Solvent effects on electronic properties, geometries and internal rotation barriers of bithiophenes. An ab initio self-consistent reaction field theoretical study

A self-consistent reaction field (SCRF) theoretical model has been used to simulate the average solvent effects on some π-conjugated organic thiophene dimers. Restricted Hartree-Fock molecular orbital calculations, using ab initio basis sets up to 6–31 + G*, are reported on geometries, total energies and rotational barriers of 2,2′-bithiophene, and its 3,3′- and 3,4′-dimethyl derivatives.