1072-63-5

Brown liquid

1-Vinylimidazole has been employed:

• as functional monomer in the synthesis of molecularly imprinted polymers
• as monomer in the preparation of magnetic-poly(divinylbenzene-1-vinylimidazole) [m-poly(DVB-VIM)] microbeads
• in the synthesis of novel ion imprinted polyvinylimidazole-silica hybrid copolymer (IIHC)
• in removal of the vinyl protecting group via isoprene-catalyzed lithiation process

Removal of the vinyl protecting group with an isoprene-catalyzed lithiation process.1

Notclassified

Poly(vinylimidazole)s, which contain heterocyclic aromatic rings on the polymer side chains, are of increasing interest for a wide variety of applications ranging from catalysis, polymeric ionic liquids to membrane material. Researcher demonstrated that well-controlled and low dispersity (as low as 1.05) poly(1VIM) could be synthesized via RAFT polymerization by using acetic acid as a special solvent. Acetic acid not only works as a solvent that allows homogeneous polymerization, it also protonates 1VIM, thereby, allowing the stabilization of propagating radicals during polymerization. The synthesis of well-controlled poly(1VIM) is expected to greatly expand the design and utility of vinyl imidazole-based materials and their applications in catalysis, membrane material, heavy metal removal, fuel cells and many other fields.