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  • Articles: DFG German National Licenses  (11)
  • 1975-1979  (11)
  • Chemistry  (8)
  • Fixed-ratio schedules  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 64 (1979), S. 1-7 
    ISSN: 1432-2072
    Keywords: Etonitazene ; Etonitazene reinforcement ; Concurrent schedules ; Choice procedures ; Rats ; Taste ; Olfaction ; Auditory stimuli ; Discriminative stimuli ; Conditioned reinforcers ; Fixed-ratio schedules
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Etonitazene and water were concurrently available to four rats during daily 1 h sessions in operant conditioning chambers equipped with two levers and two liquid dippers. A food-induced training procedure was used whereby etonitazene drinking was rapidly established by presenting rats with gradually increased drug concentrations with their daily food ration. When food was subsequently removed from the session and given post-session, etonitazene responding persisted. The rats were subsequently trained on fixed-ratio (FR) schedules with concurrent access to etonitazene and water. The number of dipper presentations compared with etonitazene concentrations (0.078–10.0 μg/ml) resulted in a typical inverted U-shaped function while etonitazene intake (μg/kg) increased directly with concentration. After drinking large quantities of etonitazene the rats showed ataxia, hyper-activity, and stereotypy. Extinction tests demonstrated that rats could discriminate between etonitazene and water on the basis of one dipper full of each liquid; the amount of etonitazene in one dipper was 0.0078 μg. Further tests showed that this discrimination was based on taste or immediate post-ingestional feedback rather than olfactory cues. An auditory stimulus was presented concurrently with responses on the drug lever; however, there was no difference in responding for the drug in the presence or absence of this stimulus except at the lowest concentration. After the extinction tests, when the lowest drug concentration was again available with concurrent water, responding was substantially higher in the presence of stimulus associated with availability of etonitazene. The results extend previous work on oral narcotic intake to a lever-press concurrent choice procedure which is sensitive to reinforcing effects of the drug at low concentrations.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 59 (1978), S. 225-229 
    ISSN: 1432-2072
    Keywords: Rhesus monkeys ; Etonitazene HCl ; Etonitazene concentration ; Etonitazene reinforcement ; Fixed-ratio schedules ; Etonitazene drinking ; Oral self-administration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Drinking of etonitazene HCl was studied in three rhesus monkeys during daily 3-h sessions. As the drug concentration was increased, the number of liquid deliveries decreased, and etonitazene intake (μg/kg body weight) increased. As fixed-ratio (FR) requirements were increased, rate of responding increased, and liquid deliveries slightly decreased. When water was substituted for the drug, there was a large increase in responding for several sessions, followed by a slow decline to low rates. When etonitazene was reintroduced, responding abruptly increased to previous drug levels. These data suggest that etonitazene can serve as a positive reinforcer when taken orally by rhesus monkeys.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 57 (1978), S. 133-136 
    ISSN: 1432-2072
    Keywords: Rhesus monkeys ; Ethanol reinforcement ; Ethanol concentration ; Blood ethanol level ; Ethanol drinking ; Fixed-ratio schedules ; Intoxication
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Ethanol deliveries maintained fixed-ratio (FR) responding of three rhesus monkeys during daily 3-h sessions. At FR values of 8 or 16, ethanol concentration was varied in the sequence 0 (water), 8, 11.3, 16, 22.6, 32, 8, and 0% (w/v). As the ethanol concentration increased, number of liquid deliveries decreased, although intake of ethanol (g/kg/session) increased somewhat. Blood ethanol levels were usually greater than 200 mg% and occasionally greater than 300 mg%.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 14 (1975), S. 173-196 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Miyazawa-Blout-Krimm (M-B-K) treatment of polypeptide absorption in the infrared is extended to the calculation of circular dichroism (CD), linear dichroism, and oriented CD for the amide I and amide II transitions. Matrix methods are applied to the α helix and β structures using measured values for the strengths and directions of the transition dipole moments and empirical values from M-B-K for the coupling constants.Relatively small aggregates, a 36-residue helix, and 8-chain × 4-residue β sheets, are large enough to show calculated absorption agreeing with M-B-K results, which are based on infinite lattices.In all cases the predicted CD is an approximately conservative couple. The strongest CD should appear in the α helix, Δε/ε ≃± 10-3 for both transitions. The amide II transition should show moderate CD couples in both β structures, Δε/ε ≃ (+2 to -1) × 10-4. The amide I transitions in β structures should show weak CD couples, Δε/ε = (+3 to -2) × 10-5, except that the negative branch in the antiparallel structure may be detectable (Δε/ε ≃ -2 × 10-4) because absorption is very low at its wavelength peak.CD on oriented samples should be enhanced over the unoriented cases, giving values as large as Δε/ε = 3 × 10-3 because particular directions of observation allow the light to avoid much of the absorption in the sample.If all three structures are considered as helices, then the larger distance of the transition dipoles from the axis in the α helix, and the orientations of the transitions in the different structures, are the factors that, in terms of our previous theoretical work [Snir and Schellman (1973) J. Phys. Chem. 77, 1653] satisfactorily explain the calculated results. Simple dipole-dipole interaction is calculated to make a substantial contribution to the coupling between groups.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 23 (1977), S. 529-538 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Previous studies of copper-ion catalyzed ascorbic acid autoxidation have indicated zero-order, first-order, or Michaelis-Menten dependence of rate on ascorbic acid or copper concentrations and first- or half-order dependence on oxygen concentration. A simple mathematical model of gas-liquid mass transfer with liquid phase reaction accounts for the various behaviors. Use of an experimental technique that eliminates the mass transfer step shows that the oxidation rate dependence is first order in copper, half order in oxygen, and Michaelis-Menten in ascorbic acid concentrations.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 19 (1975), S. 3361-3367 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 9 (1977), S. 589-592 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The carbon-fluorine coupling constants in 33 different substituted benzotrifluorides (trifluoromethyl-benzenes) have been determined. The 3J(CF) to the ortho aromatic ring carbons varied between 1.7 and 5.6 Hz and, in a given molecule, were always larger than the 5J(CF) to the para carbon, which ranged between 0.7 and 1.7 Hz. Coupling to the meta carbons, 4J(CF), was not observed and is under 0.3 Hz.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 14 (1979), S. 196-197 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chemical ionization induced fragmentations (with 2-methylpropane as reagent gas) of 4-methyl- and 4,5-dimethyl-2-phenyl-1,3,2-dioxaborolane and 4-methyl-2-phenyl-1,3,2-dioxaborinane gave in each case two fragments, a hydrocarbon ion and metaboric acid. Propeae and thence metaboric acid are eliminated from 4,6-dimethyl-2-phenyl-1,3,2-dioxaborinane. The mechanisms of the fragmentations are discussed. Under the conditions used 2-phenyl-1,3,2-dioxaborolane and 2-phenyl-1,3,2-dioxaborinane do not fragment.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 14 (1979), S. 507-511 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Consequential upon determinations of kinetic rate constants of ion/molecule reactions in methane and isobutane, simple equations are presented from which the pressures of methane and isobutane in the ion source of chemical ionization mass spectrometers can be calculated. Account is taken of the design of the ion source and it is only necessary to determine two ion currents for each gas.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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