Zobrazeno 1 - 10
of 51
pro vyhledávání: '"F. J. H. M. Jansen"'
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 113:552-562
The all-E isomers of (12,12′-13C2)-, (13,13′-13C2)-, (14,14′-13C2)-, (15,15′-13C2)- and (20,20′-13C2)astaxanthin were prepared by total synthesis starting from commercially available 99% 13C-enriched acetonitrile, acetic acid and methyl iod
Autor:
A. T. J. W. de Goede, A. U. Baldew, F. J. H. M. Jansen, E. M. M. van den Berg, Johan Lugtenburg
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 109:287-297
L-(3a-13C)- And L-(6-13C)tryptophan have been synthesized from simple labelled compounds via a single reaction scheme based on the conversion of 1,3-cyclohexanedione into indole. The labelled indoles have been converted in one step into the correspon
Autor:
Ineke van der Hoef, Jesusa S. Josue, Ronald L. Christensen, Johan Lugtenburg, Gary Wiederrecht, F. J. H. M. Jansen, James A. Bautista, Harry A. Frank
Publikováno v:
The Journal of Physical Chemistry B. 106:2083-2092
The spectroscopic properties of open-chain, all-trans-C{sub 30} carotenoids having seven, eight and nine {pi}-electron conjugated carbon-carbon double bonds were studied using steady-state absorption, fluorescence, fluorescence excitation and time-re
Autor:
Johan Lugtenburg, F. J. H. M. Jansen
Publikováno v:
European Journal of Organic Chemistry. 2000:829-836
The all-E isomer of (4,4′-13C2)astaxanthin (1a) has been prepared by total synthesis starting from commercially available 99% 13C enriched acetonitrile. The labelled astaxanthin was obtained in high purity and with high isotope incorporation. For t
Autor:
Joanna Duncan, Johan Lugtenburg, Beverly DeCoster, Ronald L. Christensen, Laurie Gallagher, Michelle Goyette, F. J. H. M. Jansen, Ineke van der Hoef
Publikováno v:
The Journal of Physical Chemistry A. 103:2399-2407
A series of apocarotenes with 5 to 11 conjugated double bonds were synthesized and all-trans isomers were isolated using HPLC techniques. Absorption, fluorescence, and fluorescence excitation spectra were obtained in 77 K glasses. As previously noted
Autor:
Michiel A. Verhoeven, Menno C. F. Monnee, A. A. C. van Wijk, F. J. H. M. Jansen, Alain F. L. Creemers, P. J. E. Verdegem, Johan Lugtenburg
Publikováno v:
Pure and Applied Chemistry. 71:2245-2251
A three-part strategy has been developed to study molecular interactions in biological systems at the atomic level. First, isotopically labeled carotenoids and retinoids are prepared by organic total synthetic schemes with labels at predetermined ato
Autor:
J. C. Merlin, Johan Lugtenburg, Jean-Paul Cornard, F. J. H. M. Jansen, George Britton, R. J. Weesie
Publikováno v:
Biospectroscopy. 5:19-33
Semiempirical AM1 calculations have been carried out for β-carotene and the three xanthophylls (zeaxanthin, canthaxanthin, and astaxanthin) containing oxygen functions (hydroxy/keto groups) found in the majority of natural pigment. The fully optimiz
Autor:
H. J. M. de Groot, Johan Lugtenburg, R. J. Weesie, J. C. Merlin, Jean-Paul Cornard, F. J. H. M. Jansen, George Britton
Publikováno v:
Biospectroscopy
Biospectroscopy, 5(6), 358-370
Biospectroscopy, 5(6), 358-370
Resonance Raman spectroscopy and quantum chemical calculations were used to investigate the molecular origin of the large redshift assumed by the electronic absorption spectrum of astaxanthin in alpha-crustacyanin, the major blue carotenoprotein from
Autor:
Harry A. Frank, Agnes Cua, Johan Lugtenburg, Ruel Z. B. Desamero, Veeradej Chynwat, Ineke van der Hoef, F. J. H. M. Jansen, Michael R. Wasielewski, David F. Bocian, David Gosztola
Publikováno v:
The Journal of Physical Chemistry B. 102:8151-8162
Spheroidene and a series of spheroidene analogues with extents of π-electron conjugation ranging from 7 to 13 carbon−carbon double bonds were incorporated into the B850 light-harvesting complex of Rhodobacter sphaeroides R-26.1. The structures and
Autor:
Harry A. Frank, F. J. H. M. Jansen, Veeradej Chynwat, David J. Gosztola, James A. Bautista, Michael R. Wasielewski, Johan Lugtenburg, Agnes Cua
Publikováno v:
Photosynthesis Research. 55:49-65
The spectroscopic and photochemical properties of the synthetic carotenoid, locked-15,15′-cis-spheroidene, were studied by absorption, fluorescence, circular dichroism, fast transient absorption and electron spin resonance spectroscopies in solutio