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A pyrene-based N‑heterocyclic carbene: study of its coordination chemistry and stereoelectronic properties

机译:基于芘的N-杂环卡宾:研究其配位化学和立体电子性质

摘要

A new pyrene-N-heterocyclic carbene ligand has been obtained and coordinated to rhodium and iridium,affording the corresponding [MCl(NHC)(COD)] and [MCl(NHC)(CO)2] complexes (M = Ir, Rh). The presence of thepyrene backbone allows the introduction of a η6-bonded [RuCp]+ fragment and facilitates the formation of the correspondingheterometallic complexes of Rh/Ru and Ir/Ru. The stereoelectronic properties of the new ligand have been studied by means ofIR spectroscopy and cyclic voltammetry and demonstrate that the introduction of the [RuCp]+ fragment results in the reductionof the electron-donating power of the ligand
机译:获得了一种新的pyr-N-杂环卡宾配体,并与相应的[MCl(NHC)(COD)]和[MCl(NHC)(CO)2]配合物(M = Ir,Rh)配位,与铑和铱配位。 backbone骨架的存在允许引入η6-键合的[RuCp] +片段,并促进Rh / Ru和Ir / Ru的相应杂金属络合物的形成。通过红外光谱和循环伏安法研究了新配体的立体电子性质,证明了[RuCp] +片段的引入导致配体的供电子能力降低。

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