钨的 1-氮杂三烯络合物的合成:金属促进二氢吡啶的开环反应

IF 2.5 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Organometallics Pub Date : 2024-04-30 DOI:10.1021/acs.organomet.4c00108
Jonathan D. Dabbs, Megan N. Ericson, Diane A. Dickie and W. Dean Harman*, 
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引用次数: 0

摘要

近一个世纪以来,化学家们一直在探索过渡金属配合物如何影响线性共轭多烯和杂多烯的物理和化学特性。虽然关于高触变性配合物(η4-η6)的研究已经很多,但人们对其 η2 类似物的化学性质却知之甚少。在此,我们介绍了一种通过 6π-azaelectrocyclic dihydropyridine ring-opening 合成 5,6-η2-(1-氮杂三烯)钨配合物的一般方法,这种方法受到 {WTp(NO)(PMe3)} 的 π 基本性质的促进。本研究包括η2-二氢吡啶和η2-1-氮杂三烯络合物的详细光谱和晶体学数据,这两种络合物都是以单一区域异构体和立体异构体的形式制备的。
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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Synthesis of 1-Azatriene Complexes of Tungsten: Metal-Promoted Ring-Opening of Dihydropyridine

For nearly a century, chemists have explored how transition-metal complexes can affect the physical and chemical properties of linear conjugated polyenes and heteropolyenes. While much has been written about higher hapticity complexes (η4–η6), less is known about the chemistry of their η2 analogues. Herein, we describe a general method for synthesizing 5,6-η2-(1-azatriene) tungsten complexes via a 6π-azaelectrocyclic dihydropyridine ring-opening that is promoted by the π-basic nature of {WTp(NO)(PMe3)}. This study includes detailed spectroscopic and crystallographic data for the η2-dihydropyridine and η2-1-azatriene complexes, both of which were prepared as single regio- and stereoisomers.

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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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