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Boletín de la Sociedad Chilena de Química

versão impressa ISSN 0366-1644

Resumo

BROVELLI, FRANCISCO; DEL VALLE, M. ANGÉLICA; DIAZ, FERNANDO R.  e  CHRISTIAN BERNEDE, J.. Bol. Soc. Chil. Quím. [online]. 2001, vol.46, n.3, pp.219-337. ISSN 0366-1644.  http://dx.doi.org/10.4067/S0366-16442001000300012.

A serie of thiophene derivatives having functional groups of different nature between 2 and 2' ring positions has been synthesized. Through ab-initio calculations using HF 6-31G basis, the geommetry was optimized and the atomic distribution of the electronic densities of each neutral molecules were determined. It was found that the electronic density depends strongly on the nature of the atoms bonded to 2 and 2' ring positions. The electro-oxidation potential of the molecules was measured by cyclic voltammetry on platinum work electrodes. An inverse relation between the electronic density and the potential was found. The electrochemical oxidation of these compounds was irreversible and the voltammetric profiles showed assymetric peaks, which can be explain by the simoultaneous oxidation of the heterocyclic rings and the bridging functional groups

Palavras-chave : electrochemical oxidation; redox potential; thiophene; thiophene derivatives; ab-initio calculations.

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