Very fast singlet and triplet energy transfers in a tri-chromophoric porphyrin dyad aided by the truxene platform

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TitreVery fast singlet and triplet energy transfers in a tri-chromophoric porphyrin dyad aided by the truxene platform
Type de publicationJournal Article
Year of Publication2015
AuteursLanglois A, Xu H-J, Karsenti P-L, Gros CP, Harvey PD
JournalJOURNAL OF PORPHYRINS AND PHTHALOCYANINES
Volume19
Pagination427-441
Date PublishedJAN-MAR
Type of ArticleArticle
ISSN1088-4246
Mots-clésDexter mechanism, energy transfer, MO coupling, palladium(II)porphyrin, ultrafast fluorescence lifetime, zinc(II)porphyrin
Résumé

A trichromophoric dyad composed of an octa-beta-alkyl-palladium(II)porphyrin (donor) and two tri-meso-aryl-zinc(II)porphyrins (acceptors) held by a truxene spacer exhibits very fast rates for triplet energy transfers at 77 (k(ET)(T-1) = 1.63 x 10(8) s(-1)) and 298 K (k(ET) (T-1) = 3.44 x 10(8) s(-1)), whereas the corresponding singlet energy transfer rates, k(ET)(S-1) = 3.9 x 10(10) s(-1) (77 K) and k(ET) (S-1) = 6.0 x 10(10) s(-1) (298 K), are also considered fast. The interpretation for these results is that the energy transfer processes proceed via a through bond Dexter mechanism (i.e. double electron exchange) supported by comparison with literature data and evidence for a moderate MO coupling between the donor and acceptor chromophores in the frontier MOs.

DOI10.1142/S1088424615500327