## Abstract For Abstract see ChemInform Abstract in Full Text.
Synthesis and Radical Polymerization of Various 2-Cyclopropylacrylates
✍ Scribed by Armin de Meijere; Viktor Bagutski; Frank Zeuner; Urs Karl Fischer; Volker Rheinberger; Norbert Moszner
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 196 KB
- Volume
- 2004
- Category
- Article
- ISSN
- 1434-193X
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A monomer having dibenzothiophene moiety, 2-vinyldibenzothiophene (1), was prepared by the Ni-catalyzed cross-coupling reaction of vinyl bromide with the Grignard reagent of 2-bromodibenzothiophene. The radical homopolymerization of 1 and the copolymerization with styrene were carried out at 60ЊC in
## Abstract New 1,1‐disubstituted 2‐vinylcyclopropanes were synthesized by reaction of the corresponding malonyl diesters with __trans__‐1,4‐dibromo‐2‐butene and of sodium hydride. The structure of the 2‐vinylcyclopropanes could be confirmed by elemental analysis, IR, ^1^H NMR and ^13^C NMR spectro
The NMR-spectra of acrylamide and polyacrylamide in various mixtures of water with DMSO have been studied as well as of N-vinylpyrrolidone and its polymer in various solvents. The results indicate that, while the carbonyl groups of acrylamide and N-vinylpyrrolidone in aqueous solution are practicall
NMR-spectral data for diethylaminoethyl methacrylate and its salts in various solvents have been considered with the kinetics of polymerization of these monomers. The data on the interaction of a monomer with a solvent obtained using NMR-spectroscopy lead to ideas about the effect of the formation o
## Abstract Multifunctional 2‐vinylcyclopropanes were synthesized by esterification of the 1‐methoxycarbonyl‐2‐vinylcyclopropane‐1‐carboxylic acid with ethylene glycol, 1,1,1‐trimethylolpropane or 1,4‐cyclohexanediol in the presence of 1,3‐dicyclohexylcarbodiimide (DCC). The structure of the new vi