Copolymerization of 2-Chloro-Substitutedp-Cyclopropylstyrenes with Styrene and Properties of the Resulting Copolymers
β Scribed by K. G. Guliev; G. Z. Ponomareva; A. M. Guliev
- Book ID
- 106518790
- Publisher
- SP MAIK Nauka/Interperiodica
- Year
- 2005
- Tongue
- English
- Weight
- 50 KB
- Volume
- 78
- Category
- Article
- ISSN
- 1070-4272
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Radical copolymerization of N-methylmaleimide (MeMI) as well as other N-alkylmaleimides (RMI) and isobutene (IB) was carried out with 2,2'-azobis(isobutyronitri1e) as an initiator a t 60Β°C. The initial rate of the copolymerization (R,) was dependent on the monomer composition and was maximum at the
Radical copolymerization of N-(alkyl-substituted pheny1)maleimides (RPhMI) with isobutene (IB) was carried out with an initiator in various solvents at 6OoC. The copolymerization of N-(2,6-diethylphenyl)maleimide (2,6-DEPhMI) with IB in benzene proceeded readily in a homogeneous system to give an al
## Abstract Summary: Ethylene and butadiene were copolymerized with a silyleneβbridged bis(fluorenyl) complex {[Me~2~Si(C~13~H~8~)~2~]NdCl} (1) in combination with various alkylating agents (BuLi/AlH(__i__Bu)~2~, (Bu)MgCl, Mg(Bu)(Oct)). Copolymers have a unique microstructure since they contain 1,2