@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 = {<p>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.</p>
},
	keywords = {zeolites},
	isbn = {0022-3654},
	doi = {Doi 10.1021/J100196a028},
	url = {<Go to ISI>://WOS:A1992JK80700028},
	author = {Mueller, K. T. and Baltisberger, J. H. and Wooten, E. W. and Pines, A.}
}
