Absorption and emission spectra of all-trans 1, 3, 5, 7-octatetraene are presented along with fluorescence quantum yields and lifetimes. In solution, a gap of about 3000 cm−1 is found between the first band of the 1 1Ag→11Bu transition and the onset of the emission spectrum. Excitation spectra of concentrated solutions at 77 K show low-lying bands in this gap, the lowest energy band being almost coincident with the highest energy fluorescence band. On the other hand, gas phase fluorescence spectra show no gap between the lowest energy 11Ag→11Bu absorption band and the first fluorescence band. The radiative lifetime in hexane is 220 ns at room temperature and 190 ns at 77 K. The radiative lifetime for the gas phase fluorescence is estimated to be longer than 150 ns. The solvent dependence of the absorption and emission spectra, the fluorescence lifetimes, and the vibrational frequencies observed in solution imply support for the conjecture of Karplus et al. that the lowest excited singlet state is of 1Ag symmetry. The solution data imply that the low-lying state is about 6400 cm−1 below the 11Bu level. On the other hand, the lack of a gap between absorption and emission and the long lifetime found for the gas phase are not compatible with this model.
Absorption spectra are reported for cis- and trans-1,3,5-hexatriene in the region between 47 000 and 69 000 cm−1. The observed transitions are compared to those predicted from Pople-Pariser-Parr pi-electron calculations using configuration interaction including both single and double excitations. The ordering of states predicted from calculations based on single excitations appears to be more plausible than that of the more extensive single-plus-double excitation calculations. Vibrational progressions associated with the higher energy ππ* transitions of the trans isomer are almost identical to those reported previously for the lowest energy allowed transition (39 000–47 000 cm−1). The linewidths of the trans isomer transitions are considerably smaller than those for the cis isomer transitions throughout the entire vacuum ultraviolet region. An ionization petential of 8.27 eV is obtained for the trans isomer from a Rydberg series extrapolation. This value compares favorably with the value (8.29 eV) obtained recently from photoelectron spectroscopy. Strong bands which could be assigned unambiguously as Rydberg transitions were not found for cis-hexatriene. However, the shape of the absorption curve in the region 62 000–68 000 cm−1 implies that the ionization potential for cis-hexatriene is probably within 0.1 eV of that for trans-hexatriene.
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