Coumarin-Tetrapyrrolic Macrocycle Conjugates: Synthesis and Applications

被引:21
作者
Cerqueira, Ana F. R.
Almodovar, Vitor A. S.
Neves, Maria G. P. M. S.
Tome, Augusto C. [1 ]
机构
[1] Univ Aveiro, Dept Chem, P-3810193 Aveiro, Portugal
关键词
coumarins; porphyrins; phthalocyanines; corroles; SUBSTITUTED METAL-FREE; PHTHALOCYANINES BEARING COUMARIN; PHOTOCHEMICAL PROPERTIES; ELECTROCHEMICAL PROPERTIES; PORPHYRIN-CORE; MESOSUBSTITUTED CORROLES; PHOTOPHYSICAL PROPERTIES; FLUORESCENCE BEHAVIOR; HIGHLY EFFICIENT; ENERGY-TRANSPORT;
D O I
10.3390/molecules22060994
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This review covers the synthesis of coumarin-porphyrin, coumarin-phthalocyanine and coumarin-corrole conjugates and their potential applications. While coumarin-phthalocyanine conjugates were obtained almost exclusively by tetramerization of coumarin-functionalized phthalonitriles, coumarin-porphyrin and coumarin-corrole conjugates were prepared by complementary approaches: (a) direct synthesis of the tetrapyrrolic macrocycle using formylcoumarins and pyrrole or (b) by functionalization of the tetrapyrrolic macrocycle. In the last approach a range of reaction types were used, namely 1,3-dipolar cycloadditions, hetero-Diels-Alder, Sonogashira, alkylation or acylation reactions. This is clearly a more versatile approach, leading to a larger diversity of conjugates and allowing the access to conjugates bearing one to up to 16 coumarin units.
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页数:26
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