Issue 3, 2002

Abstract

The mild cleavage of phosphonodiester groups supported on a silica matrix has been investigated. The use of TMSBr (bromotrimethylsilane) with diethyl phosphonates has been revisited, and interactions of phosphonoacids with silicon species are described. An alternative route utilising di-tert-butyl phosphonate group has also been studied and in this case cleavage has been demonstrated in very mild conditions.

Graphical abstract: Studies of the hydrolysis of ethyl and tert-butyl phosphonates covalently bonded to silica xerogels

Article information

Article type
Paper
Submitted
27 Jul 2001
Accepted
12 Dec 2001
First published
31 Jan 2002

J. Mater. Chem., 2002,12, 540-545

Studies of the hydrolysis of ethyl and tert-butyl phosphonates covalently bonded to silica xerogels

C. Carbonneau, R. Frantz, J. Durand, M. Granier, G. F. Lanneau and R. J. P. Corriu, J. Mater. Chem., 2002, 12, 540 DOI: 10.1039/B106838E

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