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  • 1985-1989  (23)
  • 1975-1979  (9)
  • 1970-1974  (3)
  • 1925-1929  (1)
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 40 (1975), S. 2572-2573 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    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 91 (1989), S. 778-782 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Cyanoacetylene underwent polymerization reaction in a solid phase at pressures above 1.5 GPa. The Raman study of the reaction product showed that the polymer had a conjugated linear backbone with CN pendant groups. The Raman spectra for this substituted polyacetylene demonstrated a resonance behavior similar to that reported for trans-polyacetylene. The optical gap associated with the π–π* transition in the conjugated system was smaller than that of trans-polyacetylene, probably due to the resonance interactions between the CN triple bonds and the conjugated double bonds.
    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 89 (1988), S. 529-534 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The mechanism and kinetics of the pressure-induced polymerization of acetylene were studied by Raman spectroscopy. The polymerization reaction occurred in the orthorhombic phase at room temperature and pressures above 3.5 GPa. Dominant formation of trans-polyacetylene suggested that the monomer underwent trans opening of the triple bond and polymerized along the diagonal of the bc plane of the unit cell. The reaction was described as an idealized one-step and one-dimensional growth process by an Avrami equation with an exponent 1.34.
    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 88 (1988), S. 4565-4568 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Raman spectra were measured for liquid (0–0.7 GPa), crystalline cubic (0.7–0.9 GPa), and orthorhombic (0.9–3.5 GPa) phases in C2H2 at room temperature. For the orthorhombic phase, the high-pressure behavior of the librational and internal vibrations was obtained in a wide pressure range. The frequencies of all the librational modes increased monotonically with pressure, while those of the internal modes showed a variety of frequency shifts depending on vibrational mode. These high-pressure data will be of great use for the construction of theoretical models for the intermolecular interactions in crystalline C2H2.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 2814-2817 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: At room temperature, cyanoacetylene undergoes a liquid–solid transition at 70±30 MPa and further a polymerization reaction at 1.5 GPa. Raman spectra indicates that the crystal structure of the high-pressure phase is isomorphic with the monoclinic low-temperature structure (P21/m, Z=2), in which linear cyanoacetylene molecules are joined with CH NC hydrogen bonds to form infinite one-dimensional chains. The internal stretching frequency of the C–H proton donor decreases wtih increasing pressure, while that of the C 3/4 N proton acceptor increases. The librational modes associated with the rotational motions of the rigid molecules show large shifts to higher frequencies with pressure. The observed frequency shifts are attributed to the strengthening of the CH⋅⋅⋅NC hydrogen bond in the one-dimensional molecular chain.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 52 (1988), S. 2122-2123 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The hydrogen-induced transformation from the crystalline to the amorphous state in GdFe2 has been studied by means of differential thermal analysis. GdFe2 absorbs hydrogen in the crystalline state above 420 K by an exothermic reaction. The resultant crystalline c-GdFe2H3.8 alloy transforms to the amorphous a-GdFe2H2.8 alloy above 470 K exothermally, which crystallizes to the stable phases α-Fe and GdH2 above about 700 K. The driving force for the hydrogen-induced transformation is suggested to be the difference in the enthalpy resulting from the different hydrogen occupation sites in both states of alloy.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 62 (1987), S. 3314-3317 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The influence of hydrogenation on the structural change and magnetic properties of the Laves-phase GdFe2 compound has been investigated. Crystalline c-GdFe2 absorbs 4.4 hydrogen atoms per formula unit without any change in the crystal structure below 423 K. On the other hand, GdFe2 transforms to amorphous a-GdFe2H3.6 by hydrogenation from 423 to 523 K, where the decomposition of GdFe2 into GdH2 and α-Fe is prevented. The same amount of hydrogen (3.6 atoms per formula unit) dissolves in amorphous alloys produced by both hydrogenation and rapid quenching. Hydrogenation sharply reduces the Curie temperature of the crystalline alloy from 818 to 107 K, in contrast to the Curie temperature of 443 K for the hydrogen-induced amorphous alloy. The temperature dependence of the magnetization of the hydrogen-induced amorphous alloy is identical to that of the hydrogenated rapidly quenched amorphous alloy, suggesting similarity of their structures. The magnetization of the hydrogen-induced amorphous alloy shows a broad peak around 300 K. Above 300 K the magnetization of the amorphous alloys is largely uninfluenced by hydrogen. Below the peak it is reduced by hydrogenation.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 18 (1971), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract— Seven-day-old rats were injected intraperitoneally with l-phenylalanine (1 g/kg) and the time course of brain polyribosome disaggregation and changes in brain levels of phenylalanine, tryptophan and tyrosine were determined. Disaggregation of brain polyribosomes preceded the increase in levels of phenylalanine in brain, and followed the same time course as depletion of tryptophan from brain.The effects of several metabolites of phenylalanine (which are formed in phenylketonuria) on protein synthesis in vitro was determined for brain and liver systems. None of the compounds tested was inhibitory at concentrations below 10 mM and in all cases hepatic protein synthesis was more sensitive to inhibition than was the corresponding system from brain.Ribosomal dimers, formed in brain after injection of phenylalanine, were incapable of supporting high levels of protein synthesis in vitro, a finding that suggested that the inhibition of protein synthesis in vitro in cell-free systems of brain tissue after injection of phenylalanine into young rats was mediated by disaggregation of brain polyribosomes associated with tryptophan deficiency in brain.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 24 (1975), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Clinical and experimental pharmacology and physiology 16 (1989), S. 0 
    ISSN: 1440-1681
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: 〈list xml:id="l1" style="custom"〉1To clarify whether acute changes in the properties of baroreflexes can occur in man, we evaluated the time course of baroreflex control of heart rate and cardiopulmonary baroreflex control of forearm vascular resistance (FVR) over 240 min after intravenous administration of propranolol (0.2 mg/kg) in 13 healthy young men.2Systolic and diastolic blood pressure remained unchanged after propranolol. Propranolol significantly decreased cardiac index and heart rate, and significantly increased total peripheral resistance. These effects remained unchanged for 240 min after propranolol.3Baroreflex control of heart rate was significantly augmented immediately after, and at 30, 60 min after propranolol, but partly reverted to the initial level afterwards. Cardiopulmonary baroreflex control of FVR was reduced immediately after, and at 30, 60 min after propranolol, but partly reverted to the initial level afterwards. Pressor responses to phenylephrine was reduced immediately after propranolol, but no significant differences were observed after 30 min.4These results suggest that acute changes in the properties of baroreflexes occur in man after propranolol.
    Type of Medium: Electronic Resource
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