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Palladium on Polydopamine: Its True Potential in Catalytic Transfer Hydrogenations and Heck Coupling Reactions
Author(s) -
Kunfi Attila,
Szabó Vivien,
Mastalir Ágnes,
Bucsi Imre,
Mohai Miklós,
Németh Péter,
Bertóti Imre,
London Gábor
Publication year - 2017
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.201700609
Subject(s) - catalysis , heck reaction , chemistry , transfer hydrogenation , palladium , aldehyde , nitro , coupling reaction , leaching (pedology) , heterogeneous catalysis , organic chemistry , combinatorial chemistry , photochemistry , ruthenium , alkyl , soil science , soil water , environmental science
The application of Pd–polydopamine and magnetic Fe 3 O 4 @Pd–polydopamine catalysts in catalytic transfer hydrogenation reactions and the Heck arylation is reported. The reduction of a wide range of aromatic nitro‐compounds bearing both electron‐donating and ‐withdrawing substituents to the corresponding anilines could be efficiently performed, although the reduction of carbonyl compounds was found to be less general. In the latter case, only aromatic ketones could be reduced to the corresponding alcohols, whereas aldehyde substrates were unaffected, which may be owing to their reaction with the catalyst support leading to catalyst deactivation. By using magnetic Fe 3 O 4 @Pd–polydopamine system, facilitated catalyst recovery and reuse for five consecutive cycles without considerable loss of activity in nitro‐group reduction. The efficiency of the catalyst in Heck reactions was comparable to that in transfer hydrogenation, however, no catalytic activity was observed upon reuse in this case, likely as a result of metal leaching. We also explored tandem Heck reaction/catalytic transfer hydrogenation sequences, however, the two reactions showed limited compatibility under the applied conditions.