铑
化学
原位
配体(生物化学)
催化作用
立体化学
核磁共振波谱
有机化学
受体
生物化学
作者
Saskia Möller,Christoph Kubis,Hans‐Joachim Drexler,Elisabetta Alberico,Detlef Heller
标识
DOI:10.1016/j.jorganchem.2019.121002
摘要
The often applied in situ formation of neutral dinuclear rhodium precatalysts of the type [Rh(Diphosphine)(μ2-Cl)]2 with the ligands DPEPhos and DIOP has been mechanistically investigated by NMR spectroscopy. The structural characterization of reaction intermediates [Rh2(μ2-Diphosphine)(COD)2(Cl)2] and [Rh2(Diphosphine)(COD)(μ2-Cl)2] was accomplished using X-ray crystallography. So a new and unexpected intermediate was found, which casts a new light on the mechanism of this ligand exchange. In addition, equilibria could be found which can at least influence the formation of neutral dinuclear rhodium precatalysts.
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