Comparison of electronic effects of β-Aryl substituents on optical and electrochemical properties of 5,15-diazaporphyrin φ-systems

Satoshi Omomo, Ko Furukawa, Haruyuki Nakano, Yoshihiro Matano

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10 Citations (Scopus)


The syntheses and optical/electrochemical properties of 3-Aryl-10,20-dimesityl-5,15-diazaporphyrin-metal complexes (MDAPs; mesityl = 2,4,6-trimethylphenyl; M = Ni, Zn) are reported. Treatment of 3-bromo-MDAPs with arylboronic acids in the presence of a Pd catalyst and a bulky phosphine ligand in a dioxane-water mixed solvent afforded the corresponding 3-Aryl-MDAPs in moderate to good yields. X-ray crystallographic analysis of p-EtO2CC6H4-NiDAP showed that the β-Aryl group was tilted toward the NiDAP ring, with a dihedral angle of 21.7°. In the UV-visible absorption spectra, all the Ar-MDAPs showed intense Q-bands attributable to HOMO-to-LUMO transitions. The para substituents were found to influence the HOMO energies, which eventually resulted in fine tuning of the HOMO-LUMO gaps of the diazaporphyrin chromophores. It is worth noting that the p-Ph 2NC6H4-ZnDAP showed broad absorption and emission bands in the visible-near-infrared regions. The large Stokes shifts and their linear solvation energy relationships vs. orientation polarizability show that this Ph 2N-substituted derivative has intrinsically high charge transfer from the triphenylamine (donor) to the ZnDAP (acceptor) unit. These experimental observations were supported by theoretical calculations for model Ar-ZnDAP compounds. These results confirm that the introduction of a highly electron-donating aryl group at the peripheral β-carbon is a promising strategy for enhancing the light-harvesting and light-emitting abilities of diazaporphyrin-based φ-systems in the visible-near-infrared regions.

Original languageEnglish
Pages (from-to)775-785
Number of pages11
JournalJournal of Porphyrins and Phthalocyanines
Issue number6
Publication statusPublished - Jun 1 2015

All Science Journal Classification (ASJC) codes

  • Chemistry(all)


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