Issue 8, 2014

A spiroborate-based anionic bis-N-heterocyclic carbene

Abstract

A twisted mono-cationic bis-benzimidazolium salt was serendipitously isolated from the dehydrative condensation of 5,6-dihydroxyl-1,3-dimesityl-benzimidazolium and 1,4-benzenediboronic acid. Subsequent deprotonation of the benzimidazolium salt led to the formation of a spiroborate-linked free bis-NHC, which was further transformed into the corresponding diborane adduct and the di-Rh complex.

Graphical abstract: A spiroborate-based anionic bis-N-heterocyclic carbene

Supplementary files

Article information

Article type
Communication
Submitted
13 Sep 2013
Accepted
05 Dec 2013
First published
10 Dec 2013

Dalton Trans., 2014,43, 3059-3062

Author version available

A spiroborate-based anionic bis-N-heterocyclic carbene

J. Su, G. Lee, S. Peng and C. Chiu, Dalton Trans., 2014, 43, 3059 DOI: 10.1039/C3DT52131A

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