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  • 3,4,5,6,7,8-hexahydro-4a (2H)-hydroxymethyl-2-methylenenaphthalene  (1)
  • 4-methylene-2-phenyl-1,3-dioxolane  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 3493-3497 
    ISSN: 0887-624X
    Keywords: photochromic ; difunctional monomer ; π2s + π2s photochemical cycloaddition ; 3,4,5,6,7,8-hexahydro-4a (2H)-hydroxymethyl-2-methylenenaphthalene ; 3,4,5,6,7,8-Hexahydro-4a (2H)-hydroxymethyl-2-oxo-naphthalene ; 3,4,5,6,7,8-hexahydro-4a (2H)-methyl-2-oxo-naphthalene acetate ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 2207-2219 
    ISSN: 0887-624X
    Keywords: 4-methylene-2-phenyl-1,3-dioxolane ; photoinitiated cationic polymerization ; copolymerization ; poly(alkylene ether ketone)s ; ring-opening polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photoinitiated polymerization of 4-methylene-2-phenyl-1,3-dioxolane (1) was carried out using either tris (4-methylphenyl) sulfonium hexafluoroantimonate or 4-decyloxyphenyl phenyliodonium hexafluoroantimonate as initiators. 1H-NMR analyses confirmed exclusive ring-opening while DSC and SEC were used to determine the glass transition temperatures (Tgs) and molecular weights, respectively. Photoinitiated cationic copolymerizations of 1 were investigated with several acyclic and cyclic monomers. Copolymerization of 1 with vinyl ethers and a spiroorthoester resulted in copolymers whose thermal properties were dependent on comonomer ratios. Copolymers of 1 and dihydrofuran or dihydropyran afforded soluble polymers with Tgs significantly higher than the homopolymer of 1. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 2207-2219, 1997
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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