Arikawa Yasuhiro, Tabata Itoe, Miura Yukari, Tajiri Hiroki, Seto Yudai, Horiuchi Shinnosuke, Sakuda Eri, Umakoshi Keisuke
Division of Chemistry and Materials Science, Graduate School of Engineering, Nagasaki University, Bunkyo-machi 1-14, Nagasaki, 852-8521, Japan.
Chemistry. 2020 May 4;26(25):5603-5606. doi: 10.1002/chem.201905840. Epub 2020 Apr 15.
Photocatalytic CO reduction using a ruthenium photosensitizer, a sacrificial reagent 1,3-dimethyl-2-(o-hydroxyphenyl)-2,3-dihydro-1H-benzo[d]imidazole (BI(OH)H), and a ruthenium catalyst were carried out. The catalysts contain a pincer ligand, 2,6-bis(alkylimidazol-2-ylidene)pyridine (CNC) and a bipyridine (bpy). The photocatalytic reaction system resulted in HCOOH as a main product (selectivity 70-80 %), with a small amount of CO, and H . Comparative experiments (a coordinated ligand (NCMe vs. CO) and substituents (tBu vs. Me) of the CNC ligand in the catalyst) were performed. The turnover number (TON ) of carbonyl-ligated catalysts are higher than those of acetonitrile-ligated catalysts, and the carbonyl catalyst with the smaller substituents (Me) reached TON =5634 (24 h), which is the best performance among the experiments.
使用钌光敏剂、牺牲试剂1,3-二甲基-2-(邻羟基苯基)-2,3-二氢-1H-苯并[d]咪唑(BI(OH)H)和钌催化剂进行光催化CO还原反应。催化剂包含钳形配体2,6-双(烷基咪唑-2-亚基)吡啶(CNC)和联吡啶(bpy)。光催化反应体系以HCOOH为主要产物(选择性70-80%),伴有少量CO和H。进行了对比实验(催化剂中CNC配体的配位配体(NCMe与CO)和取代基(tBu与Me))。羰基配位催化剂的周转数(TON)高于乙腈配位催化剂,取代基较小(Me)的羰基催化剂达到TON =5634(24小时),这是实验中的最佳性能。