Palladium nanoparticles, generated by hydrogen reduction of Pd acetate, coordinated to a stereocomplexed 2,20-bipyridine end-functionalized poly(lactic acid)-poly(ecaprolactone) copolymer showed enhanced catalytic activity and chemoselectivity for the partial reduction of phenylacetylene compared to the reference system which did not contain the poly(epsilon-caprolactone). The obtained heterogeneous catalyst proved to be recyclable and suitable for selective phenylacetylene hydrogenation to styrene in solution and under solventless conditions.

Palladium nanoparticles supported onto stereocomplexed poly(lactic acid)-poly(epsilon-caprolactone) copolymers for selective partial hydrogenation of phenylacetylene

Oberhauser Werner;Passaglia Elisa;Capozzoli Laura
2017

Abstract

Palladium nanoparticles, generated by hydrogen reduction of Pd acetate, coordinated to a stereocomplexed 2,20-bipyridine end-functionalized poly(lactic acid)-poly(ecaprolactone) copolymer showed enhanced catalytic activity and chemoselectivity for the partial reduction of phenylacetylene compared to the reference system which did not contain the poly(epsilon-caprolactone). The obtained heterogeneous catalyst proved to be recyclable and suitable for selective phenylacetylene hydrogenation to styrene in solution and under solventless conditions.
2017
Istituto di Chimica dei Composti OrganoMetallici - ICCOM -
Palladium Polymer Poly(lactic acid)-poly(ecaprolactone) copolymers Stereocomplex Catalysis Hydrogenation
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/356554
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