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Amino acids based on 2,4,5-triarylimidazoles: synthesis and evaluation as new chemosensors for ion recognition

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Detalhes bibliográficos
Resumo:N-tert-butyloxycarbonyl-4-formylphenylalanine methyl ester and appropriate heterocyclic diones were used in the synthesis of novel fluorescent unnatural amino acids, namely 2,4,5-triarylimidazolyl-alanines. These new compounds were fully characterised by the usual spectroscopic techniques, such as IR and NMR. The photophysical properties of the amino acids were evaluated by UV-Vis absorption and fluorescence spectroscopy in solvents of different character. Interaction studies with biologically and analytically important ions such as F-, OH-, Cu2+ and Fe3+, through spectrophotometric and spectrofluorimetric titrations were carried out to assess their potential as chemosensors.
Autores principais:Esteves, Cátia I. C.
Outros Autores:Raposo, M. Manuela M.; Costa, Susana P. G.
Assunto:2,4,5-triarylimidazoles Unnatural amino acids Chemosensors Fluorescence
Ano:2013
País:Portugal
Tipo de documento:comunicação em conferência
Tipo de acesso:acesso aberto
Instituição associada:Universidade do Minho
Idioma:inglês
Origem:RepositóriUM - Universidade do Minho
Descrição
Resumo:N-tert-butyloxycarbonyl-4-formylphenylalanine methyl ester and appropriate heterocyclic diones were used in the synthesis of novel fluorescent unnatural amino acids, namely 2,4,5-triarylimidazolyl-alanines. These new compounds were fully characterised by the usual spectroscopic techniques, such as IR and NMR. The photophysical properties of the amino acids were evaluated by UV-Vis absorption and fluorescence spectroscopy in solvents of different character. Interaction studies with biologically and analytically important ions such as F-, OH-, Cu2+ and Fe3+, through spectrophotometric and spectrofluorimetric titrations were carried out to assess their potential as chemosensors.