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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 184 (1983), S. 463-473 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Diaryliodonium salts undergo facile copper catalyzed reduction in the presence of Sn(II) compounds. Such redox couples can be employed for the in situ generation of active initiators for cationic vinyl and ring opening polymerizations. Two mechanisms are proposed for the reduction reaction to explain the stoichiometry of the reactants and nature of the products formed. The polymerizations of several representative cationically polymerizable monomers were studied.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 3293-3309 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: All aromatic polyimides bearing diarylsulfide linkages in the main chain were prepared either by condensation of a sulfur containing dianhydride with an aromatic diamine or the condensation of a sulfur containing aromatic diamine with a dianhydride. Phenylation with diphenyl iodonium salts was then used to convert the diarylsulfide groups to triarylsulfonium salts. The resulting photosensitive polyimides were shown to undergo main chain cleavage during photolysis using UV irradiation. These new polyimides are candidates for positive working, high temperature photoresist materials.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 479-503 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The preparation of a variety of silicon-containing epoxy monomers and oligomers is described and their reactivity in photoinitiated cationic polymerization examined. Monomers and oligomers having terminal cycloaliphatic epoxy groups were found to be especially reactive in cationic polymerization. These materials are attractive candidates for use in coatings, adhesives, and elastomers.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 3951-3968 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This paper describes the synthesis and characterization of a series of (4-alkoxyphenyl)phenyliodonium salts which are excellent photo- and thermal-initiators for the cationic polymerization of vinyl and heterocyclic monomers. These compounds are easily prepared by straightforward synthetic techniques and display very good solubility and photoresponse characteristics which make them especially attractive for use in UV curing applications. Those compounds with alkoxy chains of eight carbons and longer are essentially nontoxic.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 1197-1215 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This first paper on the topic of polydimethylsiloxane-vinyl block polymers describes the development of a unique class of vinyl functional silicon containing free-radical initiators which can be used in the synthesis of block polymers. Details of the synthesis and characterization of these initiators are described together with the kinetics of their thermolysis. Specific conditions are described under which these initiators can be condensed with α,ω-hydrogen functional polydimethylsiloxane oligomers by a platinum-catalyzed hydrosilylation reaction to yield macroinitiators.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermolysis of polydimethylsiloxanes containing thermally labile bis(silyl pinacolate) groups in the backbone in the presence of various vinyl monomers leads to the direct synthesis of block polymers. Depending on the monomer chosen, simple triblock or multisequence block polymers can be readily prepared. Analysis of the products of the block polymerizations using various styrenic-type monomers shows that only block polymers are obtained, i.e., no homo-polymers are formed. These block polymers display evidence of phase separation such as intense iridescence and solvent-dependent mechanical properties. The mechanical properties of these block polymers have been measured and found to be highly composition dependent. Depending on the block length and the relative portions of the hard (vinyl) and soft (polydimethylsiloxane) blocks, one can produce either thermoplastic elastomers or rubber-modified thermoplastics.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 199 (1998), S. 1003-1011 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of hydroxypropyl cellulose (HPC) derivatives with, on the average, 3, 2, 3/2, 1, 1/2, 1/3 alkyl side chains (18 carbons) on each anhydroglucose unit were synthesized. X-ray studies indicate that layered structures prevail in most of these HPC derivatives, even in the sample containing only one alkyl side chain per two rings, i.e. C18(1/6)HPC. The polymers were able to pack in better ordered arrays in the solvent-cast films than in as-made samples obtained by precipitation from a nonsolvent. Side chain melting endotherms were observed for C18(3/3), C18(2/3), C18(1/6), and C18(1/9)HPC's. In C18(1/2) and C18(1/3)HPC's, side chain melting enthalpies were negligible but isotropization enthalpies were unexpectedly large. The isotropization temperatures and the associated enthalpies remained almost constant in differential scanning calorimetry (DSC) heating/cooling cycles. Distinct morphological features were observed under the cross polarized optical microscope (POM) after shearing the samples in the molten state. The degree of side chain substitution has a profound influence on the polymer morphology.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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