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用于C-H氧化及CO环加成生成环氧化物的高活性金属间铜基电子化物催化剂。

Intermetallic Copper-Based Electride Catalyst with High Activity for C-H Oxidation and Cycloaddition of CO into Epoxides.

作者信息

Kadam Ravishankar G, Ye Tian-Nan, Zaoralová Dagmar, Medveď Miroslav, Sharma Priti, Lu Yangfan, Zoppellaro Giorgio, Tomanec Ondřej, Otyepka Michal, Zbořil Radek, Hosono Hideo, Gawande Manoj B

机构信息

Regional Centre of Advanced Technologies and Materials, Czech Advanced Technology and Research Institute (CATRIN), Palacký University Olomouc, Šlechtitelů 27, Olomouc, 779 00, Czech Republic.

Frontiers Science Center for Transformative Molecules, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai, 200240, China.

出版信息

Small. 2022 Sep;18(38):e2201712. doi: 10.1002/smll.202201712. Epub 2022 Aug 26.

Abstract

Inorganic electrides have been proved to be efficient hosts for incorporating transition metals, which can effectively act as active sites giving an outstanding catalytic performance. Here, it is demonstrated that a reusable and recyclable (for more than 7 times) copper-based intermetallic electride catalyst (LaCu Si ), in which the Cu sites activated by anionic electrons with low-work function are uniformly dispersed in the lattice framework, shows vast potential for the selective C-H oxidation of industrially important hydrocarbons and cycloaddition of CO with epoxide. This leads to the production of value-added cyclic carbonates under mild reaction conditions. Importantly, the LaCu Si catalyst enables much higher turnover frequencies for the C-H oxidation (up to 25 276 h ) and cycloaddition of CO into epoxide (up to 800 000 h ), thus exceeding most nonnoble as well as noble metal catalysts. Density functional theory investigations have revealed that the LaCu Si catalyst is involved in the conversion of N-hydroxyphthalimide (NHPI) into the phthalimido-N-oxyl (PINO), which then triggers selective abstraction of an H atom from ethylbenzene for the generation of a radical susceptible to further oxygenation in the presence of O .

摘要

无机电子化物已被证明是掺入过渡金属的有效主体,过渡金属可有效充当活性位点,展现出出色的催化性能。在此,研究表明一种可重复使用和循环利用(超过7次)的铜基金属间电子化物催化剂(LaCuSi),其中具有低功函数的阴离子电子激活的铜位点均匀分散在晶格框架中,在工业上重要的烃类的选择性C-H氧化以及CO与环氧化物的环加成反应中显示出巨大潜力。这使得在温和的反应条件下能够生产增值环状碳酸酯。重要的是,LaCuSi催化剂在C-H氧化(高达25276 h⁻¹)和CO与环氧化物的环加成反应(高达800000 h⁻¹)中具有更高的周转频率,从而超过了大多数非贵金属以及贵金属催化剂。密度泛函理论研究表明,LaCuSi催化剂参与了N-羟基邻苯二甲酰亚胺(NHPI)向邻苯二甲酰亚胺-N-氧基(PINO)的转化,然后在O₂存在下引发从乙苯中选择性提取一个H原子,以生成易于进一步氧化的自由基。

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