Frontispiz: CO2 Reduction at a Borane-Modified Iron Complex: A Secondary Coordination Sphere Strategy

Connor S. Durfy, Joseph A. Zurakowski, Dr. Marcus W. Drover
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Abstract

Bifunctional complex design can enable selective activation of the strong C=O bonds in CO2. Much like a fiddler crab, the {Fe-H/Cp*-BCy2} complex employed by Marcus W. Drover and co-workers in their Research Article (e202421599), features two distinct "claws". This study highlights that cooperativity between the iron hydride and pendant Lewis acidic borane is integral to facilitate the reduction of CO2 to a C1 product.

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双功能复合物设计可以选择性地激活二氧化碳中的强 C=O 键。Marcus W. Drover 及其合作者在其研究文章(e202421599)中采用的{Fe-H/Cp*-BCy2}复合物就像大闸蟹一样,具有两个不同的 "爪子"。这项研究强调,铁氢化物与悬挂的路易斯酸硼烷之间的合作性是促进 CO2 还原成 C1 产物不可或缺的因素。
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来源期刊
Angewandte Chemie
Angewandte Chemie 化学科学, 有机化学, 有机合成
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审稿时长
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期刊最新文献
Frontispiz: Rapid N2O Formation from N2 on Water Droplet Surfaces Frontispiz: CO2 Reduction at a Borane-Modified Iron Complex: A Secondary Coordination Sphere Strategy Frontispiz: Chemical Synthesis of ~1 nm Multilevel Capacitor-like Particles with Atomic Precision Frontispiz: Divergent Activity Shifts of Tin-Based Catalysts for Electrochemical CO2 Reduction: pH-Dependent Behavior of Single-Atom Versus Polyatomic Structures Rücktitelbild: Air-Mediated Biomimetic Synthesis of Polyhydroxyalkanoate with C4 Diol (Angew. Chem. 8/2025)
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