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  • Polymer and Materials Science  (11)
  • Binding assay  (1)
  • Computational Chemistry and Molecular Modeling  (1)
  • 1
    ISSN: 1432-0584
    Keywords: B-CLL, IL-2, IL-2 receptor ; Binding assay ; Affinity cross linking
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Functional and structural characteristics of interleukin 2 (IL-2) receptors on B-cell chronic lymphocytic leukemia (B-CLL) cells were analyzed by a proliferation assay, IL-2 binding assay and cross-linking study. In the3H-thymidine incorporation assay, purified B-CLL cells from four out of sixteen cases, in which the percentage of Tac antigen (Tac Ag) positive cells in peripheral blood lymphocytes ranged from 0 to 48.8%, responded to IL-2 (100 U/ml) after both 3- and 6-day incubation. No relationship was found between the responsiveness to IL-2 and the percentage of Tac Ag positive cells. In the radiolabeled IL-2 binding assay, however, B-CLL cells from all seven cases examined, including three cases with mitogenic response to IL-2 and four cases without mitogenic response, were shown to have both high- and low-affinity receptors. The number of high- and low-affinity receptors per cell ranged from 29–186 and from 420 to 1,800, respectively. Furthermore, with the affinity cross-linking method p55 (Tac Ag) and p70/75 were found even in cases without mitogenic response in their B-CLL cells. In conclusion, the B-CLL cells so far examined possessed high-affinity IL-2 receptors consisting of p55 and p70/75; nevertheless, this was not sufficient to respond to the mitogenic signal of IL-2.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 23 (1983), S. 387-397 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Accurate Hellmann-Feynman force method for the first and second derivatives of energy has been applied to the studies of the chemical reaction systems. We have studied (1) the electronic origins of the structure-reactivity correlations in the reactions CH3 + H → CH4 and CH3 + CH3 → C2H6 and (2) the geometries and force constants in the reaction intermediate and the transition state of the reactions F- + HF → [FHF]- → FH + F- and H- + CH4 → CH4 + H-, respectively. An intuitive simplicity of the underlying concepts of the first and second derivatives of the present approach is shown in the analysis.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 49 (1961), S. S11 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 14 (1954), S. 312-314 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 20 (1956), S. 537-550 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Several problems in the process of radical polymerization, e.g., the relation between the chemical structure of vinyl monomer and its chemical reactivity, the prevalence of head-to-tail configuration, the reactivity of initiator radicals, the alternation tendency in heteropolymerization, and the relative ease of coupling in several cases of homopolymerization, are treated by the theory previously proposed by the present authors, in which reactivity is represented by the magnitude of stabilization energy due to π conjugation between a monomer and a radical in the transition state. In addition, a brief discussion on the existing theories of reactivity and some applications of Hush's method to the problem of termination are presented. The agreement between results of calculation and experiment is shown to be almost statisfactory.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 26 (1957), S. 311-321 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The stabilization energy due to the conjugation taking place between a monomer and an ion in the transition state is calculated by the LCAO perturbation theory, in the same way in which the reactivity in radical copolymerization has previously been treated. In terms of this stabilization energy, the reactivity ratios of several monomer pairs in ionic copolymerization are satisfactorily interpreted. It is noted that, by the present method, both the radical and ionic copolymerization can be treated in a unified manner, whereas it is difficult in existing empirical methods. The positions of attack in polymer ions as well as in monomers, which are predicted by the frontier electron densities, are shown to agree well with experimental facts. The relative reactivities of vinyl monomers in ionic homopolymerization is also explained successfully by the magnitude of the localization energy computed by the LCAO method.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 39 (1959), S. 487-492 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A theoretical interpretation of the mechanism of stereospecific cationic polymerization in a homogeneous system at low temperature is given. The existance of a counterion in the vicinity of a charged carbon atom of a growing polymer ion is assumed and a repulsive interaction is considered to be between the substituent of the attacking monomer and that of the polymer. The most probable geometrical conformation of a monomer and a polymer ion in the transition state is determined by the magnitude of stabilization due to the overlap between atomic orbitals of ion and monomer. Our experimental results can be explained satisfactorily by this mechanism.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 42 (1960), S. 535-544 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The present investigation is concerned with the relationship between P, the reactivity of a radical, and Q that of a monomer in the propagation reaction. At first, P values are calculated from the accumulated data of the rate constants of the propagation reaction. From these results, the relation is shown to be represented by the following equation: \documentclass{article}\pagestyle{empty}\begin{document}$ \log {\rm }P = kQ + a(k 〈 0) $\end{document} where k and a are constants. The P values in the termination reaction (Pt) are also calculated, and the relation between these values and Q values are examined. The results show that the similar relation found in the propagation reaction holds in this step too. By applying the method of Evans and co-workers, a sufficient explanation for this equation is not obtained, but the analogous equation can be derived. The present authors suggest that the inverse proportion between log P and Q appears to be based on the following different principles: (1) the inverse proportion between the magnitude of localization energy of the radical and that of monomer, and (2) the linear free energy relationship found in organic chemistry.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 7 (1969), S. 23-26 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 2215-2222 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A model is proposed for the transition state of the anionic copolymerization of styrene and p-methylstyrene in hydrocarbon solvent with lithium counterion. An LCAO-MO treatment which considers the effect of the positive counterion on the negative chain end is used to calculate the electrostatic and the π electron resonance contributions to the activation energies of the four propagation reactions. The electron contributions to the activation energies are also calculated for the propagation reactions of free ions, i.e., in the absence of a counterion. The previously determined rate constants in benzene and tetrahydrofuran are then compared with the results of these calculations.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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