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Energy transfer in a supramolecular complex­assembled via sapphyrin dimer-mediated­dicarboxylate anion chelation

✍ Scribed by Stacy L. Springs; Andrei Andrievsky; Vladinír Král; Jonathan L. Sessler


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
220 KB
Volume
02
Category
Article
ISSN
1088-4246

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✦ Synopsis


The synthesis of a new terephthalate-strapped porphyrin is described. This porphyrin, prepared in the form of the free base and corresponding zinc(II) complex, was designed to act as the photo-donor portion of a novel, non-covalent artificial light-harvesting complex, the other, acceptor component of which is comprised of a covalently linked sapphyrin dimer. UV-vis and 1 H NMR spectroscopic analyses were used to establish that strong complexes are formed between the porphyrin terephthalate and sapphyrin dimer components (affinity constants on the order of 10 5 M À1 in dichloromethane). In these complexes the dicarboxylate portion of the strapped porphyrin is sandwiched between two sapphyrins of an individual dimer. Steady state fluorescence studies of the resulting ensembles support the conclusion that, upon photoexcitation of the porphyrin subunit, energy transfer from the porphyrin to the sapphyrin dimer occurs efficiently. This intra-ensemble, anion-chelation-based energy transfer can be inhibited by the addition of fluoride anion.