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The Kinetic Features of the Palladium‐Catalyzed Hydrogenolysis of Nitriles and Amines
Author(s) -
Yap Aaron J.,
Masters Anthony F.,
Maschmeyer Thomas
Publication year - 2012
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201100472
Subject(s) - hydrogenolysis , benzonitrile , benzylamine , chemistry , catalysis , palladium , organic chemistry
A model of the kinetics underlying the hydrogenolysis of nitriles and amines, catalysed by Pd/C, has been derived. Benzonitrile and benzylamine were used as archetypical compounds to better understand the various reaction pathways involved in these processes. The reaction order under mild conditions (80 °C, 1 bar H 2 ) for the hydrogenolysis of benzylamine was zero order in benzylamine, indicating strong adsorption of benzylamine to the catalyst, whereas the hydrogenation of benzonitrile was found to be first order in benzonitrile, owing to mass transport limitations, explaining the observed selectivities toward hydrogenolysis versus hydrogenation. Significantly, benzylamine itself was found to reversibly poison the hydrogenolysis function of the catalyst, preventing high yields of hydrogenolysis products at low catalyst loadings.