, CS and Finbloom, JA and Jeong, K and Bruns, CJ and Wemmer, DE and Pines, A and Francis, MB} } @article {1941, title = {Rotaxane-mediated suppression and activation of cucurbit[6]uril for molecular detection by 129Xe hyperCEST NMR}, journal = {ChemComm}, year = {2016}, author = {Joel A. Finbloom and Clancy C. Slack and Carson J. Bruns and Keunhong Jeong and David E. Wemmer and Alexander Pines and Matthew B. Francis} } @article {2074, title = {Targeted Molecular Imaging of Cancer Cells using MS2-Based 129Xe NMR}, journal = {Bioconjugate Chemistry}, volume = {27}, year = {2016}, month = {07/2016}, chapter = {1796}, doi = {10.1021/acs.bioconjchem.6b00275}, url = {http://pubs.acs.org/doi/abs/10.1021/acs.bioconjchem.6b00275}, author = {Keunhong Jeong and Chawita Netirojjanakul and Henrik K Munch and Jinny Sun and Joel A Finbloom and David E Wemmer and Alexander Pines and Matthew B Francis} } @article {1863, title = {Decoherence-protected transitions of nitrogen-vacancy centers in 99\% 13C-enriched diamond}, journal = {arXiv:1506.05484}, year = {2015}, month = {06/2015}, author = {Anna J. Parker and Hai-Jing Wang and Yiran Li and Alexander Pines and Jonathan P. King} } @article {1866, title = {Investigation of DOTA-Metal Chelation Effects on 129Xe Chemical Shift}, journal = {ChemPhysChem}, year = {2015}, author = {Keunhong Jeong and Clancy C. Slack and Christophoros C. Vassiliou and Phuong Dao and Muller D Gomes and Daniel J. Kennedy and Ashley E. Truxal and Lindsay J Sperling and Matthew B. Francis and David E. Wemmer and Alexander Pines} } @article {1875, title = {Room temperature in situ nuclear spin hyperpolarization from optically pumped nitrogen vacancy centers in diamond}, journal = {Nature Communications}, year = {2015}, author = {Jonathan P. King and Keunhong Jeong and Christophoros C. Vassiliou and Chang S. Shin and Ralph H. Page and Claudia E. Avalos and Hai-Jing Wang and Alexander Pines} } @article {1451, title = {Molecular Sensing Using Hyperpolarized Xenon NMR Spectroscopy}, journal = {Israel Journal of Chemistry}, volume = {54}, year = {2014}, pages = {104-112}, doi = {10.1002/ijch.201300128}, author = {Palaniappan, K.K. and Francis, M.B. and Pines, A. and Wemmer, D.E.} } @article {1476, title = {Optically detected cross-relaxation spectroscopy of electron spins in diamonds}, journal = {Nature Communication}, volume = {5}, year = {2014}, month = {06/2014}, pages = {4135}, doi = {10.1038/ncomms5135}, author = {Wang, H. J. and Shin, C. S. and Seltzer, S. J. and Avalos, C. E. and Pines, A. and Bajaj, V. S.} } @article {1477, title = {Optically-detected nuclear quadrupolar interaction of 14N in nitrogen-vacancy centers in diamond}, journal = {Physical Review B}, volume = {89}, year = {2014}, pages = {205202}, doi = {10.1103/PhysRevB.89.205202}, author = {Shin, C. S. and Butler, M. C. and Wang, H. J. and Avalos, C. E. and Seltzer, S. J. and Liu, R. and Pines, A. and Bajaj, V.S.} } @article {243, title = {HyperCEST detection of a 129Xe-based contrast agent composed of cryptophane-A molecular cages on a bacteriophage scaffold}, journal = {Magnetic Resonance in Medicine}, volume = {69}, year = {2013}, pages = {1245-1252}, author = {Stevens, T.K. and Palaniappan, K.K. and Ramirez, R.M. and Francis, M.B. and Wemmer, D.E. and Pines, A.} } @article {1350, title = {Hyperpolarized xenon-based molecular sensors for label-free detection of analytes}, journal = {Journal of the American Chemical Society}, volume = {136}, year = {2013}, month = {12/2013}, pages = {164-168}, doi = {10.1021/ja406760r}, author = {Garimella, Praveena and Meldrum, Tyler and Witus, Leah Suzanne and Smith, Monica and Bajaj, Vikram and Wemmer, David E. and Francis, Matthew B. and Pines, Alexander} } @article {244, title = {Molecular imaging of cancer cells using a bacteriophage-based (129) xe NMR biosensor.}, journal = {Angewandte Chemie-International Edition}, volume = {52}, year = {2013}, pages = {4849-4853}, edition = {2013 Mar 28}, doi = {10.1002/anie.201300170}, author = {Palaniappan, K. K. and Ramirez, R.M. and Bajaj, V.S. and Wemmer, D.E. and Pines, A. and Francis, M.B.} } @article {1074, title = {Sensitive magnetic control of ensemble nuclear spin hyperpolarization in diamond}, journal = {Nature Communications}, volume = {4}, year = {2013}, note = {Nature communicationsWang, Hai-JingShin, Chang SAvalos, Claudia ESeltzer, Scott JBudker, DmitryPines, AlexanderBajaj, Vikram SengEngland2013/06/06 06:00Nat Commun. 2013 Jun 5;4:1940. doi: 10.1038/ncomms2930.}, month = {June 5, 2013}, pages = {1940}, chapter = {1940}, abstract = {

Dynamic nuclear polarization, which transfers the spin polarization of electrons to nuclei, is routinely applied to enhance the sensitivity of nuclear magnetic resonance. This method is particularly useful when spin hyperpolarization can be produced and controlled optically or electrically. Here we show complete polarization of nuclei located near optically polarized nitrogen-vacancy centres in diamond. Close to the ground-state level anti-crossing condition of the nitrogen-vacancy electron spins, (13)C nuclei in the first shell are polarized in a pattern that depends sensitively upon the magnetic field. Based on the anisotropy of the hyperfine coupling and of the optical polarization mechanism, we predict and observe a reversal of the nuclear spin polarization with only a few millitesla change in the magnetic field. This method of magnetic control of high nuclear polarization at room temperature can be applied in sensitivity enhanced nuclear magnetic resonance of bulk nuclei, nuclear-based spintronics, and quantum computation in diamond.

}, isbn = {2041-1723 (Linking)}, doi = {10.1038/ncomms2930}, url = {http://www.ncbi.nlm.nih.gov/pubmed/23736952}, author = {Wang, H. J. and Shin, C. S. and Avalos, C. E. and Seltzer, S. J. and Budker, D. and Pines, A. and Bajaj, V. S.} } @article {1318, title = {Suppression of electron spin decoherence of the diamond NV center by a transverse magnetic field}, journal = {Physical Review B}, volume = {88}, year = {2013}, month = {10/2013}, abstract = {

We demonstrate that the spin decoherence of nitrogen vacancy (NV) centers in diamond can be suppressed by a transverse magnetic field if the electron spin bath is the primary decoherence source. The NV spin coherence, created in \“a decoherence-free subspace,\” is protected by the transverse component of the zero-field splitting, increasing the spin-coherence time about twofold. The decoherence due to the electron spin bath is also suppressed at magnetic fields stronger than \∼25 G when applied parallel to the NV symmetry axis. Our method can be used to extend the spin-coherence time of similar spin systems for applications in quantum computing, field sensing, and other metrologies.

}, doi = {10.1103/PhysRevB.88.161412}, url = {http://prb.aps.org/abstract/PRB/v88/i16/e161412}, author = {Shin, Chang S. and Avalos, Claudia E. and Butler, Mark C. and Wang, Hai-Jing and Seltzer, Scott J. and Liu, Ren-Bao and Pines, Alexander and Bajaj, Vikram S.} } @article {257, title = {Band-selective chemical exchange saturation transfer imaging with hyperpolarized xenon-based molecular sensors}, journal = {Journal of Magnetic Resonance}, volume = {213}, year = {2011}, note = {J Magn Reson847UKTimes Cited:3Cited References Count:29}, month = {Dec}, pages = {14-21}, abstract = {

Molecular imaging based on saturation transfer in exchanging systems is a tool for amplified and chemically specific magnetic resonance imaging. Xenon-based molecular sensors are a promising category of molecular imaging agents in which chemical exchange of dissolved xenon between its bulk and agent-bound phases has been use to achieve sub-picomolar detection sensitivity. Control over the saturation transfer dynamics, particularly when multiple exchanging resonances are present in the spectra, requires saturation fields of limited bandwidth and is generally accomplished by continuous wave irradiation. We demonstrate instead how band-selective saturation sequences based on multiple pulse inversion elements can yield saturation bandwidth tuneable over a wide range, while depositing less RF power in the sample. We show how these sequences can be used in imaging experiments that require spatial-spectral and multispectral saturation. The results should be applicable to all CEST experiments and, in particular, will provide the spectroscopic control required for applications of arrays of xenon chemical sensors in microfluidic chemical analysis devices. (C) 2011 Elsevier Inc. All rights reserved.

}, keywords = {xe-129}, isbn = {1090-7807}, doi = {Doi 10.1016/J.Jmr.2011.06.027}, url = {://WOS:000296997800002}, author = {Meldrum, T. and Bajaj, V. S. and Wemmer, D. E. and Pines, A.} } @article {256, title = {Relaxivity of Gadolinium Complexes Detected by Atomic Magnetometry}, journal = {Magnetic Resonance in Medicine}, volume = {66}, year = {2011}, note = {Magn Reson Med799AVTimes Cited:1Cited References Count:23}, month = {Aug}, pages = {605-608}, abstract = {

Laser atomic magnetomeby is a portable and low-cost yet highly sensitive method for low magnetic field detection. In this work, the atomic magnetometer was used in a remote-detection geometry to measure the relaxivity of aqueous gadolinium-diethylenetriamine pentaacetic acid Gd(DTPA) at the Earth\&$\#$39;s magnetic field (40 mu T). The measured relaxivity of 9.7 +/- 2.0 s(-1) mM(-1) is consistent with field-cycling experiments measured at slightly higher magnetic fields, but no cryogens or strong and homogeneous magnetic field were required for this experiment. The field-independent sensitivity of 80 fT Hz(-1/2) allowed an in vitro detection limit of similar to 10 mu M Gd(DTPA) to be measured in aqueous buffer solution. The low detection limit and enhanced relaxivity of Gd-containing complexes at Earth\&$\#$39;s field motivate continued development of atomic magnetometry toward medical applications. Magn Reson Med 66:605-608, 2011. (C) 2011 Wiley-Liss, Inc.

}, keywords = {nmr}, isbn = {0740-3194}, doi = {Doi 10.1002/Mrm.22811}, url = {://WOS:000293256800033}, author = {Michalak, D. J. and Xu, S. J. and Lowery, T. J. and Crawford, C. W. and Ledbetter, M. and Bouchard, L. S. and Wemmer, D. E. and Budker, D. and Pines, A.} } @article {261, title = {MRI Thermometry Based on Encapsulated Hyperpolarized Xenon}, journal = {Chemphyschem}, volume = {11}, year = {2010}, note = {Chemphyschem691LFTimes Cited:2Cited References Count:25}, month = {Nov 15}, pages = {3529-3533}, abstract = {

A new approach to MRI thermometry using encapsulated hyperpolarized xenon is demonstrated The method is based on the temperature dependent chemical shift of hyperpolarized xenon in a cryptophane-A cage This shift is linear with a slope of 029 ppm degrees C(-1) which is perceptibly higher than the shift of the proton resonance frequency of water (ca 0 01 ppm degrees C(-1)) that is currently used for MRI thermometry Using spectroscopic imaging techniques, we collected temperature maps of a phantom sample that could discriminate by direct NMR detection between temperature differences of 0 1 degrees C at a sensor concentration of 150 mu M Alternatively, the xenon-in-cage chemical shift was determined by indirect detection using saturation transfer techniques (Hyper-CEST) that allow detection of nanomolar agent concentrations Thermometry based on hyperpolarized xenon sensors improves the accuracy of currently available MRI thermometry methods, potentially giving rise to biomedical applications of biosensors functionalized for binding to specific target molecules

}, keywords = {xe-129}, isbn = {1439-4235}, doi = {Doi 10.1002/Cphc.201000507}, url = {://WOS:000285080600023}, author = {Schilling, F. and Schroder, L. and Palaniappan, K. K. and Zapf, S. and Wemmer, D. E. and Pines, A.} } @article {263, title = {A Xenon-Based Molecular Sensor Assembled on an MS2 Viral Capsid Scaffold}, journal = {Journal of the American Chemical Society}, volume = {132}, year = {2010}, note = {J Am Chem Soc589OATimes Cited:20Cited References Count:23}, month = {May 5}, pages = {5936-+}, abstract = {

In MRI, anatomical structures are most often differentiated by variations in their bulk magnetic properties. Alternatively, exogenous contrast agents can be attached to chemical moieties that confer affinity to molecular targets; the distribution of such contrast agents can be imaged by magnetic resonance. Xenon-based molecular sensors are molecular imaging agents that rely on the reversible exchange of hyperpolarized xenon between the bulk and a specifically targeted host-guest complex. We have incorporated similar to 125 xenon sensor molecules in the interior of an MS2 viral capsid, conferring multivalency and other properties of the viral capsid to the sensor molecule. The resulting signal amplification facilitates the detection of sensor at 0.7 pM, the lowest to date for any molecular imaging agent used in magnetic resonance. This amplification promises the detection of chemical targets at much lower concentrations than would be possible without the capsid scaffold.

}, keywords = {nmr}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja100319f}, url = {://WOS:000277158500007}, author = {Meldrum, T. and Seim, K. L. and Bajaj, V. S. and Palaniappan, K. K. and Wu, W. and Francis, M. B. and Wemmer, D. E. and Pines, A.} } @article {264, title = {Xenon-based molecular sensors in lipid suspensions}, journal = {Journal of Magnetic Resonance}, volume = {205}, year = {2010}, note = {J Magn Reson627SZTimes Cited:8Cited References Count:23}, month = {Aug}, pages = {242-246}, abstract = {

There have been many proposals to use xenon-based molecular sensors in biological settings. Fundamental to understanding the properties of these sensors in vivo is characterizing their behavior in lipid environments. We report the investigation of xenon-based molecular sensors in suspensions of lipid vesicles with a size comparable to cells. We detail spectroscopic properties of sensors associated with lipid vesicles as well as those in equilibrium in the surrounding solution. We characterize the dependence of the spectral parameters on temperature, relevant for studies at physiological temperatures. We also demonstrate the ability to perform selective saturation transfer (Hyper-CEST) between sensor, both lipid bound and unbound, and the bulk solution. Lastly, we demonstrate the applicability of saturation transfer in the heterogeneous medium as an imaging modality. (C) 2010 Elsevier Inc. All rights reserved.

}, keywords = {binding}, isbn = {1090-7807}, doi = {Doi 10.1016/J.Jmr.2010.05.005}, url = {://WOS:000280064500008}, author = {Meldrum, T. and Schroder, L. and Denger, P. and Wemmer, D. E. and Pines, A.} } @article {268, title = {Optical detection of NMR J-spectra at zero magnetic field}, journal = {Journal of Magnetic Resonance}, volume = {199}, year = {2009}, note = {J Magn Reson456YJTimes Cited:19Cited References Count:26}, month = {Jul}, pages = {25-29}, abstract = {

Scalar couplings of the form JI(1) . I(2) between nuclei impart valuable information about molecular structure to nuclear magnetic-resonance spectra. Here we demonstrate direct detection of J-spectra due to both heteronuclear and homonuclear J-coupling in a zero-field environment where the Zeeman interaction is completely absent. We show that characteristic functional groups exhibit distinct spectra with straightforward interpretation for chemical identification. Detection is performed with a microfabricated optical atomic magnetometer, providing high sensitivity to samples of microliter volumes. We obtain 0.1 Hz linewidths and measure scalar-coupling parameters with 4-mHz statistical uncertainty. We anticipate that the technique described here will provide a new modality for high-precision\" J spectroscopy\" using small samples oil microchip devices for multiplexed Screening, assaying, and sample identification in chemistry and biomedicine. (C) 2009 Elsevier Inc. All rights reserved.

}, keywords = {cells}, isbn = {1090-7807}, doi = {Doi 10.1016/J.Jmr.2009.03.008}, url = {://WOS:000266890300004}, author = {Ledbetter, M. P. and Crawford, C. W. and Pines, A. and Wemmer, D. E. and Knappe, S. and Kitching, J. and Budker, D.} } @article {272, title = {Picomolar sensitivity MRI and photoacoustic imaging of cobalt nanoparticles}, journal = {Proceedings of the National Academy of Sciences of the United States of America}, volume = {106}, year = {2009}, note = {P Natl Acad Sci USA420HDTimes Cited:43Cited References Count:41}, month = {Mar 17}, pages = {4085-4089}, abstract = {

Multimodality imaging based on complementary detection principles has broad clinical applications and promises to improve the accuracy of medical diagnosis. This means that a tracer particle advantageously incorporates multiple functionalities into a single delivery vehicle. In the present work, we explore a unique combination of MRI and photoacoustic tomography (PAT) to detect picomolar concentrations of nanoparticles. The nanoconstruct consists of ferromagnetic (Co) particles coated with gold (Au) for biocompatibility and a unique shape that enables optical absorption over a broad range of frequencies. The end result is a dual-modality probe useful for the detection of trace amounts of nanoparticles in biological tissues, in which MRI provides volume detection, whereas PAT performs edge detection.

}, keywords = {cancer}, isbn = {0027-8424}, doi = {Doi 10.1073/Pnas.0813019106}, url = {://WOS:000264278800008}, author = {Bouchard, L. S. and Anwar, M. S. and Liu, G. L. and Hann, B. and Xie, Z. H. and Gray, J. W. and Wang, X. D. and Pines, A. and Chen, F. F.} } @article {276, title = {Temperature response of (129)Xe depolarization transfer and its application for ultrasensitive NMR detection}, journal = {Physical Review Letters}, volume = {100}, year = {2008}, note = {Phys Rev Lett320JWTimes Cited:12Cited References Count:8}, month = {Jun 27}, abstract = {

Trapping xenon in functionalized cryptophane cages makes the sensitivity of hyperpolarized (HP) (129)Xe available for specific NMR detection of biomolecules. Here, we study the signal transfer onto a reservoir of unbound HP xenon by gating the residence time of the nuclei in the cage through the temperature-dependant exchange rate. Temperature changes larger than similar to 0.6 K are detectable as an altered reservoir signal. The temperature response is adjustable with lower concentrations of caged xenon providing more sensitivity at higher temperatures. Ultrasensitive detection of functionalized cryptophane at 310 K is demonstrated with a concentration of 10 nM, corresponding to a similar to 4000-fold sensitivity enhancement compared to conventional detection. This makes HPNMR capable of detecting such constructs in concentrations far below the detection limit of benchtop uv-visible light absorbance.

}, keywords = {biosensors}, isbn = {0031-9007}, doi = {Doi 10.1103/Physrevlett.100.257603}, url = {://WOS:000257230500066}, author = {Schroeder, L. and Meldrum, T. and Smith, M. and Lowery, T. J. and Wemmer, D. E. and Pines, A.} } @article {277, title = {Temperature-controlled molecular depolarization gates in nuclear magnetic resonance}, journal = {Angewandte Chemie-International Edition}, volume = {47}, year = {2008}, note = {Angew Chem Int Edit308BXTimes Cited:13Cited References Count:19}, pages = {4316-4320}, keywords = {mri}, isbn = {1433-7851}, doi = {Doi 10.1002/Anie.200800382}, url = {://WOS:000256364400007}, author = {Schroder, L. and Chavez, L. and Meldrum, T. and Smith, M. and Lowery, T. J. and Wemmer, D. E. and Pines, A.} } @article {289, title = {Sensitivity enhancement by exchange mediated magnetization transfer of the xenon biosensor signal}, journal = {Journal of Magnetic Resonance}, volume = {184}, year = {2007}, note = {J Magn Reson127EUTimes Cited:7Cited References Count:18}, month = {Jan}, pages = {72-77}, abstract = {

Hyperpolarized xenon associated with ligand derivatized cryptophane-A cages has been developed as a NMR based biosensor. To optimize the detection sensitivity we describe use of xenon exchange between the caged and bulk dissolved xenon as an effective signal amplifier. This approach, somewhat analogous to \&$\#$39;remote detection\&$\#$39; described recently, uses the chemical exchange to repeatedly transfer spectroscopic information from caged to bulk xenon, effectively integrating the caged signal. After an optimized integration period, the signal is read out by observation of the bulk magnetization. The spectrum of the caged xenon is reconstructed through use of a variable evolution period before transfer and Fourier analysis of the bulk signal as a function of the evolution time. (c) 2006 Elsevier Inc. All rights reserved.

}, keywords = {resonance}, isbn = {1090-7807}, doi = {Doi 10.1016/J.Jmr.2006.09.010}, url = {://WOS:000243568900009}, author = {Garcia, S. and Chavez, L. and Lowery, T. J. and Han, S. I. and Wemmer, D. E. and Pines, A.} } @article {294, title = {Molecular imaging using a targeted magnetic resonance hyperpolarized biosensor}, journal = {Science}, volume = {314}, year = {2006}, note = {Science096MWTimes Cited:109Cited References Count:20}, month = {Oct 20}, pages = {446-449}, abstract = {

A magnetic resonance approach is presented that enables high-sensitivity, high-contrast molecular imaging by exploiting xenon biosensors. These sensors link xenon atoms to specific biomolecular targets, coupling the high sensitivity of hyperpolarized nuclei with the specificity of biochemical interactions. We demonstrated spatial resolution of a specific target protein in vitro at micromolar concentration, with a readout scheme that reduces the required acquisition time by \>3300-fold relative to direct detection. This technique uses the signal of free hyperpolarized xenon to dramatically amplify the sensor signal via chemical exchange saturation transfer (CEST). Because it is similar to 10,000 times more sensitive than previous CEST methods and other molecular magnetic resonance imaging techniques, it marks a critical step toward the application of xenon biosensors as selective contrast agents in biomedical applications.

}, keywords = {agents}, isbn = {0036-8075}, doi = {Doi 10.1126/Science.1131847}, url = {://WOS:000241382500036}, author = {Schroder, L. and Lowery, T. J. and Hilty, C. and Wemmer, D. E. and Pines, A.} } @article {299, title = {Optimization of xenon biosensors for detection of protein interactions}, journal = {Chembiochem}, volume = {7}, year = {2006}, note = {Chembiochem003SDTimes Cited:39Cited References Count:25}, month = {Jan}, pages = {65-73}, abstract = {

Hyperpolarized Xe-129 NMR spectroscopy can detect the presence of specific low-concentration biomolecular analytes by means of a xenon biosensor that consists of a water-soluble, targeted cryptophane-A cage that encapsulates the xenon. In this work, we use the prototypical biotinylated xenon biosensor to determine the relationship between the molecular composition of the xenon biosensor and the characteristics of protein-bound resonances. The effects of diastereomer overlap, dipole-dipole coupling, chemical-shift anisotropy, xenon exchange, and biosensor conformotional exchange on the protein-bound biosensor signal were assessed. It was found that an optimal protein-bound biosensor signal can be obtained by minimizing the number of biosensor diastereomers and using a flexible linker of appropriate length. Both the line width and sensitivity of chemical shift to protein binding of the xenon biosensor were found to be inversely proportional to linker length.

}, keywords = {complexes}, isbn = {1439-4227}, doi = {Doi 10.1002/Cbic.200500327}, url = {://WOS:000234701000012}, author = {Lowery, T. J. and Garcia, S. and Chavez, L. and Ruiz, E. J. and Wu, T. and Brotin, T. and Dutasta, J. P. and King, D. S. and Schultz, P. G. and Pines, A. and Wemmer, D. E.} } @article {300, title = {Solid-state NMR structural studies of the fibril form of a mutant mouse prion peptide PrP89-143(P101L)}, journal = {Solid State Nuclear Magnetic Resonance}, volume = {29}, year = {2006}, note = {Solid State Nucl Mag999VATimes Cited:22Cited References Count:34}, month = {Feb}, pages = {183-190}, abstract = {

The peptide fragment 89-143 of the prion protein (carrying a P101L mutation) is biologically active in transgenic mice when in a fibrillar form. Injection of these fibrils into transgenic mice (expressing full length PrP with the P101L mutation) induces a neurodegenerative prion disease (Kaneko et al., J. Mol. Biol. 295 (2000) 997). Here we present solid-state NMR studies of PrP89-143(P101L) fibrils, probing the conformation of residues in the hydrophobic segment 112-124 with chemical shifts. The conformations of glycine residues were analyzed using doubly C-13 = 0 labeled peptides by two-dimensional (2D) double-quantum correlation, and double-quantum filtered dephasing distance measurements. MQ-NMR experiments were carried out to probe the relative alignment of the individual peptides fibrils. These NMR studies indicate that the 112-124 segment adopts an extended beta-sheet conformation, though not in a parallel, in register alignment. There is evidence for conformational variability at Gly 113. DQ correlation experiments provide useful information in regions with conformational heterogeneity. (c) 2005 Elsevier Inc. All rights reserved.

}, keywords = {identification}, isbn = {0926-2040}, doi = {Doi 10.1016/J.Ssnmr.2005.09.017}, url = {://WOS:000234417500020}, author = {Lim, K. H. and Nguyen, T. N. and Damo, S. M. and Mazur, T. and Ball, H. L. and Prusiner, S. B. and Pines, A. and Wemmer, D. E.} } @article {301, title = {Spectrally resolved magnetic resonance imaging of a xenon biosensor}, journal = {Angewandte Chemie-International Edition}, volume = {45}, year = {2006}, note = {Angew Chem Int Edit997CZTimes Cited:48Cited References Count:14}, pages = {70-73}, keywords = {delivery}, isbn = {1433-7851}, doi = {Doi 10.1002/Anie.200502693}, url = {://WOS:000234223900007}, author = {Hilty, C. and Lowery, T. J. and Wemmer, D. E. and Pines, A.} } @article {297, title = {Xenon biosensor amplification via dendrimer-cage supramolecular constructs}, journal = {Journal of the American Chemical Society}, volume = {128}, year = {2006}, note = {J Am Chem Soc043HFTimes Cited:37Cited References Count:21}, month = {May 17}, pages = {6334-6335}, keywords = {chemistry}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja061735s}, url = {://WOS:000237590400033}, author = {Mynar, J. L. and Lowery, T. J. and Wemmer, D. E. and Pines, A. and Frechet, J. M. J.} } @article {313, title = {Distinguishing multiple chemotaxis Y protein conformations with laser-polarized Xe-129 NMR}, journal = {Protein Science}, volume = {14}, year = {2005}, note = {Protein Sci907SSTimes Cited:23Cited References Count:27}, month = {Apr}, pages = {848-855}, abstract = {

The chemical shift of the Xe-129 NMR signal has been shown to be extremely sensitive to the local environment around the atom and has been used to follow processes such as ligand binding by bacterial periplasmic binding proteins. Here we show that the Xe-129 shift can sense more subtle changes: magnesium binding, BeF3- activation, and peptide binding by the Escherichia coli chemotaxis Y protein. H-1-N-15 correlation spectroscopy and X-ray crystallography were used to identify two xenon-binding cavities in CheY that are primarily responsible for the shift changes. One site is near the active site, and the other is near the peptide binding site.

}, keywords = {cavity}, isbn = {0961-8368}, doi = {Doi 10.1110/Ps.041231005}, url = {://WOS:000227738900002}, author = {Lowery, T. J. and Doucleff, M. and Ruiz, E. J. and Rubin, S. M. and Pines, A. and Wemmer, D. E.} } @article {316, title = {Isotropic proton-detected local-field nuclear magnetic resonance in solids}, journal = {Journal of Chemical Physics}, volume = {122}, year = {2005}, note = {J Chem Phys899JFTimes Cited:1Cited References Count:31}, month = {Feb 15}, abstract = {

A nuclear magnetic resonance method is presented which produces linear, isotropic proton-detected local-field spectra for INS spin systems in powdered samples. The method, heteronuclear isotropic evolution (HETIE), refocuses the anisotropic portion of the heteronuclear dipolar coupling frequencies by evolving the system under a series of specially designed Hamiltonians and evolution pathways. The theory behind HETIE is presented along with experimental studies conducted on a powdered sample of ferrocene, demonstrating the methodology outlined in this paper. Applications of HETIE for use in structure determination in the solid state are discussed. (C) 2005 American Institute of Physics.

}, keywords = {spectra}, isbn = {0021-9606}, doi = {Doi 10.1063/1.1844296}, url = {://WOS:000227140000043}, author = {Havlin, R. H. and Walls, J. D. and Pines, A.} } @article {317, title = {NMR-based biosensing with optimized delivery of polarized Xe-129 to solutions}, journal = {Analytical Chemistry}, volume = {77}, year = {2005}, note = {Anal Chem942GLTimes Cited:30Cited References Count:37}, month = {Jul 1}, pages = {4008-4012}, abstract = {

Laser-enhanced (LE) Xe-129 nuclear magnetic resonance (NMR) is an exceptional tool for sensing extremely small physical and chemical changes; however, the difficult mechanics of bringing polarized xenon and samples of interest together have limited applications, particularly to biological molecules. Here we present a method for accomplishing solution Xe-129 biosensing based on flow (bubbling) of LE Xe-129 gas through a solution in situ in the NMR probe, with pauses for data acquisition. This overcomes fundamental limitations of conventional solution-state LE Xe-129 NMR, e.g., the difficulty in transferring hydrophobic xenon into aqueous environments, and the need to handle the sample to refresh LE Xe-129 after an observation pulse depletes polarization. With this new method, we gained a factor of \> 100 in sensitivity due to improved xenon transfer to the solution and the ability to signal average by renewing the polarized xenon. Polarized xenon in biosensors was detected at very low concentrations, \<= 250 nanomolar, while retaining all the usual information from NMR. This approach can be used to simultaneously detect multiple sensors with different chemical shifts and is also capable of detecting signals from opaque, heterogeneous samples, which is a unique advantage over optical methods. This general approach is adaptable for sensing minute quantities of xenon in heterogeneous in vitro samples, in miniaturized devices and should be applicable to certain in-vivo environments.

}, keywords = {blood}, isbn = {0003-2700}, doi = {Doi 10.1021/Ac0500479}, url = {://WOS:000230270800035}, author = {Han, S. I. and Garcia, S. and Lowery, T. J. and Ruiz, E. J. and Seeley, J. A. and Chavez, L. and King, D. S. and Wemmer, D. E. and Pines, A.} } @article {333, title = {Design of a conformation-sensitive xenon-binding cavity in the ribose-binding protein}, journal = {Angewandte Chemie-International Edition}, volume = {43}, year = {2004}, note = {Angew Chem Int Edit877MVTimes Cited:10Cited References Count:20}, pages = {6320-6322}, keywords = {probe}, isbn = {1433-7851}, doi = {Doi 10.1002/Anie.200460629}, url = {://WOS:000225575600015}, author = {Lowery, T. J. and Rubin, S. M. and Ruiz, E. J. and Pines, A. and Wemmer, D. E.} } @article {325, title = {Development of a functionalized xenon biosensor}, journal = {Journal of the American Chemical Society}, volume = {126}, year = {2004}, note = {J Am Chem Soc872UHTimes Cited:60Cited References Count:76}, month = {Nov 24}, pages = {15287-15294}, abstract = {

NMR-based biosensors that utilize laser-polarized xenon offer potential advantages beyond current sensing technologies. These advantages include the capacity to simultaneously detect multiple analytes, the applicability to in vivo spectroscopy and imaging, and the possibility of \"remote\" amplified detection. Here, we present a detailed NMR characterization of the binding of a biotin-derivatized caged-xenon sensor to avidin. Binding of \"functionalized\" xenon to avidin leads to a change in the chemical shift of the encapsulated xenon in addition to a broadening of the resonance, both of which serve as NMR markers of ligand-target interaction. A control experiment in which the biotin-binding site of avidin was blocked with native biotin showed no such spectral changes, confirming that only specific binding, rather than nonspecific contact, between avidin and functionalized xenon leads to the effects on the xenon NMR spectrum. The exchange rate of xenon (between solution and cage) and the xenon spin-lattice relaxation rate were not changed significantly upon binding. We describe two methods for enhancing the signal from functionalized xenon by exploiting the laser-polarized xenon magnetization reservoir. We also show that the xenon chemical shifts are distinct for xenon encapsulated in different diastereomeric cage molecules. This demonstrates the potential for tuning the encapsulated xenon chemical shift, which is a key requirement for being able to multiplex the biosensor.

}, keywords = {drug discovery}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja0483037}, url = {://WOS:000225233600051}, author = {Spence, M. M. and Ruiz, E. J. and Rubin, S. M. and Lowery, T. J. and Winssinger, N. and Schultz, P. G. and Wemmer, D. E. and Pines, A.} } @article {343, title = {Applications of Laser-Polarized 129 XE NMR to Biomolecular Assays}, journal = {Magnetic Resonance Imaging}, year = {2003}, pages = {1235-1239}, doi = {10.1016/J.Mri.2003.08.025}, author = {Lowery, T.J. and Rubin, S.M. and Ruiz, E.J. and Spence, M.M. and Winssinger, N. and Schultz, P.G. and Pines, A. and Wemmer, D.E.} } @article {352, title = {Creating isotropic dipolar spectra for a pair of dipole coupled spins in high-field}, journal = {Chemical Physics Letters}, volume = {363}, year = {2002}, note = {Chem Phys Lett595CVTimes Cited:3Cited References Count:20}, month = {Sep 9}, pages = {372-380}, abstract = {

In the absence of a strong magnetic field, the dipolar interaction between two nuclear spins is independent of orientation leading to sharp lines. However, in high magnetic fields the Zeeman interaction breaks the symmetry of space and spin producing an anisotropic dipolar spectra. In the following Letter, a method that yields isotropic dipolar spectra for a pair of dipole-coupled spins is presented. This is accomplished through a suitable choice of coherence pathways and average Hamiltonians. We present a theoretical explanation as well as an experimental verification for this novel methodology. (C) 2002 Elsevier Science B.V. All rights reserved.

}, keywords = {angle}, isbn = {0009-2614}, doi = {Doi 10.1016/S0009-2614(02)01188-0}, url = {://WOS:000178090000027}, author = {Walls, J. D. and Blanton, W. B. and Havlin, R. H. and Pines, A.} } @article {354, title = {Detection and characterization of xenon-binding sites in proteins by Xe-129 NMR spectroscopy}, journal = {Journal of Molecular Biology}, volume = {322}, year = {2002}, note = {J Mol Biol597PTTimes Cited:53Cited References Count:54}, month = {Sep 13}, pages = {425-440}, abstract = {

Xenon-binding sites in proteins have led to a number of applications of xenon in biochemical and structural studies. Here we further develop the utility of Xe-129 NMR in characterizing specific xenon-protein interactions. The sensitivity of the Xe-129 chemical shift to its local environment and the intense signals attainable by optical pumping make xenon a useful NMR reporter of its own interactions with proteins. A method for detecting specific xenon-binding interactions by analysis of Xe-129 chemical shift data is illustrated using the maltose binding protein (MBP) from Escherichia coli as an example. The crystal structure of MBP in the presence of 8 atm of xenon confirms the binding site determined from NMR data. Changes in the structure of the xenon-binding cavity upon the binding of maltose by the protein can account for the sensitivity of the Xe-129 chemical shift to MBP conformation. Xe-129 NMR data for xenon in solution with a number of cavity containing phage T4 lysozyme mutants show that xenon can report on cavity structure. In particular, a correlation exists between cavity size and the binding-induced Xe-129 chemical shift. Further applications of Xe-129 NMR to biochemical assays, including the screening of proteins for xenon binding for crystallography are considered. (C) 2002 Elsevier Science Ltd. All rights reserved

}, keywords = {nonpolar cavity}, isbn = {0022-2836}, doi = {Doi 10.1016/S0022-2836(02)00739-8}, url = {://WOS:000178230500014}, author = {Rubin, S. M. and Lee, S. Y. and Ruiz, E. J. and Pines, A. and Wemmer, D. E.} } @article {359, title = {Investigations of low-amplitude radio frequency pulses at and away from rotary resonance conditions for I=5/2 Nuclei}, journal = {Solid State Nuclear Magnetic Resonance}, volume = {22}, year = {2002}, note = {Solid State Nucl Mag613WLTimes Cited:8Cited References Count:40}, month = {Sep-Nov}, pages = {97-109}, abstract = {

Additional experimental evidence of rotary resonance effects for multiple-quantum coherence conversion in a spin-5/2 system is presented. Two-dimensional plots of the relative efficiency of MQ excitation and conversion are given as a function of radio frequency (rf) amplitude and pulse width. Data are presented for the excitation of five-quantum coherence (5QC), as well as for 5QC to three-quantum coherence (3QC) conversion, 5QC to 1QC (the central transition coherence) conversion, and 3QC to 1 QC conversion. A two-fold increase in the signal-to-noise ratio is achieved by substituting low amplitude rf pulses in place of hard rf pulses for 5QC excitation and 5QC to 3QC conversion in a mixed multiple-quantum magic angle spinning (MAS) (MMQMAS) experiment. The anisotropic line shape for the low-amplitude rf pulse version of the MMQMAS experiment was observed to be distorted from the MAS line shape. The cause and implications of the distortion are discussed. (C) 2002 Elsevier Science (USA).

}, keywords = {solid-state}, isbn = {0926-2040}, doi = {Doi 10.1006/Snmr.2002.0084}, url = {://WOS:000179154400003}, author = {Logan, J. W. and Urban, J. T. and Walls, J. D. and Lim, K. H. and Jerschow, A. and Pines, A.} } @article {346, title = {Laser-polarized Xe-129 NMR and MRI at ultralow magnetic fields}, journal = {Journal of Magnetic Resonance}, volume = {157}, year = {2002}, note = {J Magn Reson600EJTimes Cited:23Cited References Count:25}, month = {Aug}, pages = {235-241}, abstract = {

Laser-polarized Xe-129 and a high-T-c superconducting quantum interference device (SQUID) are used to obtain magnetic resonance images in porous materials at a magnetic field of 2.3 mT, corresponding to a Larmor frequency of 27 kHz. Image resolution of 1 mm is obtained with gradients of only 1 mT/m. The resolution of xenon chemical shifts in different physicochemical environments at ultralow fields is also demonstrated. Details of the circulating flow optical pumping apparatus and the SQUID spectrometer are presented. (C) 2002 Elsevier Science (USA).

}, keywords = {atoms}, isbn = {1090-7807}, doi = {Doi 10.1006/Jmre.2002.2592}, url = {://WOS:000178377400009}, author = {Wong-Foy, A. and Saxena, S. and Moule, A. J. and Bitter, H. M. L. and Seeley, J. A. and McDermott, R. and Clarke, J. and Pines, A.} } @article {358, title = {Measurement of dipolar couplings in partially oriented molecules by local field NMR spectroscopy with low-power decoupling}, journal = {Journal of Magnetic Resonance}, volume = {158}, year = {2002}, note = {J Magn Reson619VETimes Cited:8Cited References Count:23}, month = {Sep-Oct}, pages = {52-59}, abstract = {

Low-power phase-modulated Lee-Goldburg homonuclear decoupling was used to record PDLF spectra of fluorine-substituted benzene derivatives dissolved in nematic thermotropic liquid crystalline solvents. The low-power decoupling minimizes sample heating during RE irradiation while still achieving highly resolved PDLF spectra. The method is illustrated by recording spectra for 1,3-dichloro-4-fluoro-5-nitrobenzene, 1,3-dichloro-4-fluorobenzene, and 1, 2-difluoro benzene dissolved in different nematic solvents. (C) 2002 Elsevier Science (USA). All rights reserved.

}, keywords = {resolution}, isbn = {1090-7807}, doi = {Doi 10.1016/S1090-7807(02)00059-9}, url = {://WOS:000179497500006}, author = {Marjanska, M. and Castiglione, F. and Walls, J. D. and Pines, A.} } @article {348, title = {Reintroducing anisotropic interactions in magic-angle-spinning NMR of half-integer quadrupolar nuclei: 3D MQMAS}, journal = {Journal of the American Chemical Society}, volume = {124}, year = {2002}, note = {J Am Chem Soc591GWTimes Cited:14Cited References Count:21}, month = {Sep 11}, pages = {10652-10653}, keywords = {redor}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja027043v}, url = {://WOS:000177872200011}, author = {Wi, S. and Heise, H. and Pines, A.} } @article {347, title = {Rotary resonance recoupling for half-integer quadrupolar nuclei in solid-state nuclear magnetic resonance spectroscopy}, journal = {Journal of Chemical Physics}, volume = {117}, year = {2002}, note = {J Chem Phys599CVTimes Cited:22Cited References Count:53}, month = {Oct 15}, pages = {7024-7033}, abstract = {

Investigations were made of rotary resonance recouplings (R-3) of chemical shift anisotropy (CSA), heteronuclear dipolar (HTD), and homonuclear dipolar (HMD) couplings involving half-integer quadrupolar nuclei under magic-angle sample spinning condition. Under rotary resonance conditions provided by a low amplitude rf field and a high spinning speed, the spectrum of the central transition coherence of half-integer quadrupolar nuclei shows recouplings of CSA, HTD, and HMD interactions that depend on the ratio of the rf field to the spinning speed. These new properties can be used to extract electronic and structural information about the sample that are otherwise difficult to extract in the presence of a dominant quadrupolar interaction. An average Hamiltonian theory is used to explain the recoupling properties of various interactions. Experimental implementations of the R-3 are demonstrated on model compounds with spin-3/2 systems. (C) 2002 American Institute of Physics.

}, keywords = {polarization}, isbn = {0021-9606}, doi = {Doi 10.1063/1.1506907}, url = {://WOS:000178317300016}, author = {Wi, S. and Logan, J. W. and Sakellariou, D. and Walls, J. D. and Pines, A.} } @article {349, title = {Selective excitation in dipole coupled systems}, journal = {Chemical Physics Letters}, volume = {357}, year = {2002}, note = {Chem Phys Lett558GVTimes Cited:5Cited References Count:22}, month = {May 10}, pages = {241-248}, abstract = {

In this Letter the possibility of selective excitation in coupled multispin systems is studied theoretically. A general method of transforming any selective pulse developed for uncoupled systems into a form that is selective in coupled systems is presented. This is accomplished by adding a small perturbation to a decoupling radiofrequency (RF) field. When viewed in an interaction frame given by the decoupling RF field, this method generates, in an averaged sense, a propagator similar to the propagator of uncoupled spins under a shaped RF pulse. Preliminary experimental results are presented for the case of selective excitation in proton nuclear magnetic resonance in liquid crystals. (C) 2002 Elsevier Science B.V. All rights reserved.

}, keywords = {spin-diffusion}, isbn = {0009-2614}, doi = {Doi 10.1016/S0009-2614(02)00493-1}, url = {://WOS:000175958700012}, author = {Walls, J. D. and Marjanska, M. and Sakellariou, D. and Castiglione, F. and Pines, A.} } @article {360, title = {Sensitivity enhancement in multiple-quantum NMR experiments with CPMG detection}, journal = {Journal of Magnetic Resonance}, volume = {157}, year = {2002}, note = {J Magn Reson589DHTimes Cited:12Cited References Count:12}, month = {Jul}, pages = {160-162}, abstract = {

We present a modified multiple-quantum (MQ) experiment, which implements the Carr-Purcell-Meiboom-Gill (CPMG) detection scheme in the static MQ NMR experiment proposed by W. S. Warren et al. (1980, J. Chem. Phys. 73, 2084-2099) and exploited further by O. N. Antzutkin and R. Tycko (1999, J. Chem. Phys. 110, 2749-2752). It is demonstrated that a significant enhancement in the sensitivity can be achieved by acquiring echo trains in the MQ experiments for static powder samples. The modified scheme employing the CPMG detection was superior to the original MQ experiment, in particular for the carbonyl carbon with a very large chemical shift anisotropy. (C) 2002 Elsevier Science (USA).

}, keywords = {dynamics}, isbn = {1090-7807}, doi = {Doi 10.1006/Jmre.2002.2578}, url = {://WOS:000177742400019}, author = {Lim, K. H. and Nguyen, T. and Mazur, T. and Wemmer, D. E. and Pines, A.} } @article {351, title = {Theoretical investigations of I=5/2 quadrupolar spin dynamics in the sudden-passage regime}, journal = {Journal of Chemical Physics}, volume = {117}, year = {2002}, note = {J Chem Phys566JRTimes Cited:3Cited References Count:44}, month = {Jul 8}, pages = {518-532}, abstract = {

The theoretical approach utilizing bimodal Floquet theory in the quadrupolar/central-transition interaction frame, presented in an earlier article [J. D. Walls, K. H. Lim, and A. Pines, J. Chem. Phys. 116, 79 (2002)], is extended to describe the more complicated spin dynamics of I=5/2 spin systems. Rotary resonance effects occur when the strength of the radio-frequency irradiation, omega(1), matches the sample spinning speed, omega(r), at the conditions omega(1) = 2/3nomega(r) (n integral). At these conditions, conversions of both triple-quantum and five-quantum coherences to central-quantum coherence are observed. Between rotary resonance conditions [ 2n/3omega(r)\<ω(1)\<[2(n+1)]/3ω(r)], five-quantum as well as triple-quantum coherences can be created from equilibrium z-magnetization via a nutation mechanism. In addition, effective transfer between five-quantum and triple-quantum coherences also is observed in between rotary resonance conditions. These effects have been investigated theoretically and verified by both numerical calculations and experimental results. (C) 2002 American Institute of Physics.

}, keywords = {SPECTROSCOPY}, isbn = {0021-9606}, doi = {Doi 10.1063/1.1483256}, url = {://WOS:000176424800003}, author = {Walls, J. D. and Lim, K. H. and Logan, J. W. and Urban, J. T. and Jerschow, A. and Pines, A.} } @article {350, title = {Theoretical studies of the spin dynamics of quadrupolar nuclei at rotational resonance conditions}, journal = {Journal of Chemical Physics}, volume = {116}, year = {2002}, note = {J Chem Phys503ECTimes Cited:12Cited References Count:20}, month = {Jan 1}, pages = {79-90}, abstract = {

A theory of the spin dynamics of I=3/2 quadrupolar nuclei in the sudden-passage limit is discussed in relation to the recently observed rotational resonance (RR) effects on the excitation and conversion of triple-quantum coherence in the FASTER multiple-quantum magic-angle spinning (MQMAS) experiments [T. Vosegaard, P. Florian, D. Massiot, and P. J. Grandinetti, J. Chem. Phys. 114, 4618 (2001)]. A novel interaction frame, which combines the quadrupolar interaction with the central transition radio frequency irradiation, is shown to be useful in understanding the complex spin dynamics at and away from RR conditions. Analytical expressions for the Hamiltonian obtained from bimodal Floquet theory are included in order to provide insight into the spin dynamics observed in the FASTER MQMAS experiments. Numerical simulations have been performed and were found to support the theoretical formalism. (C) 2002 American Institute of Physics.

}, keywords = {solids}, isbn = {0021-9606}, doi = {Doi 10.1063/1.1421613}, url = {://WOS:000172784700010}, author = {Walls, J. D. and Lim, K. H. and Pines, A.} } @article {366, title = {Characterization of the effects of nonspecific xenon-protein interactions on Xe-129 chemical shifts in aqueous solution: Further development of xenon as a biomolecular probe}, journal = {Journal of Magnetic Resonance}, volume = {152}, year = {2001}, note = {J Magn Reson472QDTimes Cited:37Cited References Count:34}, month = {Sep}, pages = {79-86}, abstract = {

The sensitivity of Xe-129 chemical shifts to weak nonspecific xenon-protein interactions has suggested the use of xenon to probe biomolecular structure and interactions. The realization of this potential necessitates a further understanding of how different macromolecular properties influence the Xe-129 chemical shift in aqueous solution. Toward this goal, we have acquired Xe-129 NMR spectra of xenon dissolved in amino acid, peptide, and protein solutions under both native and denaturing conditions. In general, these cosolutes induce Xe-129 chemical shifts that are downfield relative to the shift in water, as they deshield the xenon nucleus through weak, diffusion-mediated interactions. Correlations between the extent of deshielding and molecular properties including chemical identity, structure, and charge are reported. Xenon deshielding was found to depend linearly on protein size under denaturing solution conditions; the denaturant itself has a characteristic effect on the Xe-129 chemical shift that likely results from a change in the xenon solvation shell structure. In native protein solutions, contributions to the overall Xe-129 chemical shift arise from the presence of weak xenon binding either in cavities or at the protein surface. Potential applications of xenon as a probe of biological systems including the detection of conformational changes and the possible quantification of buried surface area at protein-protein interfaces are discussed. (C) 2001 Academic Press.

}, keywords = {gas}, isbn = {1090-7807}, doi = {Doi 10.1006/Jmre.2001.2389}, url = {://WOS:000170995700009}, author = {Rubin, S. M. and Spence, M. M. and Pines, A. and Wemmer, D. E.} } @article {367, title = {Detection of a conformational change in maltose binding protein by Xe-129 NMR spectroscopy}, journal = {Journal of the American Chemical Society}, volume = {123}, year = {2001}, note = {J Am Chem Soc467XNTimes Cited:28Cited References Count:28}, month = {Sep 5}, pages = {8616-8617}, keywords = {blood}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja0110325}, url = {://WOS:000170729200029}, author = {Rubin, S. M. and Spence, M. M. and Dimitrov, I. E. and Ruiz, E. J. and Pines, A. and Wemmer, D. E.} } @article {373, title = {An experimental and theoretical investigation of the chemical shielding tensors of C-13(alpha) of alanine, valine, and leucine residues in solid peptides and in proteins in solution}, journal = {Journal of the American Chemical Society}, volume = {123}, year = {2001}, note = {J Am Chem Soc486FTTimes Cited:47Cited References Count:31}, month = {Oct 24}, pages = {10362-10369}, abstract = {

We have carried out a solid-state magic-angle sample-spinning (MAS) nuclear magnetic resonance (NMR) spectroscopic investigation of the C-13(alpha), chemical shielding tensors of alanine, valine, and leucine residues in a series of crystalline peptides of known structure. For alanine and leucine, which are not branched at the beta -carbon, the experimental chemical shift anisotropy (CSA) spans (Omega) are large, about 30 ppm, independent of whether the residues adopt helical or sheet geometries, and are in generally good accord with Omega values calculated by using ab initio Hartree-Fock quantum chemical methods. The experimental Omegas for valine C-alpha in two peptides (in sheet geometries) are also large and in good agreement with theoretical predictions. In contrast, the \"CSAs\" (Delta sigma*) obtained from solution NMR data for alanine, valine, and leucine residues in proteins show major differences, with helical residues having Delta sigma* values of similar to6 ppm while sheet residues have Delta sigma* approximate to 27 ppm. The origins of these differences are shown to be due to the different definitions of the CSA, When defined in terms of the solution NMR CSA, the solid-state results also show small helical but large sheet CSA values. These results are of interest since they lead to the idea that only the beta -branched amino acids threonine, valine, and isoleucine can have small (static) tensor spans, Omega (in helical creometries), and that the small helical \"CSAs\" seen in solution NMR are overwhelmingly dominated by changes in tensor orientation, from sheet to helix. These results have important implications for solid-state NMR structural studies which utilize the CSA span, Omega, to differentiate between helical and sheet residues. Specifically, there will be only a small degree of spectral editing possible in solid proteins since the spans, Omega, for the dominant nonbranched amino acids are quite similar. Editing on the basis of Omega will, however, be very effective for many Thr, Val, and Hen residues, which frequently have small (similar to 15-20 ppm) helical CSA (Omega) spans.

}, keywords = {threonine}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja0115060}, url = {://WOS:000171808300025}, author = {Havlin, R. H. and Laws, D. D. and Bitter, H. M. L. and Sanders, L. K. and Sun, H. H. and Grimley, J. S. and Wemmer, D. E. and Pines, A. and Oldfield, E.} } @article {364, title = {Functionalized xenon as a biosensor}, journal = {Proceedings of the National Academy of Sciences of the United States of America}, volume = {98}, year = {2001}, note = {P Natl Acad Sci USA472CZTimes Cited:112Cited References Count:29}, month = {Sep 11}, pages = {10654-10657}, abstract = {

The detection of biological molecules and their interactions is a significant component of modern biomedical research. In current biosensor technologies, simultaneous detection is limited to a small number of analytes by the spectral overlap of their signals. We have developed an NMR-based xenon biosensor that capitalizes on the enhanced signal-to-noise, spectral simplicity, and chemical-shift sensitivity of laser-polarized xenon to detect specific biomolecules at the level of tens of nanomoles. We present results using xenon \"functionalized\" by a biotin-modified supramolecular cage to detect biotin-avidin binding. This biosensor methodology can be extended to a multiplexing assay for multiple analytes.

}, keywords = {mri}, isbn = {0027-8424}, doi = {Doi 10.1073/Pnas.191368398}, url = {://WOS:000170966800030}, author = {Spence, M. M. and Rubin, S. M. and Dimitrov, I. E. and Ruiz, E. J. and Wemmer, D. E. and Pines, A. and Yao, S. Q. and Tian, F. and Schultz, P. G.} } @article {365, title = {Resolution of Xe-129 chemical shifts at ultralow magnetic field}, journal = {Journal of the American Chemical Society}, volume = {123}, year = {2001}, note = {J Am Chem Soc463TWTimes Cited:9Cited References Count:39}, month = {Aug 22}, pages = {8133-8134}, keywords = {adsorption}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja011064s}, url = {://WOS:000170494200027}, author = {Saxena, S. and Wong-Foy, A. and Moule, A. J. and Seeley, J. A. and McDermott, R. and Clarke, J. and Pines, A.} } @article {370, title = {Solid-state NMR studies of the secondary structure of a mutant prion protein fragment of 55 residues that induces neurodegeneration}, journal = {Proceedings of the National Academy of Sciences of the United States of America}, volume = {98}, year = {2001}, note = {P Natl Acad Sci USA476PCTimes Cited:51Cited References Count:26}, month = {Sep 25}, pages = {11686-11690}, abstract = {

The secondary structure of a 55-residue fragment of the mouse prion protein, MoPrP(89-143), was studied in randomly aggregated (dried from water) and fibrillar (precipitated from water/ acetonitrile) forms by C-13 solid-state NMR. Recent studies have shown that the fibrillar form of the P101L mutant of MoPrP(89-143) is capable of inducing prion disease in transgenic mice, whereas unaggregated or randomly aggregated samples do not provoke disease. Through analysis of C-13 chemical shifts, we have determined that both wild-type and mutant sequence MoPrP(89-143) form a mixture of beta -sheet and alpha -helical conformations in the randomly aggregated state although the beta -sheet content in MoPrP(89-143, P101L) is significantly higher than in the wild-type peptide. In a fibrillar state, MoPrP(89-143, P101L) is completely converted into beta -sheet, suggesting that the formation of a specific beta -sheet structure may be required for the peptide to induce disease. Studies of an analogous peptide from Syrian hamster PrP verify that sequence alterations in residues 101-117 affect the conformation of aggregated forms of the peptides.

}, keywords = {diseases}, isbn = {0027-8424}, doi = {Doi 10.1073/Pnas.201404298}, url = {://WOS:000171237100125}, author = {Laws, D. D. and Bitter, H. M. L. and Liu, K. and Ball, H. L. and Kaneko, K. and Wille, H. and Cohen, F. E. and Prusiner, S. B. and Pines, A. and Wemmer, D. E.} } @article {375, title = {Evidence of nonspecific surface interactions between laser-polarized xenon and myoglobin in solution}, journal = {Proceedings of the National Academy of Sciences of the United States of America}, volume = {97}, year = {2000}, note = {P Natl Acad Sci USA345XMTimes Cited:40Cited References Count:35}, month = {Aug 15}, pages = {9472-9475}, abstract = {

The high sensitivity of the magnetic resonance properties of xenon to its local chemical environment and the large Xe-129 NMR signals attainable through optical pumping have motivated the use of xenon as a probe of macromolecular structure and dynamics. In the present work, we report evidence for nonspecific interactions between xenon and the exterior of myoglobin in aqueous solution, in addition to a previously reported internal binding interaction. Xe-129 chemical shift measurements in denatured myoglobin solutions and under native conditions with varying xenon concentrations confirm the presence of nonspecific interactions. Titration data are modeled quantitatively with treatment of the nonspecific interactions as weak binding sites. Using laser-polarized xenon to measure Xe-129 spin-lattice relaxation times (T-1), we observed a shorter T-1 in the presence of 1 mM denatured apomyoglobin in 6 M deuterated urea (T-1 = 59 +/- 1 s) compared with that in 6 M deuterated urea alone (T-1 = 291 +/- 2 s), suggesting that nonspecific xenon-protein interactions can enhance Xe-129 relaxation. An even shorter T1 was measured in ? mM apomyoglobin in D2O (T-1 = 15 +/- 0.3 s), compared with that in D2O alone (T-1 = 506 +/- 5 s). This difference in relaxation efficiency likely results from couplings between laser-polarized xenon and protons in the binding cavity of apomyoglobin that may permit the transfer of polarization between these nuclei via the nuclear Overhauser effect.

}, keywords = {binding}, isbn = {0027-8424}, doi = {Doi 10.1073/Pnas.170278897}, url = {://WOS:000088840500026}, author = {Rubin, S. M. and Spence, M. M. and Goodson, B. M. and Wemmer, D. E. and Pines, A.} } @article {382, title = {High-T-c SQUIDs for low-field NMR and MRI of room temperature samples}, journal = {Ieee Transactions on Applied Superconductivity}, volume = {9}, year = {1999}, note = {Ieee T Appl SuperconPart 3225MCTimes Cited:5Cited References Count:18}, month = {Jun}, pages = {4424-4427}, abstract = {

We have constructed a high-T-c SQUID spectrometer to detect NMR signals from samples at room temperature in magnetic fields up to 3 mT. The multiloop SQUID magnetometer has a system noise of about 30 fT/Hz(1/2) at the relevant frequencies of 2 to 100 kHz, The magnetometer is operated in vacuum at 77 K, and is separated from the sample, which is less than 1.5 mm away, by a sapphire window, In a magnetic field of 2 mT we can detect the proton spin echo at 86 kHz without signal averaging. This sensitivity enables us to obtain one-dimensional images. In addition, we present data on hyperpolarized Xe-129, which has an optically pumped polarization of several percent.

}, keywords = {frequencies}, isbn = {1051-8223}, doi = {Doi 10.1109/77.784006}, url = {://WOS:000081964500386}, author = {Schlenga, K. and McDermott, R. F. and Clarke, J. and de Souza, R. E. and Wong-Foy, A. and Pines, A.} } @article {383, title = {Low-field magnetic resonance imaging with a high-T-c dc superconducting quantum interference device}, journal = {Applied Physics Letters}, volume = {75}, year = {1999}, note = {Appl Phys Lett259URTimes Cited:49Cited References Count:19}, month = {Dec 6}, pages = {3695-3697}, abstract = {

A spectrometer incorporating a high transition temperature dc superconducting quantum interference device (SQUID) is used to obtain nuclear magnetic resonance signals from protons in mineral oil at room temperature in fields up to 3 mT. The spatial separation between the SQUID magnetometer at 77 K and the sample at room temperature is less than 1 mm. At 2 mT, the signal is easily resolved in a single scan. Two-dimensional images of samples consisting of pieces of lucite or glass immersed in mineral oil are obtained at 2 mT. (C) 1999 American Institute of Physics. [S0003-6951(99)03649-9].

}, keywords = {mri}, isbn = {0003-6951}, doi = {Doi 10.1063/1.125432}, url = {://WOS:000083912800035}, author = {Schlenga, K. and McDermott, R. and Clarke, J. and de Souza, R. E. and Wong-Foy, A. and Pines, A.} } @article {387, title = {NMR and MRI obtained with high transition temperature DC SQUIDs}, journal = {Journal of the Brazilian Chemical Society}, volume = {10}, year = {1999}, note = {J Brazil Chem Soc259BETimes Cited:11Cited References Count:30}, month = {Jul-Aug}, pages = {307-312}, abstract = {

We have measured nuclear magnetic resonance (NMR) signals from several samples at room temperature in magnetic fields ranging from about 0.05 mT to 2 mT using a spectrometer based on a high-T-c de SQUID (high transition temperature de Superconducting QUantum Interference Device). We are able to observe proton signals from 1 mL of mineral oil in 2 mT in a single transient. The sensitivity of this system has also allowed the detection of proton NMR at magnetic fields as low as 0.059 mT, which is comparable to the Earth\&$\#$39;s field. Such results make possible a number of new experiments in magnetic resonance imaging (MRI). We present a two-dimensional image of a phantom filled with mineral oil obtained in a field of 2 mT.

}, keywords = {system}, isbn = {0103-5053}, url = {://WOS:000083873500009}, author = {de Souza, R. E. and Schlenga, K. and Wong-Foy, A. and McDermott, R. and Pines, A. and Clarke, J.} } @article {405, title = {Low field magnetic resonance images of polarized noble gases obtained with a dc superconducting quantum interference device}, journal = {Applied Physics Letters}, volume = {72}, year = {1998}, note = {Appl Phys LettZg930Times Cited:37Cited References Count:24}, month = {Apr 13}, pages = {1908-1910}, abstract = {

Using a low transition temperature superconducting quantum interference device as a detector, we have obtained magnetic resonance images of laser-polarized He-3 gas and solid Xe-129 at 4.2 K in magnetic fields as low as 0.54 mT (He-3) and 1 mT (Xe-129), corresponding to Larmor frequencies of 17.6 and 11.8 kHz, respectively. The experimental resolution of the images is similar to 500 mu m for He-3 ill the gas phase and similar to 950 mu m for Xe-129 in the solid state. (C) 1998 American Institute of Physics.

}, keywords = {mri}, isbn = {0003-6951}, doi = {Doi 10.1063/1.121223}, url = {://WOS:000073054300038}, author = {Augustine, M. P. and Wong-Foy, A. and Yarger, J. L. and Tomaselli, M. and Pines, A. and TonThat, D. M. and Clarke, J.} } @article {418, title = {Determination of dihedral angles in peptides through experimental and theoretical studies of alpha-carbon chemical shielding tensors}, journal = {Journal of the American Chemical Society}, volume = {119}, year = {1997}, note = {J Am Chem SocXt037Times Cited:90Cited References Count:57}, month = {Aug 20}, pages = {7827-7831}, abstract = {

A simple method for the determination of backbone dihedral angles in peptides and proteins is presented. The chemical-shift anisotropies (CSA) of the central alanine alpha-carbon in powdered crystalline tripeptides, whose structures have been determined previously by X-ray crystallography, were measured by cross-polarization magic-angle-spinning nuclear magnetic resonance. The experimental CSA values were correlated with ab initio chemical-shielding calculations over Ramanchandran phi/psi space on an N-formyl-L-alanine amide fragment. Using this correlation, phi/psi probability surfaces for one of the tripeptides were calculated based only on the alpha-carbon CSA, allowing a prediction of backbone angles. Dihedral angles predicted by these calculations fall within +/-12 degrees of the values determined by crystallography. This approach should be useful in the determination of solid-slate protein structure.

}, keywords = {crystal-structure}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja970124k}, url = {://WOS:A1997XT03700025}, author = {Heller, J. and Laws, D. D. and Tomaselli, M. and King, D. S. and Wemmer, D. E. and Pines, A. and Havlin, R. H. and Oldfield, E.} } @article {406, title = {Multiple-quantum magic-angle spinning and dynamic-angle spinning NMR spectroscopy of quadrupolar nuclei}, journal = {Solid State Nuclear Magnetic Resonance}, volume = {8}, year = {1997}, note = {Solid State Nucl MagWy629Times Cited:60Cited References Count:40}, month = {Mar}, pages = {1-16}, abstract = {

Several aspects of the Multiple-Quantum Magic-Angle Spinning (MQMAS) technique (L, Frydman and J,S, Harwood, J, Am, Chem, Sec., 117 (1995) 5367) are compared with Dynamic-Angle Spinning (DAS), Examples of MQMAS spectra are shown for I = 3/2 nuclei with C-Q up to 3.6 MHz, and for: Al-27 (I = 5/2) with C-Q up to 10 MHz. The MQMAS linewidth is largely independent of the magnitude of the homonuclear dipolar interaction, while the spinning sideband manifold is similar to that observed in DAS experiments, MQMAS is technically simple and routinely useful for studying nuclei with short spin-lattice relaxation times, but care must be taken in its use for quantitative studies as the excitation of the triple-quantum coherence is not uniform, In this regard, MQMAS is most useful for samples with small quadrupolar coupling constants, In the specific case of O-17, DAS would give spectra with excellent resolution in comparison to MQMAS, The different advantages of DAS and MQMAS make them useful complementary techniques in many cases,Two additional methods are also presented for extracting the chemical shift anisotropy (CSA) directly for quadrupolar nuclei using the multiple-quantum scheme, (C) 1997 Elsevier Science B,V.

}, keywords = {rb-87}, isbn = {0926-2040}, doi = {Doi 10.1016/S0926-2040(96)01277-5}, url = {://WOS:A1997WY62900001}, author = {Wang, S. H. and Xu, Z. and Baltisberger, J. H. and Bull, L. M. and Stebbins, J. F. and Pines, A.} } @article {410, title = {Optical magnetic resonance imaging of Rb vapor in low magnetic fields}, journal = {Physics Letters A}, volume = {226}, year = {1997}, note = {Phys Lett AWf939Times Cited:12Cited References Count:19}, month = {Feb 10}, pages = {69-74}, abstract = {

By applying magnetic field gradients to alkali vapor cells, images of the spatial distribution of spin-polarized Rb atoms were obtained. Optical pumping is used to produce precessing spin-polarization in the ground state. Detection of the coherent spin transients is performed in the time-domain by a single optical probe beam covering the whole sample cell. Spatial resolution of better than 1 mm has been achieved by a projection-reconstruction method.

}, keywords = {xe-129}, isbn = {0375-9601}, doi = {Doi 10.1016/S0375-9601(96)00927-9}, url = {://WOS:A1997WF93900012}, author = {Skalla, J. and Wackerle, G. and Mehring, M. and Pines, A.} } @article {428, title = {Application of rotational resonance to inhomogeneously broadened systems}, journal = {Chemical Physics Letters}, volume = {251}, year = {1996}, note = {Chem Phys LettUd924Times Cited:17Cited References Count:28}, month = {Mar 22}, pages = {223-229}, abstract = {

A protocol is presented for the determination of internuclear distances using rotational-resonance magnetization-exchange NMR in systems with inhomogeneously broadened lines. Non-linear least-square fitting procedures are used to obtain the distance, the inhomogeneous broadening, the zero-quantum relaxation time, and error estimates for these parameters. We apply this procedure to a biological system of unknown structure.

}, keywords = {nmr}, isbn = {0009-2614}, doi = {Doi 10.1016/0009-2614(96)00098-X}, url = {://WOS:A1996UD92400015}, author = {Heller, J. and Larsen, R. and Ernst, M. and Kolbert, A. C. and Baldwin, M. and Prusiner, S. B. and Wemmer, D. E. and Pines, A.} } @article {422, title = {Determination of quadrupolar and chemical shielding tensors using solid-state two-dimensional NMR spectroscopy}, journal = {Journal of Chemical Physics}, volume = {105}, year = {1996}, note = {J Chem PhysVv625Times Cited:18Cited References Count:40}, month = {Dec 1}, pages = {9412-9420}, abstract = {

The quadrupolar and chemical shift tensors, as well as the relative orientation of the two principle axis systems, are accurately determined using a two-dimensional nuclear magnetic resonance technique. Good agreement between experimental and simulated two-dimensional spectra is obtained for a series of rubidium and sodium compounds at multiple magnetic field strengths. Extension of this technique to correlate the quadrupolar and dipolar interactions, as well as the incorporation of a purely isotropic dimension resulting in a three-dimensional experiment is also discussed. (C) 1996 American Institute of Physics.

}, keywords = {line-shapes}, isbn = {0021-9606}, doi = {Doi 10.1063/1.472776}, url = {://WOS:A1996VV62500003}, author = {Shore, J. S. and Wang, S. H. and Taylor, R. E. and Bell, A. T. and Pines, A.} } @article {429, title = {Solid-state NMR studies of the prion protein H1 fragment}, journal = {Protein Science}, volume = {5}, year = {1996}, note = {Protein SciVa138Times Cited:74Cited References Count:53}, month = {Aug}, pages = {1655-1661}, abstract = {

Conformational changes in the prion protein (PrP) seem to be responsible for prion diseases. We have used conformation-dependent chemical-shift measurements and rotational-resonance distance measurements to analyze the conformation of solid-state peptides lacking long-range order, corresponding to a region of PrP designated H1. This region is predicted to undergo a transformation of secondary structure in generating the infectious form of the protein. Solid-state NMR spectra of specifically C-13-enrrched samples of H1, residues 109-122 (MKHMAGAAAAGAVV) of Syrian hamster PrP, have been acquired under cross-polarization and magic-angle spinning conditions. Samples lyophilized from 50\% acetonitrile/50\% water show chemical shifts characteristic of a beta-sheet conformation in the region corresponding to residues 112-121, whereas samples lyophilized from hexafluoroisopropanol display shifts indicative of alpha-helical secondary structure in the region corresponding to residues 113-117. Complete conversion to the helical conformation was not observed and conversion from alpha-helix back to beta-sheet, as inferred from the solid-state NMR spectra, occurred when samples were exposed to water. Rotational-resonance experiments were performed on seven doubly C-13-labeled H1 samples dried from water. Measured distances suggest that the peptide is in an extended, possibly beta-strand, conformation. These results are consistent with the experimental observation that PrP can exist in different conformational states and with structural predictions based on biological data and theoretical modeling that suggest that H1 may play a key role in the conformational transition involved in the development of prion diseases.

}, keywords = {alpha-helices}, isbn = {0961-8368}, url = {://WOS:A1996VA13800019}, author = {Heller, J. and Kolbert, A. C. and Larsen, R. and Ernst, M. and Bekker, T. and Baldwin, M. and Prusiner, S. B. and Pines, A. and Wemmer, D. E.} } @inbook {436, title = {Synthetic Peptides Model α - Helix - β - Sheet Conformational Changes in the Prion Protien}, booktitle = {Peptides: Chemistry, Structure and Biology}, year = {1996}, pages = {468-470}, publisher = {Mayflower Scientific Ltd.}, organization = {Mayflower Scientific Ltd.}, author = {Baldwin, M.A. and Zhang, H. and Bekker, T. and Zhou, S. and Nguyen, J. and Kolbert, A.C. and Heller, J. and James, T.L. and Wemmer, D.E. and Pines, A. and Cohen, F.E. and Prusiner, S.B.}, editor = {Hidges, Pravin T.P Kaumaya and Robert S.} } @article {435, title = {Triple-quantum two-dimensional Al-27 magic-angle spinning nuclear magnetic resonance spectroscopic study of aluminosilicate and aluminate crystals and glasses}, journal = {Journal of the American Chemical Society}, volume = {118}, year = {1996}, note = {J Am Chem SocVa026Times Cited:139Cited References Count:31}, month = {Jul 31}, pages = {7209-7214}, abstract = {

A new two-dimensional magic-angle spinning NMR experiment(1,2) using multiple-quantum coherences of half-integer quadrupolar nuclei was used to study Al-27 sites in crystalline samples of leucite (KAlSi2O6), anorthite (CaAl2Si2O8), and kyanite (Al2SiO5), as well as CaAl2Si2O8 glass and a magnesium aluminoborate glass. In the crystals, multiple sites are partially resolved and new results for isotropic chemical shifts and quadrupolar parameters are derived, using data collected at a single magnetic field. Data for both leucite and anorthite are consistent with previous results that correlate chemical shifts with mean intertetrahedral bond angle. Signal can be obtained from sites with quadrupolar coupling constants as large as 9 MHz, but intensities are reduced. In the aluminoborate glass, peaks for sites with different Al coordination numbers are well separated. The lack of such features in CaAl2Si2O8 glass rules out the presence of significant quantities of AlO5 and AlO6 groups.

}, keywords = {anorthite}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja9606586}, url = {://WOS:A1996VA02600027}, author = {Baltisberger, J. H. and Xu, Z. and Stebbins, J. F. and Wang, S. H. and Pines, A.} } @article {452, title = {Solid-State O-17 Magic-Angle and Dynamic-Angle Spinning Nmr-Study of the Sio2 Polymorph Coesite}, journal = {Journal of Physical Chemistry}, volume = {99}, year = {1995}, note = {J Phys Chem-UsRn706Times Cited:95Cited References Count:41}, month = {Aug 10}, pages = {12341-12348}, abstract = {

Five distinctly resolved O-17 solid-state NMR resonances in room temperature coesite, an SiO2 polymorph, have been observed and assigned using dynamic-angle spinning (DAS) at 11.7 T along with magic-angle spinning (MAS) spectra at 9.4 and 11.7 T. The O-17 quadrupolar parameters for each of the five oxygen environments in coesite are correlated with the Si-O-Si bridging bond angles determined by diffraction experiments. The sign of e(2)qQ/h along with the orientation of the electric field gradient for oxygen in the Si-O-Si linkage were determined from a Townes-Dailey analysis of the data.

}, keywords = {oxygen}, isbn = {0022-3654}, doi = {Doi 10.1021/J100032a045}, url = {://WOS:A1995RN70600045}, author = {Grandinetti, P. J. and Baltisberger, J. H. and Farnan, I. and Stebbins, J. F. and Werner, U. and Pines, A.} } @article {438, title = {Xe-129 Nmr-Studies of Hyper-Cross-Linked Polyarylcarbinols - Rigid Versus Flexible Structures}, journal = {Chemistry of Materials}, volume = {7}, year = {1995}, note = {Chem MaterRk993Times Cited:27Cited References Count:30}, month = {Jul}, pages = {1325-1332}, abstract = {

Xenon NMR is used with adsorption measurements to infer information about the microstructure of some novel hyper-cross-linked polyarylcarbinols. It is shown that rigidrod connecting units are necessary for microporosity in these systems, as hyper-cross-linked polymers based on flexible structures are found to have conventional surface areas and xenon NMR spectra. A microporous polymer based on rigid triarylcarbinol monomers shows high xenon uptake and a linear chemical shift variation with pressure at room temperature. Spin-lattice relaxation and cross-polarization dynamics are studied at low temperatures. In this regime the xenon has extremely long equilibration times, and the adsorption dynamics are complicated but give important insight into the polymer topology. The data are compared with two possible models of the polymer microstructwre.

}, keywords = {adsorption}, isbn = {0897-4756}, doi = {Doi 10.1021/Cm00055a008}, url = {://WOS:A1995RK99300008}, author = {Urban, C. and Mccord, E. F. and Webster, O. W. and Abrams, L. and Long, H. W. and Gaede, H. and Tang, P. and Pines, A.} } @article {465, title = {Cross Polarization and Dynamic-Angle Spinning of O-17 in L-Alanine}, journal = {Bulletin of Magnetic Resonance}, volume = {16}, year = {1994}, pages = {68-72}, author = {Gann, S.L. and Baltisberger, J.H. and Wooten, E.W. and Zimmerman, H. and Pines, A.} } @article {456, title = {N-14 Squid Nqr of L-Ala-L-His and of Serine}, journal = {Zeitschrift Fur Naturforschung Section a-a Journal of Physical Sciences}, volume = {49}, year = {1994}, note = {Z Naturforsch AQh740Times Cited:2Cited References Count:15}, month = {Dec}, pages = {1188-1192}, abstract = {N-14 nuclear quadrupole resonance spectroscopy, detected with a Superconducting Quantum Interference Device, makes possible the study of nitrogen environments in amino acids and small peptides. The present experiments characterize: 1) the effects of intermolecular interactions upon the amino nitrogen of serine upon cocrystallization of the stereoisomers in a range of concentrations; 2) the changes of the amino and imidazole nitrogen environments brought about by combining L-Alanine and L-Histidine into the dipeptide L-Ala-L-His.}, keywords = {n-14}, isbn = {0932-0784}, url = {://WOS:A1994QH74000013}, author = {Wernerzwanziger, U. and Ziegeweid, M. and Black, B. and Pines, A.} } @article {455, title = {SQUID-NQR of N-14}, journal = {NQI Newsletter}, volume = {3}, year = {1994}, pages = {24-25}, author = {Ziegeweid, M. and Werner, U. and Black, B. and Pines, A.} } @article {470, title = {Effects of Double Rotation on Homonuclear Spin Systems}, journal = {Journal of Magnetic Resonance Series A}, volume = {102}, year = {1993}, note = {J Magn Reson Ser AKz354Times Cited:3Cited References Count:13}, month = {Mar}, pages = {29-33}, keywords = {solids}, isbn = {1064-1858}, doi = {Doi 10.1006/Jmra.1993.1064}, url = {://WOS:A1993KZ35400005}, author = {Wu, Y. and Peng, Z. Y. and Olejniczak, Z. and Sun, B. Q. and Pines, A.} } @article {478, title = {Pure-Absorption-Mode Lineshapes and Sensitivity in 2-Dimensional Dynamic-Angle Spinning Nmr}, journal = {Journal of Magnetic Resonance Series A}, volume = {103}, year = {1993}, note = {J Magn Reson Ser ALj625Times Cited:98Cited References Count:20}, month = {Jun 1}, pages = {72-81}, keywords = {nuclei}, isbn = {1064-1858}, doi = {Doi 10.1006/Jmra.1993.1132}, url = {://WOS:A1993LJ62500010}, author = {Grandinetti, P. J. and Baltisberger, J. H. and Llor, A. and Lee, Y. K. and Werner, U. and Eastman, M. A. and Pines, A.} } @article {471, title = {Squid-Nqr of N-14 in Amino-Acids and Small Peptides}, journal = {Chemical Physics Letters}, volume = {209}, year = {1993}, note = {Chem Phys LettLh246Times Cited:7Cited References Count:13}, month = {Jun 25}, pages = {17-21}, abstract = {

We present a technique for the study of nuclear quadrupole resonance of N-14 interacting with low electric field gradients as found, for example, in amino acids. A superconducting quantum interference device (SQUID) is used to detect directly small NMR signals via cross relaxation of the N-14 polarization to adjacent proton spins, eliminating the need for field cycling. When one nitrogen quadrupolar transition matches the proton Zeeman splitting, the remaining two quadrupolar transitions can be observed by sweeping a saturating rf field through resonance. In addition, signal enhancement by simultaneous excitation of two nitro n resonances helps to identify connected transitions.

}, keywords = {resonance}, isbn = {0009-2614}, doi = {Doi 10.1016/0009-2614(93)87194-8}, url = {://WOS:A1993LH24600003}, author = {Werner, U. and Black, B. and Ziegeweid, M. and Pines, A.} } @article {494, title = {Adsorption Effects in Aluminophosphate Molecular-Sieves Studied by Al-27 Double-Rotation Nmr}, journal = {Catalysis Letters}, volume = {15}, year = {1992}, note = {Catal LettJj259Times Cited:18Cited References Count:17}, pages = {65-73}, abstract = {

Al-27 double rotation NMR (DOR) spectroscopy is used to investigate structural changes in the framework of several aluminophosphate molecular sieves upon adsorption of water. The shapes, widths, and positions of the spectral lines yield information on the aluminum environments, adsorption sites, and degree of structural disorder undergone upon water adsorption.

}, keywords = {alpo4-8}, isbn = {1011-372X}, doi = {Doi 10.1007/Bf00770899}, url = {://WOS:A1992JJ25900008}, author = {Jelinek, R. and Chmelka, B. F. and Wu, Y. and Davis, M. E. and Ulan, J. G. and Gronsky, R. and Pines, A.} } @article {492, title = {Isotropic Chemical-Shifts and Quadrupolar Parameters for O-17 Using Dynamic-Angle Spinning Nmr}, journal = {Journal of Physical Chemistry}, volume = {96}, year = {1992}, note = {J Phys Chem-UsJk807Times Cited:66Cited References Count:48}, month = {Aug 20}, pages = {7001-7004}, abstract = {

Several oxygen-17-enriched silicates were studied using dynamic-angle spinning (DAS) NMR spectroscopy at two magnetic field strengths. The DAS method averages second-order quadrupolar interactions by reorienting a sample about a time-dependent axis, thereby yielding high-resolution spectra for half-odd integer spin quadrupolar nuclei such as oxygen-17. A narrow spectral line is observed for each distinct oxygen site in a powdered sample at the sum of the isotropic chemical shift and the field-dependent isotropic second-order quadrupolar shift. Using equations for the total shift observed at two field strengths, the chemical shift is uniquely determined together with a product of the quadrupolar coupling constant (C(Q) = e2qQ/h) and the quadrupolar asymmetry parameter (eta). For one silicate, we demonstrate aa computer program that uses the isotropic shifts and quadrupolar products as constraints and provides simulations of overlapped magic-angle spinning line shapes. In this way the quadrupolar parameters, C(Q) and eta, are determined separately for each crystallographic site. The silicates studied include the discrete orthosilicates larnite (Ca2SiO4) and forsterite (Mg2SiO4), as well as diopside (CaMgSi2O6), wollastonite (CaSiO3), and clinoenstatite (MgSiO3), which are minerals composed of chains of silicon-oxygen tetrahedra.

}, keywords = {zeolites}, isbn = {0022-3654}, doi = {Doi 10.1021/J100196a028}, url = {://WOS:A1992JK80700028}, author = {Mueller, K. T. and Baltisberger, J. H. and Wooten, E. W. and Pines, A.} } @article {484, title = {New Angles in Nuclear-Magnetic-Resonance Sample Spinning}, journal = {Accounts of Chemical Research}, volume = {25}, year = {1992}, note = {Accounts Chem ResHu248Times Cited:41Cited References Count:29}, month = {May}, pages = {209-215}, keywords = {axis}, isbn = {0001-4842}, doi = {Doi 10.1021/Ar00017a001}, url = {://WOS:A1992HU24800001}, author = {Wooten, E. W. and Mueller, K. T. and Pines, A.} } @article {487, title = {Nmr-Studies of the Surface-Structure and Dynamics of Semiconductor Nanocrystals}, journal = {Chemical Physics Letters}, volume = {198}, year = {1992}, note = {Chem Phys LettJt385Times Cited:77Cited References Count:27}, month = {Oct 16}, pages = {431-436}, abstract = {

H-1 NMR studies of thiophenol capping groups on cadmium sulfide nanocrystals demonstrate that the coverage of the capping molecule depends on the size of the nanocrystal. Data are presented which show that as the size of the nanocrystal increases, the coverage of thiophenol decreases. In addition, information about the overall tumbling of the nanocrystal and the motion of the capping groups relative to the surface can be obtained from linewidth studies, indicating that the rotation of the capping groups is hindered in the smaller nanocrystals (r almost-equal-to 12 angstrom) and becomes less so in larger nanocrystals (r almost-equal-to 20 angstrom). The coverage data are related to the electronic properties of this important class of compounds.

}, keywords = {relaxation}, isbn = {0009-2614}, doi = {Doi 10.1016/0009-2614(92)80023-5}, url = {://WOS:A1992JT38500001}, author = {Sachleben, J. R. and Wooten, E. W. and Emsley, L. and Pines, A. and Colvin, V. L. and Alivisatos, A. P.} } @article {498, title = {Quantification of the Disorder in Network-Modified Silicate-Glasses}, journal = {Nature}, volume = {358}, year = {1992}, note = {NatureJb341Times Cited:169Cited References Count:32}, month = {Jul 2}, pages = {31-35}, abstract = {

Local order in silicate glasses has been observed by many experimental techniques to be similar to that in crystalline materials. Details of the intermediate-range order are more elusive, but essential for understanding the lack of long-range symmetry in glasses and the effect of composition on glass structure. Two-dimensional O-17 dynamic-angle-spinning nuclear magnetic resonance experiments reveal intermediate-range order in the distribution of inter-tetrahedral (Si-O-Si) bond angles and a high degree of order in the disposition of oxygen atoms around the network-modifying cations.

}, keywords = {time}, isbn = {0028-0836}, doi = {Doi 10.1038/358031a0}, url = {://WOS:A1992JB34100043}, author = {Farnan, I. and Grandinetti, P. J. and Baltisberger, J. H. and Stebbins, J. F. and Werner, U. and Eastman, M. A. and Pines, A.} } @article {500, title = {Rb-87 Dynamic-Angle Spinning Nmr-Spectroscopy of Inorganic Rubidium Salts}, journal = {Journal of the American Chemical Society}, volume = {114}, year = {1992}, note = {J Am Chem SocJm979Times Cited:39Cited References Count:28}, month = {Sep 9}, pages = {7489-7493}, abstract = {

Five inorganic rubidium salts, RbCl, RbClO4, Rb2SO4, Rb2CrO4, and RbNO3, were examined using Rb-87 NMR spectroscopy. Significant line narrowing occurs under dynamic-angle spinning (DAS) compared to magic-angle spinning (MAS) or variable-angle spinning (VAS). From DAS spectra acquired at various magnetic field strengths, isotropic chemical shifts and isotropic second-order quadrupolar shifts were obtained. By simulations of single-site line shapes obtained from MAS-detected DAS experiments, complete chemical shift and quadrupolar parameters were determined for each of the three crystallographically distinct rubidium sites in RbNO3.

}, keywords = {cesium}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja00045a023}, url = {://WOS:A1992JM97900023}, author = {Baltisberger, J. H. and Gann, S. L. and Wooten, E. W. and Chang, T. H. and Mueller, K. T. and Pines, A.} } @article {485, title = {Sidebands in dynamic angle spinning (DAS) and double rotation (DOR) NMR}, journal = {Solid State Nuclear Magnetic Resonance}, volume = {1}, year = {1992}, note = {Solid State Nucl MagV26htTimes Cited:63Cited References Count:29}, month = {Dec}, pages = {267-295}, abstract = {

A theory of dynamic angle spinning (DAS) and double rotation (DOR) NMR is described using average Hamiltonian and irreducible tensor methods. Sideband intensities in DAS and DOR spectra are analyzed by both the moment and Bessel function methods, and general formulae are derived. Results show that the DAS moments depend on the relative rotor phase between the first and the second evolution periods, whereas the second and third DOR moments are independent of the relative phase between the inner and outer rotors. Sideband intensities in DAS spectra also depend on the relative rotor phases between evolution at the first and second angles, as well as on the ratio of time spent at each angle. Sideband intensities and phases in DOR spectra are related to the relative rotor phases between the inner and outer rotors, and the sideband pattern is determined by the ratio of the inner and outer rotor spinning speeds. An inversion symmetry of the odd numbered DOR sidebands at the relative rotor phase gamma(r) = 0 degrees. 180 degrees permits the elimination of these sidebands. Finally, numerical simulations are implemented and shown to agree with experimental results. Quadrupolar parameters can therefore be recovered either by calculating the second and third moments or by simulating the sideband intensities and phases.

}, keywords = {central transition}, isbn = {0926-2040}, doi = {Doi 10.1016/0926-2040(92)90047-D}, url = {://WOS:000208537400006}, author = {Sun, B. Q. and Baltisberger, J. H. and Wu, Y. and Samoson, A. and Pines, A.} } @conference {509, title = {Framework ordering in aluminophosphate molecular sieves studied by (27)Al double rotation NMR}, volume = {69}, year = {1991}, month = {1991}, pages = {435-442}, publisher = {Elsevier}, organization = {Elsevier}, author = {Chmelka, B.F. and Wu, Y. and Jelinek, R. and Davis, M.E. and Pines, A.}, editor = {P.A. Jacobs, N.I. Jaeger, L. Kubelkova, and B. Wichterlov} } @article {504, title = {High-Resolution O-17 Nmr of Solid Silicates}, journal = {Journal of the American Chemical Society}, volume = {113}, year = {1991}, note = {J Am Chem SocEr082Times Cited:90Cited References Count:39}, month = {Jan 2}, pages = {32-38}, abstract = {

Several O-17-enriched silicates were studied by use of dynamic angle spinning (DAS) and double rotation (DOR) nuclear magnetic resonance spectroscopy. These methods average away second-order quadrupolar interactions by reorienting a sample about a time-dependent axis, thereby yielding high-resolution spectra of oxygen-17 nuclei. A narrow spectral line is observed for each distinct oxygen site at the sum of the isotropic chemical shift and the field-dependent isotropic second-order quadrupolar shift. Resolution is increased by up to 2 orders of magnitude compared to conventional magic angle spinning (MAS) spectra. Crystallographically inequivalent oxygens are now observable as distinct resonances in spectra of polycrystalline silicates such as diopside (CaMgSi2(17)O6), wollastonite (CaSi17O3), clinoenstatite (MgSi17O3), larnite (Ca2Si17O4),and forsterite (Mg2Si17O4).

}, keywords = {spectra}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja00001a006}, url = {://WOS:A1991ER08200006}, author = {Mueller, K. T. and Wu, Y. and Chmelka, B. F. and Stebbins, J. and Pines, A.} } @article {505, title = {Pure-Absorption-Phase Dynamic-Angle Spinning}, journal = {Journal of Magnetic Resonance}, volume = {92}, year = {1991}, note = {J Magn ResonFj100Times Cited:30Cited References Count:15}, month = {May}, pages = {620-627}, keywords = {nuclei}, isbn = {0022-2364}, doi = {Doi 10.1016/0022-2364(91)90359-2}, url = {://WOS:A1991FJ10000018}, author = {Mueller, K. T. and Wooten, E. W. and Pines, A.} } @article {508, title = {Study of the Aluminophosphates Alpo4-21 and Alpo4-25 by Al-27 Double-Rotation Nmr}, journal = {Journal of the American Chemical Society}, volume = {113}, year = {1991}, note = {J Am Chem SocFn005Times Cited:53Cited References Count:16}, month = {May 22}, pages = {4097-4101}, abstract = {

Aluminum-27 double-rotation NMR in a magnetic field of 11.7 T distinguishes the extremely distorted five-coordinated aluminum sites in the molecular sieve precursor ALPO4(-21). Upon calcination, ALPO4(-21) transforms to ALPO4(-25), which has two tetrahedral aluminum sites with similar isotropic chemical shifts that cannot be resolved in an 11.7 T field. The two tetrahedral environments, however, have a different quadrupole coupling constants and are distinguished by double rotation at 4.2 T field. The quadrupole coupling constants obtained for these sites indicates that the tetrahedral aluminum environments are less distorted in the hydrated material.

}, keywords = {nuclei}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja00011a007}, url = {://WOS:A1991FN00500007}, author = {Jelinek, R. and Chmelka, B. F. and Wu, Y. and Grandinetti, P. J. and Pines, A. and Barrie, P. J. and Klinowski, J.} } @article {515, title = {High-Resolution Al-27 Nmr-Spectroscopy of the Aluminophosphate Molecular-Sieve Vpi-5}, journal = {Nature}, volume = {346}, year = {1990}, note = {NatureDt679Times Cited:97Cited References Count:12}, month = {Aug 9}, pages = {550-552}, isbn = {0028-0836}, doi = {Doi 10.1038/346550a0}, url = {://WOS:A1990DT67900067}, author = {Wu, Y. and Chmelka, B. F. and Pines, A. and Davis, M. E. and Grobet, P. J. and Jacobs, P. A.} } @article {514, title = {Nmr Experiments with a New Double Rotor}, journal = {Journal of Magnetic Resonance}, volume = {89}, year = {1990}, note = {J Magn ResonDu813Times Cited:113Cited References Count:13}, month = {Sep}, pages = {297-309}, isbn = {0022-2364}, doi = {Doi 10.1016/0022-2364(90)90236-3}, url = {://WOS:A1990DU81300008}, author = {Wu, Y. and Sun, B. Q. and Pines, A. and Samoson, A. and Lippmaa, E.} } @article {518, title = {Nuclear Magnetic Resonance}, journal = {Spectroscopy}, volume = {5}, year = {1990}, pages = {34-35}, author = {Pines, A. and Wu, Y.} } @article {516, title = {A suggestion for detecting rotational tunnelling of CD3: Groups by mulitple quantum spectroscopy}, journal = {Bulletin of Magnetic Resonance}, volume = {12}, year = {1990}, pages = {9-14}, author = {Werner, U. and Muller-Warmuth, W. and Pines, A.} } @article {551, title = {Nuclear Magnetic-Resonance with Dc Squid Preamplifiers}, journal = {Ieee Transactions on Magnetics}, volume = {25}, year = {1989}, note = {Ieee T MagnT6706Times Cited:21Cited References Count:23}, month = {Mar}, pages = {1193-1199}, isbn = {0018-9464}, doi = {Doi 10.1109/20.92510}, url = {://WOS:A1989T670600113}, author = {Fan, N. Q. and Heaney, M. B. and Clarke, J. and Newitt, D. and Wald, L. L. and Hahn, E. L. and Bielecki, A. and Pines, A.} } @article {554, title = {O-17 Nmr in Solids by Dynamic-Angle Spinning and Double Rotation}, journal = {Nature}, volume = {339}, year = {1989}, note = {NatureU4451Times Cited:177Cited References Count:15}, month = {May 4}, pages = {42-43}, isbn = {0028-0836}, doi = {Doi 10.1038/339042a0}, url = {://WOS:A1989U445100054}, author = {Chmelka, B. F. and Mueller, K. T. and Pines, A. and Stebbins, J. and Wu, Y. and Zwanziger, J. W.} } @article {558, title = {Observation of Molecular-Reorientation in Ice by Proton and Deuterium Magnetic-Resonance}, journal = {Journal of the American Chemical Society}, volume = {110}, year = {1988}, note = {J Am Chem SocP7649Times Cited:80Cited References Count:16}, month = {Aug 17}, pages = {5668-5671}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja00225a013}, url = {://WOS:A1988P764900013}, author = {Wittebort, R. J. and Usha, M. G. and Ruben, D. J. and Wemmer, D. E. and Pines, A.} } @article {574, title = {Multiple-Quantum Nmr-Study on Correlation of 2 Methyl-Groups}, journal = {Scientia Sinica Series a-Mathematical Physical Astronomical \& Technical Sciences}, volume = {30}, year = {1987}, note = {Sci China Ser AG8059Times Cited:2Cited References Count:12}, month = {Feb}, pages = {157-164}, url = {://WOS:A1987G805900005}, author = {Tang, J. and Wang, J. F. and Pines, A.} } @article {610, title = {Multiple Quantum Spectrum of Oriented Hexane-D6}, journal = {Chemical Physics}, volume = {108}, year = {1986}, note = {Chem PhysE1754Times Cited:7Cited References Count:27}, month = {Oct 1}, pages = {179-185}, isbn = {0301-0104}, doi = {Doi 10.1016/0301-0104(86)85039-X}, url = {://WOS:A1986E175400001}, author = {Drobny, G. and Weitekamp, D. P. and Pines, A.} } @article {622, title = {A Sharp Method for High-Resolution Nmr of Heteronuclear Spin Systems in Inhomogeneous Fields}, journal = {Journal of Magnetic Resonance}, volume = {63}, year = {1985}, note = {J Magn ResonAmg38Times Cited:18Cited References Count:30}, pages = {431-437}, isbn = {1090-7807}, doi = {Doi 10.1016/0022-2364(85)90341-5}, url = {://WOS:A1985AMG3800028}, author = {Gochin, M. and Weitekamp, D. P. and Pines, A.} } @article {617, title = {Zero-Field Nmr and Nqr}, journal = {Journal of Chemical Physics}, volume = {83}, year = {1985}, note = {J Chem PhysAtt21Times Cited:105Cited References Count:184}, pages = {4877-4905}, isbn = {0021-9606}, doi = {Doi 10.1063/1.449748}, url = {://WOS:A1985ATT2100005}, author = {Zax, D. B. and Bielecki, A. and Zilm, K. W. and Pines, A. and Weitekamp, D. P.} } @article {633, title = {Computer-Simulations of Multiple-Quantum Nmr Experiments .1. Nonselective Excitation}, journal = {Journal of Magnetic Resonance}, volume = {60}, year = {1984}, note = {J Magn ResonTw096Times Cited:58Cited References Count:50}, pages = {205-235}, isbn = {1090-7807}, doi = {Doi 10.1016/0022-2364(84)90327-5}, url = {://WOS:A1984TW09600005}, author = {Murdoch, J. B. and Warren, W. S. and Weitekamp, D. P. and Pines, A.} } @article {628, title = {Computer-Simulations of Multiple-Quantum Nmr Experiments .2. Selective Excitation}, journal = {Journal of Magnetic Resonance}, volume = {60}, year = {1984}, note = {J Magn ResonTw096Times Cited:11Cited References Count:23}, pages = {236-256}, isbn = {1090-7807}, doi = {Doi 10.1016/0022-2364(84)90328-7}, url = {://WOS:A1984TW09600006}, author = {Warren, W. S. and Murdoch, J. B. and Pines, A.} } @article {635, title = {Fourier-Transform Pure Nuclear-Quadrupole Resonance by Pulsed Field Cycling}, journal = {Journal of Chemical Physics}, volume = {80}, year = {1984}, note = {J Chem PhysSh432Times Cited:34Cited References Count:23}, pages = {2232-2234}, isbn = {0021-9606}, doi = {Doi 10.1063/1.446915}, url = {://WOS:A1984SH43200068}, author = {Bielecki, A. and Murdoch, J. B. and Weitekamp, D. P. and Zax, D. B. and Zilm, K. W. and Zimmermann, H. and Pines, A.} } @article {642, title = {Spin Diffusion between Inequivalent Quadrupolar Nuclei by Double-Quantum Flip-Flops}, journal = {Chemical Physics Letters}, volume = {99}, year = {1983}, note = {Chem Phys LettRb604Times Cited:13Cited References Count:13}, pages = {35-40}, isbn = {0009-2614}, doi = {Doi 10.1016/0009-2614(83)80265-6}, url = {://WOS:A1983RB60400008}, author = {Eckman, R. and Pines, A. and Tycko, R. and Weitekamp, D. P.} } @article {641, title = {Total Spin Coherence Transfer Echo Spectroscopy}, journal = {Journal of Chemical Physics}, volume = {79}, year = {1983}, note = {J Chem PhysRr565Times Cited:25Cited References Count:43}, pages = {5301-5310}, isbn = {0021-9606}, doi = {Doi 10.1063/1.445692}, url = {://WOS:A1983RR56500011}, author = {Garbow, J. R. and Weitekamp, D. P. and Pines, A.} } @article {640, title = {Zero-Field Nuclear Magnetic-Resonance}, journal = {Physical Review Letters}, volume = {50}, year = {1983}, note = {Phys Rev LettQr621Times Cited:103Cited References Count:21}, pages = {1807-1810}, isbn = {0031-9007}, doi = {Doi 10.1103/Physrevlett.50.1807}, url = {://WOS:A1983QR62100025}, author = {Weitekamp, D. P. and Bielecki, A. and Zax, D. and Zilm, K. and Pines, A.} } @article {648, title = {Bilinear Rotation Decoupling of Homonuclear Scalar Interactions}, journal = {Chemical Physics Letters}, volume = {93}, year = {1982}, note = {Chem Phys LettPw861Times Cited:358Cited References Count:22}, pages = {504-509}, isbn = {0009-2614}, doi = {Doi 10.1016/0009-2614(82)83229-6}, url = {://WOS:A1982PW86100020}, author = {Garbow, J. R. and Weitekamp, D. P. and Pines, A.} } @article {645, title = {Determination of Dipole Coupling-Constants Using Heteronuclear Multiple Quantum Nmr}, journal = {Journal of Chemical Physics}, volume = {77}, year = {1982}, note = {J Chem PhysPf412Times Cited:119Cited References Count:44}, pages = {2870-2883}, isbn = {0021-9606}, doi = {Doi 10.1063/1.444180}, url = {://WOS:A1982PF41200024}, author = {Weitekamp, D. P. and Garbow, J. R. and Pines, A.} } @article {644, title = {Search Procedure for Optimizing High-Order Multiple-Quantum Transition Intensities}, journal = {Journal of Magnetic Resonance}, volume = {46}, year = {1982}, note = {J Magn ResonNc063Times Cited:24Cited References Count:11}, pages = {529-534}, isbn = {1090-7807}, doi = {Doi 10.1016/0022-2364(82)90104-4}, url = {://WOS:A1982NC06300015}, author = {Weitekamp, D. P. and Garbow, J. R. and Pines, A.} } @article {646, title = {Simple Pulse Sequences for Selective Multiple-Quantum Excitation}, journal = {Chemical Physics Letters}, volume = {88}, year = {1982}, note = {Chem Phys LettNs759Times Cited:15Cited References Count:12}, pages = {441-443}, isbn = {0009-2614}, doi = {Doi 10.1016/0009-2614(82)83042-X}, url = {://WOS:A1982NS75900018}, author = {Warren, W. S. and Pines, A.} } @article {653, title = {Analogy of Multiple-Quantum Nmr to Isotopic Spin Labeling}, journal = {Journal of the American Chemical Society}, volume = {103}, year = {1981}, note = {J Am Chem SocLk271Times Cited:43Cited References Count:40}, pages = {1613-1617}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja00397a001}, url = {://WOS:A1981LK27100001}, author = {Warren, W. S. and Pines, A.} } @article {651, title = {C-13 Chemical-Shifts in Solid Metal Sandwich Compounds}, journal = {Journal of the American Chemical Society}, volume = {103}, year = {1981}, note = {J Am Chem SocKy444Times Cited:40Cited References Count:8}, pages = {34-36}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja00391a007}, url = {://WOS:A1981KY44400007}, author = {Wemmer, D. E. and Pines, A.} } @article {650, title = {C-13 Nmr-Studies of Coal and Coal Extracts}, journal = {Philosophical Transactions of the Royal Society a-Mathematical Physical and Engineering Sciences}, volume = {300}, year = {1981}, note = {Philos T R Soc ALj670Times Cited:50Cited References Count:25}, pages = {15-41}, isbn = {1364-503X}, doi = {Doi 10.1098/Rsta.1981.0045}, url = {://WOS:A1981LJ67000002}, author = {Wemmer, D. E. and Pines, A. and Whitehurst, D. D.} } @article {654, title = {Experiments on Selective Excitation of Multiple-Quantum Transitions in Nmr-Spectroscopy}, journal = {Journal of Chemical Physics}, volume = {74}, year = {1981}, note = {J Chem PhysLg574Times Cited:57Cited References Count:23}, pages = {2808-2818}, isbn = {0021-9606}, doi = {Doi 10.1063/1.441452}, url = {://WOS:A1981LG57400021}, author = {Warren, W. S. and Pines, A.} } @article {652, title = {High-Resolution Nmr-Spectra in Inhomogeneous Magnetic-Fields - Application of Total Spin Coherence Transfer Echoes}, journal = {Journal of the American Chemical Society}, volume = {103}, year = {1981}, note = {J Am Chem SocLt874Times Cited:64Cited References Count:10}, pages = {3578-3579}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja00402a057}, url = {://WOS:A1981LT87400057}, author = {Weitekamp, D. P. and Garbow, J. R. and Murdoch, J. B. and Pines, A.} } @article {649, title = {Nmr-Study of Molecular-Reorientation under Fivefold Symmetry - Solid Permethylferrocene}, journal = {Journal of the American Chemical Society}, volume = {103}, year = {1981}, note = {J Am Chem SocKy444Times Cited:68Cited References Count:21}, pages = {28-33}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja00391a006}, url = {://WOS:A1981KY44400006}, author = {Wemmer, D. E. and Ruben, D. J. and Pines, A.} } @article {656, title = {Selectivity in Multiple-Quantum Spectroscopy}, journal = {Philosophical Transactions of the Royal Society a-Mathematical Physical and Engineering Sciences}, volume = {299}, year = {1981}, note = {Philos T R Soc ALj669Times Cited:19Cited References Count:17}, pages = {585-592}, isbn = {1364-503X}, doi = {Doi 10.1098/Rsta.1981.0036}, url = {://WOS:A1981LJ66900008}, author = {Drobny, G. and Pines, A. and Sinton, S. and Warren, W. S. and Weitekamp, D. P.} } @article {658, title = {High-Order Selective Sequences in Multiple-Quantum Nmr}, journal = {Journal of Magnetic Resonance}, volume = {40}, year = {1980}, note = {J Magn ResonKh908Times Cited:21Cited References Count:3}, pages = {581-583}, isbn = {1090-7807}, doi = {Doi 10.1016/0022-2364(80)90015-3}, url = {://WOS:A1980KH90800015}, author = {Warren, W. S. and Weitekamp, D. P. and Pines, A.} } @article {657, title = {Theory of Selective Excitation of Multiple-Quantum Transitions}, journal = {Journal of Chemical Physics}, volume = {73}, year = {1980}, note = {J Chem PhysKh292Times Cited:159Cited References Count:26}, pages = {2084-2099}, isbn = {0021-9606}, doi = {Doi 10.1063/1.440403}, url = {://WOS:A1980KH29200011}, author = {Warren, W. S. and Weitekamp, D. P. and Pines, A.} } @article {664, title = {Viscosity and Temperature-Dependence of the Magnetic Isotope Effect}, journal = {Journal of Chemical Physics}, volume = {73}, year = {1980}, note = {J Chem PhysKx295Times Cited:53Cited References Count:35}, pages = {5493-5499}, isbn = {0021-9606}, doi = {Doi 10.1063/1.440068}, url = {://WOS:A1980KX29500010}, author = {Sterna, L. and Ronis, D. and Wolfe, S. and Pines, A.} } @article {672, title = {Selective Excitation of Multiple-Quantum Coherence in Nuclear Magnetic-Resonance}, journal = {Physical Review Letters}, volume = {43}, year = {1979}, note = {Phys Rev LettHw700Times Cited:85Cited References Count:14}, pages = {1791-1794}, isbn = {0031-9007}, doi = {Doi 10.1103/Physrevlett.43.1791}, url = {://WOS:A1979HW70000008}, author = {Warren, W. S. and Sinton, S. and Weitekamp, D. P. and Pines, A.} } @article {676, title = {5-Quantum and 6-Quantum Nmr-Spectra of Oriented Benzene}, journal = {Bulletin of the American Physical Society}, volume = {23}, year = {1978}, note = {B Am Phys SocEg455Times Cited:27Cited References Count:3}, pages = {21-21}, isbn = {0003-0503}, url = {://WOS:A1978EG45500071}, author = {Pines, A. and Wemmer, D. and Tang, J. and Sinton, S.} } @article {679, title = {Fourier transform multiple quantum nuclear magnetic resonance}, journal = {Faraday Symposia of the Chemical Society}, volume = {13}, year = {1978}, pages = {49-55}, abstract = {

The excitation and detection of multiple quantum transitions in systems of coupled spins offers, among other advantages, an increase in resolution over single quantum n.m.r. since the number of lines decreases as the order of the transition increases. This paper reviews the motivation for detecting multiple quantum transitions by a Fourier transform experiment and describes an experimental approach to high resolution multiple quantum spectra in dipolar systems along with results on some protonated liquid crystal systems. A simple operator formalism for the essential features of the time development is presented and some applications in progress are discussed.

}, isbn = {0301-5696}, url = {http://dx.doi.org/10.1039/FS9781300049}, author = {Drobny, Gary and Pines, Alexander and Sinton, Steven and Weitekamp, Daniel P. and Wemmer, David} } @inbook {682, title = {Double quantum NMR in solids}, booktitle = {Magnetic Resonance in Condensed Matter: Recent developments}, year = {1977}, pages = {127-129}, publisher = {University of Ljubljana Press}, organization = {University of Ljubljana Press}, author = {Pines, A. and Vega, S. and Ruben, D.J. and Shattuck, T.W. and Wemmer, D.}, editor = {Lahajanr, R. Blinc and G.} } @proceedings {683, title = {Application of novel NMR techniques to coal structure}, journal = {Coal Chemistry Workshop}, year = {1976}, pages = {229}, address = {Stanford}, author = {Wemmer, D. and Whitehurst, D. and Pines, A.} } @article {689, title = {C-13 Chemical Shielding in Oxalic-Acid, Oxalic-Acid Dihydrate, and Diammonium Oxalate}, journal = {Journal of Chemical Physics}, volume = {63}, year = {1975}, note = {J Chem PhysAk998Times Cited:49Cited References Count:20}, pages = {1267-1271}, isbn = {0021-9606}, doi = {Doi 10.1063/1.431418}, url = {://WOS:A1975AK99800034}, author = {Griffin, R. G. and Pines, A. and Pausak, S. and Waugh, J. S.} } @article {688, title = {Observation of C-13-N-14 Dipolar Couplings in Single-Crystals of Glycine}, journal = {Journal of Chemical Physics}, volume = {63}, year = {1975}, note = {J Chem PhysAt263Times Cited:24Cited References Count:10}, pages = {3676-3677}, isbn = {0021-9606}, doi = {Doi 10.1063/1.431768}, url = {://WOS:A1975AT26300072}, author = {Griffin, R. G. and Pines, A. and Waugh, J. S.} } @article {703, title = {C-13 and N-15 chemical shielding anisotropy in acetonitrile}, journal = {Chemical Physics Letters}, year = {1974}, pages = {78}, author = {Kaplan, S. and Pines, A. and Griffin, R.G. and Waugh, J.S.} } @article {704, title = {Chemical Shielding Anisotropy of C-13 and N-15 in Acetonitrile}, journal = {Chemical Physics Letters}, volume = {25}, year = {1974}, note = {Chem Phys LettS5222Times Cited:46Cited References Count:8}, pages = {78-79}, isbn = {0009-2614}, doi = {Doi 10.1016/0009-2614(74)80336-2}, url = {://WOS:A1974S522200017}, author = {Kaplan, S. and Pines, A. and Griffin, R. G. and Waugh, J. S.} } @article {695, title = {Chemical Shielding Tensors of C-13 in Oxalates}, journal = {Bulletin of the American Physical Society}, volume = {19}, year = {1974}, note = {B Am Phys SocS5575Times Cited:0Cited References Count:1}, pages = {486-487}, isbn = {0003-0503}, url = {://WOS:A1974S557500422}, author = {Pines, A. and Griffin, R. G. and Waugh, J. S.} } @article {692, title = {Dipolar Spin Temperature in a Periodically Perturbed Nuclear Spin System}, journal = {Physics Letters A}, volume = {A 47}, year = {1974}, note = {Phys Lett AS7970Times Cited:11Cited References Count:5}, pages = {337-338}, isbn = {0375-9601}, doi = {Doi 10.1016/0375-9601(74)90192-3}, url = {://WOS:A1974S797000033}, author = {Pines, A. and Waugh, J. S.} } @article {710, title = {C-13 Chemical Shielding Tensors in Single-Crystal Durene}, journal = {Journal of Chemical Physics}, volume = {59}, year = {1973}, note = {J Chem PhysQ3293Times Cited:124Cited References Count:22}, pages = {591-595}, isbn = {0021-9606}, doi = {Doi 10.1063/1.1680062}, url = {://WOS:A1973Q329300002}, author = {Pausak, S. and Pines, A. and Waugh, J. S.} } @article {707, title = {Proton-Enhanced Nmr of Dilute Spins in Solids}, journal = {Journal of Chemical Physics}, volume = {59}, year = {1973}, note = {J Chem PhysQ3293Times Cited:2144Cited References Count:119}, pages = {569-590}, isbn = {0021-9606}, doi = {Doi 10.1063/1.1680061}, url = {://WOS:A1973Q329300001}, author = {Pines, A. and Gibby, M. G. and Waugh, J. S.} } @article {720, title = {Anisotropic Nuclear Spin Relaxation of C-13 in Solid Benzene}, journal = {Chemical Physics Letters}, volume = {16}, year = {1972}, note = {Chem Phys LettN8559Times Cited:53Cited References Count:17}, pages = {296-\&}, isbn = {0009-2614}, doi = {Doi 10.1016/0009-2614(72)80276-8}, url = {://WOS:A1972N855900018}, author = {Gibby, M. G. and Waugh, J. S. and Pines, A.} } @article {722, title = {High-Resolution Nmr of N-15 in Solids}, journal = {Chemical Physics Letters}, volume = {17}, year = {1972}, note = {Chem Phys LettO4215Times Cited:47Cited References Count:17}, pages = {80-84}, isbn = {0009-2614}, doi = {Doi 10.1016/0009-2614(72)80330-0}, url = {://WOS:A1972O421500021}, author = {Gibby, M. G. and Griffin, R. G. and Pines, A. and Waugh, J. S.} } @article {718, title = {Homogeneous and Inhomogeneous Nuclear Spin Echoes in Solids}, journal = {Journal of Magnetic Resonance}, volume = {6}, year = {1972}, note = {J Magn ResonM2264Times Cited:33Cited References Count:32}, pages = {457-\&}, isbn = {1090-7807}, doi = {Doi 10.1016/0022-2364(72)90154-0}, url = {://WOS:A1972M226400001}, author = {Pines, A. and Rhim, W. and Waugh, J. S.} } @article {719, title = {P-31 Chemical Shielding Anisotropy in Solids - Single-Crystal and Powder Studies at 99.4 Mhz}, journal = {Journal of Chemical Physics}, volume = {56}, year = {1972}, note = {J Chem PhysL3043Times Cited:33Cited References Count:21}, pages = {991-\&}, isbn = {0021-9606}, doi = {Doi 10.1063/1.1677259}, url = {://WOS:A1972L304300043}, author = {Gibby, M. G. and Waugh, J. S. and Pines, A. and Rhim, W. K.} } @proceedings {714, title = {Proton-enhance NMR of dilute spins in solids, proceedings of the congress ampere}, journal = {The Congress Ampere}, year = {1972}, pages = {11-17}, publisher = {North Holland Publishers}, address = {Turku, Finland}, author = {Waugh, J.S. and Gibby, M.G. and Kaplan, S. and Pines, A.} } @article {716, title = {Proton-Enhanced Nuclear Induction Spectroscopy C-13 Chemical Shielding Anisotropy in Some Organic Solids}, journal = {Chemical Physics Letters}, volume = {15}, year = {1972}, note = {Chem Phys LettN5315Times Cited:290Cited References Count:10}, pages = {373-\&}, isbn = {0009-2614}, doi = {Doi 10.1016/0009-2614(72)80191-X}, url = {://WOS:A1972N531500014}, author = {Pines, A. and Waugh, J. S. and Gibby, M. G.} } @article {715, title = {Proton-Enhanced Nuclear Induction Spectroscopy - Method for High-Resolution Nmr of Dilute Spins in Solids}, journal = {Journal of Chemical Physics}, volume = {56}, year = {1972}, note = {J Chem PhysL5803Times Cited:520Cited References Count:10}, pages = {1776-\&}, isbn = {0021-9606}, doi = {Doi 10.1063/1.1677439}, url = {://WOS:A1972L580300054}, author = {Pines, A. and Waugh, J. S. and Gibby, M. G.} } @article {721, title = {Proton-Enhanced Nuclear Induction Spectroscopy - Silicon-29 Chemical Shielding Anisotropy in Some Organosilicon Compounds}, journal = {Journal of the American Chemical Society}, volume = {94}, year = {1972}, note = {J Am Chem SocN2839Times Cited:31Cited References Count:5}, pages = {6231-\&}, isbn = {0002-7863}, doi = {Doi 10.1021/Ja00772a071}, url = {://WOS:A1972N283900071}, author = {Gibby, M. G. and Pines, A. and Waugh, J. S.} } @article {717, title = {Quantitative Aspects of Coherent Averaging - Simple Treatment of Resonance Offset Processes in Multiple-Pulse Nmr}, journal = {Journal of Magnetic Resonance}, volume = {8}, year = {1972}, note = {J Magn ResonO1700Times Cited:34Cited References Count:38}, pages = {354-\&}, isbn = {1090-7807}, doi = {Doi 10.1016/0022-2364(72)90053-4}, url = {://WOS:A1972O170000009}, author = {Pines, A. and Waugh, J. S.} } @article {713, title = {Spin Echoes and Loschmidt{\textquoteright}s paradox}, journal = {Journal Pure Applied Chemistry}, volume = {32}, year = {1972}, pages = {317-324}, author = {Waugh, J.S. and Rhim, W.-K. and Pines, A.} } @article {724, title = {C-13 Chemical Shielding Anisotropy in Solids - Cs2 and Caco3}, journal = {Journal of Chemical Physics}, volume = {54}, year = {1971}, note = {J Chem PhysJ6303Times Cited:30Cited References Count:17}, pages = {5438-\&}, isbn = {0021-9606}, doi = {Doi 10.1063/1.1674855}, url = {://WOS:A1971J630300070}, author = {Pines, A. and Rhim, W. K. and Waugh, J. S.} } @article {726, title = {High Resolution Nmr of Dilute Spins in Solids}, journal = {Bulletin of the American Physical Society}, volume = {16}, year = {1971}, note = {B Am Phys SocL0382Times Cited:0Cited References Count:3}, pages = {1408-\&}, isbn = {0003-0503}, url = {://WOS:A1971L038200080}, author = {Pines, A. and Gibby, M. G. and Waugh, J. S.} } @article {728, title = {Spectrometers for multiple pulse NMR}, journal = {Advances in Magnetic Resonance}, volume = {5}, year = {1971}, pages = {117-175}, author = {Ellett, J.D., Jr. and Gibby, M.G. and Haeberlen, U. and Huber, L.M. and Mehring, M. and Pines, A. and Waugh, J.S.} } @article {727, title = {Spin-Decoupling in Resolution of Chemical Shifts in Solids by Pulsed Nmr}, journal = {Journal of Chemical Physics}, volume = {54}, year = {1971}, note = {J Chem PhysJ1849Times Cited:49Cited References Count:9}, pages = {3239-\&}, isbn = {0021-9606}, doi = {Doi 10.1063/1.1675324}, url = {://WOS:A1971J184900070}, author = {Mehring, M. and Pines, A. and Rhim, W. K. and Waugh, J. S.} } @article {723, title = {Time-Reversal Experiments in Dipolar-Coupled Spin Systems}, journal = {Physical Review B}, volume = {3}, year = {1971}, note = {Phys Rev BI5979Times Cited:281Cited References Count:36}, pages = {684-\&}, doi = {Doi 10.1103/Physrevb.3.684}, url = {://WOS:A1971I597900016}, author = {Rhim, W. K. and Pines, A. and Waugh, J. S.} } @article {729, title = {Violation of Spin-Temperature Hypothesis}, journal = {Physical Review Letters}, volume = {25}, year = {1970}, note = {Phys Rev LettG8549Times Cited:140Cited References Count:17}, pages = {218-\&}, isbn = {0031-9007}, doi = {Doi 10.1103/Physrevlett.25.218}, url = {://WOS:A1970G854900007}, author = {Rhim, W. K. and Pines, A. and Waugh, J. S.} } @article {1925, title = {Non-disruptive dissolution of hp-129Xe in viscou aqueous and organic liquid crystalline environments}, author = {Ashley E. Truxal and Clancy C. Slack and Muller D. Gomes and Christophoros C. Vassiliou and David E. Wemmer and Alexander Pines} }