Photolytic release of bioactive carboxylic acids from fused pyran conjugates. (January 2018)

• Record Type: Journal Article
• Authors: Conceição, Rafaela; Hungerford, Graham; Costa, Susana P.G.; Gonçalves, M. Sameiro T.
• Is Part Of: Dyes and pigments. Volume 148(2018)
• Page Start: 368
• Page End: 379
• Publication Date: 2018-01
• Subjects: Phototriggers -- Caging groups -- Neurotransmitters -- Coumarins -- Photolysis; Dyes and dyeing -- Periodicals; Pigments -- Periodicals; 667.2
• DOI: 10.1016/j.dyepig.2017.09.023
• Languages: English
• ISSNs: 0143-7208

Abstract

Abstract: New ester cages bearing the coumarin (2 H -benzopyran-2-one) skeleton with extended π-systems as phototriggers, for glycine and β-alanine, as models of carboxylic acid bifunctional molecules with biological relevance, were evaluated under photolysis conditions at 254, 300, 350 and 419 nm of irradiation in a RPR-100 photochemical reactor. The processes were followed by HPLC-UV detection and 1 H NMR with collection of kinetic data. The results showed a correlation between the photolysis efficiency and the increasing extension of the conjugation for both glycine and β-alanine, showing that the 7-aminocoumarin afforded the best results at all wavelengths tested. From a study of the time-resolved fluorescence behaviour, these compounds were also found to exhibit more complex fluorescence decay kinetics. This was attributed to the presence of conjugated and non-conjugated coumarin species. Graphical abstract: Highlights: Coumarins with amino and aryl substituents were synthesized and used in the derivatization of glycine and β-alanine. The new ester cages, as models of carboxylic acid bioactive molecules, revealed to be interesting photo-responsive units. A remarkable behaviour towards irradiation at higher wavelengths occurred in conjugates bearing the styryl-coumarin. Time-resolved fluorescence studies revealed different fluorescing species by the determination of decay associated spectra. This study shows new promising alternative moieties for the development of photoactivable fluorescent acid prodrugs.