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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 768-774 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The cooling process of DNA gel (20 wt./wt.%–40 wt./wt.%) with various counterions has been investigated by low frequency Raman spectroscopy and differential scanning calorimetry (DSC). We have found that the dynamics of water of hydration is different among counterion species below 0 °C. For K-, Rb-, Sr-, and Ba-DNA gels, a part of nonfreezing water slowly changes its dynamical structure, when the gel is kept at ∼−30 °C after cooling below −50 °C. This relaxation process can be monitored both by the frequency increment of the lowest Raman band from ∼17 to ∼20 cm−1 and by the intensity increment of an extra endothermic peak in DSC heating curves. We propose that this relaxation process corresponds to the crystallization of a part of nonfreezing water and is caused by the rearrangement of the secondary hydrated water including counterions when the temperature is held at ∼−30 °C. This relaxation process cannot be observed for NH4- and Li-DNA gels. For Na-, Mg-, and Ca-DNA gels, this phenomenon is more complicated. The dynamical behavior of water of hydration in DNA gels is thus concluded to be different among counterion species.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 100 (1994), S. 2407-2412 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Low-frequency depolarized Raman spectra of aqueous solutions of D-glucose and D-galactose have been investigated in the frequency region from −250 cm−1 to 250 cm−1 at 30.0 °C as a function of concentration up to 0.04 molar ratio. The dynamical structure of water in aqueous solution is analyzed by using the reduced Raman spectrum χ‘(ν¯), which corresponds to the imaginary part of the dynamical susceptibility. The reduced spectrum is fitted with the superposition of one Cole–Cole type relaxation mode and two damped harmonic oscillator modes by a nonlinear least-squares fitting. The effects of D-glucose and D-galactose on the dynamical structure of water in aqueous solution are similar. The relaxation time of hydrogen bond among water molecules becomes slower with increasing sugar concentration. The characteristic frequencies of stretching-like and bending-like vibrations among water molecules do not change in both D-glucose and D-galactose aqueous solutions.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 3453-3458 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Depolarized low-frequency Raman spectra of aqueous electrolyte solutions (ACl and BCl2; A=Li, Na, K, Rb and B=Mg, Ca) in the frequency region from −250 to 250 cm−1 have been investigated over a wide concentration range. The spectra were analyzed with one Cole–Cole type relaxation mode and two damped harmonic oscillators. A broad relaxation mode was found below 20 cm−1. For the present aqueous electrolyte solutions, with increasing salt concentration each relaxation time τ becomes longer than that of liquid water τwater. The relaxation time is considered to correspond to the duration time of the tetrahedral structure of bulk water. We have found that the concentration dependence of the ratio τ/τwater is equivalent to the ratio η/ηwater, where η is the viscosity of aqueous solutions.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 104 (1996), S. 7377-7381 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The low-frequency Raman spectra of dioxane aqueous solutions have been analyzed from a dynamical aspect of water structure. The reduced Raman spectra χ″(ν¯) of the dioxane aqueous solutions are well explained by a superposition of three characteristic modes of water and one Gaussian mode (∼60 cm−1) of dioxane. The concentration dependence of χ″(ν¯) spectra shows that the 190 cm−1 mode of water disappears below about 0.8 molar fraction of water. This molar fraction corresponds to the ratio of four water molecules to one dioxane molecule. This means that the tetrahedral-like structure of water which is formed by five water molecules is almost destroyed below about 0.8 molar fraction. Thus the basic idea of the five water molecules model of liquid water has been confirmed from Raman spectroscopic point of view. © 1996 American Institute of Physics.
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 104 (1996), S. 1-6 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Depolarized low-frequency Raman spectra of aqueous solutions of L-xyloascorbic acid and its epimer D-araboascorbic acid have been investigated as a function of concentration at 30 °C. The influence of fluorescence in the low-frequency Raman spectral intensity of D-araboascorbic acid aqueous solution was removed by the background correction. The reduced χ″(ν¯) spectrum, which corresponds to the imaginary part of the dynamical susceptibility due to the dynamical structure of water in aqueous solutions, was analyzed with the superposition of one Cole–Cole type relaxation mode and two damped harmonic oscillator modes. The effect of L-xyloascorbic acid on the dynamical structure of water is less than that of D-araboascorbic acid. © 1996 American Institute of Physics.
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 102 (1995), S. 9474-9479 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The hydration structure of L-xylo and D-arabo ascorbic acids in aqueous solutions were investigated by a dielectric relaxation measurement over a wide frequency range from 10 MHz to 10 GHz from a standpoint on the difference of biological activity at 25 °C. In order to clarify the hydration structure the concentration dependence of dielectric relaxation was investigated not only in aqueous solution but in water–ethanol mixtures. Two kinds of dielectric relaxation processes were observed in each isomerism solution. The low frequency process is assigned to cooperative motions of ascorbic acid molecules and hydrated water. The high frequency process is assigned to reorientational motions of bulk water. From the results of the dehydration process out of the ascorbic acid surface by ethanol it is concluded that the amount of hydrated water of the L-xylo ascorbic acid is more than that of the D-arabo ascorbic acid. © 1995 American Institute of Physics.
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  • 7
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 19 (1986), S. 1604-1612 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 1558-1568 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The low-frequency Raman spectra of alkali halide AX (A=Na, K, Rb; X=Cl, Br) aqueous solutions with various temperatures and concentrations are investigated. We have found that at the supercooled temperature region the relaxation time of the KX and RbX aqueous solutions becomes shorter than that of pure water. Since in these solutions the viscosity decreases with increasing concentration, this result suggests that the relaxation time of the electrolytic solutions in the Raman region is strongly correlated with the viscosity. Moreover, through comparing the spectral profiles of the relaxation mode among AX aqueous solutions we demonstrate that the pattern of the concentration dependence of the relaxation mode parameters such as the activation energy changes between NaX and (KX, RbX) aqueous solutions. © 1999 American Institute of Physics.
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 83 (1985), S. 5972-5975 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Low frequency Raman spectra (±50 cm−1) of DNA gels from 0 to −140 °C have been obtained. A drastic spectral change near −20 °C has been observed, and this is well explained by the model of coupled dynamics between the collective vibrational mode of the DNA and the relaxational mode of the secondary hydration shell. The obtained relaxation time of the secondary hydration shell at 0 °C is τ(approximate)4×10−12 s which is the same order as that of bulk water.
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