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Analysis of two novel 1-4 quinolinone structures with bromine and nitrobenzyl ligands.
Michelini, Lidiane J; Vaz, Wesley F; D'Oliveira, Giulio D C; Pérez, Caridad N; Napolitano, Hamilton B.
Afiliação
  • Michelini LJ; Instituto de Química, Universidade Federal de Goiás, Goiânia, GO, Brazil.
  • Vaz WF; Instituto Federal de Ciência, Educação e Tecnologia Goiano, Iporá, GO, Brazil.
  • D'Oliveira GDC; Ciências Exatas e Tecnológicas, Universidade Estadual de Goiás, Anápolis, GO, Brazil.
  • Pérez CN; Instituto de Química, Universidade Federal de Goiás, Goiânia, GO, Brazil.
  • Napolitano HB; Instituto de Química, Universidade Federal de Goiás, Goiânia, GO, Brazil.
J Mol Model ; 25(3): 55, 2019 Feb 08.
Article em En | MEDLINE | ID: mdl-30734868
The scientific community has shown particular interest in the study of quinolinones-a class of bicyclic organic compounds. An example of these compounds are the 4-quinolinones, considered to be very useful building blocks, since they can adapt their molecular structures with different ligands for applications in various fields such as pharmacy, medicine, physics and engineering. The compounds (E)-3-(benzylidene)-2-(3-nitrophenyl)-2,3-dihydro-1-(phenylsulfonyl)-quinolin-4-(1H)-one (NFQ) and (E)-3-(benzylidene)-2-(4-bromophenyl)-2,3-dihydro-1-(phenylsulfonyl) quinolin-4-(1H)-one (BFQ) were synthesized and characterized by infrared spectroscopy, 1H and 13C NMR, and melting point. NFQ crystallized in the orthorhombic Pbca space group while BFQ appears in the monoclinic P21/n space group. X-ray diffraction was used to evaluate their crystallographic structures, and Hirshfeld surface evaluates the intermolecular interactions, supramolecular arrangement and packaging. Theoretical vibrational assignments and calculated electronic properties also demonstrate acceptable agreement between experimental and theoretical results.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Mol Model Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Brasil País de publicação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Mol Model Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Brasil País de publicação: Alemanha