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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1965-1973 
    ISSN: 0887-6266
    Keywords: poly(p-phenylenebenzobisthiazole) ; Lewis acid ; Lewis base ; complexation ; mediated solubilization ; aluminum chloride ; nitromethane ; aprotic solvent ; electron donor-acceptor complex ; processing ; spectroscopic evidence ; structural changes ; stability of the complex ; decomplexation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Investigations on aluminum chloride-mediated solubilization of poly(p-phenylenebenzo-bisthiazole), PBZT, in nitromethane revealed that, in general, dilute solutions of the polymer prepared in nitromethane with a large molar excess of the Lewis acid with respect to PBZT were relatively stable and thus suitable for processing into films and coatings via regeneration with hydroxylic nosolvents while polymer solutions with minimum stoichiometrically required (PBZT:AlCl3 molar ratio 1:4) or marginal molar excess of AlCl3 relative to PBZT tended to gel during handling. Structural studies on polymer-Lewis acid complex solutions were performed using 1H and 27Al NMR. 1H NMR of the protonated structure of the model compound 2,6-diphenylbenzo [1,2-d:4,5-d′] bisthiazole was useful for confirming the 1H NMR assignments of PBZT-AlCl3 complex solution in CD3NO2. 27Al NMR was particularly useful in probing the different tetrahedrally coordinated environments of the Al nucleus in the polymer solution, pointing to a complexation interaction between the polymer molecule and the Lewis acid and also between the solvent and the Lewis acid. Direct evidence in the solid state for the presence of a reversible electron donor-acceptor complex (EDA complex) was obtained from FTIR spectra of complexed films, isolated and handled in an inert atmosphere. The structural changes upon PBZT complexation caused significant frequencly shifts in both aromatic as well as heteroring stretching modes relative to PBZT itself, and intensity variations indicative of changes in the resonance configuration between the 1,4-phenylene moiety and the aromatic heterocyclic ring were also observed upon complexation. A preliminary comparison between the pristine PBZT fibers and regenerated PBZT by dilute solution viscometry indicates that the process results, to some extent, in polymer degradation leading to a decrease in the molecular weight of the polymer © 1993 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 8 (1976), S. 205-214 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The oxidation of α-hydroxy acids and α-hydroxy ketones by Br(V) follows the rate-law \documentclass{article}\pagestyle{empty}\begin{document}$$\frac{{- d[{\rm Br(V)}]}}{{dt}} = k_2 [{\rm Br(V)}][{\rm substrate}]$$\end{document}However, the former reaction exhibits a second-order dependence on hydrogen ion concentration while the latter reaction has a third-order dependence. A mechanism involving a slow formation of a bromate ester of the α-hydroxy acid followed by a fast decomposition is proposed. A rate-determining formation of a bromate ester from the conjugate acid of benzoin, followed by a rapid decomposition of the bromate ester, explains the kinetic data for the oxidation of benzoin.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 883-897 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The oxidation of fluorene by vanadium(V) in aqueous acetic acid containing sulfuric acid (1.0M) at 50°C produces fluorenone and 2-hydroxy diphenyl 2′-carboxaldehyde. The order with respect to each reactant is found to be 1. The order dependence on sulfuric acid concentration is 4, indicating that V(OH)23+ could be the active species. An increase in the acetic acid percentage in the solvent medium increases the rate of the reaction. The effect of solvent variation has been discussed in the light of the acidity function and the polarity of the medium. The effect of substituents on the rate has been studied for seven substituted fluorenes, and a linear relationship exists between log k versus σ values with the slope ρ = -3.2. A small isotope effect is observed for the oxidation of the parent compound (kH/kD = 1.2). The effect of temperature on the rate of the reaction has been studied, and the activation parameters are discussed. A mechanism involving the rate-limiting formation of a cation-radical intermediate is proposed.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 773-776 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 10 (1978), S. 581-589 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of thallation of fluorene with thallium triacetate (TTA) in HOAc-H2SO4 solutions led to the rate expression \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm rate = [TTA]}^{\rm 2} [{\rm fluorene}] $$\end{document}The rate of thallation is found to increase with increasing acid concentration, and a sixth-order dependence on [H2SO4] is observed. Decrease in solvent polarity increases the rate of thallation. The effect of substituents is in accord with the electrophilic substitution at an aromatic system. Thallation occurs at 4-position. A mechanism similar to aromatic bromination is proposed for the thallation of fluorene.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 103-110 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the alkaline hydrolysis of five diol monoesters and related esters in aqueous DMSO, aqueous acetone, and aqueous ethanol are reported. A novel solvent dependency of the reactivity pattern of the various esters is noticed. The results are explained on the basis of an internal stabilization of the transition state and the influences of the various solvent systems on such transition states. It is suggested that such dipolar aprotic-protic solvent influences on reaction rates can be used as a criterion in the assessment of anchimeric assistance in such reactions.
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
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