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Synthesis and characterization of IPrMe-containing silver(I), gold(I) and gold(III) complexes

机译:含IPrMe的银(I),金(I)和金(III)配合物的合成与表征

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摘要

The compounds 4,5-dimethyl-N, N'-bis(2,6-diisopropylphenyl) imidazol-2-ylidene silver chloride [AgCl(IPrMe)] 3 and 4,5-dimethyl-N, N'-bis(2,6-diisopropylphenyl) imidazol-2-ylidene gold(I) chloride [AuCl(IPrMe)] 4 have been synthesized. The attempted synthesis of the corresponding 4,5-dimethyl-N, N'-bis(2,6-diisopropylphenyl) imidazol-2-ylidene gold(III) chloride by oxidative addition of chlorine gas on 4 allowed for the formation of the expected complex, concomitantly with 6, resulting from a chlorination of a methyl group situated in the backbone of the NHC (N-heterocyclic carbene). Additionally, the buried volume %V-bur of the IPrMe ligand in [AgCl(IPrMe)] 3 and [AuCl(IPrMe)] 4 complexes was calculated and compared to %V-bur of more classical NHCs. This quanti. cation of the steric hinderance of the IPrMe ligand reveals the influence of the substituent modulation in the backbone of NHCs.
机译:化合物4,5-二甲基-N,N'-双(2,6-二异丙基苯基)咪唑-2-亚烷基氯化银[AgCl(IPrMe)] 3和4,5-二甲基-N,N'-双(2合成了,6-二异丙基苯基)咪唑-2-亚烷基氯化金(I)[AuCl(IPrMe)] 4。尝试通过在4上氧化添加氯气来合成相应的4,5-二甲基-N,N'-双(2,6-二异丙基苯基)咪唑-2-亚甲基氯化金(III),从而形成了预期的氯化物与NHC(N-杂环卡宾)的主链中的甲基发生氯化反应,与6形成络合物。另外,计算了[AgCl(IPrMe)] 3和[AuCl(IPrMe)] 4复合物中IPrMe配体的掩埋体积%V-bur,并将其与更多经典NHC的%V-bur进行了比较。这个数量。 IPrMe配体的空间位阻阳离子揭示了NHCs骨架中取代基调节的影响。

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