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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 2631-2643 
    ISSN: 0887-624X
    Keywords: macroporous beads ; poly(chloromethylstyrene) ; chiral separation ; HPLC ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactive monodisperse porous poly(chloromethylstyrene-co-styrene-co-divinylbenzene) beads have been prepared by a staged templated suspension polymerization method with different concentrations of linear polystyrene porogen and chloromethylstyrene in the polymerization mixture. The presence of a small amount of linear polystyrene in the polymerization mixture leads to a dramatic increase in both the pore size and the pore volume of the resulting beads. In contrast, addition of chloromethylstyrene leads to lower surface areas and smoother surfaces due to the reduced compatibility between the polystyrene porogen and the newly formed crosslinked chains. The modification of chloromethylstyrene beads by Gabriel synthesis to obtain aminated beads has also been studied. The final number of primary amino groups is related to the starting concentration of functional benzyl chloride moieties rather than to the porous properties. Both π-basic and π-acidic type chiral selectors, (R)-1-(1-naphthyl)-ethylamine and (R)-N-(3,5-dinitrobenzoyl)phenylglycine, respectively, have been attached to the amino functionalized beads, and the resulting chiral beads have been used in the model HPLC separations of enantiomers. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 2631-2643 1997
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0887-624X
    Keywords: monodisperse beads ; 2,3-epoxypropyl vinylbenzyl ether ; divinylbenzene ; copolymers ; macroporous ; chromatography ; HPLC ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In search for HPLC separation media with new surface chemistries, a styrene-based monomer, 2,3-epoxypropyl vinylbenzyl ether, containing reactive epoxide groups has been syn-thesized and copolymerized with divinylbenzene in a suspension polymerization. The process involves the use of size monodisperse particles that are swollen with monomer and then polymerized in the presence of a porogenic diluent consisting of a mixture of 4-methyl-2-pentanol and octane. The effect of concentration of divinylbenzene on the pore size dis-tribution and the specific surface area of the resulting uniformly sized porous poly(2,3-epoxypropyl vinylbenzyl ether-co-divinylbenzene) beads has been studied. The epoxide groups of the copolymer have been hydrolyzed and the beads used for reversed-phase chro-matography of both small molecules and proteins to show the effect of hydrophobicity of the matrix on the separation properties. Reversed-phase chromatography of alkylbenzenes follows the expected pattern while for proteins the hydrolyzed beads with the highest content of the crosslinking monomer exhibit a remarkable deviation from the predicted retention characteristics. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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