Isolation of a C5-Deprotonated Imidazolium, a Crystalline “Abnormal” N-Heterocyclic Carbene

Author:

Aldeco-Perez Eugenia1,Rosenthal Amos J.1,Donnadieu Bruno1,Parameswaran Pattiyil2,Frenking Gernot2,Bertrand Guy1

Affiliation:

1. University of California Riverside–CNRS Joint Research Chemistry Laboratory (UMI 2957), Department of Chemistry, University of California Riverside, Riverside, CA 92521-0403, USA.

2. Fachbereich Chemie, Philipps-Universitat Marburg, Hans-Meerwein-Strasse, 35032 Marburg, Germany.

Abstract

Stretching Carbene Versatility Stable N-heterocyclic carbene (NHC) molecules are versatile catalysts for organic reactions (see the Perspective by Albrecht ). Lavallo and Grubbs (p. 559 ) now show that these molecules can also catalyze organometallic transformations. Specifically, the carbenes induce coupling of monomeric iron olefin complexes to form clusters incorporating three or four bonded iron centers. Initial coordination of carbene to iron may facilitate formation of an iron-iron bond with a second complex. In a related development, Aldeco-Perez et al. (p. 556 ) prepared an NHC isomer in which the divalent carbon is shifted so that it no longer lies between the nitrogens. The compound forms stable complexes with both gold and CO 2 .

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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