0000000000484835

AUTHOR

Tom Reimers

0000-0001-8583-1855

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Introducing a 1,1-diphenylethylene analogue for vinylpyridine: anionic copolymerisation of 3-(1-phenylvinyl)pyridine (m-PyPE)

2021

3-(1-Phenylvinyl)pyridine (m-PyPE), prepared by Wittig reaction from the readily available 3-benzoylpyridine, represents a structural analog of 1,1-diphenylethylene (DPE), one phenyl group being replaced by pyridine. The suitability of m-PyPE for the copolymerisation with vinylpyridine is reflected by the 13C NMR shifts of the β-carbon of 2-vinylpyridine (2-VP; 118.32 ppm) and m-PyPE (115.83 ppm, measured in CDCl3), which possess predictive character for carbanionic copolymerisation. In analogy to DPE and its manifold reported derivatives, carbanionic homopolymerisation of m-PyPE was not possible, due to its steric bulk. Copolymers of 2-VP and m-PyPE with varied composition have been synthe…

Steric effectsPolymers and PlasticsOrganic ChemistryBioengineeringBiochemistrychemistry.chemical_compoundMonomerchemistryPolymer chemistryWittig reactionPyridineCopolymerPhenyl groupGlass transitionStructural analogPolymer Chemistry
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