## 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
Polymerization of cyclic monomers, 4. Synthesis and radical polymerization of bi- and trifunctional 2-vinylcyclopropanes
✍ Scribed by Norbert Moszner; Frank Zeuner; Volker Rheinberger
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 271 KB
- Volume
- 18
- Category
- Article
- ISSN
- 1022-1336
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✦ Synopsis
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 vinylcyclopropanes was confirmed by elemental analysis, IR, ^1^H NMR and ^13^C NMR spectroscopy. The radical polymerization of the 2‐vinylcyclopropanes in bulk with 2,2′‐azoisobutyronitrile (AIBN) results in transparent crosslinked polymers. The polymerization of the liquid monomers is accompanied by a low shrinkage in volume.
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1,3-Bis[(1-alkoxycarbonyl-2-vinylcyclopropane-1-yl)carboxy]benzenes 1 [RO: CH 3 O (a), C 2 H 5 O (b)] were synthesized by the esterification of the corresponding 1-alkoxycarbonyl-2-vinylcyclopropane-1-carboxylic acids with resorcinol. The structure of the new vinylcyclopropanes was confirmed by elem
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