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将 Pd(I) 非循环物种转化为高效交叉偶联催化剂。

Conversion of Pd(I) off-cycle species into highly efficient cross-coupling catalysts.

机构信息

Department of Chemistry and Center for Sustainable Chemistry, Ghent University, Krijgslaan 281 (S-3), 9000, Ghent, Belgium.

KAUST Catalysis Centre, KCC, King Abdullah University of Science and Technology, Thuwal-23955-6900, Saudi Arabia.

出版信息

Dalton Trans. 2021 Apr 28;50(16):5420-5427. doi: 10.1039/d1dt00929j.

Abstract

We report on the facile conversion of [Pd2(μ-Cl)(μ-η3-R-allyl)(NHC)2] complexes, which are commonly considered undesirable off-cycle species in cross-coupling reactions, into active [PdCl(μ-Cl)(NHC)]2 pre-catalysts. All reactions proceed under mild conditions (40 °C, 1-2 hours in acetone) using inexpensive HCl as both an oxidant and chloride source. DFT calculations were performed to explore the possible mechanism of this transformation, which appears to involve a combination of two different pathways. Moreover this study provides insights into factors favoring and hindering Pd(i) dimer formation undesirable in catalysis.

摘要

我们报告了一种简便的方法,可将通常被认为是交叉偶联反应中不需要的[Pd2(μ-Cl)(μ-η3-R-allyl)(NHC)2]配合物转化为活性[PdCl(μ-Cl)(NHC)]2预催化剂。所有反应均在温和条件下(40°C,在丙酮中 1-2 小时)进行,使用廉价的 HCl 作为氧化剂和氯源。进行了 DFT 计算以探索这种转化的可能机制,该机制似乎涉及两种不同途径的结合。此外,这项研究深入了解了有利于和阻碍在催化中不希望出现的 Pd(i)二聚体形成的因素。

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