Synthesis and study of fluorine-functionalized ZnTPPs

Abstract

Five fluorinated zinc tetraphenyl porphyrins derivatives, fluorinated either on all ortho positions of the meso phenyl rings (Zn(II)-5,10,15,20-tetrakis(2,6-difluorophenyl)porphyrin) or in [Formula: see text]-positions with two, four, six or eight fluorine groups (2,3-difluoro-5,10,15,20-tetraphenylporphyrin, 7, 8,17,18-tetrafluoro-5,10,15,20-tetraphenylporphyrin, 7,8,12,13,17,18-hexafluoro-5,10,15,20-tetraphenyl- porphyrin and 2,3,7,8,12,13,17,18-octafluoro-5,10,15,20-tetraphenylporphyrin, respectively), were studied to probe the effect of fluorine in on-surface synthesis approaches. Additionally, bulkier substituents have been used in 7,8,17,18-tetrabromo-5,10,15,20-tetraphenylporphyrin and 7,8,17,18-tetramethyl-5,10,15,20-tetraphenylporphyrin, for a direct comparison with the corresponding fluorinated compounds. Reported are the synthesis and electronic structure characterization of the compounds, using UV-vis absorption and fluorescence spectroscopies as well as electronic structure calculations of the ground state molecular properties. Steric and electronic effects of fluorination are explored. For all molecules studied, substitution with fluorine maintains a planar tetrapyrrole macrocycle and shifts in the absorption spectra were consistent with calculated changes in the HOMOs and LUMOs energies of the molecules. In contrast, the bromo and methyl-substituted derivatives exhibit chemical instability and spectral shifts, compared to parent compound ZnTPP, consistent with structural distortions and accounted for calculations. The site-specific effects of fluorination on the electronic structure are discussed in detail.