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Synthesis of meso-tetrakis(4-chlorocoumarin-3-yl)porphyrins

✍ Scribed by M. Amaravathi; B. Rajitha; M. Kanakalingeswara Rao; P. Sitadevi


Publisher
Journal of Heterocyclic Chemistry
Year
2007
Tongue
English
Weight
454 KB
Volume
44
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

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meso‐Tetrakis(4‐chlorocoumarin‐3‐yl)porphyrins were prepared by condensation of corresponding 4‐chlorocoumarin‐3‐carboxaldehydes and pyrrole in the presence of trifluoro acetic acid (TFA) in dichloromethane followed by oxidation with 2,3‐dichloro‐5,6‐dicyano‐1,4‐benzoquinone (DDQ). These porphyrins exhibited the atropisomerism due to ortho substituent of meso aryl groups. The atropisomers of meso‐tetrakis(4‐chloro‐6‐methylcoumarin‐3‐yl)porphyrin were separated and identified by ^1^H‐nmr spectra. Zinc complexes of these porphyrins were synthesized and characterized by ms, ^1^H nmr, ir and uv‐vis spectra.


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