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  • General Chemistry  (2)
  • Cationic amphiphiles  (1)
  • Physical Chemistry  (1)
  • Solvent effects  (1)
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  • 1
    ISSN: 1434-193X
    Keywords: Cationic amphiphiles ; Transfection ; Pyridinium salts ; Vesicles ; Lipoplex ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Pyridinium amphiphiles have found practical use for the delivery of DNA into cells. Starting from 4-methylpyridine, a general synthesis has been devised for the production of pyridinium amphiphiles which allows variation in both the hydrophobic part and in the headgroup area of the compounds. By means of differential scanning microcalorimetry, zeta potential, particle size measurements and cryo electron microscopy, some characteristics of the pyridinium amphiphile/DNA complexes have been determined.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    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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  • 3
    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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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 32 (1993), S. 1545-1579 
    ISSN: 0570-0833
    Keywords: Hydrophobic effect ; Water ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The term hydrophobic interactions denotes the tendency of relatively apolar molecules to stick together in aqueous solution. These interactions are of importance in many chemical disciplines, including the chemistry of in vivo processes. Enzyme-substrate interactions, the assembly of lipids in biomembranes, surfactant aggregation, and kinetic solvent effects in water-rich solutions are all predominantly governed by hydrophobic interactions. Despite extensive research efforts, the hydration of apolar molecules and the noncovalent interactions between these molecules in water are still poorly understood. In fact, the question as to what the driving force for hydrophobic intractions is shifts the study into a quest for a detailed understanding of the remarkable properties of liquid water. This review highlights some of the novel insights that have been obtained in the past decade. The emphasis is on both hydrophobic hydration and hydrophobic interactions since both phenomena are intimately connected. Several traditional views have been found to be deeply unsatisfactory, and courageous attempts have been made to conceptualize the driving force behind pairwise and bulk hydrophobic interactions. The review presents an admittedly personal selection of the recent experimental and theoretical developments, and when necessary, reference is made to relevant studies of earlier date.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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