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.
📜 SIMILAR VOLUMES
## Absbwl: The synrhesis of a new family of meso-terrakis (glycosylated) porphyrins is reported. Uqfonunately. the porphyrins 4 and 5 bearing glycosykqvnethylene sabstituents are unstable.
## Abstract __meso__‐Tetrakis‐(__p__‐methoxyphenyl)porphyrin rare earth chlorides, Ln(TMOPP)Cl (Ln: Dy, Ho, Tm, Yb, Lu and H~2~TMOPP: tetrakis‐(__p__‐methoxyphenyl)porphyrin), were synthesized and characterized. Their composition, structure and properties were studied by elemental analyses, ultra‐v