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School of Chemistry & Chemical Biology, University College Dublin, Belfield, Dublin 4, Ireland
E-mail: martin.albrecht@ucd.ie
; Fax: +353 17162501
; Tel: +353 17162504
Dalton Trans., 2013,42, 7424-7432
DOI:
10.1039/C3DT32939A
Received
07 Dec 2012,
Accepted
17 Jan 2013
First published online
18 Jan 2013
A series of RuII (η6-arene) complexes with 1,2,3-triazolylidene ligands comprising different aryl and alkyl wingtip groups have been prepared and characterized by NMR spectroscopy, microanalysis, and in one case by X-ray diffraction. All complexes are active catalyst precursors for the oxidation of alcohols to the corresponding aldehydes/ketones without the need of an oxidant or base as additive. The wingtip groups have a direct impact on the catalytic activity, alkyl wingtips providing the most active species while aryl wingtip groups induce lower activity. An N-bound phenyl group was the most inhibiting wingtip group due to cyclometalation. Arene dissociation was observed as a potential catalyst deactivation pathway.
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