Through-bond indirect and through-space direct dipolar coupling 31P MAS NMR constraints for spectral assignment in the cubic 3 x 3 x 3 superstructure of Ti2O7

被引:42
作者
Helluy, X
Marichal, C
Sebald, A
机构
[1] Univ Bayreuth, Bayer Geoinst, D-95440 Bayreuth, Germany
[2] Aventis Pharma, Dept Pharmaceut Sci, Res Ctr Vitry Alfortville, F-94403 Vitry, France
[3] Lab Mat Mineraux, F-68093 Mulhouse, France
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2000年 / 104卷 / 13期
关键词
D O I
10.1021/jp993626o
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
A P-31 solid-state NMR study of TiP2O7 is reported. The combined constraints from one-dimensional P-31 MAS NMR experiments and from P-31 2D MAS NMR experiments probing through-bond P-O-P connectivities via homonuclear J coupling interactions (TOBSY experiments), positively identify the cubic space group Pa(3) over bar with a 3 x 3 x 3 superstructure. Additional P-31 2D MAS NMR experiments, probing spatial connectivities between phosphorus sites via homonuclear dipolar coupling interactions (P-31 single-quantum-double-quantum correlation MAS NMR experiments), subsequently lead to complete assignment of the ii distinct crystallographic P sites in the structure of TiP2O7 to the corresponding eight resolved resonances in P-31 MAS NMR spectra of TiP2O7, while P-31 RIL ZQT and C7 DQT MAS NMR experiments confirm that TiP2O7 and the cubic phase of SiP2O7 are isostructural.
引用
收藏
页码:2836 / 2845
页数:10
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