Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/107973
Title: Towards mild conditions by predictive catalysis via sterics in the Ru-catalyzed hydrogenation of thioesters
Authors: Tomasini, Michele
Duran, Josep
Simon, Silvia
Azofra, Luis Miguel 
Poater, Albert
UNESCO Clasification: 221001 Catálisis
Keywords: Homogeneous catalysis
Ruthenium catalysis
Thioesters
Reaction mechanisms
Density functional theory (DFT)
Issue Date: 2021
Journal: Molecular Catalysis 
Abstract: The Milstein's reported discovery of hydrogenation of thioesters directly toward thiols and alcohols catalyzed by a Ru-acridine complex has been studied here by DFT calculations to know the origin of the different performance depending on the nature of the substituents. Unveiling the reaction mechanism leads to a deeper understanding of the steric and electronic properties on the nature of the limiting step of the reaction. Steric maps and Conceptual DFT have been the tools to rationalize the reactivity patterns. In addition, the nature of the catalyst has been studied, replacing the substituents on the phosphorous atoms by less sterically demanding groups with the aim to move to milder reaction conditions.
URI: http://hdl.handle.net/10553/107973
ISSN: 2468-8231
DOI: 10.1016/j.mcat.2021.111692
Source: Molecular Catalysis [ISSN 2468-8231], v. 510, 111692 (junio 2021)
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