TY - JOUR
T1 - Electronic spectrum of anthracene
T2 - An ab-initio molecular orbital calculation combined with a valence bond interpretation
AU - Zilberg, Shmuel
AU - Haas, Yehuda
AU - Shaik, Sason
PY - 1995
Y1 - 1995
N2 - The properties of the two lowest excited singlet states of anthracene, S1(1B1u) and S2(1B2u), and the first triplet state, T1(3B1u), were calculated at the CIS/3-21G level of theory. The main structural changes are described, and the calculated vibrational levels are compared with available experimental data. The assignment of the two-photon observed transition at about 28 000 cm-1 to the S2 state is confirmed, as well as some recent argon matrix vibronic bands (Wolf, J.; Hohlneicher, G. Chem. Phys. 1994, 181, 185). The calculation suggests some changes in the vibrational assignment, and correlation with the ground state vibrational modes shows that one b2u mode undergoes a large frequency increase upon electronic excitation to S2. This change is similar to that observed for Kekulé-type modes of benzene, naphthalene, and their derivatives. It is compatible with the notion that the π electrons of these molecules tend to distort the molecule to a Kekulé structure.
AB - The properties of the two lowest excited singlet states of anthracene, S1(1B1u) and S2(1B2u), and the first triplet state, T1(3B1u), were calculated at the CIS/3-21G level of theory. The main structural changes are described, and the calculated vibrational levels are compared with available experimental data. The assignment of the two-photon observed transition at about 28 000 cm-1 to the S2 state is confirmed, as well as some recent argon matrix vibronic bands (Wolf, J.; Hohlneicher, G. Chem. Phys. 1994, 181, 185). The calculation suggests some changes in the vibrational assignment, and correlation with the ground state vibrational modes shows that one b2u mode undergoes a large frequency increase upon electronic excitation to S2. This change is similar to that observed for Kekulé-type modes of benzene, naphthalene, and their derivatives. It is compatible with the notion that the π electrons of these molecules tend to distort the molecule to a Kekulé structure.
UR - http://www.scopus.com/inward/record.url?scp=0000638857&partnerID=8YFLogxK
U2 - 10.1021/j100045a012
DO - 10.1021/j100045a012
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AN - SCOPUS:0000638857
SN - 0022-3654
VL - 99
SP - 16558
EP - 16565
JO - Journal of Physical Chemistry
JF - Journal of Physical Chemistry
IS - 45
ER -