Coordination-induced axial chirality controls the metal-centred configuration in a stereogenic-at-iron catalyst.

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chemical Communications Pub Date : 2025-01-23 DOI:10.1039/d4cc06227b
Benedikt Buchberger, Nemrud Demirel, Xiulan Xie, Sergei I Ivlev, Eric Meggers
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引用次数: 0

Abstract

A new approach is introduced to control the metal-centred configuration of stereogenic-at-iron catalysts by utilizing axial ligand chirality, which becomes locked upon metal coordination. This strategy is applied to an iron catalyst containing two chelating N-(2-pyridyl)-substituted triazol-5-ylidene mesoionic carbenes (MICs) resulting in a helical topology with a stereogenic iron centre.

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配位诱导的轴向手性控制了立体铁催化剂的金属中心构型。
介绍了一种利用轴向配体手性控制金属中心构型的新方法,该方法被金属配位锁定。该策略应用于含有两个螯合N-(2-吡啶基)取代三唑-5-酰基介离子羰基(MICs)的铁催化剂,产生具有立体性铁中心的螺旋拓扑结构。
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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
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