Flash Communication: Ligand Centered Cooperative O–H Bond Splitting by a Mo(CO)5(phosphine) Complex

IF 2.9 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Organometallics Pub Date : 2025-01-22 DOI:10.1021/acs.organomet.4c00507
Sotirios Pavlidis,  and , Josh Abbenseth*, 
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引用次数: 0

Abstract

The synthesis and reactivity of a molybdenum carbonyl complex ligated by geometrically constrained phosphorus trisamide are reported. Reaction with potassium tert-butoxide or methanol triggers ligand-centered substrate activation, leading to planarization of the phosphine donor ligand. P–O bond formation, decarbonylation, and insertion of the molybdenum center into a ligand P–N bond result in the formation of molybdenum tetracarbonyl complexes ligated by rigid N,P-chelate ligands.

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闪光通讯:Mo(CO)5(膦)配合物以配体为中心的协同o -氢键分裂
本文报道了一种由几何约束三胺磷连接的钼羰基配合物的合成及其反应性。与叔丁二氧化钾或甲醇反应触发配体中心底物活化,导致磷化氢供体配体平面化。P-O键的形成、脱羰基化和钼中心插入配体P-N键,形成由刚性N、p螯合配体连接的钼四羰基配合物。
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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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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