TY - JOUR
T1 - Highly efficient additive-free dehydrogenation of neat formic acid
AU - Kar, Sayan
AU - Rauch, Michael
AU - Leitus, Gregory
AU - Ben-David, Yehoshoa
AU - Milstein, David
N1 - Funding Information:
This research was supported by the European Research Council (ERC AdG 692775). D.M. holds the Israel Matz Professorial Chair of Organic Chemistry. S.K. acknowledges the Sustainability and Energy Research Initiative (SAERI) of the Weizmann Institute of Science for a research fellowship. M.R. acknowledges the Zuckerman STEM Leadership Program for a research fellowship. S.K. thanks M. Montag for useful discussions and for carefully proofreading the manuscript. M.R. thanks N. von Wolff and M. Iron for computational assistance and helpful discussions.
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2021/3
Y1 - 2021/3
N2 - Formic acid (FA) is a promising hydrogen carrier that can play an instrumental role in the overall implementation of a hydrogen economy. In this regard, it is important to generate H2 gas from neat FA without any solvent and/or additive, for which existing systems are scarce. Here we report the remarkable catalytic activity of a ruthenium 9H-acridine pincer complex for this process. The catalyst is unusually stable and robust in FA, even at high temperatures, and can catalyse neat FA dehydrogenation for over a month, with a total turnover number of 1,701,150. It can also generate high H2/CO2 gas pressures from neat FA (tested up to 100 bars). Mechanistic investigations and density functional theory studies are conducted to fully understand the molecular mechanism of the process. Overall, the high activity, stability, selectivity, simplicity and versatility of the system to generate a CO-free H2/CO2 gas stream and high pressure from neat FA makes it promising for large-scale implementation. [Figure not available: see fulltext.].
AB - Formic acid (FA) is a promising hydrogen carrier that can play an instrumental role in the overall implementation of a hydrogen economy. In this regard, it is important to generate H2 gas from neat FA without any solvent and/or additive, for which existing systems are scarce. Here we report the remarkable catalytic activity of a ruthenium 9H-acridine pincer complex for this process. The catalyst is unusually stable and robust in FA, even at high temperatures, and can catalyse neat FA dehydrogenation for over a month, with a total turnover number of 1,701,150. It can also generate high H2/CO2 gas pressures from neat FA (tested up to 100 bars). Mechanistic investigations and density functional theory studies are conducted to fully understand the molecular mechanism of the process. Overall, the high activity, stability, selectivity, simplicity and versatility of the system to generate a CO-free H2/CO2 gas stream and high pressure from neat FA makes it promising for large-scale implementation. [Figure not available: see fulltext.].
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U2 - 10.1038/s41929-021-00575-4
DO - 10.1038/s41929-021-00575-4
M3 - Article
AN - SCOPUS:85101189687
VL - 4
SP - 193
EP - 201
JO - Nature Catalysis
JF - Nature Catalysis
SN - 2520-1158
IS - 3
ER -