Title: Amino derivatives of symmetrical 1,3,5-triphenylbenzene - nature of the polar singlet excited-state
Authors: Verbeek, G ×
Depaemelaere, S
Van der Auweraer, Mark
Deschryver, Fc
Vaes, A
Terrell, D
Demeutter, S #
Issue Date: Jan-1993
Publisher: Elsevier science bv
Series Title: Chemical physics vol:176 issue:1 pages:195-213
Abstract: The solvent dependence of the fluorescence spectra of (dialkylamino) and (diarylamino) substituted triphenylbenzene derivatives indicates that the emission occurs from a highly polar excited state. The exponential fluorescence decays, obtained with time correlated single photon timing, suggest that equilibration between the different excited species occurs within the time resolution of the experimental set-up. For 5'-(3-(diethylamino)phenyl)-N,N,N',N'-tetrakisethyl-(1,1': 3,1''-terphenyl)-3,3''-diamine the size of the excited state dipole moment excludes the formation of a TICT state. For (4(bis(4-ethyphenyl)amino)phenyl)-N,N,N',N'-tetrakis(4-ethylphenyl)(1,1':3',1''-terphenyl)-4,4''-diamine the large fluorescent rate constant in polar solvents suggests the formation of a conjugated intramolecular charge transfer state. Only for (4-(diethylamino)phenyl)-N,N,N',N'-tetrakis-ethyl-(1,1':3',1''-terphenyl)-4,4''-diamine the experimental evidence does not allow to exclude either the formation of a TICT state or a delocalized ICT state.
ISSN: 0301-0104
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Molecular Imaging and Photonics
× corresponding author
# (joint) last author

Files in This Item:

There are no files associated with this item.

Request a copy


All items in Lirias are protected by copyright, with all rights reserved.

© Web of science