Study of cationic N-isopropylacrylamide-styrene copolymer latex particles using fluorescent probes

• Autor(a) principal: Castanheira, Elisabete M. S.
• Data de Publicação: 1999
• Outros Autores: Martinho, J. M.G., Duracher, D., Charreyre, M. T., Elaïssari, A., Pichot, C.
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
• Texto Completo: http://hdl.handle.net/1822/63058

Monodisperse cationically charged core-shell poly[styrene/N-isopropylacrylamide] latexes, differing in their shell structure, were studied at temperatures around the lower critical solution temperature (LCST) of poly[N-isopropylacrylamide]. Near the LCST, a transition on the latex dimensions was observed by quasi-elastic light scattering measurements. The same transition could also be detected using the intensity ratio of the pyrene fluorescence vibronic bands, I1/I3, and the excimer to monomer fluorescence intensity ratio of 1,10-bis(1-pyrenyl)decane. The fluorescence spectra and decay curve measurements of 1,10-bis-(1-pyrenyl)decane provided a better understanding of both the hydrophilic-hydrophobic variation and the conformational changes occurring in the poly[N-isopropylacrylamide] shell of the latex particles upon temperature variation.