Synthesis and spectroscopic properties of beta-meso directly linked porphyrin-corrole hybrid compounds
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY, cilt.14, ss.187-193, 2017 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 14
- Basım Tarihi: 2017
- Doi Numarası: 10.3762/bjoc.14.13
- Dergi Adı: BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.187-193
- Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
- Gazi Üniversitesi Adresli: Hayır
Özet
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.