Palladium nanoparticles, generated by hydrogen reduction of Pd acetate, coordinated to a stereocomplexed 2,2′-bipyridine end-functionalized poly(lactic acid)-poly(ε-caprolactone) copolymer showed enhanced catalytic activity and chemoselectivity for the partial reduction of phenylacetylene compared to the reference system which did not contain the poly(ε-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(ε-caprolactone) copolymers for selective partial hydrogenation of phenylacetylene / Frediani, Marco; Oberhauser, Werner; Rosi, Luca; Bartoli, Mattia; Passaglia, Elisa; Capozzoli, Laura. - In: ATTI DELLA ACCADEMIA NAZIONALE DEI LINCEI. RENDICONTI LINCEI. SCIENZE FISICHE E NATURALI. - ISSN 1720-0776. - ELETTRONICO. - 117:(2017), pp. 1-8. [10.1007/s12210-017-0600-8]

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

FREDIANI, MARCO;ROSI, LUCA;BARTOLI, MATTIA;
2017

Abstract

Palladium nanoparticles, generated by hydrogen reduction of Pd acetate, coordinated to a stereocomplexed 2,2′-bipyridine end-functionalized poly(lactic acid)-poly(ε-caprolactone) copolymer showed enhanced catalytic activity and chemoselectivity for the partial reduction of phenylacetylene compared to the reference system which did not contain the poly(ε-caprolactone). The obtained heterogeneous catalyst proved to be recyclable and suitable for selective phenylacetylene hydrogenation to styrene in solution and under solventless conditions.
2017
117
1
8
Frediani, Marco; Oberhauser, Werner; Rosi, Luca; Bartoli, Mattia; Passaglia, Elisa; Capozzoli, Laura
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1075247
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