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多孔配位聚合物的微孔对 Ru 配合物催化 CO 还原产物选择性的影响。

Effect of Micropores of a Porous Coordination Polymer on the Product Selectivity in Ru Complex-catalyzed CO Reduction.

机构信息

Institute for Integrated Cell-Material Sciences (KUIAS/iCeMS), Kyoto University, Yoshida Ushinomiyacho, Sakyo-Ku, Kyoto, 606-8501, Japan.

Department of Chemistry, Graduate School of Science, Osaka City University, Sumiyoshi-Ku, Osaka, 558-8585, Japan.

出版信息

Chem Asian J. 2021 Nov 2;16(21):3341-3344. doi: 10.1002/asia.202100813. Epub 2021 Sep 22.

Abstract

To develop an efficient CO2 reduction catalyst, hybridizing a molecular catalyst and a porous coordination polymer (PCP) is a promising strategy because it can combine both advantages of the precise reactivity control of the former and the CO2 adsorption property of the latter. Although several PCP hybrid catalysts have been reported to date, the CO2 sorption behavior and the CO2 reduction reactivity have been investigated separately, and the CO2 enrichment during the catalysis is still unclear. We report CO2 photoreduction under different temperatures and pressures using a PCP-RuII complex hybrid catalyst. The product selectivity (CO or HCOOH) varied depending on the reaction conditions. The altered selectivity could be interpreted in terms of the CO2 capture in the micropores of a PCP.

摘要

为了开发高效的 CO2 还原催化剂,将分子催化剂和多孔配位聚合物(PCP)进行杂交是一种很有前途的策略,因为它可以结合前者的精确反应性控制和后者的 CO2 吸附性能的优势。尽管迄今为止已经报道了几种 PCP 混合催化剂,但 CO2 的吸附行为和 CO2 还原反应性是分别进行研究的,并且在催化过程中 CO2 的富集情况尚不清楚。我们使用 PCP-RuII 配合物混合催化剂在不同温度和压力下报道了 CO2 的光还原。产物选择性(CO 或 HCOOH)取决于反应条件而变化。可以根据 PCP 微孔中 CO2 的捕获来解释选择性的变化。

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