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Well-defined N-heterocyclic carbene silver halides of 1-cyclohexyl-3- arylmethylimidazolylidenes: Synthesis, structure and catalysis in A 3-reaction of aldehydes, amines and alkynes  ( EI收录)  

文献类型:期刊文献

英文题名:Well-defined N-heterocyclic carbene silver halides of 1-cyclohexyl-3- arylmethylimidazolylidenes: Synthesis, structure and catalysis in A 3-reaction of aldehydes, amines and alkynes

作者:Li, Yanbo[1]; Chen, Xiaofeng[1]; Song, Yin[1]; Fang, Ling[1]; Zou, Gang[1]

机构:[1] Department of Fine Chemicals, East China University of Science and Technology, Shanghai, China

年份:2011

卷号:40

期号:9

起止页码:2046

外文期刊名:Dalton Transactions

收录:EI(收录号:20110813681814)

语种:英文

外文关键词:Chlorine compounds - Catalyst activity - Hydrogen bonds - Nitrates - Organic compounds - X ray diffraction - Crystal structure - Sodium nitrate - Synthesis (chemical) - Ligands - Single crystals - Catalysis - Binary alloys - Silver oxides

摘要:Structurally well-defined N-heterocyclic carbene silver chlorides and bromides supported by 1-cyclohexyl-3-benzylimidazolylidene (CyBn-NHC) or 1-cyclohexyl-3-naphthalen-2-ylmethylimidazolylidene (CyNaph-NHC) were synthesized by reaction of the corresponding imidazolium halides with silver(i) oxide while cationic bis(CyBn-NHC) silver nitrate was isolated under similar conditions using imidazolium iodide in the presence of sodium nitrate. Single-crystal X-ray diffraction revealed a dimeric structure through a nonpolar weak-hydrogen-bond supported Ag-Ag bond for 1-cyclohexyl-3- benzylimidazolylidene silver halides [(CyBn-NHC)AgX]2 (X = Cl, 1; Br, 2) but a monomeric structure for N-heterocyclic carbene silver halides with the more sterically demanding 1-cyclohexyl-3-naphthalen-2-ylmethylimidazolylidene ligand (CyNaph-NHC)AgX (X = Cl, 4; Br, 5). Cationic biscarbene silver nitrate [(CyBn-NHC)2Ag]+NO3-3 assumed a cis orientation with respect to the two carbene ligands. The monomeric complexes (CyNaph-NHC)AgX 4 and 5 showed higher catalytic activity than the dimeric [(CyBn-NHC)AgX]21 and 2 as well as the cationic biscarbene silver nitrate 3 in the model three component reaction of 3-phenylpropionaldehyde, phenylacetylene and piperidine with chloride 4 performing best and giving product in almost quantitative yield within 2 h at 100 °C. An explanation for the structure-activity relationship in N-heterocyclic carbene silver halide catalyzed three component reaction is given based on a slightly modified mechanism from the one in literature. ? The Royal Society of Chemistry 2011.

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