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AbstractAbstract
[en] In order to develop probes of the structure of chromophores, the author introduces isotopic modifications at specific chromophoric positions as structural probes. To obtain bacteriorhodopsin, rhodopsin and their photoproducts labelled in the chromophore at selected positions, bacterioopsin and opsin were reacted with the appropriate labelled a11-trans and 11-cis retinals. The author describes the synthesis of a11-trans retinal selectively 13C labelled at different positions. The characterization of these labelled a11-trans retinals by mass spectrometry, 300 MHz 1H NMR and 75 MHz 13C NMR spectroscopy is given. The photochemical preparation and isolation of the pure 9-, 11- and 13-cis forms is described in the experimental part. (Auth.)
Source
5 Jun 1986; 175 p; Includes Dutch summary; Includes previously published material; 366 refs.; 58 figs.; 25 schemes; 26 tabs.; Proefschrift (Dr.).
Record Type
Miscellaneous
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Thesis/Dissertation
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