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

ABSTRACT: 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.

SUBMITTER: Temelli B 

PROVIDER: S-EPMC5789387 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature