Abstract
Ab initio complete active space self-consistent field (CASSCF) calculations combined with polarized continuum model (PCM) have been performed to examine the charge transfer (CT) state formation of trans-4-dimethylamino,4'-cyanostilbene (DCS) in a solvent. In a polar solvent, the globally stable geometry in S1 takes a twisted conformation where the electron-donating dimethylanilino group is highly twisted against the other part of the electron-withdrawing 4-cyanostyryl group. In addition, skeletal relaxation where the aromatic benzene rings turn to be a nonaromatic quinoid structure is essential to stabilize the CT state. In a nonpolar solvent, the stable geometry in S1 takes a nontwisted conformation, though the skeletal relaxation is also an essential factor. By means of the free energy decomposition analysis, it is found that the stable CT geometry which depends on solvent polarity mainly comes from two factors: the linkage bond between the dimethylanilino and the 4-cyanostyryl group and the electrostatic interaction. In a polar solvent, the linkage bond has a single bond character to slightly prevent the torsional motion. This twist geometrically assists the charge separation so as to reinforce the electrostatic interaction. In consequence, the twisted internal CT (TICT) conformation is stable. In a nonpolar solvent, on the other hand, a nontwisted CT state is stable because the linkage bonds greatly increase a double bond character so as to prevent the torsional motion, while the electrostatic interaction is not so enhanced even by the geometrical twist.
Published Version
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