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Synthesis and spectroscopic properties of ?-meso directly linked porphyrin-corrole hybrid compounds.

ABSTRACT: The preparation of ?-meso directly linked porphyrin-corrole hybrids was realized for the first time via an InCl3-catalyzed condensation reaction of 2-formyl-5,10,15,20-tetraphenylporphyrins with meso-substituted dipyrromethanes. Hybrid compounds have been characterized by 1H NMR, 13C NMR, 2D NMR, UV-vis absorption and fluorescence spectroscopy.

SUBMITTER: Temelli B

PROVIDER: S-EPMC5789387 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature

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Synthesis and spectroscopic properties of β-meso directly linked porphyrin-corrole hybrid compounds.

Temelli Baris B Kalkan Hilal H

Beilstein journal of organic chemistry 20180122

The preparation of β-meso directly linked porphyrin-corrole hybrids was realized for the first time via an InCl3-catalyzed condensation reaction of 2-formyl-5,10,15,20-tetraphenylporphyrins with meso-substituted dipyrromethanes. Hybrid compounds have been characterized by 1H NMR, 13C NMR, 2D NMR, UV-vis absorption and fluorescence spectroscopy. ...[more]

PMID: 29441141

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