Journal
CHEMSUSCHEM
Volume 12, Issue 1, Pages 179-184Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.201802275
Keywords
dehydrogenation; energy conversion; hydrogen; iridium; N ligands
Funding
- China Scolarship Council
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The selective dehydrogenation of formic acid by iridium(III) Cp*(dipyridylamine) catalysts is reported. The electron-enriched catalyst [(IrCp)-Cp-III*{(4-dimethylaminopyridin-2-yl-kappa N)(pyridin-2 '-yl-kappa N)amine}(OSO3)] gave the best performances enabling the base free dehydrogenation of aqueous and neat formic acid. In both cases the reaction was selective with no carbon monoxide detectable. The Ir-III complex demonstrated latent behavior, which may be of practical utility. Experimental results suggest an outer-sphere interaction with the ligand.
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