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ESR study of photoexcited triplets of some tetra(4-sulfonatophenyl)porphyrin dimers

✍ Scribed by T.K. Chandrashekar; Hans Van Willigen


Publisher
Elsevier Science
Year
1984
Tongue
English
Weight
469 KB
Volume
106
Category
Article
ISSN
0009-2614

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✦ Synopsis


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 values of the zero field splitting paramctcrs of the triplets. This contrasts with what has been reported for photoescitcd triplets oi 3 series of covalcntlylinked tctrapyrrolcs.The expcrimcntal data indicate that the dimerizntion cffcct on the TPPS triplet pxmtctcrs must be attributed to charge transfer contributions to the triplet electronic state.


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✍ Tatiana L. Simándi; Antal Rockenbauer; LászlóI. Simándi 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 316 KB

## IReactions of 3,3',5,5'-tetra-ferz-butylstilbene-4,4'-quinone with free radicals from the decomposition of azo compounds and peroxides (R') have been studied by ESR spectroscopy. Relatively stable phenoxyl+,pe free radicals are formed via addition of R' across the exo C=C bond. Their coupling c