4.5 Article

Picosecond Dynamics of Dimer Formation in a Pyrene Labeled Polymer

期刊

JOURNAL OF PHYSICAL CHEMISTRY B
卷 114, 期 39, 页码 12439-12447

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jp1020214

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资金

  1. Portuguese Science Foundation (FCT) [SFRH/BPD/47181/2008, SFRH/BPD/25269/2005]
  2. Fundação para a Ciência e a Tecnologia [SFRH/BPD/47181/2008] Funding Source: FCT

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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.

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