Cyclic oligothiophenes: Novel organic materials and models for polythiophene. A theoretical study

Sanjio S. Zade, Michael Bendikov

Research output: Contribution to journalArticle

56 Citations (Scopus)

Abstract

Cyclic oligothiophenes (CnT, n = 6-30, even only) in syn- and anti-conformations are studied theoretically at the B3LYP/6-31G(d) level of theory. Strain energies, ionization potentials, HOMO-LUMO gaps, bond length alternations, NICS values, and IR and Raman spectra have been studied. The properties of anti-conformers change systematically with increasing ring size and were studied in detail in neutral, radical cation, and dication forms. In syn-conformation, the oligomers lose their nearly planar ring shape and bend significantly for n > 14, and thus properties cannot be related to ring size. The HOMO-LUMO gap in C14T-syn is even lower than polythiopehene. IR and Raman spectra calculated at the B3LYP/6-31G(d) level are used to differentiate syn- from anti-conformations. The properties of cyclic oligomers are compared to those of the linear system, and cyclic oligothiophenes are revealed as good models for polythiophene. To assist the experimental study of known cyclic oligomers having dibutyl substituents on alternate thiophene rings, the corresponding dimethyl-substituted oligomers are also studied. The experimentally evaluated HOMO-LUMO gaps for alternately dibutyl-substituted cyclic oligomers match the calculated values; however, they are significantly higher than those of the unsubstituted analogues.

Original languageEnglish
Pages (from-to)2972-2981
Number of pages10
JournalJournal of Organic Chemistry
Volume71
Issue number8
DOIs
Publication statusPublished - Apr 14 2006

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Oligomers
Conformations
Raman scattering
Thiophenes
Ionization potential
Bond length
Strain energy
Linear systems
Cations
polythiophene

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Cyclic oligothiophenes : Novel organic materials and models for polythiophene. A theoretical study. / Zade, Sanjio S.; Bendikov, Michael.

In: Journal of Organic Chemistry, Vol. 71, No. 8, 14.04.2006, p. 2972-2981.

Research output: Contribution to journalArticle

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