Cyclic (Amino)(aryl)carbenes (CAArCs) as Strong σ‐Donating and π‐Accepting Ligands for Transition Metals |
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| Authors: | Bin Rao Huarong Tang Prof?Dr Xiaoming Zeng Liu Liu Dr Mohand Melaimi Prof?Dr Guy Bertrand |
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| Affiliation: | 1. Frontier Institute of Science and Technology, Xi'an Jiaotong University, Xi'an, Shaanxi, 710054 (P.R. China);2. State Key Laboratory of Elemento‐organic Chemistry, Nankai University, Tianjin 300071 (P.R. China);3. UCSD‐CNRS Joint Research Chemistry Laboratory (UMI 3555), Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, CA 92093‐0358 (USA) |
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| Abstract: | Cyclic (amino)(aryl)carbenes (CAArCs) result from the replacement of the alkyl substituent of cyclic (alkyl)(amino) carbenes (CAACs) by an aryl group. This structural modification leads to enhanced electrophilicity of the carbene center with retention of the high nucleophilicity of CAACs, and therefore CAArCs feature a small singlet–triplet gap. The isoindolium precursors are readily prepared in good yields, and deprotonation at low temperature, in the presence of RhCl(cod)]2 and (Me2S)AuCl] lead to air‐stable rhodium and gold CAArC‐supported complexes, respectively. The rhodium complexes promote the 3+2] cycloaddition of diphenylcyclopropenone with ethyl phenylpropiolate, and induce the addition of 2‐vinylpyridine to alkenes by CH activation. The gold complexes allow for the catalytic three‐component preparation of 1,2‐dihydroquinolines from aniline and phenyl acetylene. These preliminary results illustrate the potential of CAArC ligands in transition‐metal catalysis. |
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| Keywords: | electronic properties gold homogeneous catalysis N‐heterocyclic carbenes rhodium |
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