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.
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Temelli, B., & Kalkan, H. (2017). Synthesis and spectroscopic properties of β-meso directly linked porphyrin-corrole hybrid compounds. Beilstein Journal of Organic Chemistry, 14, 187–193. https://doi.org/10.3762/bjoc.14.13
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