Charge transfer interaction in the acetic acid-benzene cation complex

Geometrical and electronic structures of the acetic acid-benzene cation com plex, (CH3COOH). (C6H6)(+), are studied experimentally and theoretically. E xperimentally, a vibrational spectrum of (CH3COOH). (C6H6)(+) in the supers onic jet is measured in the 3000-3680 cm(-1) region using an ion-trap photo dissociation spectrometer. An electronic spectrum is also observed with thi s spectrometer in the 12 000-29 600 cm(-1) region. Theoretically, ab initio molecular orbital calculations are performed for geometry optimization and evaluation of vibrational frequencies and electronic transition energies. The vibrational spectrum shows two distinct bands in the O-H stretching vib rational region. The frequency of the strong band (3577 cm(-1)) is close to that of the O-H stretching vibration of acetic acid and the weak one is lo cated at 3617 cm(-1). On the basis of geometry optimizations and frequency calculations, the strong band is assigned to the O-H stretching vibration o f the cis-isomer of acetic acid in the hydrogen-bonded complex (horizontal cis-isomer). The weak one is assigned to the vertical trans-isomer where th e trans-isomer of acetic acid interacts with the pi -electron system of the benzene cation. The weakness of the high frequency band in the photodissoc iation spectrum is attributed to the binding energy larger than the photon energy injected. Only hot vertical trans-isomers can be dissociated by the IR excitation. The electronic spectrum exhibits two bands with intensity ma xima at 17 500 cm(-1) and 24 500 cm(-1). The calculations of electronic exc itation energies and oscillator strengths suggest that charge transfer band s of the vertical trans-isomer can be observed in this region in addition t o a local excitation band of the horizontal cis-isomer. We assign the 17 50 0 cm(-1) band to the charge transfer transition of the vertical trans-isome r and the 24 500 cm(-1) band to the pi-pi transition of the horizontal cis- isomer. The calculations also suggest that the charge transfer is induced t hrough the intermolecular C . . .O=C bond formed between a carbon atom of b enzene and the carbonyl oxygen atom of acetic acid. (C) 2001 American Insti tute of Physics.