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氮杂环卡宾催化的P=C键复分解反应

Metathesis of P=C Bonds Catalyzed by N-Heterocyclic Carbenes.

作者信息

Han Zeyu, Gates Derek P

机构信息

Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, BC, V6T 1Z1, Canada.

出版信息

Chemistry. 2021 Oct 21;27(59):14594-14599. doi: 10.1002/chem.202102384. Epub 2021 Sep 21.

Abstract

The catalytic metathesis of C=C bonds is a textbook reaction that has no parallel in the widely studied area of multiple bonds involving heavier p-block elements. A high-yielding P=C bond metathesis of phosphaalkenes (ArP=CPh , Ar=Mes, o-Tol, Ph) has been discovered that is catalyzed by N-heterocyclic carbenes (NHC=Me IMe, Me I Pr). The products are cyclic oligomers formally derived from ArP=PAr [i. e. cyclo-(ArP) ; n=3, 4, 5, 6] and Ph C=CPh . Preliminary mechanistic studies of this remarkable transformation have established NHC=PAr (Ar=Mes, o-Tol, Ph) as key phosphinidene transfer agents. In addition, novel cyclic intermediates, such as, cyclo-(ArP) CPh and cyclo-(ArP) CPh have also been observed. This work represents a rare application of non-metal-based catalysts for transformations involving main-group elements.

摘要

碳 - 碳双键的催化复分解反应是一种常见的教科书式反应,在广泛研究的涉及较重p区元素的多重键领域中尚无类似反应。现已发现,氮杂环卡宾(NHC = Me IMe、Me I Pr)可催化磷亚烯(ArP = CPh,Ar = Mes、o - Tol、Ph)进行高产率的磷 - 碳双键复分解反应。产物是形式上由ArP = PAr [即环 - (ArP)ₙ;n = 3、4、5、6] 和Ph₂C = CPh₂衍生而来的环状低聚物。对这一显著转化的初步机理研究已确定NHC = PAr(Ar = Mes、o - Tol、Ph)为关键的磷烯转移试剂。此外,还观察到了新型环状中间体,如环 - (ArP)₂CPh₂和环 - (ArP)₃CPh₂。这项工作代表了基于非金属的催化剂在涉及主族元素转化中的罕见应用。

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