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Addition-Fragmentation Reactions for Cationic Polymerization using a Novel Allyloxy-picolinium Salt

✍ Scribed by Reetz, Ivo; Bacak, Vildan; Yagci, Yusuf


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
270 KB
Volume
43
Category
Article
ISSN
0959-8103

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✦ Synopsis


A novel allyloxy-picolinium salt, N-[2-(methyl)allyloxy]-a-picolinium hexaÑuoroantimonate, has been synthesized and used as additionÈfragmentation agent for radical promoted thermal and photochemical cationic polymerization of monomers such as cyclohexene oxide, p-methoxystyrene and various vinyl ethers. Polymerization by heat was achieved using the allylic salt in conjunction with benzoyl peroxide (BPO), phenylazotriphenylmethane (PAT) and 2-2@-azobisisobutyronitrile (AIBN). Polymerization rates were found to drop in the order PAT [ BPO [ AIBN. Photopolymerization was carried out by irradiating the allyloxy-picolinium salt in the presence of monomer at 280 nm. Upon adding benzoin as free radical source, the spectral response was extended to 370 nm. The initiation mechanism is explained in terms of an additionÈfragmentation scheme.


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✍ Bacak, Vildan; Reetz, Ivo; Yagci, Yusuf; Schnabel, Wolfram 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 240 KB 👁 1 views

Allyloxy-pyridinium salts with various substituents on the allylic moiety are shown to be very efficient coinitiators in radical promoted cationic polymerization of cyclohexene oxide. Depending upon the radical initiator chosen, cationic polymerizations may be initiated by either heat or light. For