The photoexcited triplet states of mono-and di-thi'aporphyrins and their protonated derivatives are investigated by ESR spectroscopy. A comparison of the magnitude of the zero-field splitting parameters (D and E) of neutral thiaporphyrins with H,TPP indicates no significant alterations in the triple
Photoexcited triplet ESR studies on water-soluble thiaporphyrins
β Scribed by T.K. Chandrashekar; Hans van Willigen
- Book ID
- 103034302
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 284 KB
- Volume
- 198
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
Triplet state characteristics of monomer and dimer of two core modified thiaporphyrins (STPPS and S2TPPS) are reported. Introduction of heavy sulfur atom (s) into the porphyrin core does not alter the zero-field splitting parameters significantly and the ESP pattern remains the same as in analogous H2TPPS. This is possibly due to similarities in the structures of the porphyrin core of STPPS, S2TPPS and H2TPPS. However, there is a strong dimerization effect on the D value similar to those observed for dimerization of HzTPPS.
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Tc1r~(l-sulfon~1ophcnyl)porphyrin (H,TPPS), and the mct;tlloporph~rinsZnTPPS and PdTPPS dimctir in ;~qusous solution. An ESR study has been made of the photocscited ~rrplrrs oi the [ZnTPPS12. [H2TPPS/Z~TPPS] and [HzTPPS/PdTPPS] dimers. It is found that there is n strong dimcrization effect on the va
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