James Kegere, Shaikha S. Alneyadi, Alejandro Perez Paz, Lamia A. Siddig, Afra Alblooshi, Mohamed A. Alnaqbi, Ahmed Alzamly and Yaser E. Greish
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引用次数: 0
摘要
大气中二氧化碳含量的升高一直是环境科学家关注的主要问题。捕获二氧化碳气体并随后将其转化为有用的有机化合物,是过去十年中被广泛研究的途径之一。二氧化碳的光催化环加成法是有效捕获二氧化碳并生产环碳酸盐等高附加值化学品的一种很有前景的方法。MOF-901 是一种钛基金属有机框架,具有六角形层和亚胺链节,本研究利用 Oxone 成功地将其氧化为含有酰胺链节的 MOF-997。这两种 MOF 在温和的条件下(包括适度的温度和可见光照射),在 CO2 环加成反应中都表现出了显著的光催化活性。尤其值得一提的是,MOF-997 在供体-受体活性位点方面表现出卓越的性能,在溶剂条件下催化环氧苯乙烯到碳酸苯乙烯的 CO2 转化率达到 99.9%。
Titanium metal–organic frameworks for photocatalytic CO2 conversion through a cycloaddition reaction†
The elevated levels of CO2 in the atmosphere have been a major concern for environmental scientists. Capturing CO2 gas and its subsequent conversion to useful organic compounds is one of the avenues that have been extensively studied in the last decade. The photocatalytic cycloaddition of CO2 is a promising approach for effective CO2 capture and the production of value-added chemicals such as cyclic carbonates. MOF-901, a titanium-based metal–organic framework with hexagonal layers and imine linkages, was successfully oxidized in this study to MOF-997, incorporating amide linkages using Oxone. Both MOFs displayed remarkable photocatalytic activity in CO2 cycloaddition under mild conditions, including moderate temperatures and visible light exposure. Particularly noteworthy is MOF-997, exhibiting superior performance with donor–acceptor active sites, achieving a 99.9% yield in catalyzing CO2 conversion from styrene epoxide to styrene carbonate under solvent conditions.