The conversions of photophysical and nonlinear optical (NLO) properties in [32]octaphyrins(1.0.1.0.1.0.1.0) following macrocyclic isomerization between Huckel and Mobius topologies have been studied in detail by means of quantum chemistry calculations.… Click to show full abstract
The conversions of photophysical and nonlinear optical (NLO) properties in [32]octaphyrins(1.0.1.0.1.0.1.0) following macrocyclic isomerization between Huckel and Mobius topologies have been studied in detail by means of quantum chemistry calculations. Compared to their quasi-planar analogues, the twisted Mobius and the figure-eight Huckel conformers exhibit red- and blue-shifted absorptions, respectively. The fluorescence emissions of Huckel topological molecules are likely to be from the second excited state, while the Mobius ones should emit photons from the first excited state by following Kasha’s rule. The average polarizabilities of octaphyrins reveal certain regularity with regard to their topologies, but is not particularly large; with the π-conjugation enhanced, the polarizability value increased moderately. The static first- and second-order hyperpolarizabilities of Mobius conformations are almost all much higher than those of Huckel conformers, and the figure-eight Huckel structures exhibit rel...
               
Click one of the above tabs to view related content.