Directivity of the Intramolecular O→Si Bond in Pentacoordinate Organosilicone Compounds

被引:2
|
作者
Aksamentova, T. N. [1 ]
Chipanina, N. N. [1 ]
Voronkov, M. G. [1 ]
Trofimova, O. M. [1 ]
Zelbst, E. A. [2 ]
Turchaninov, V. K. [1 ]
机构
[1] Russian Acad Sci, Favorskii Irkutsk Inst Chem, Siberian Branch, Irkutsk 664033, Russia
[2] Irkutsk State Pedag Univ, Irkutsk 664011, Russia
关键词
MOLECULAR-STRUCTURE; CRYSTAL-STRUCTURE; SILICON-COMPOUNDS; AB-INITIO; STEREOELECTRONIC STRUCTURE; NUCLEOPHILIC-SUBSTITUTION; COORDINATION; (BENZOYLOXYMETHYL)TRIFLUOROSILANE; (AROYLOXYMETHYL)TRIFLUOROSILANES; REACTIVITY;
D O I
10.1134/S1070363209110085
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
According to the data of X-ray diffraction analysis and quantum chemical calculations, in the hypervalent silicon compounds where the coordination cycle is closed by the C=O-->Si-F fragment, the O-->Si interatomic distance is governed by the orientation of the silicon atom determined by the C=O-->Si angle. This is an indication of a directivity of the coordination bond O-->Si; a regular variation in the nature of the latter is reflected in the observed dependence of the O-->Si distance on the C=O-->Si angle.
引用
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页码:2328 / 2338
页数:11
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