4.7 Article

Lead-Decorated Titanium Oxide Compound with a High Performance in Catalytic CO2 Insertion to Epoxides

Journal

INORGANIC CHEMISTRY
Volume 62, Issue 5, Pages 1901-1910

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.2c01315

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A high-nuclearity titanium oxide cluster (TOC) with main-group element Pb2+ was synthesized and showed high catalytic activities for CO2 cycloaddition under visible-light irradiation. The cluster not only helps reduce greenhouse gas emissions, but also produces valuable industrial materials. The study demonstrates the potential of heterometal-decorated TOCs in cost-effective and efficient CO2 capture and storage.
The CO2 cycloaddition to epoxides is an efficient method for CO2 capture and storage, important not only for reducing greenhouse gas emission but also for producing cyclic carbonates, which are valuable industrial materials. In this study, we report a novel high-nuclearity titanium oxide cluster (TOC) inlayed with main-group element Pb2+, H2Ti16Pb9O24(SA)18(DMF)10(OH2)2 (denoted as 1; SA = salicylate; DMF = N,N-dimethylformamide), which has the property of visible-light absorption and has shown high catalytic activities for cycloadditions of CO2 under visible-light irradiation. The cluster was synthesized in a high yield in a facial solvothermal process. Its structure and electronic structure were characterized by single-crystal X-ray diffraction, density functional theory calculations, and complementary techniques. The cycloaddition reactions were performed under solvent-free conditions. While the catalytic activity due to the Lewis acidity was moderate, visible-light irradiation further folded the reaction rates. The turnover number reached 3400 with a turnover frequency of 120 h-1. Mechanism studies indicated a synergistic effect of the Lewis acidity and photogenerated charge carriers. The performance of 1 in reversible I2 uptake was also investigated. This study demonstrates the high potential of heterometal-decorated TOCs in the cost-effective and efficient CO2 cycloaddition reaction under mild conditions.

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