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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Triazole vs. triazolium carbene ligands in the site-selective cyclometallation of o-carboranes by M(III) (M = Ir, Rh) complexes
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Triazole vs. triazolium carbene ligands in the site-selective cyclometallation of o-carboranes by M(III) (M = Ir, Rh) complexes

机译:三唑与三唑鎓卡宾配体在现场选择性环荷组合,由M(III)(M = IR,RH)复合物

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摘要

Ir(III) and Rh(III)-mediated site-selective cage B-H and C-H bond activation in o-carboranylmethyl derivatives has been achieved. The selectivity of the reaction is related to the electron donating properties of the ligand. 1,2,3-Triazole-derivatives use the N2 position of the triazole ring to direct the selective o-carborane B-H bond activation, whereas the corresponding triazolylidene derivatives lead to the cage C-H bond activation with complete site-selectivity.
机译:已经实现了IR(III)和RH(III)介导的位点选择性笼B-H和C-H键活化在O-碳硼酰甲基甲基衍生物中。 反应的选择性与配体的电子捐赠性质有关。 1,2,3-三唑 - 衍生物使用三唑环的N2位置,以指示选择性O-碳硼烷B-H键活化,而相应的三唑基衍生物导致笼式C-H键活化,具有完全的位点选择性。

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