Spectroscopic properties of spheroidene analogs having different extents of π-electron conjugation

Harry A. Frank, Ruel Z B Desamero, Veeradej Chynwat, Ronald Gebhard, Ineke Van Der Hoef, Frans Jos Jansen, Johan Lugtenburg, David Gosztola, Michael R Wasielewski

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Abstract

The spectroscopic properties of spheroidene and a series of spheroidene analogs with extents of π-electron conjugation ranging from 7 to 13 carbon-carbon double bonds were studied using steady-state absorption, fluorescence, fluorescence excitation, and time-resolved absorption spectroscopy. The spheroidene analogs studied here were 5′,6′-dihydro-7′,8′-didehydrospheroidene, 7′,8′-didehydrospheroidene, and 1′,2′-dihydro3′,4′,7′,8′- tetradehydrospheroidene and taken together with data from 3,4,7,8-tetrahydrospheroidene, 3,4,5,6-tetrahydrospheroidene, 3,4-dihydrospheroidene already published (DeCoster, B.; Christensen, R. L.; Gebhard, R.; Lugtenburg, J.; Farhoosh, R.; Frank, H. A. Biochim. Biophys. Acta 1992, 1102, 107) provide a systematic series of molecules for understanding the molecular features that control energy transfer to bacteriochlorophyll in photosynthetic bacterial light-harvesting complexes. All of the molecules were purified by high-pressure liquid chromatographic techniques prior to the spectroscopic experiments. The absorption spectra of the molecules were observed to red-shift with increasing extent of π-electron conjugation. The room temperature fluorescence data show a systematic crossover from dominant S1 → S0 (21Ag → 11Ag) emission to dominant S2 → S0 (11Bu → 11Ag) with increasing extent of conjugation. The S2 fluorescence quantum yields of all the carotenoids in the series were measured here and indicate that 3,4-dihydrospheroidene with nine carbon - carbon double bonds has an S2 quantum yield of (2.7 ± 0.3) × 10-4 which is the highest value in the series. The lifetimes of the S1 states of the molecules were determined from time-resolved transient absorption spectroscopy and found to decrease as the conjugated chain length increases. The transient data are discussed in terms of the energy gap law for radiationless transitions which allows a prediction of the S1 energies of the molecules. The implications of these results for the process of light harvesting by carotenoids in photosynthesis are discussed.

Original languageEnglish
Pages (from-to)149-157
Number of pages9
JournalJournal of Physical Chemistry A
Volume101
Issue number2
Publication statusPublished - Jan 9 1997

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conjugation
analogs
Carbon
Molecules
Fluorescence
Electrons
fluorescence
carotenoids
carbon
molecules
Quantum yield
Carotenoids
electrons
Absorption spectroscopy
absorption spectroscopy
Bacteriochlorophylls
photosynthesis
Photosynthesis
Electron transitions
Chain length

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry

Cite this

Frank, H. A., Desamero, R. Z. B., Chynwat, V., Gebhard, R., Van Der Hoef, I., Jansen, F. J., ... Wasielewski, M. R. (1997). Spectroscopic properties of spheroidene analogs having different extents of π-electron conjugation. Journal of Physical Chemistry A, 101(2), 149-157.

Spectroscopic properties of spheroidene analogs having different extents of π-electron conjugation. / Frank, Harry A.; Desamero, Ruel Z B; Chynwat, Veeradej; Gebhard, Ronald; Van Der Hoef, Ineke; Jansen, Frans Jos; Lugtenburg, Johan; Gosztola, David; Wasielewski, Michael R.

In: Journal of Physical Chemistry A, Vol. 101, No. 2, 09.01.1997, p. 149-157.

Research output: Contribution to journalArticle

Frank, HA, Desamero, RZB, Chynwat, V, Gebhard, R, Van Der Hoef, I, Jansen, FJ, Lugtenburg, J, Gosztola, D & Wasielewski, MR 1997, 'Spectroscopic properties of spheroidene analogs having different extents of π-electron conjugation', Journal of Physical Chemistry A, vol. 101, no. 2, pp. 149-157.
Frank HA, Desamero RZB, Chynwat V, Gebhard R, Van Der Hoef I, Jansen FJ et al. Spectroscopic properties of spheroidene analogs having different extents of π-electron conjugation. Journal of Physical Chemistry A. 1997 Jan 9;101(2):149-157.
Frank, Harry A. ; Desamero, Ruel Z B ; Chynwat, Veeradej ; Gebhard, Ronald ; Van Der Hoef, Ineke ; Jansen, Frans Jos ; Lugtenburg, Johan ; Gosztola, David ; Wasielewski, Michael R. / Spectroscopic properties of spheroidene analogs having different extents of π-electron conjugation. In: Journal of Physical Chemistry A. 1997 ; Vol. 101, No. 2. pp. 149-157.
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