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Symmetry lowering in triindoles: Impact on the electronic and photophysical properties

AuthorsRuiz, Constanza ; García-Frutos, Eva M. ; Silva Filho, Demetrio A. da; López Navarrete, Juan T.; Ruiz Delgado, M. Carmen; Gómez-Lor, Berta
Issue Date2014
PublisherAmerican Chemical Society
CitationJournal of Physical Chemistry C 118(10): 5470-5477 (2014)
AbstractThe electronic and photophysical properties of 6,11-dihydro-5H-diindolo[2, 3-a:2′,3′-c]carbazole, an asymmetric cyclic dehydrotrimer of indole, have been explored and compared to its symmetric analogue, 10,15-dihydro-5H- diindolo[3,2-a:3′,2′-c]carbazole (triindole), a well-known high hole mobility semiconductor. To this purpose, we use a joint experimental and theoretical approach that combines absorption and emission spectroscopies, cyclic voltammetry, and spectroelectrochemistry with DFT calculations. Lowering the symmetry of the triindole platform causes a red-shift of the absorption edge and emission maxima and improved the fluorescence quantum yield. Cyclic voltammetry and spectroelectrochemistry reveal the reversible nature of the two observable oxidation processes in the alkylated asymmetric triindoles together with an increase in the stabillity of their oxidized species. On the other hand, the insertion of alkyl groups on the nitrogen atoms results in a further fluorescence enhancement although larger reorganization energies are found. DFT and time-dependent (TD-DFT) calculations successfully support the experimental data and aid in the understanding of the tuning of the physicochemical properties of the triindole platform upon symmetry lowering toward their incorporation in electronic devices. © 2014 American Chemical Society.
Identifiersdoi: 10.1021/jp412129m
e-issn: 1932-7455
issn: 1932-7447
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