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乙烯与基于钳形的硼基铱单元发生可逆加成反应,形成桥连亚乙基。

Reversible addition of ethylene to a pincer-based boryl-iridium unit with the formation of a bridging ethylidene.

作者信息

Cao Yihan, Shih Wei-Chun, Bhuvanesh Nattamai, Ozerov Oleg V

机构信息

Department of Chemistry, Texas A&M University 3255 TAMU, College Station Texas 77842 USA

出版信息

Chem Sci. 2020 Oct 5;11(40):10998-11002. doi: 10.1039/d0sc04748a.

Abstract

This report examines reactions of a series of Ir complexes supported by the diarylboryl/bis(phosphine) PBP pincer ligand with ethylene: (PBP)IrH (), (PBP)IrH(CO) (), and (PBP)Ir(CO) (). The outcomes of these reactions differ from those typical for Ir complexes supported by other pincer ligands and do not give rise to simple ethylene adducts or products of insertion of Ir into the C-H bond of ethylene. Instead, the elements of ethylene are incorporated into the molecules to result in B-C bonds. In the case of and , ethylene addition results in the formation of B/Ir bridging ethylidene complexes and . For , the addition of ethylene (and the analogous addition of 1-hexene) is shown to be partially reversible. Addition of ethylene to and is remarkable because they are saturated at Ir and yet the net outcome is such that ethylene binds without replacing any ligands already present. A mechanistic inquiry suggests that dissociation of CO from or is necessary in order for the addition or loss of ethylene to proceed.

摘要

本报告研究了一系列由二芳基硼基/双(膦)PBP钳形配体支持的Ir配合物与乙烯的反应:(PBP)IrH()、(PBP)IrH(CO)()和(PBP)Ir(CO)()。这些反应的结果不同于其他钳形配体支持的Ir配合物的典型反应结果,不会产生简单的乙烯加合物或Ir插入乙烯C-H键的产物。相反,乙烯的元素被并入分子中形成B-C键。在和的情况下,乙烯加成导致形成B/Ir桥连亚乙基配合物和。对于,乙烯的加成(以及1-己烯的类似加成)显示部分可逆。乙烯加成到和上很显著,因为它们在Ir处是饱和的,但最终结果是乙烯在不取代任何已存在配体的情况下结合。机理研究表明,为了使乙烯的加成或消除得以进行,CO从或中解离是必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b2e/8162418/201de02fde74/d0sc04748a-s1.jpg

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