Picosecond Dynamics of Dimer Formation in a Pyrene Labeled Polymer

resumo

A commercial poly(acrylic acid) (PAA, M(n) = 450 000 g mol(-1)) has been labeled with high levels (9.1 mol %) of pyretic by reaction with 1-pyrenylmethylamine in the presence of boric acid. The modified polymer was found to display an unusual photophysical behavior closely resembling that found for pyrene in constrained environments. The appearance of a band at longer wavelengths in the excitation spectra when collected at the long wavelength emission band was attributed to the spectra of a dimer. The emission of this dimer was particularly enhanced in dioxane:water solvent mixtures with low dioxane content. From time-resolved fluorescence measurements in the picosecond time domain, two decay components were obtained: a fast. decay (4-10 ps) at short wavelengths, which becomes a rising component at longer wavelengths, and a second exponential (2-4 ns) related to the emission of the relaxed dimer. Time-resolved emission spectra were seen to change with time, revealing the emission contribution of two species. This is one of the first reports where the dynamics of dimer formation in a pyrene derivative have been observed.

palavras-chave

STEADY-STATE FLUORESCENCE; WATER-SOLUBLE POLYMERS; EXCIMER FORMATION; CONFORMATIONAL RELAXATION; POLY(ETHYLENE OXIDE); POLY(ACRYLIC ACID)S; CHAIN DYNAMICS; ASSOCIATION; SPECTROSCOPY; PHOTOPHYSICS

categoria

Chemistry

autores

Costa, T; de Melo, JSS; Castro, CS; Gago, S; Pillinger, M; Goncalves, IS

nossos autores

agradecimentos

Financial support from the Portuguese Science Foundation (FCT) through FEDER and FOCI is acknowledged. T.C. and S.G. thank the FCT for Ph.D. (SFRH/BPD/47181/2008) and postdoctoral (SFRH/BPD/25269/2005) grants, respectively.

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