Lv Wen-Rui, Li Rong-Jian, Liu Zhen-Jiang, Jin Yan, Yao Zi-Jian
School of Chemical and Environmental Engineering, Shanghai Institute of Technology, Shanghai 201418, China.
Key Laboratory of Wireless Sensor Network&Communication, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, Shanghai 200050, China.
Inorg Chem. 2021 Jun 7;60(11):8181-8188. doi: 10.1021/acs.inorgchem.1c00820. Epub 2021 May 13.
A series of -coordinate iridium(III) complexes with a half-sandwich motif bearing Schiff base ligands for catalytic hydrogenation of nitro and carbonyl substrates have been synthesized. All iridium complexes showed efficient catalytic activity for the hydrogenation of ketones, aldehydes, and nitro-containing compounds using clean H as reducing reagent. The iridium catalyst displayed the highest TON values of 960 and 950 in the hydrogenation of carbonyl and nitro substrates, respectively. Various types of substrates with different substituted groups afforded corresponding products in excellent yields. All -coordinate iridium(III) complexes - were well characterized by IR, NMR, HRMS, and elemental analysis. The molecular structure of complex was further characterized by single-crystal X-ray determination.
已经合成了一系列具有半夹心结构且带有席夫碱配体的 - 配位铱(III)配合物,用于催化硝基和羰基底物的氢化反应。所有铱配合物在使用纯净氢气作为还原剂时,对酮、醛和含硝基化合物的氢化反应均表现出高效的催化活性。铱催化剂在羰基和硝基底物的氢化反应中分别显示出最高的TON值,分别为960和950。各种具有不同取代基的底物都能以优异的产率得到相应的产物。所有 - 配位铱(III)配合物均通过红外光谱(IR)、核磁共振(NMR)、高分辨质谱(HRMS)和元素分析进行了充分表征。配合物 的分子结构通过单晶X射线测定进一步表征。