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: RENDICONTI LINCEI. SCIENZE FISICHE E NATURALI. - ISSN 2037-4631. - STAMPA. - 28:S1(2017), pp. 51-58. [10.1007/s12210-017-0600-8]
Palladium nanoparticles supported onto stereocomplexed poly(lactic acid)-poly(ε-caprolactone) copolymers for selective partial hydrogenation of phenylacetylene
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.Pubblicazioni consigliate
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https://hdl.handle.net/11583/2710234
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