Ultrafast transient lens spectroscopy of various C40 carotenoids:: lycopene, β-carotene, (3R,3′R)- zeaxanthin, (3R,3′R,6′R)-lutein, echinenone, canthaxanthin, and astaxanthin

被引:30
|
作者
Kopczynski, M
Lenzer, T
Oum, K
Seehusen, J
Seidel, MT
Ushakov, VG
机构
[1] Univ Gottingen, Inst Chem Phys, D-37077 Gottingen, Germany
[2] Max Planck Inst Biophys Chem, Abt Spektroskopie & Photochem Kinet 10100, D-37077 Gottingen, Germany
关键词
D O I
10.1039/b506574g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The ultrafast internal conversion ( IC) dynamics of seven C-40 carotenoids have been investigated at room temperature in a variety of solvents using two- color transient lens ( TL) pump - probe spectroscopy. We provide comprehensive data sets for the carbonyl carotenoids canthaxanthin, astaxanthin, and - for the. first time - echinenone, as well as new data for lycopene, beta- carotene, ( 3R, 3'R)- zeaxanthin and ( 3R, 3'R, 6'R)- lutein in solvents which have not yet been investigated in the literature. Measurements were carried out to determine, how the IC processes are influenced by the conjugation length of the carotenoids, additional substituents and the polarity of the solvent. TL signals were recorded at 800 nm following excitation into the high energy edge of the carotenoid S-2 band at 400 nm. For the S-2 lifetime solvent- independent upper limits on the order of 100 - 200 fs are estimated for all carotenoids studied. The S-1 lifetimes are in the picosecond range and increase systematically with decreasing conjugation length. For instance, in the sequence canthaxanthin/ echinenone/ b- carotene ( 13/ 12/ 11 double bonds) one. finds tau(1) approximate to 5, 7.7 and 9 ps for the S-1 -> S-0 IC process, respectively. Hydroxyl groups not attached to the conjugated system have no apparent influence on tau(1), as observed for canthaxanthin/ astaxanthin ( tau(1) approximate to 5 ps in both cases). For all carotenoids studied, tau(1) is found to be insensitive to the solvent polarity. This is particularly interesting in the case of echinenone, canthaxanthin and astaxanthin, because earlier measurements for other carbonyl carotenoids like, e. g., peridinin partly showed dramatic differences. The likely presence of an intramolecular charge transfer state in the excited state manifold of C-40 carbonyl carotenoids, which is stabilized in polar solvents, has obviously no influence on the measured tau(1).
引用
收藏
页码:2793 / 2803
页数:11
相关论文
共 50 条
  • [1] An efficient conversion of (3R,3′R,6′R)-lutein to (3R,3′S,6′R)-lutein (3′-epilutein) and (3R,3′R)-zeaxanthin
    Khachik, F
    [J]. JOURNAL OF NATURAL PRODUCTS, 2003, 66 (01): : 67 - 72
  • [2] Chronic ingestion of (3R, 3′R, 6′R)-lutein and (3R, 3′R)-zeaxanthin in the female rhesus macaque
    Khachik, Frederick
    London, Edra
    de Moura, Fabiana F.
    Johnson, Mary
    Steidl, Scott
    DeTolla, Louis
    Shipley, Steven
    Sanchez, Rigoberto
    Chen, Xue-Qing
    Flaws, Jodi
    Lutty, Gerard
    McLeod, Scott
    Fowler, Bruce
    [J]. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2006, 47 (12) : 5476 - 5486
  • [3] A supplementation study in human subjects with a combination of meso-zeaxanthin, (3R,3′R)-zeaxanthin and (3R,3′R,6′R)-lutein
    Thurnham, David I.
    Tremel, Aurelie
    Howard, Alan N.
    [J]. BRITISH JOURNAL OF NUTRITION, 2008, 100 (06) : 1307 - 1314
  • [4] Synthesis of (3R,3′R)-Zeaxanthin and Its meso-Stereoisomer from (3R,3′R,6′R)-Lutein via (3R)-3′,4′-Anhydrolutein
    Khachik, Frederick
    [J]. SYNTHESIS-STUTTGART, 2012, 44 (03): : 453 - 459
  • [5] Partial synthesis of (3R,6′R)-α-cryptoxanthin and (3R)-β-cryptoxanthin from (3R,3′R,6′R)-lutein
    Khachik, Frederick
    Chang, An-Ni
    Gana, Audry
    Mazzola, Eugene
    [J]. JOURNAL OF NATURAL PRODUCTS, 2007, 70 (02): : 220 - 226
  • [6] A Simple and Efficient Method for the Partial Synthesis of Pure (3R,3′S)-Astaxanthin from (3R,3′R,6′R)-Lutein and Lutein Esters via (3R,3′S)-Zeaxanthin and Theoretical Study of Their Formation Mechanisms
    Rodriguez-deLeon, Eloy
    Jimenez-Halla, J. Oscar. C.
    Baez, Jose E.
    Bah, M. Moustapha
    [J]. MOLECULES, 2019, 24 (07)
  • [7] SEPARATION OF (3R,3'R)-ZEAXANTHIN, (3R,3'S - MESO)-ZEAXANTHIN, (3S,3'S)-ZEAXANTHIN, (3R,3'R,6'R)-LUTEIN, (3R,3'S,6'S)-LUTEIN AND (3S,3'S,6'S)-LUTEIN VIA THE DICARBAMATES OF (S)-(+)-ALPHA-(1-NAPHTHYL) ETHYL ISOCYANATE
    RUTTIMANN, A
    SCHIEDT, K
    VECCHI, M
    [J]. JOURNAL OF HIGH RESOLUTION CHROMATOGRAPHY & CHROMATOGRAPHY COMMUNICATIONS, 1983, 6 (11): : 612 - 616
  • [8] Transformation of naturally occurring (3R,3′R,6′R)-lutein and its fatty acid esters to (3 R)-β-cryptoxanthin and (3R,6′R)-α-cryptoxanthin
    Khachik, Frederick
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2018, 653 : 107 - 112
  • [9] Metabolism of lutein and zeaxanthin in rhesus monkeys:: Identification of (3R,6′R)- and (3R,6′S)-3′-dehydro-lutein as common metabolites and comparison to humans
    Albert, Gesa I.
    Hoeller, Ulrich
    Schierle, Joseph
    Neuringer, Martha
    Johnson, Elizabeth J.
    Schalch, Wolfgang
    [J]. COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 2008, 151 (01): : 70 - 78
  • [10] Preparation of (3R, 3′R)-astaxanthin monoester and (3R, 3′R)-astaxanthin from Antarctic krill (Euphausia superba Dana)
    Shasha Zhang
    Xiaoyun Sun
    Daicheng Liu
    [J]. European Food Research and Technology, 2015, 240 : 295 - 299