Synthesis and Spectroscopic Properties of Β-Meso Directly Linked Porphyrin–Corrole Hybrid Compounds

dc.contributor.author	Temelli, Baris
dc.contributor.author	Kalkan, Hilal
dc.date.accessioned	2019-12-13T11:04:56Z
dc.date.available	2019-12-13T11:04:56Z
dc.date.issued	2018
dc.identifier.issn	1860-5397
dc.identifier.uri	https://doi.org/10.3762/bjoc.14.13
dc.identifier.uri	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789387/
dc.identifier.uri	http://hdl.handle.net/11655/18978
dc.description.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.
dc.relation.isversionof	10.3762/bjoc.14.13
dc.rights	info:eu-repo/semantics/openAccess
dc.title	Synthesis and Spectroscopic Properties of Β-Meso Directly Linked Porphyrin–Corrole Hybrid Compounds
dc.type	info:eu-repo/semantics/article
dc.type	info:eu-repo/semantics/publishedVersion
dc.relation.journal	Beilstein Journal of Organic Chemistry
dc.contributor.department	Kimya Mühendisliği
dc.identifier.volume	14
dc.identifier.startpage	187
dc.identifier.endpage	193
dc.description.index	PubMed
dc.description.index	WoS
dc.description.index	Scopus