Artigo Revisado por pares

Excitation energies of terthiophene and its dioxide derivative: a first-principles study

2001; Elsevier BV; Volume: 339; Issue: 5-6 Linguagem: Inglês

10.1016/s0009-2614(01)00332-3

ISSN

1873-4448

Autores

Fabio Della Sala, Habbo Hait Heinze, Andreas Görling,

Tópico(s)

Free Radicals and Antioxidants

Resumo

The excitation spectra of terthiophene and terthiophene-S,S-dioxide are investigated by time-dependent density-functional theory (TD-DFT) calculated data are compared with recent experimental results. The second singlet–triplet excitation energy (T2) is calculated above the first singlet–singlet (S1) one. In terthiophene-S,S-dioxide the formation of a bonding interaction in the lowest unoccupied molecular orbital decreases its kinetic energy and explains the red-shift of the excitation spectrum. The inter-system crossing (ISC) rate in terthiophene-S,S-dioxide is expected to be lower than in terthiophene due to the increased T2–S1 energy gap, which is also found to not decrease with inter-ring torsion as in terthiophene.

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