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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1997 (1997), S. A1 
    ISSN: 0947-3440
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0947-3440
    Keywords: Hetero Diels-Alder reaction ; Water chemistry ; Solvent effects ; Cosolvent effects ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The adduct of the Diels-Alder reaction of nitrosobenzene with cyclopentadiene is not stable in solution. The equilibrium constant for the reaction depends strongly on the medium and water induces a spectacular shift to the adduct. Comparison with the bimolecular addition of nitrosobenzene to 1,3-cyclohexadiene enables separation of the effect of the aqueous medium on the rate constants for the forward and reverse reaction. In water, the former reaction is accelerated and the latter is retarded. The deceleration of the retro reaction in water is due to hydrogen-bond stabilization of the adduct. The influence of cosolvents and micelles on the cycloreversion is discussed.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0947-3440
    Keywords: Cyclic phosphate amphiphiles ; Micellization ; Vesicle fusion ; Bilayer packing ; Vesicles ; Amphiphiles ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Herein we describe the synthesis and aggregation of the sodium salts of a series of 5-alkyl-2-hydroxy-1,3,2-dioxaphosphorinan-2-ones and 5,5-dialkyl-2-hydroxy-1,3,2-dioxaphosphorinan-2-ones in aqueous solution. The results are compared with properties of previously studied sodium di-n-alkyl phosphates. The single-tailed surfactants (6a, b, g) form micelles whereas the double-tailed ones (6f, h-k) form vesicles, as revealed by transmission electron microscopy (TEM). Critical micelle concentrations (CMC) for 6a, b, g were determined using different techniques: UV spectroscopy, microcalorimetry, and conductometry. Phase transition temperatures of the bilayers were measured by differential scanning calorimetry (DSC) and by fluorescence depolarization. Fusion of the vesicles was studied employing the resonance energy transfer (RET) assay based on lipid mixing and TEM. Vesicles of 6h-k fuse upon addition of Ca2+ or Mg2+ ions, to almost the same extent in each case. Fusion only takes place above the phase transition temperature (Tc) of the different bilayers. The threshold concentrations of Ca2+ and Mg2+ ions for fusion of the different vesicles are below 0.1 mM. The initial rate of fusion is high and precludes the measurement of accurate rate constants. Upon addition of calcium chloride different processes occur. Vesicle fusion, crystallization, and formation of multilamellar sheets were observed, as was apparent from experiments with vesicles formed from 6h. Leakage through the vesicular bilayer of 6h was determined by measuring the carboxyfluorescein release from the aqueous compartment of the vesicles. All data are consistent with the notion that the alkyl chain packing in the bilayers of the vesicles formed from the cyclic phosphates is less efficient than that in the bilayers of vesicles composed of di-n-alkyl phosphates.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 5 (1992), S. 451-456 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This paper describes a fluorescence depolarization and 31P NMR spectroscopic study of the phase transition behaviour of a series of identical and mixed-chain di-n-alkyl phosphate vesicles in the presence of different counterions (Na+,K+,Me4N+,Ca2+). Using trans, trans, trans-1, 6-diphenyl-1, 3, 5-hexatriene (DPH) as a fluorescent probe, the fluorescence polarization (P) was measured for the identical-chain vesicles (Na+, K+, Me4N+) as a function of temperature. The temperature for the main phase transition (Tm) only responded to variation of the counterion in the case of the longer-chain di-n-alkyl phosphates, with Tm decreasing in the sequence Na+ 〉 K+ 〉 Me4N+. This result is rationalized in terms of a decreasing counterion binding, which affects chain ordening in the core of the bilayer. Peak intensities and line widths of the 31P NMR resonances for the bilayer vesicles suggest a more complex phase behaviour, but the overall results are reconcilable with the picture emerging from the fluorescence depolarization experiments. Fluorescence depolarization measurements were also carried out with vesicles formed from the sodium di-n-alkyl phosphates and in the presence of various concentrations of Ca2+ (0-6 mM) at temperatures above Tm. For both the identical-chain and mixed-chain di-n-alkyl phosphate vesicles, a steep increase in P was found between ca 1.0 and 1.4 mM Ca2+, indicative of a strong Ca2+-induced ordening of the alkyl chains.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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