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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 4 (1992), S. 19-26 
    ISSN: 1040-0397
    Keywords: Amalgam electrode ; cadmium ; macrocyclic complexes ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electrochemical oxidation of cadmium amalgam was studied in the nonaqueous solvents CH2Cl2, 1,2-C2H4Cl2 and propylene carbonate. Significant coordination effects were observed between the electrogenerated Cd(II) ions and 18-membered macromonocyclic ligands, each containing six Lewis bases heteroatoms: 18-O6, 18-S6, 18-N2O4, and 18-N6. The stoichiometries and the stabilities of the resulting complexes were determined. These stabilities increase from 18-O6 or 18-S6 to 18-N6.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 1 (1989), S. 493-499 
    ISSN: 1040-0397
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of 12 macrocycles containing 4, 6, or 8 N, S, and O heteroatoms (with increasing size from 14 to 24 atoms in the cycle) was studied to ascertain size and heteroatoms effects on the formation and 14 redox characteristics of their mercuric complexes. The concentration dependence of anodic currents at mercury electrodes in solutions of these ligands led to the determination of the formation constants of the complexes generated according to the folling of \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm Hg} \mathbin{\lower.3ex\hbox{$\buildrel\textstyle\rightarrow\over {\smash{\leftarrow}\vphantom{_{\vbox to.5ex{\vss}}}}$}} {\rm Hg}^{{\rm 2 + }} {\rm + 2e}^{\rm - } {\rm,}\,{\rm Hg}^{{\rm 2 + }} {\rm + jL} \mathbin{\lower.3ex\hbox{$\buildrel\textstyle\rightarrow\over {\smash{\leftarrow}\vphantom{_{\vbox to.5ex{\vss}}}}$}} {\rm (HgL}_{\rm j} {\rm)}^{{\rm 2 + }} $$\end{document} In propylene carbonate, the resulting mercuric complexes were stable (log Ks up to 40) mono- and dinuclear species. Their stability depends both on the nature of the heteroatoms and on the size of the macrocycle. For identical ligand sizes, the stability sequence N 〉 S 〉 O was established for mercuric complexes.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 16 (1955), S. 549-576 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymerization in solution of a variety of water-soluble monomers with a variety of water-soluble redox initiators is described and a detailed study is reported on the polymerization, in aqueous solution, of methyl vinyl ketone and of methyl methacrylate under the influence of potassium sulfate-silver nitrate. Keeping the persulfate concentration constant and varying the silver nitrate or, conversely, keeping the silver nitrate constant and varying the persulfate, it is found that, except at very high concentration of catalyst, both the rate of polymerization and the molecular weight of the polymer bear a linear relation to the square root of the catalyst concentration, in harmony with the general theory of catalyzed bulk and emulsion polymerization. The molecular weight of the polymer formed diminishes with increase in the temperature of polymerization. The study of redox polymerization in water, without emulsifier, has been extended to the case of a mixture of a water-soluble and a water-insoluble monomer, and it has been found that copolymerization proceeds at a reasonable rate and frequently forms a stable latex. The copolymerization of styrene and 5 or 10 per cent of its weight of methacrylonitrile in water under the influence of a water-soluble persulfate-bisulfite redox pair has been examined with some closeness. Polymerization is apparently initiated in the aqueous solution, since, contrary to the state of affairs in emulsion polymerization, water-soluble retarders are more effective than oil-soluble ones, when the retarder is added at the outset. If the retarder is added at a later stage of polymerization, oil-soluble reagents are more effective than water-soluble ones. The water-soluble monomer enters into the polymer at a greater rate than the water-insoluble one, but it appears that, even at the earliest stage at which it is practicable to take samples co-polymerization occurs. The influence of catalyst concentration on the rate of polymerization, the molecular weight of the polymer, and the latex particle size was examined.
    Additional Material: 20 Ill.
    Type of Medium: Electronic Resource
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