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Cooperative Initiation in a Dinuclear Indium Complex for CO2 Epoxide Copolymerization

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INORGANIC CHEMISTRY
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AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.2c03192

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Dinuclear indium complexes have been synthesized and characterized. The neutral indium chloride complex [(ONapNiN)InCl2]2 (4) showed high conversion and selectivity for the alternating copolymerization of cyclohexene oxide and CO2. The reactivity of the dinuclear indium chloride complex 4 differs significantly from that of the mononuclear indium chloride complex 5, suggesting a cooperative initiation mechanism involving the two indium centers in 4.
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 CO2 and cyclohexene oxide. In particular, the neutral indium chloride complex (+/-)-[(ONapNiN)InCl2]2 (4) showed high conversion of cyclohexene oxide and selectivity for poly(cyclohexene carbonate) formation without cocatalysts at 80 degrees C under various CO2 pressures (2-30 bar). Importantly, the reactivity of the dinuclear indium chloride complex 4 is drastically different from that of the mononuclear indium chloride complex (+/-)-(NNiOtBu)InCl2 (5), suggesting a cooperative initiation mechanism involving the two indium centers in 4.

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