Prospects for the Creation of a Photocontrolled Supramolecular Machine Based on a 1,4-Di(azastyryl)benzene Derivative and Cucurbit[7]uril

The photophysical processes and photochemical reactions of 1,4-di(azastyryl)benzene (1) derivative {[(E,E)-1](ClO4)2} were investigated by absorption, luminescence, and laser kinetic spectroscopy in the water solution. The observed photo processes include dimerization, E-Z isomerization, and intersystem crossing to the triplet state, as well as the complexation [(E,E)-1](ClO4)2 with cucurbit[7]uril (CB[7]). The [(E,E)-1](ClO4)2 dye dimerization was shown to be energetically more favorable in the excited state than in the ground state. The reversible photoinduced migration of the dye dication in the CB[7] cavity takes place as a result of partial exit of the [(E,E)-1]2+ from the cavity and its subsequent conversion to the (E,Z)-isomer in the excited state, which undergoes conversion to the initial complex of {[(E,E)-1]@CB[7]}2+ after returning to the ground state. This photoprocess is of interest in relation to the scientific problem of designing photocontrolled supramolecular machines.