Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/337677
Type: Artigo
Title: A theoretical investigation on the aminolysis of pyromellitic and 1,4,5,8-naphthalenetetracarboxylic dianhydrides
Author: Schneider, Felipe S. S.
Setiadi, Jeffry
Felisberti, Maria Isabel
Vazquez, Pedro A. M.
da Conceicao, Thiago Ferreira
Heinzelmann, Germano
Caramori, Giovanni Finoto
Abstract: Aniline aminolysis reaction of pyromellitic (PMDA) and 1,4,5,8-naphthalenetetracarboxylic (NTDA) dianhydrides is investigated by means of density functional theory (BP86-D3(BJ)/def2-TZVP). The concerted mechanism is shown to be more favorable for both substrates, in comparison to the stepwise one, with the aminolysis of PMDA presenting lower activation energy than the reaction of NTDA. This result is shown to be related to the lower ring tension in NTDA. Solvation also shows significant influence on the kinetics and thermodynamics of these reactions, as determined by two different methods, implicit with the universal solvation model SMD, and explicit with alchemical FEP molecular dynamics simulations. The comparison between SMD and FEP enables us to explore possible inaccuracies on the SMD model, and examine the suitability of the FEP approach as a physics-based method for the calculation of the solvent contribution in different reactions
Subject: Mecanismo de reação
Country: Países Baixos
Editor: Elsevier
Rights: Fechado
Identifier DOI: 10.1016/j.comptc.2018.11.008
Address: https://www.sciencedirect.com/science/article/pii/S2210271X18305905
Date Issue: 2019
Appears in Collections:IQ - Artigos e Outros Documentos

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