Issue 12, 2002

Silicon–carbon bond cleavage of organosilicon amines MenN[CH2Si(OCH2CH2)3N]3–n (n = 1, 2) by phenols

Abstract

Anomalously high basicity of organosilicon amines MenN[CH2Si(OCH2CH2)3N]3–n determines the ease of nucleophilic cleavage of the Si–C bond by phenols even at room temperature. The conversion of silatrane increases both with phenol acidity and basicity of the exocyclic nitrogen atom.

Article information

Article type
Paper
Submitted
23 Jul 2002
Accepted
18 Sep 2002
First published
25 Oct 2002

J. Chem. Soc., Perkin Trans. 2, 2002, 2083-2086

Silicon–carbon bond cleavage of organosilicon amines MenN[CH2Si(OCH2CH2)3N]3–n (n = 1, 2) by phenols

N. F. Lazareva, E. I. Brodskaya and G. V. Ratovsky, J. Chem. Soc., Perkin Trans. 2, 2002, 2083 DOI: 10.1039/B207208D

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