UV, FL and IR spectroscopic analysis of N-confused meso-tetra(methoxyphenyl)porphyrins

UV, FL and IR spectra of isomer A (in DCM) and isomer B (in DMAc) of N-confused 5,10,15,20-tetra([Formula: see text]-methoxyphenyl)porphyrin ([Formula: see text]-isomer, 1), N-confused 5,10,15,20-tetra([Formula: see text]-methoxyphenyl)porphyrin ([Formula: see text]-isomer, 2) and N-confused 5,10,15,20-tetra([Formula: see text]-methoxyphenyl)porphyrin ([Formula: see text]-isomer, 3) were investigated. Significant red shifts are observed from [Formula: see text]-isomer (1) to [Formula: see text]-isomer (3) in UV-vis absorption and fluorescence spectra. The fluorescence lifetime ([Formula: see text] of isomer A and isomer B of the samples (1, 2 and 3) are ca. 1.39[Formula: see text]1.79 ns and 1.68[Formula: see text]2.09 ns, respectively. In addition, the order of fluorescence quantum yield for isomer A is 1 >2 > 3, but for isomer B it is 1 < 3 <2. The isomer B of 2shows the strongest emission in accord with the strongest absorption. The isomer A of 1shows the strongest emission with the fluorescence quantum yield of 0.045, which is nearly double that of 3. The introduction of the methoxy group at the orthoposition increases steric hindrance, the molecular rigidity and the flow of [Formula: see text]-electron, thereby favourable to the fluorescence enhancement. The IR absorption peaks of 1, 2 and 3 were investigated and empirically assigned. The effects of the position of the substituents on the absorption frequency were also discussed. The absorption frequency of the C=C phenyl stretching in plane changed obviously by conjugative effect and steric effect when the methoxy group was at the orthoormetaposition in comparison with paraposition.