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Intramolecular hydrogen bonds interactions in the isomers of the bilirubin molecule: DFT and QTAIM analysis

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Autor(es):
Cruz, allefe Barbosa ; de Brito, Livia Gabriela ; Leal, Paulo Vitor Brandao ; Ramos, Welyson Tiano dos Santos ; Pereira, Douglas Henrique
Número total de Autores: 5
Tipo de documento: Artigo Científico
Fonte: Journal of Molecular Modeling; v. 29, n. 10, p. 9-pg., 2023-10-01.
Resumo

Context Bilirubin is an important molecule, used as a marker of some liver diseases, and it can also be toxic and cause jaundice, especially in newborns. The main treatment for neonatal jaundice is phototherapy with blue light, which is still widely studied because the photophysical processes involved are not fully understood. Methods Calculations based on the density functional theory ( DFT) at M062X/6-31G(d,p) level were performed in order to evaluate the structural, electronic, and topological properties of bilirubin isomers. It was found that the ZZ conformation can form a greater number of hydrogen bonds, which gives the isomer greater energy stabilization compared to the other ZE, EZ, and EE isomers, and that the EE isomer is the conformer with the lowest energy of stabilization. The hydrogen bonds were characterized by the quantum theory of atoms in molecules ( QTAIM) and for the ZZ isomer four hydrogen bonds (HBs) were found classified as intermediate, del(2) p(r) > 0, H(r) > 0. The ZE, EZ, and EE isomers show weak HBs, del(2) p(r) > 0, H(r) > 0. (AU)

Processo FAPESP: 13/08293-7 - CECC - Centro de Engenharia e Ciências Computacionais
Beneficiário:Munir Salomao Skaf
Modalidade de apoio: Auxílio à Pesquisa - Centros de Pesquisa, Inovação e Difusão - CEPIDs
Processo FAPESP: 17/11485-6 - Desenvolvimentos computacionais e teóricos baseados em métodos ab initio e na Teoria do Funcional de Densidade
Beneficiário:Rogério Custodio
Modalidade de apoio: Auxílio à Pesquisa - Regular