Cooperative Activation of CO and Pyridine by an Aluminum(I) Complex Ligated with a Silylene-Borane Ligand.

Jinghuang Lv, Xiao Fang, Fanshu Cao, Zhenbo Mo
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Abstract

Cooperative main-group systems based on alumylenes are highly attractive due to their potential for activating and transforming inert chemical bonds and small molecules. However, their development has been hindered by the scarcity of suitable supporting ligands. Herein, we report the synthesis of an amphiphilic carboranyl silylene-borane ligand (1) and demonstrate its effectiveness in stabilizing an aluminum(I) complex 2. Complex 2 has been unambiguously characterized by spectroscopic analysis, X-ray diffraction analysis, and DFT calculations, which reveals a unique structure featuring both silicon(II)→aluminum(I) and aluminum(I)→boron(III) donor-acceptor bonds. The synergistic interplay between the silylene-borane ligand and the aluminum(I) center in 2 drives its unusual reactivity toward CO and pyridine activation, facilitating cleavage of the C≡O bond and dearomatization of pyridine.

硅硼烷配体连接铝(I)配合物对CO和吡啶的协同活化。
基于铝烯的协同主基团体系由于具有激活和转化惰性化学键和小分子的潜力而具有很高的吸引力。然而,由于缺乏合适的配体,它们的发展一直受到阻碍。本文报道了一种两亲性碳硼基硅硼烷配体(1)的合成,并证明了其稳定铝(1)配合物2的有效性。通过光谱分析、x射线衍射分析和DFT计算对配合物2进行了明确的表征,揭示了配合物2具有硅(II)→铝(I)和铝(I)→硼(III)供体-受体键的独特结构。值得注意的是,硅硼烷配体与2中的铝(I)中心之间的协同相互作用驱动了其对CO和吡啶活化的异常反应性,促进了C≡O键的断裂和吡啶的脱芳构化。
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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