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  • 1995-1999  (2)
  • Chemistry  (2)
  • emulsion polymerization  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 989-1006 
    ISSN: 0887-624X
    Keywords: emulsion polymerization ; molecular weight distribution ; styrene ; morphology ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Styrene ab initio emulsion polymerizations were conducted at 70°C in an automated reaction calorimeter. Two polymerizations were performed, one above and the other below the critical micelle concentration (CMC) of the surfactant, thus ensuring differing polymerization kinetics between the two: the system below the CMC gave large particles that were expected to follow pseudobulk kinetics, while that above the CMC gave small particles that were expected to follow zero-one kinetics. The evolutions of the molecular weight distributions (MWDs) were characterized by removing samples periodically during the course of the reactions and analyzing with gel permeation chromatography. Interpretation of the data used average molecular weights, the GPC MWDs, and the number MWDs, as functions of conversion. It was found that all of the number MWDs (plotted as ln (number of polymer chains) vs. molecular weight of polymer chains) were concave-up at low molecular weights and become nearly linear at molecular weights (≥3-4 × 106); this linearity is expected from theory. The slope of the high molecular weight region was consistent with theory for the dominant mode for chain stoppage: termination and transfer for the pseudobulk system and (predominantly) chain transfer to monomer for the zero-one system. The most likely explanation for the concavity of the number MWDs is a heterogeneity of radicals: some surface anchored with sulfate end groups and others (with hydrogen end groups arising from transfer to monomer and/or reentry) being more mobile. Thus, two types of termination are proposed: slow reaction-diffusion for the less mobile surface anchored chains, and rapid short-long (center of mass) termination for the more mobile hydrogen-terminated chains. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 989-1006, 1997
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0899-0042
    Keywords: diastereomeric salts ; molecular recognition ; hydrogen bonding ; polymorphism ; thermal analysis ; crystallography ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Binary diastereomeric (-) (1R,2S)-ephedrine salts of various mandelic acids obtained from 95% ethanol show considerable differences in solubility. Structures and some properties of the less-soluble (L) and more-soluble (M) solid phases of (-)-ephedrine with unsubstituted mandelic acid, 2-, 3-, and 4-monosubstituted halo (F, Cl, Br) mandelic acids, and 3- and 4-methylmandelic acids have been determined. Salts were found to be binary, without solvent of crystallization, and composed of double-layered arrays of alternating anions and cations linked by H-bonds normal to the layers. H-bonding links charged donors and acceptors usually along a crystallographic 2-fold screw axis. A striking discrimination is evident in that the (2R)-mandelate salts typically display a compact four-atom chain as the H-bonding repeating unit [+N - H…O( - C- - O)…H-N′, C21(4)] while the (2S)-mandelate salts adopt a more dimensionally variable six-atom chain repeating unit [+N - H…O - C- - O…H - N′, C22(6)]. Two distinct packing schemes display the shorter H-bonding chain of the (2R)-mandelates which always occurs with ephedrinium ions in the fully extended conformation. Slightly greater packing efficiency and H-bonding energies of the (2R)-mandelate salts correlates with increased fusion points, lower solubilities (95% ethanol), and higher heats of fusion relative to the phase adopted by their diastereoisomers. In contrast, (2S)-mandelate salts exhibit considerably more structural variability involving all three major ephedrinium conformations, and at least four distinct packing motifs. Mandelates with larger 3′-substituents (Cl, Br, methyl) show similar property discriminations, but these occur with an opposing trend, that is, between phases in which the less-soluble salts contain (2S)-mandelates. Salts with 2-bromomandelate do not show property disparities and their structures are dissimilar to the other phases. © 1995 Wiley-Liss, Inc.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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