The cationic copolymerization of cyclo-octa-1, 3-diene with styrene and p-chlorostyrene
β Scribed by M.A.S. Mondal; R.N. Young
- Publisher
- Elsevier Science
- Year
- 1971
- Tongue
- English
- Weight
- 260 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0014-3057
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
In contrast to recent claims by Rhodes and Glidewell, comparison of both ESR and electronic absorption spectra shows that the photoproduct of the recently characterized radical cation of bicyclo[ 3.3.0]octa-2,6-diene-4,8-diyl is identical to the 1,4dihydropentalene radical cation, i.e. a linear conj
A study was made of the effect of varying the amount of 3-(methacrylamidinopropyl)trimethylammonium chloride (MAD) on the emulsion copolymerization of styrene and MAD with azo-bis(isobutyramidine hydrochloride) as initiator. The addition of MAD accelerated the polymerization and decreased the partic
Al~traet--Copolymers of 4-methylpentene-1 and styrene were prepared (TiCla-AliBu3, 70 Β°) and their structure investigated. Monomer reactivity ratios calculated from the copolymer compositions were found to be 3"92 and 0"98. Comparison of the i.r.-spectra of copolymers thus prepared and of isotactic
## Abstract The reaction of acetylene (A) with cyclohexaβ1,3βdiene (CHD) has been studied between 450 and 592 K. The pressures of A ranged from 25 to 112 torr and those of CHD from 8 to 62 torr. The reaction yields only ethene (E) and benzene (B) instead of bicyclo[2.2.2]octaβ2,5βdiene (BOD), the p