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
Photoexcited triplet ESR studies on thiaporphyrins and their protonated derivatives
β Scribed by R.P. Pandian; T.K. Chandrashekar; Hans van Willigen
- Book ID
- 103030985
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 458 KB
- Volume
- 202
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
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 triplet spin density. However, the protonated derivatives show large decreases in D (30%-40%) and E (40%-50%) values. The electron spin polarization pattern (ESP) indicates dominance of an in-plane spin sub-level with respect to the population and decay process for neutral species, while a redirection of spin sub-level activity is observed for protonated species. The structural change accompanying the protonation process accounts for most of these observations.
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