Ultrafast energy transfer within cyclic self-assembled chlorophyll tetramers

Richard F. Kelley, Randall H. Goldsmith, Michael R Wasielewski

Research output: Contribution to journalArticle

56 Citations (Scopus)

Abstract

We have prepared a zinc chlorophyll (ZC) derivative that self-assembles into a cyclic tetramer as evidenced by small-angle X-ray scattering studies in solution using a synchrotron source. This cyclic tetramer exhibits intramolecular energy transfer rates determined from singlet-singlet annihilation and transient absorption anisotropy studies that are comparable to those observed previously only for covalent ring structures. The larger transition dipole moment for the lowest energy electronic transition of ZC compared to that of metalloporphyrins increases the rate of Förster (through-space) energy transfer between the chlorophylls. Our synthetic and self-assembly strategy makes it possible to design larger monodisperse chlorophyll rings for energy transfer in artificial photosynthetic systems.

Original languageEnglish
Pages (from-to)6384-6385
Number of pages2
JournalJournal of the American Chemical Society
Volume129
Issue number20
DOIs
Publication statusPublished - May 23 2007

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Energy Transfer
Chlorophyll
Energy transfer
Zinc
Metalloporphyrins
Synchrotrons
Anisotropy
Dipole moment
X ray scattering
Self assembly
X-Rays
Derivatives

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Ultrafast energy transfer within cyclic self-assembled chlorophyll tetramers. / Kelley, Richard F.; Goldsmith, Randall H.; Wasielewski, Michael R.

In: Journal of the American Chemical Society, Vol. 129, No. 20, 23.05.2007, p. 6384-6385.

Research output: Contribution to journalArticle

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