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通过钌 - 镍(环胺)配合物的光活化实现二氧化碳还原

Carbon dioxide reduction via light activation of a ruthenium-Ni(cyclam) complex.

作者信息

Herrero Christian, Quaranta Annamaria, El Ghachtouli Sanae, Vauzeilles Boris, Leibl Winfried, Aukauloo Ally

机构信息

Institut de Chimie Moléculaire et des Matériaux d'Orsay, UMR 8182, Univ. Paris-Sud and CNRS, F-91405 Orsay, France.

出版信息

Phys Chem Chem Phys. 2014 Jun 28;16(24):12067-72. doi: 10.1039/c3cp54946a.

Abstract

In this paper we report the synthesis of a chromophore-catalyst assembly designed for the photoreduction of carbon dioxide. The chromophore unit is made up of a ruthenium trisbipyridyl-like unit covalently attached to a nickel cyclam (cyclam = 1,4,8,11-tetraazacyclotetradecane) via a triazole ring. The intramolecular electron transfer activation of the catalyst unit by visible light was studied by nanosecond flash photolysis and EPR spectroscopy. In aqueous solutions (pH = 6.5), activation of the Ru(II)-Ni(II) modular assembly with 450 nm visible light in the presence of a sacrificial electron donor accomplishes the reduction of CO2 into CO and H2 in a ratio of 2.7 to 1.

摘要

在本文中,我们报道了一种设计用于光还原二氧化碳的发色团-催化剂组件的合成。发色团单元由一个通过三唑环与镍环戊二烯(环戊二烯=1,4,8,11-四氮杂环十四烷)共价连接的三(联吡啶)钌类单元组成。通过纳秒级闪光光解和电子顺磁共振光谱研究了可见光对催化剂单元的分子内电子转移活化作用。在水溶液(pH = 6.5)中,在牺牲电子供体存在的情况下,用450 nm可见光对Ru(II)-Ni(II)模块化组件进行活化,可将CO2还原为CO和H2,其比例为2.7比1。

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