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

   Temelli, Baris; Kalkan, Hilal

The preparation of beta-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 H-1 NMR, C-13 NMR, 2D NMR, UV-vis absorption and fluorescence spectroscopy.

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