## 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
Synthesis and polymerization studies of N-cyanomethanimine monomers
✍ Scribed by Dallas D. Parker; Anne Buyle Padias; H. K. Hall Jr.
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 129 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0887-624X
No coin nor oath required. For personal study only.
✦ Synopsis
New imine monomers containing C-aryl and N-cyano substituents were synthesized and polymerized by both radical and anionic initiation. Homopolymerization yielded low molecular weight polymers ( M n õ 2100). Higher yields were obtained with anionic initiation rather than radical initiation. Radical initiated copolymerization with p-methoxystyrene gave low yields of low molecular weight copolymers. Radical initiated copolymerization with methyl acrylate gave copolymers of 15,000-32,000 molecular weight in moderate yields, but with rather low incorporation of the imine monomer. The C-substituent affected the anionic and free radical reactivity similarly. ᭧ 1997
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