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  • Photochemical reactions of biomolecules biochemical reaction mechanisms and kinetics, model reactions  (1)
  • equilibrationtime  (1)
  • Springer  (2)
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  • Springer  (2)
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  • 1
    Digitale Medien
    Digitale Medien
    Vectorial photoinduced electron transfer in phospholipid vesicles and LB bilayers (1994)
    Springer
    Il nuovo cimento della Società Italiana di Fisica 16 (1994), S. 1471-1477 
    Details
    ISSN: 0392-6737
    Schlagwort(e): Photochemical reactions of biomolecules biochemical reaction mechanisms and kinetics, model reactions ; Conference proceedings
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Summary Photoinduced electron transfer (PET) was studied in phospholipid vesicles and in Langmuir-Blodgett bilayers in the attempt to produce a model for electron transfer processes in biological media. Spatial organization of the reaction centers in lipid membranes needs to be controlled in order to provide high efficiency of light-to-chemical energy conversion. We designed a phospholipid system where the donor is localized in the inner bilayer whereas the acceptor is at the polar groups-water interface. We used dipalmitoylphosphatidic acid vesicles containing low molar fractions of dipalmitoylphosphatidylcholine with pyrene (donor) bound to one of the alkyl chains. Methylviologen (acceptor) was added to the external aqueous phase; upon photoexcitation of the donor we observed the electron transfer to take place in a unidirectional manner from the inside of the bilayer to the interface. Information about the location of the donor was obtained studying the photophysical properties of the pyrene chromophore in vesicles and in LB layers. The photoinduced electron transfer reaction was evidenced by quenching of pyrene fluorescence in the presence of increasing concentrations of acceptor, the process was studied both with steady-state and time-resolved fluorescence emission. Fluorescence intensity was found to decrease with increasing concentration of methylviologen, similar results were obtained for vesicles and LB layers of analog composition immersed in a methylviologen solution. Lifetimes of the excited species were found to be of the same order of magnitude in vesicle and LB-layer systems.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/BF02462031
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Fluorescence and viscometry study of complexation of poly(acrylic acid) with poly(acrylamide) and hydrolysed poly(acrylamide) (1991)
    Springer
    Colloid & polymer science 269 (1991), S. 131-137 
    Details
    ISSN: 1435-1536
    Schlagwort(e): Interpolymercomplexation ; excimerfluorescence ; cooperativebinding ; equilibrationtime ; meanstoichiometry
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Notizen: Abstract Interpolymer complexation of poly(acrylic acid) with poly(acrylamide) and hydrolysed poly(acrylamide) was studied by fluorescence spectroscopy and viscometry in dilute aqueous solutions. Changes in chain conformation and flexibility due to the interpolymer association are reflected in the intramolecular excimer fluorescence of pyrene groups covalently attached to the polymer chain. Both poly(acrylamide) and hydrolysed poly(acrylamide) form stable complexes with poly(acrylic acid) at low pH. The molecular weight of poly(acrylic acid) and solution properties such as pH and ionic strength were found to influence the stability and the structure of the complexes. In addition, the polymer solutions mixing time showed an effect on the mean stoichiometry of the complex. The intrinsic viscosity of the solutions of mixed polymers at low pH suggested a compact polymer structure for the complex.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/BF00660302
    Standort Signatur Erwartet Verfügbarkeit
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    Artikel (Nationallizenzen)
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