N-chlorocarbonyl dibenz[b,f] azepine in conjunction with AgSbF6 initiated the cationic polymerization of c(-methylstyrene in methylene chloride. Polymer samples obtained this way contained terminal dibenzazepine units. Chain extension occurred upon irradiating these polymers with u.v. in benzene so
Synthesis and reactions of polymers with photoactive terminal groups—3. The use of radical promoted cationic polymerization for the synthesis of poly(n-butyl vinylether) with n-acyl dibenz(b, f)azepine terminal units
✍ Scribed by Yusuf Yagci; Wolfram Schnabel; Anthony Ledwith
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- English
- Weight
- 252 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0014-3057
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✦ Synopsis
The free radical promoted cationic polymerization of n-butyl vinyl-ether (BVE) was achieved by the thermal decompositon of N-[4,4-azobis-(4-cyanopentanoyl)]-bisdibenz(b, f)azepine (ADBA) in the presence of diphenyliodonium hexafluorophosphate (Ph2I+PF6) or silver hexafluorophosphate (AgPF6). Polymer samples prepared in the presence of AgPF 6 contained a significant number of terminal dibenzazepine units. Chain extension via dimerization of the dibenzazepine units occurred upon irradiating these polymers with u.v. light (2 = 366 nm) in CH2CI 2 solution containing a triplet sensitizer (benzophenone or benzil), Polymer samples prepared in the presence of the iodonium salt contained only a very small fraction of macromolecules having dibenzazepine end-groups and were, therefore, not appropriate for the chain extension procedure.
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