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双核铟配合物协同引发 CO 环氧化物共聚。

Cooperative Initiation in a Dinuclear Indium Complex for CO Epoxide Copolymerization.

机构信息

Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver V6T 1Z1, British Columbia, Canada.

出版信息

Inorg Chem. 2023 Feb 6;62(5):1968-1977. doi: 10.1021/acs.inorgchem.2c03192. Epub 2023 Jan 23.

Abstract

Dinuclear indium complexes have been synthesized and characterized. These include neutral and cationic indium complexes supported by a Schiff base ligand bearing a binaphthol linker. The new compounds were investigated for alternating copolymerization of CO and cyclohexene oxide. In particular, the neutral indium chloride complex (±)-[(ONN)InCl] () showed high conversion of cyclohexene oxide and selectivity for poly(cyclohexene carbonate) formation without cocatalysts at 80 °C under various CO pressures (2-30 bar). Importantly, the reactivity of the dinuclear indium chloride complex is drastically different from that of the mononuclear indium chloride complex (±)-(NNO)InCl (), suggesting a cooperative initiation mechanism involving the two indium centers in .

摘要

双核铟配合物已被合成和表征。这些配合物包括由带有联萘酚连接基的席夫碱配体支撑的中性和阳离子铟配合物。新化合物被用于 CO 和环氧化环己烯的交替共聚研究。特别是,中性氯化铟配合物(±)-(ONN)InCl在 80°C 下在各种 CO 压力(2-30 巴)下无需助催化剂即可实现环氧化环己烯的高转化率和聚(环己烯碳酸酯)的选择性。重要的是,双核氯化铟配合物的反应性与单核氯化铟配合物(±)-(NNO)InCl()截然不同,这表明存在涉及两个铟中心的协同引发机制。

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