Mujahed Shrouq, Hey-Hawkins Evamarie, Gelman Dmitri
Institute of Chemistry, Edmond J. Safra Campus, The Hebrew University of Jerusalem, Jerusalem, 9190401, Israel.
Faculty of Chemistry and Mineralogy, Institute of Inorganic Chemistry, Leipzig University, Johannisallee 29, 04103, Leipzig, Germany.
Chemistry. 2022 Jul 6;28(38):e202201098. doi: 10.1002/chem.202201098. Epub 2022 Jun 21.
Low-valent metals traditionally dominate the domain of catalytic hydrogenation. However, metal-ligand cooperating (MLC) catalytic systems, operating through heterolytic H-H bond splitting by a Lewis acidic metal and a basic ligand site, do not require an electron-rich metal. On the contrary, high-valent metals that induce weaker back donation facilitate heterolytic bond activation. Here we report, for the first time, the efficient hydrogenation of carbonyl and carboxyl compounds under molecular hydrogen catalyzed by a structurally well-defined Ru catalyst bearing a bifunctional PCP pincer ligand. The catalyst exhibits reactivity toward molecular hydrogen superior to that of the low-valent analog and allows hydrogen activation even at room temperature.
传统上,低价金属主导着催化氢化领域。然而,通过路易斯酸性金属和碱性配位点进行异裂H-H键断裂来运行的金属-配体协同(MLC)催化体系并不需要富电子金属。相反,能引起较弱反馈作用的高价金属有利于异裂键活化。在此,我们首次报道了在分子氢存在下,由带有双功能PCP钳形配体的结构明确的Ru催化剂催化羰基和羧基化合物的高效氢化反应。该催化剂对分子氢的反应活性优于低价类似物,甚至在室温下也能实现氢活化。