Electronic effect of and mutual polarizability in groups attached to oxygen via their C, Si, Ge, and B atoms

Author:

Pola Josef,Chvalovský Václav

Abstract

Relative acidity of triphenylhydroxy substituted germane and stannane is consistent with superior electrondonating effect of (C6H5)3Ge and (C6H5)3Sn groups in these compounds. Relative basicity data of alkyl(alkoxy) boranes, methanes, silanes, and germanes (RO)nZRm (Z = B, C, Si, and Ge) are compiled. The variation of the electronic effect parameter σ of fully alkylated RmZ-groups upon substitution of their alkyl with ethoxy substituent appears for Z=B and Si to be influenced by mutual polarizability effect of ethoxy substituents. Mutual polarizability of ethoxy substituents attached to carbon and germanium is negligible.

Publisher

Institute of Organic Chemistry & Biochemistry

Subject

General Chemistry

Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Untersuchungen zu Substituenteneffekten in Tris(methylorganophenylsiloxy)silanen (RMePhSiO)3SiH;Zeitschrift für Chemie;2010-08-31

2. Hydrogen bonding involving the siloxane group;Journal of Molecular Structure;1992-07

3. Reply;Journal of the American Ceramic Society;1988-09

4. The System Boron-Oxygen;B Boron Compounds;1986

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