Thin solid films of 14 sexithiophenes variously substituted at the terminal R,?-positions were electrochemically deposited on electrodes by anodic coupling of the corresponding half-capped terthiophenes. Sexithiophene films were investigated by cyclic voltammetry, EQCM, in situ ESR, and in situ conductivity. Reversible oxidation is composed by two separate one-electron steps, the first of which is split into two 0.5-electron steps for most 3,4-ethylenedioxy-substituted terthiophenes. ESR indicates strong magnetic dimerization for the one-electron oxidized species. Conductivity (in the range 10-4- 10-1 S cm-1) is redox type and develops at the neutral-cation (neutral-polaron) and cation-dication (polaron-bipolaron) levels with values 5-10 times higher for the latter. The influence of steric, electron donor-acceptor, and conjugative effects on conductivity was evaluated by a suitable choice of endcapping substituents.

Electrochemical, magnetic, and electrical properties of a,w-capped sexithiohene films. 1. Neutral-polaron and polaron-bipolaron conductivities

Zotti G;Zecchin S;Vercelli B;Berlin A;
2005

Abstract

Thin solid films of 14 sexithiophenes variously substituted at the terminal R,?-positions were electrochemically deposited on electrodes by anodic coupling of the corresponding half-capped terthiophenes. Sexithiophene films were investigated by cyclic voltammetry, EQCM, in situ ESR, and in situ conductivity. Reversible oxidation is composed by two separate one-electron steps, the first of which is split into two 0.5-electron steps for most 3,4-ethylenedioxy-substituted terthiophenes. ESR indicates strong magnetic dimerization for the one-electron oxidized species. Conductivity (in the range 10-4- 10-1 S cm-1) is redox type and develops at the neutral-cation (neutral-polaron) and cation-dication (polaron-bipolaron) levels with values 5-10 times higher for the latter. The influence of steric, electron donor-acceptor, and conjugative effects on conductivity was evaluated by a suitable choice of endcapping substituents.
2005
Istituto di Chimica della Materia Condensata e di Tecnologie per l'Energia - ICMATE
Istituto di Scienze e Tecnologie Molecolari - ISTM - Sede Milano
Istituto per lo Studio delle Macromolecole - ISMAC - Sede Milano
Oligothiophene
electrochemistry
conductivity
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/29260
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact