Use este identificador para citar ou linkar para este item:
Título : Theoretical spectroscopic studies and identification of metal-citrate (Cd and Pb) complexes by ESI-MS in aqueous solution
Autor: Bertoli, Alexandre C.
Carvalho, Ruy
Freitas, Matheus P.
Ramalho, Teodorico C.
Mancini, Daiana T.
Oliveira, Maria C.
Varennes, Amarílis de
Dias, Ana
Palavras-chave: Cd/Pb complexes
Electrospray ionization mass spectrometry (ESI-MS)
Density functional theory (DFT)
Publicador: Elsevier
Data da publicação: Fev-2015
Referência: BERTOLI, A. C. et al. Theoretical spectroscopic studies and identification of metal-citrate (Cd and Pb) complexes by ESI-MS in aqueous solution. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, [S.l.], v. 137, p. 271-280, Feb. 2015. DOI: 10.1016/j.saa.2014.08.053.
Abstract: The combined use of ESI-MS, FTIR-ATR and theoretical calculations for the determination of metal-citrate (metal = Cd and Pb) structures are reported. Mass spectrometry allowed to determine the stoichiometry 1:1 and 2:1 of the complexes, corroborating the theoretical calculations. The species found in the ratio 2:1 had their molecular structures readjusted, since the deprotonation of citric acid differed from what was simulated. The calculations of thermodynamic stability (ΔH0(aq.)) for the complexes obtained by B3LYP/LANL2DZ were more exoenergetic than those found by PM6. However, for both methods, the stability of the complexes follows a trend, that is, the lowest-energy isomers in PM6 are also the most stable in B3LYP/LANL2DZ. The infrared analysis suggested that carboxyl groups are complexation sites and hydrogen bonds can help in the stability of the complexes. The vibrational frequencies in B3LYP/LANL2DZ had a good correlation with the experimental infrared results.
Idioma: en_US
Aparece nas coleções:DQI - Artigos publicados em periódicos

Arquivos associados a este item:
Não existem arquivos associados a este item.

Os itens no repositório estão protegidos por copyright, com todos os direitos reservados, salvo quando é indicado o contrário.