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An experimental study of the electronic absorption and fluorescence spectral properties of new p-substituted-N-phenylpyrroles and their electrosynthesized polymers

Electronic absorption and fluorescence spectral properties of new p-substituted-N-phenylpyrroles (N-PhPys), including HOPhPy, MeOPhPy, ThPhPy, PhDPy, DPhDPy, PyPhThThPhPy, and their available, electrosynthesized polymers were investigated. Electronic absorption spectra, fluorescence excitation and emission spectra, fluorescence quantum yields (UF) and lifetimes (sF), and other photophysical parameters of these N-PhPy derivatives and their polymers were measured in DMF, DMSO diluted solutions and/ or solid state at room temperature. The electronic absorption spectra of N-PhPy derivatives and their polymers included one to several bands, located in the 270–395 nm region, according to the p-phenyl substituent electron-donating effect and conjugated heteroaromatic system length. The fluorescence excitation spectra were characterized by one broad main peak, with, in most cases, one (or more) poorly resolved shoulder (s), appearing in the 270–405 nm region, and their emission spectra were generally constituted of several bands located in the 330–480 nm region. No significant shift of the absorption, fluorescence excitation and emission spectra wavelengths was found upon going from the monomers to the corresponding polymers. UF values were high, varying between 0.11 and 0.63, according to the nature of substituents(s) and to the conjugated system extension. Fluorescence decays were mono-exponential for the monomers and poly-exponential for PyPhThThPhPy and for polymers. sF values were relatively short (0.35–5.17 ns), and markedly decreased with the electron-donor character of the phenyl group p-substituent and the conjugated system extension.


Auteur(s) : A.K. D. Diaw, D. Gningue-Sall, A. Yassar, J.-C. Brochon, E.Henry, J.-J. Aaron,
Pages : 1107–1114
Année de publication : 2015
Revue : Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy
N° de volume : 135
Type : Article
Statut Editorial : Elsevier B.V.
Mise en ligne par : DIAW Abdou Karim Diagne