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Synthesis and radical polymerization behavior of bifunctional vinyl monomer derived from N‐vinylacetamide and p‐chloromethylstyrene
Authors:Takeru Iwamura  Tomoyuki Nakagawa  Takeshi Endo
Abstract:The radical polymerization of N‐(p‐vinylbenzyl)‐N‐vinylacetamide ( 1 ) prepared by the reaction of N‐vinylacetamide with p‐chloromethylstyrene was carried out by using radical initiators such as AIBN or BPO in benzene, chlorobenzene, or bulk. As a result, poly 1 was successfully isolated by dialysis (yield, 10–36%). The crosslinking reaction of poly 1 was carried out at 60–100 °C for 8 h. By using a radical initiator such as AIBN or BPO (3 mol %), the crosslinking reaction proceeded (yield, 63–79%). Moreover, the crosslinking reaction of poly 1 proceeded at 100 °C without a radical initiator in 50% yield. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 2714–2723, 2006
Keywords:chemical modification  crosslinking reaction  N‐vinylacetamide  p‐chloromethylstyrene  radical polymerization
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