Wang Lin, Onishi Naoya, Murata Kazuhisa, Hirose Takuji, Muckerman James T, Fujita Etsuko, Himeda Yuichiro
Research Institute of Energy Frontier, Department of Energy and Environment, National Institute of Advanced Industrial Science and Technology, Tsukuba Central 5, 1-1-1 Higashi, Tsukuba, Ibaraki, 305-8565, Japan.
Graduate School of Science and Engineering, Saitama University, 255 Shimo-ohkubo, Sakura-ku, Saitama, Japan.
ChemSusChem. 2017 Mar 22;10(6):1071-1075. doi: 10.1002/cssc.201601437. Epub 2016 Dec 28.
A series of new imidazoline-based iridium complexes has been developed for hydrogenation of CO and dehydrogenation of formic acid. One of the proton-responsive complexes bearing two -OH groups at ortho and para positions on a coordinating pyridine ring (3 b) can catalyze efficiently the chemical fixation of CO and release H under mild conditions in aqueous media without using organic additives/solvents. Notably, hydrogenation of CO can be efficiently carried out under CO and H at atmospheric pressure in basic water by 3 b, achieving a turnover frequency of 106 h and a turnover number of 7280 at 25 °C, which are higher than ever reported. Moreover, highly efficient CO-free hydrogen production from formic acid in aqueous solution employing the same catalyst under mild conditions has been achieved, thus providing a promising potential H -storage system in water.
已开发出一系列基于咪唑啉的新型铱配合物用于一氧化碳的氢化和甲酸的脱氢反应。其中一种质子响应型配合物在配位吡啶环的邻位和对位带有两个 -OH 基团(3 b),在不使用有机添加剂/溶剂的水性介质中,能在温和条件下有效催化一氧化碳的化学固定并释放氢气。值得注意的是,3 b 能在碱性水溶液中于大气压下的一氧化碳和氢气氛围下高效进行一氧化碳的氢化反应,在 25 °C 时实现了 106 h⁻¹ 的周转频率和 7280 的周转数,这比以往报道的都要高。此外,使用相同催化剂在温和条件下已实现了从水溶液中的甲酸高效无一氧化碳制氢,从而为水中有前景的潜在储氢系统提供了可能。