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Room-Temperature Hydration of Alkynes Catalyzed by Different Carbene Gold Complexes and their Precursors

机译:不同卡宾金配合物催化的炔烃的室温水合及其前体

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摘要

The room-temperature hydration of alkynes catalyzed by NHC-gold(I) (NHC=N-heterocyclic carbene), NAC-gold(I) (NAC=nitrogen acyclic carbene), and isocyanide gold(I) complexes was investigated carefully in the presence of different weakly coordinating anions. NHC(IPr)-AuCl/KB(C6F5)(4) (NHC(IPr)=1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene) was found to be the most active catalyst at room temperature, and the room-temperature hydration of different alkynes could be completed in 7 h using only 0.5 mol% NHC(IPr)-AuCl/KB(C6F5)(4). It was further demonstrated that the catalyst system could be simply reused at least six times without a noticeable loss of catalytic activity.
机译:仔细研究了NHC-金(I)(NHC = N-杂环碳切菜),NAC-金(I)(NAC =氮环纤维碳切菜)的炔烃的室温水合,并仔细研究了异氰化物金(I)复合物 存在不同的弱协调阴离子。 NHC(IPR)-auCl / Kb(C6F5)(4)(NHC(IPR)= 1,3-双(2,6-二异丙基苯基)咪唑-2- ylidene)被发现是室温下最活性的催化剂, 而不同alkynes的室温水合可以在7小时内完成0.5mol%NHC(IPR)-aucl / Kb(C6F5)(4)。 进一步证明了催化剂体系可以简单地重复使用至少六次,而不明显催化活性损失。

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