New Strategies in Enantioselective Hydrogenation on Supported Transition Metal Catalyst: Effects of Metal Sintering and Support Swelling

Carrara N.R.; Badano J.M.; Mendow G.; Ruiz D.; Vera C.R.; Quiroga M.E.

Abstract

The effect of noble metal catalysts supported on an ionic exchange resin for the enantioselective hydrogenation of ethyl pyruvate to ethyl lactate was studied. High activity and moderate enantioselectivity levels were obtained. Pt was the best enantioselective metallic phase, followed by Pd and Au; Rh was the less enantioselective metallic phase. The effect of the active site was evaluated for the most enantioselective catalyst: 2Pt-WA30 (prefix indicates the metal loading). A novel method for sintering the Pt metal particles by nitriles reduction was used, and a controlled migration of the metal particles to the surface layers was observed. There existed an optimal particle size with maximization of the enantiomeric excess, corresponding to 24 h sintering. The hydrogenation of ethyl pyruvate to ethyl lactate was found to be structure-sensitive and the importance of the metal particle size for the adsorption of the chiral modifier was proved. Two different chirality induction methods were tried for the 2Pt-WA30 catalyst: (i) the addition of the chiral modifier (CM) to the reaction media, or (ii) the modification of the catalyst in a swelling medium prior to the reaction in order to encapsulate CM. Lower activity but higher enantioselectivity levels were obtained with method (ii). Finally, the reuse of the catalysts was also assessed by means of consecutive reaction tests.

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Título según WOS: New Strategies in Enantioselective Hydrogenation on Supported Transition Metal Catalyst: Effects of Metal Sintering and Support Swelling
Título según SCOPUS: New strategies in enantioselective hydrogenation on supported transition metal catalyst: Effects of metal sintering and support swelling
Título de la Revista: JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY
Volumen: 30
Número: 8
Editorial: SOC BRASILEIRA QUIMICA
Fecha de publicación: 2019
Página de inicio: 1678
Página final: 1687
Idioma: English
DOI:

10.21577/0103-5053.20190069

Notas: ISI, SCOPUS