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

The preparation of β-meso directly linked porphyrin–corrole hybrids was realized for the first time via an InCl(3)-catalyzed condensation reaction of 2-formyl-5,10,15,20-tetraphenylporphyrins with meso-substituted dipyrromethanes. Hybrid compounds have been characterized by (1)H NMR, (13)C NMR, 2D N...

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Detalles Bibliográficos
Autores principales: Temelli, Baris, Kalkan, Hilal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789387/
https://www.ncbi.nlm.nih.gov/pubmed/29441141
http://dx.doi.org/10.3762/bjoc.14.13
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author Temelli, Baris
Kalkan, Hilal
author_facet Temelli, Baris
Kalkan, Hilal
author_sort Temelli, Baris
collection PubMed
description The preparation of β-meso directly linked porphyrin–corrole hybrids was realized for the first time via an InCl(3)-catalyzed condensation reaction of 2-formyl-5,10,15,20-tetraphenylporphyrins with meso-substituted dipyrromethanes. Hybrid compounds have been characterized by (1)H NMR, (13)C NMR, 2D NMR, UV–vis absorption and fluorescence spectroscopy.
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spelling pubmed-57893872018-02-13 Synthesis and spectroscopic properties of β-meso directly linked porphyrin–corrole hybrid compounds Temelli, Baris Kalkan, Hilal Beilstein J Org Chem Full Research Paper The preparation of β-meso directly linked porphyrin–corrole hybrids was realized for the first time via an InCl(3)-catalyzed condensation reaction of 2-formyl-5,10,15,20-tetraphenylporphyrins with meso-substituted dipyrromethanes. Hybrid compounds have been characterized by (1)H NMR, (13)C NMR, 2D NMR, UV–vis absorption and fluorescence spectroscopy. Beilstein-Institut 2018-01-22 /pmc/articles/PMC5789387/ /pubmed/29441141 http://dx.doi.org/10.3762/bjoc.14.13 Text en Copyright © 2018, Temelli and Kalkan https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Temelli, Baris
Kalkan, Hilal
Synthesis and spectroscopic properties of β-meso directly linked porphyrin–corrole hybrid compounds
title Synthesis and spectroscopic properties of β-meso directly linked porphyrin–corrole hybrid compounds
title_full Synthesis and spectroscopic properties of β-meso directly linked porphyrin–corrole hybrid compounds
title_fullStr Synthesis and spectroscopic properties of β-meso directly linked porphyrin–corrole hybrid compounds
title_full_unstemmed Synthesis and spectroscopic properties of β-meso directly linked porphyrin–corrole hybrid compounds
title_short Synthesis and spectroscopic properties of β-meso directly linked porphyrin–corrole hybrid compounds
title_sort synthesis and spectroscopic properties of β-meso directly linked porphyrin–corrole hybrid compounds
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789387/
https://www.ncbi.nlm.nih.gov/pubmed/29441141
http://dx.doi.org/10.3762/bjoc.14.13
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