双核 Ir(III)双(硫代磷酸)配合物通过不寻常的元-C-H 活化形成的钳形配体

IF 2.5 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Organometallics Pub Date : 2024-05-28 DOI:10.1021/acs.organomet.4c00118
Alexander Linke, Hans-Joachim Drexler and Torsten Beweries*, 
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引用次数: 0

摘要

PC(H)P 钳形配体在晚过渡金属上的氧化加成通常是通过配体 2 位上的 C-H 活化发生的,从而产生 [(PCP)MHX] 型钳形配合物(X = 单阴离子配体)。我们介绍了双核 Ir(III) 复合物 [(iPrPSCSPiPr)Ir(H)(MeCN)2]2[OTf]2的形成,这是钳形配体上元-C-H 活化的一个罕见实例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A Dinuclear Ir(III) Bis(thiophosphinite) Complex Formed by Unusual meta-C–H Activation at a Pincer Ligand

Oxidative addition of PC(H)P pincer ligands at late transition metals typically occurs via C–H activation in the 2-position of the ligand, yielding [(PCP)MHX] type pincer complexes (X = monoanionic ligand). We present formation of the dinuclear Ir(III) complex [(iPrPSCSPiPr)Ir(H)(MeCN)2]2[OTf]2 as a rare example of meta-C–H activation at a pincer ligand.

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来源期刊
Organometallics
Organometallics 化学-无机化学与核化学
CiteScore
5.60
自引率
7.10%
发文量
382
审稿时长
1.7 months
期刊介绍: Organometallics is the flagship journal of organometallic chemistry and records progress in one of the most active fields of science, bridging organic and inorganic chemistry. The journal publishes Articles, Communications, Reviews, and Tutorials (instructional overviews) that depict research on the synthesis, structure, bonding, chemical reactivity, and reaction mechanisms for a variety of applications, including catalyst design and catalytic processes; main-group, transition-metal, and lanthanide and actinide metal chemistry; synthetic aspects of polymer science and materials science; and bioorganometallic chemistry.
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