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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 505-512 
    ISSN: 0887-624X
    Keywords: cationic polymerization ; benzylpyridinium salts ; benzylanilinium salts ; cationic initiators ; thermal latency ; latent catalysts ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Novel cationic initiators, p-substituted benzylanilinium SbF-6 salts (1), were synthesized from the corresponding benzylchloride and N,N-dimethylaniline, where Cl- was exchanged with SbF-6. Their catalytic activities in the cationic polymerization of glycidyl phenyl ether (GPE) were examined and compared to that of benzylpyridinium SbF-6 salts (2), latent thermal initiators previously reported by Endo et al. It was found that 1 acted as a latent thermal initiator in the cationic polymerization of glycidyl phenyl ether (GPE) above 80°C for 10 min. Furthermore, 1 showed higher activity than 2 having the same p-substituents, except for a p-Cl group in the cationic polymerization of GPE. Both the GPE polymer structure and the benzyl group reactivity in 1 or 2 indicate that 1 generates benzyl cations that are active species for the cationic polymerization of GPE, and that in cationic polymerization using 2, side reactions generating active species other than benzyl cations occur. © 1995 John Wiley & Sons, Inc.
    Additional Material: 12 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 34 (1996), S. 475-480 
    ISSN: 0887-624X
    Keywords: α,α-dimethylbenzylpyridinium SbF6 ; cationic polymerization ; thermal latency ; latent catalysts ; cationic initiator ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-Methylbenzylpyridinium SbF6(1a) and α,α-dimethylbenzylpyridinium SbF6(1b) were prepared and the effect of α-methyl groups on the active species and the activity of 1a, 1b during the cationic polymerization of glycidyl phenyl ether (GPE) was evaluated. 1b was prepared by the reaction of α,α-dimethylbenzyl alcohol with pyridinium hexafluoroantimonate (2) in several solvents, and the yield depended on the dipole moment of the solvents, although it was poor for the reaction of α,α-dimethylbenzyl chloride with pyridine for the steric hindrance of the α-methyl groups followed by exchange with NaSbF6. Both 1a and 1b acted as a latent thermal initiator during the cationic polymerization of GPE and 1b showed higher activity during cationic polymerization with the higher steric effect of the α-methyl groups than 1a. The 1H-NMR analysis of the obtained poly GPE indicated that the active species of 1b changed from the benzyl cation to H+, depending on the reaction temperature, although 1a released benzyl cations as active species in the cationic polymerization of GPE. © 1996 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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