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Well-Defined Ir/Pd Complexes with a Triazolyl-diylidene Bridge as Catalysts for Multiple Tandem Reactions

机译:定义明确的Ir / Pd配合物与三唑基-二亚甲基桥作为多级联反应的催化剂

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摘要

The ligand 1,2,4-trimethyl-triazolyl-diylidene has been used for the preparation of a series of three iridium/palladium heterometallic complexes that have been fully characterized. The presence of the two different metals allows tandem processes to be designed by combining reactions that are typically catalyzed by Ir and Pd. Three tandem reactions have been studied: dehalogenation/transfer hydrogenation of haloacetophenones, Suzuki-coupling/transfer hydrogenation of p-bromoacetophenone, and Suzuki-coupling/α-alkylation of p-bromoacetophenone. All three reactions yielded excellent outcomes to the corresponding final products, with the relevant feature that the heterodimetallic complexes are more active than the sum of the corresponding homodimetallic species. All three catalytic reactions reported here constitute unprecedented examples of tandem approaches to complex organic molecules.
机译:配体1,2,4-三甲基-三唑基-二亚甲基已用于制备一系列三种已充分表征的铱/钯杂金属配合物。两种不同金属的存在允许通过组合通常由Ir和Pd催化的反应来设计串联工艺。已研究了三个串联反应:卤代乙酰苯的脱卤/转移氢化,对溴苯乙酮的Suzuki偶联/转移氢化和对溴苯乙酮的Suzuki偶联/α-烷基化。这三个反应均对相应的最终产物产生了优异的结果,其相关特征是异双金属配合物比相应的同双金属物种的总和更具活性。此处报道的所有三个催化反应都构成了复杂有机分子串联方法的空前实例。

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  • 来源
    《Journal of the American Chemical Society》 |2009年第40期|14531-14537|共7页
  • 作者单位

    Departamento de Quimica Inorgdnica y Orgdnica, Universitat Jaume I, Avda. Vicente Sos Baynat s, Castellon, E-12071 Spain;

    Departamento de Quimica Inorgdnica y Orgdnica, Universitat Jaume I, Avda. Vicente Sos Baynat s, Castellon, E-12071 Spain;

    Departamento de Quimica Inorgdnica y Orgdnica, Universitat Jaume I, Avda. Vicente Sos Baynat s, Castellon, E-12071 Spain;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:17:23

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