Solvent-dependent aromatic versus antiaromatic conformational switching in meso-(heptakis)pentafluorophenyl [32]heptaphyrin

We have investigated conformational switching dynamics of meso-heptakis(pentafluorophenyl) 32]heptaphyrin(1.1.1.1.1.1.1) in various solvents using steady-state, time-resolved, and temperature-dependent spectroscopy. Absorption and fluorescence spectra of 32]heptaphyrin are quite sensitive to solvent environments. In nonpolar toluene, the antiaromatic figure-of-eight conformation is dominant, as seen in the X-ray crystallography, based on broad and weak absorption bands without any fluorescence and moderate paratropic ring current. On the other hand, a well-resolved sharp absorption spectrum, strong fluorescence, and diatropic ring current in the 1H NMR spectrum in slightly polar THF indicate that most of 32]heptaphyrin molecules take significantly distorted M?bius conformation with aromatic character. By using transient absorption (TA) spectroscopy, the lowest singlet excited-state lifetimes have been revealed to decay biexponentially with the time constants of 5 and 65 ps for figure-of-eight and M?bius conformations, respectively. Based on these results along with vertical excitation energy calculations, we are able to assign two conformers as Hückel antiaromatic and M?bius aromatic species, respectively; it shoulf be noted that the aromaticity/antiaromaticity does not change with temperature variation. Interestingly, in moderately polar solvent, ethyl ether, we find out that these two conformational isomers coexist with a dynamic equilibrium, as revealed by excitation-wavelength-dependent TA, temperature-dependent absorption and 1H NMR spectra. Through our findings, we have demonstrated that the conformational switching dynamics between Hckel antiaromatic and M?bius aromatic conformers in 32]heptaphyrin(1.1.1.1.1.1.1) are strongly affected by solvent medium as well as temperature.