Full Paper
A New Class of Modular Oxazoline-NHC Ligands and Their Coordination Chemistry with Platinum Metals
Article first published online: 14 NOV 2008
DOI: 10.1002/ejic.200800908
Copyright © 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Schneider, N., Bellemin-Laponnaz, S., Wadepohl, H. and Gade, L. H. (2008), A New Class of Modular Oxazoline-NHC Ligands and Their Coordination Chemistry with Platinum Metals. Eur. J. Inorg. Chem., 2008: 5587–5598. doi: 10.1002/ejic.200800908
Publication History
- Issue published online: 9 DEC 2008
- Article first published online: 14 NOV 2008
- Manuscript Received: 10 SEP 2008
Funded by
- Deutsche Forschungsgemeinschaft (DFG). Grant Number: SFB 623
- Deutsch-Französische Hochschule (DFH-UFA)
- Abstract
- Article
- References
- Cited By
Keywords:
- Carbenes;
- Oxazolines;
- Platinum;
- Rhodium
Abstract
A novel family of enantiomerically pure imidazolium salts [(NHC-Ox)H]+X– (2a–g) has been generated bearing an oxazoline unit and in which both heterocycles are connected by a (dimethyl)methylene bridge. Deprotonation of the imidazolium salt 2f and subsequent reaction of the resulting free carbene with [Rh(nbd)Cl]2 (nbd = norbornadiene) afforded the neutral rhodium(I) complex [(NHC-Ox)Rh(nbd)Br] (3) in which the ligand was found to be monodentate. Bromide abstraction lead to the air-stable cationic complex [(NHC-Ox)Rh(nbd)]PF6 (4) with the expected bidentate coordination mode of the ligand. Reaction of the imidazolium salt 2d with Karstedt's catalyst and one equivalent of KOtBu gave the trigonal planar platinum(0) complex [(NHC-Ox)Pt(dvtms)] (5) (dvtms = divinyltetramethylsiloxane), which was oxidized by CsBr3 to give the square planar platinum(II) complex [(NHC-Ox)PtBr2] (6). Complex [(NHC-Ox)PtCl2] (7) was directly prepared by reaction of the imidazolium salt with Ag2O followed by the addition of [PtCl2(1,5-cod)]. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)

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