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

---

TEMELLİ B., Kalkan H.

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.