Artigo Revisado por pares

Fluorescence quenching of indolo[3,2-b]carbazole compounds by conformational motions of attached substituents

2016; Elsevier BV; Volume: 133; Linguagem: Inglês

10.1016/j.dyepig.2016.05.040

ISSN

1873-3743

Autores

Simona Streckaitė, Renata Karpicz, Alytis Gruodis, Wim Dehaen, Sven Van Snick, Mindaugas Kirkus, Saulius Grigalevičius, Juozas V. Gražulevičius, Vidmantas Gulbinas,

Tópico(s)

Porphyrin and Phthalocyanine Chemistry

Resumo

The influence of substituents on spectral properties and the excited state relaxation of indolo[3,2-b]carbazole derivatives has been studied by means of steady-state and time-resolved spectroscopy and quantum chemical calculations. Conformational motions of the substituents in solutions were found to cause a significant acceleration of the non-radiative excited state relaxation and concomitant fluorescence quenching of the studied compounds in comparison with their solid films, where the conformational mobility is suppressed. Although the substituents also strongly influence the radiative relaxation rates, these rates are not sensitive to the conformations of the substituents.

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