CASTEX, M.C.; OLIVERO, C.; PICHLER, G.; ADÈS, D.; CLOUTET, Eric; SIOVE, A.

doi:10.1016/S0379-6779(00)01362-X

Métadonnées

Afficher la notice complète

Licence d’utilisation du document

CASTEX, M.C.
Laboratoire de Physique des Lasers [LPL]

OLIVERO, C.

PICHLER, G.

Langue

Article de revue

Ce document a été publié dans

Synthetic Metals. 2001, vol. 122, n° 1, p. 59-61

Elsevier

Résumé en anglais

Absorption and emission features of various chromophores both in the solid amorphous state and in solution are presented. These 1-(N-ethyl-carbazolyl)-2-substituted-2-cyanovinylene molecules contain in their structure the electron-donor carbazole nucleus and cyanovinylene bearing different acceptor moieties such as either another nitrile function, a methylester, a phenyl, or a para-nitro-phenyl group. It is shown that depending on the strength of the donor–acceptor internal charge transfer, both the absorption and emission spectra are more or less red-shifted. It is found that the methylester derivative displays the best relative photoluminescence efficiency among all the samples. From solvatochromic studies we showed that the remarkable luminescence of the cyanoester derivative can be attributed to a strong dipole moment in the excited state. Furthermore, cyanoester microcrystallites exhibited spectral narrowing which was attributed to an amplified spontaneous emission.< Réduire

Métadonnées

Partager cette publication !

Licence d’utilisation du document

Photoluminescence of donor–acceptor carbazole chromophores

Langue

Ce document a été publié dans

Résumé en anglais

URI

DOI

Origine

Unités de recherche