Abstract
Control of open-shell character of meso-meso linked porphyrin meso-oxy radical dimers has been demonstrated by core metalation. Namely, NiII -porphyrin dimer 6Ni exhibits a clear 1 H NMR spectrum and a distorted but rather coplanar quinonoidal structure consisting of two ruffled porphyrin rings, in accordance with the previous report. Freebase dimer 6H2 shows a similar quinonoidal structure in the solid state but displays slightly broader and temperature-dependent 1 H NMR spectra, indicating a partial diradical character in solution that increases at high temperature. In sharp contrast, bis-imidazole-coordinated ZnII -porphyrin dimer 6ZnIm2 exhibits a perpendicular structure consisting of two planar ZnII -porphyrins and has been characterized as a distinct open-shell diradical on the basis of its non-observable 1 H NMR signals, a clear ESR signal, and a characteristic absorption spectrum reaching about 1700 nm. Despite the distinct diradical character, 6ZnIm2 is an extremely stable molecule.
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