Synthesis, characterization and catalytic performances of ruthenium-based catalysts for the acceptorless dehydrogenative coupling of butanol


Autoria(s): Bernardi, Andrea
Contribuinte(s)

Nanni, Daniele

Data(s)

27/03/2015

Resumo

A growing interest towards new sources of energy has led in recent years to the development of a new generation of catalysts for alcohol dehydrogenative coupling (ADC). This green, atom-efficient reaction is capable of turning alcohol derivatives into higher value and chemically more attractive ester molecules, and it finds interesting applications in the transformation of the large variety of products deriving from biomass. In the present work, a new series of ruthenium-PNP pincer complexes are investigated for the transformation of 1-butanol, one of the most challenging substrates for this type of reactions, into butyl butyrate, a short-chain symmetrical ester widely used in flavor industries. Since the reaction kinetics depends on hydrogen diffusion, the study aimed at identifying proper reactor type and right catalyst concentration to avoid mass transfer interferences and to get dependable data. A comparison between catalytic activities and productivities has been made to establish the role of the different ligands bonded both to the PNP binder and to the ruthenium metal center, and hence to find the best catalyst for this type of reaction.

Formato

application/pdf

Identificador

http://amslaurea.unibo.it/8521/1/Bernardi_Andrea_Tesi.pdf

Bernardi, Andrea (2015) Synthesis, characterization and catalytic performances of ruthenium-based catalysts for the acceptorless dehydrogenative coupling of butanol. [Laurea magistrale], Università di Bologna, Corso di Studio in Chimica industriale [LM-DM270] <http://amslaurea.unibo.it/view/cds/CDS0884/>

Relação

http://amslaurea.unibo.it/8521/

Direitos

info:eu-repo/semantics/openAccess

Palavras-Chave #dehydrogenative coupling ruthenium catalysts butanol #scuola :: 843899 :: Scienze #cds :: 0884 :: Chimica industriale [LM-DM270] #sessione :: terza
Tipo

PeerReviewed