Nucleophilic Cleavage of Substituted Benzyltrimethylsilanes using Tetraalkylammonium Fluoride in DMSO-H2O Media
Publication Type
Original research
Authors
  • F.M.Mahmoud
  • Mohammed Al-Nuri
  • J. A. Daraghmah
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The nucleophilic cleavage of substituted benzyltrimethyl-silanes in DMSO-H2O media using tetraalkylammonium fluoride, TAAF, has been studied. The observed rate constants, pseudo first order rate constants, activation, and thermodynamic parameters have been reported. A mechanism for such cleavage has been proposed. The results fit well Hammett equation. The reaction constant, p, value of (6.7) has been reported. The p value is consistent with a substantial negative charge developing in the transition state.
Journal
Title
Journal of Applied Sciences
Publisher
--
Publisher Country
Palestine
Publication Type
Both (Printed and Online)
Volume
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Year
2003
Pages
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