SOLID-STATE O-17 MAGIC-ANGLE AND DYNAMIC-ANGLE SPINNING NMR-STUDY OF THE SIO2 POLYMORPH COESITE

被引:112
作者
GRANDINETTI, PJ
BALTISBERGER, JH
FARNAN, I
STEBBINS, JF
WERNER, U
PINES, A
机构
[1] BEREA COLL,DEPT CHEM,BEREA,KY 40404
[2] STANFORD UNIV,DEPT GEOL & ENVIRONM SCI,STANFORD,CA 94305
[3] UNIV CALIF BERKELEY,LAWRENCE BERKELEY LAB,DIV SCI MAT,BERKELEY,CA 94720
[4] UNIV CALIF BERKELEY,DEPT CHEM,BERKELEY,CA 94720
关键词
D O I
10.1021/j100032a045
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
引用
收藏
页码:12341 / 12348
页数:8
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