Protic NNN and NCN Pincer‐Type Ruthenium Complexes Featuring (Trifluoromethyl)pyrazole Arms: Synthesis and Application to Catalytic Hydrogen Evolution from Formic Acid |
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| Authors: | Yoshiko Nakahara Tatsuro Toda Prof Dr Asuka Matsunami Prof Dr Yoshihito Kayaki Prof Dr Shigeki Kuwata |
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| Institution: | 1. Department of Chemical Science and Engineering, School of Materials and Chemical Technology, Tokyo Institute of Technology, Tokyo, Japan;2. Present address: Department of Chemistry and Biological Science, College of Science and Engineering, Aoyama Gakuin University, Sagamihara, Japan;3. PRESTO Japan Science and Technology Agency (JST), Saitama, Japan |
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| Abstract: | NNN and NCN pincer‐type ruthenium(II) complexes featuring two protic pyrazol‐3‐yl arms with a trifluoromethyl (CF3) group at the 5‐position were synthesized and structurally characterized to evaluate the impact of the substitution on the properties and catalysis. The increased Brønsted acidity by the highly electron‐withdrawing CF3 pendants was demonstrated by protonation–deprotonation experiments. By contrast, the IR spectra of the carbonyl derivatives as well as the cyclic voltammogram indicated that the electron density of the ruthenium atom is negligibly influenced by the CF3 group. Catalysis of these complexes in the decomposition of formic acid to dihydrogen and carbon dioxide was also examined. The NNN pincer‐type complex 1 a with the CF3 group exhibited a higher catalytic activity than the tBu‐substituted analogue 1 b . In addition, the bis(CF3‐pyrazolato) ammine derivative 4 catalyzed the reaction even in the absence of base additives. |
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| Keywords: | dehydrogenation homogeneous catalysis N ligands ruthenium tridentate ligands |
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