Use este identificador para citar ou linkar para este item: http://repositorio.ufla.br/jspui/handle/1/35324
Título : Structure and bonding in NbX5 X = (F, Cl, Br and I) complexes: a molecular orbital perspective in the C-H bond activation
Autor: Silva, Telles Cardoso
Pires, Maíra dos Santos
Castro, Alexandre Alves de
Lacerda, Lívia Clara Tavares
Rocha, Marcus Vinícius Juliaci
Ramalho, Teodorico Castro
Palavras-chave: Niobium pentahalide complexes
Energy decomposition analysis (EDA)
QTAIM
C-H bond activation
Ligands effects
Niobium complexes
Quantum theory of atoms in molecules (QTAIM)
Publicador: Springer
Data da publicação: Nov-2018
Referência: SILVA, T. C. et al. Structure and bonding in NbX5 X = (F, Cl, Br and I) complexes: a molecular orbital perspective in the C-H bond activation. Theoretical Chemistry Accounts, [S.l], v. 137, p. 146-159, Nov. 2018. DOI: 10.1007/s00214-018-2348-3.
Abstract: In the present work, theoretical studies of the reactivity and stability of the NbX5 complexes (X = F, Cl, Br and I) were carried out in the methane C–H bond activation. To study the chemical bonds formation of these complexes, an energy decomposition analysis was performed together with QTAIM calculations. The main results indicated that the interaction and binding energies are higher for NbF5 in relation to the halogen series. The niobium complexes gaps are influenced by the electronegativity of the halogens and the Nb–X bonding lengths. According to the energy diagram, the electrons less connected to the bond are σNb–I; on the other hand, the best electron acceptor is σ*Nb–F. The QTAIM calculations confirmed stronger Nb–X chemical bonds in NbF5 complexes. Regarding the reactivity of the niobium complexes, the overall results indicate better thermodynamic and kinetic conditions for the NbF5 complex.
URI: https://link.springer.com/article/10.1007/s00214-018-2348-3
http://repositorio.ufla.br/jspui/handle/1/35324
Idioma: en_US
Aparece nas coleções:DQI - Artigos publicados em periódicos

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