Cis-Trans Photoisomerization of the 1, 6-Diphenyl-1, 3, 5-hexatrienes in the Triplet State. The Quantum Chain Mechanism and the Structure of the Triplet State

摘要

Fluorenone sensitization in solution interconverts all-trans-1, 6-diphenyl-1, 3, 5-hexatriene (ttt-DPH) with its trans, cis, trans, cis, trans, trans, and cis, cis, trans (trace) isomers, tct-, ctt-, and cct-DPH, respectively. Photo-isomerization quantum yields are reported for the three major isomers in degassed and air-saturated benzene. In degassed solutions the quantum yields are strongly concentration dependent due to quantum chain processes. The presence of air eliminates the quantum chain processes, as all DPH triplets are deactivated by oxygen. Triplet-triplet absorption spectra observed in the microsecond time scale starting from these three DPH isomers are identical. The concentration dependence of the DPH triplet lifetime is consistent with the concentration dependence of the isomerization quantum yields. The results indicate that in benzene DPH triplets exist as an equilibrium mixture of ttt, tct, and ctt isomers whose composition at 20 ℃, 94% ttt, 5% tct, and 1% ctt is revealed by isomerization quantum yields in the presence of air. Photoisomerization quantum yields in the presence of air show that the isomeric triplets are fully equilibrated within less than 100 ns.