## Abstract The thermal reaction of 1,3βbutadiene (BD) has been studied between 464 and 557Β°K at pressures between 49 and 450 torr. The products are 4βvinylcyclohexene (VCH) and __cis__, __cis__βcyclooctaβ1,5βdiene (COD), and their formations are second order. The rate constant (in 1/mol Β· sec) for
The cationic polymerization of CIS, CIS cycloocta-1,3-diene
β Scribed by M.A.S. Mondal; R.N. Young
- Publisher
- Elsevier Science
- Year
- 1971
- Tongue
- English
- Weight
- 832 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0014-3057
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The title molecule, C 28 H 22 , is centrosymmetric with an inversion centre at the mid-point of the central C-C bond. In the crystal structure, there are two intermolecular C phenyl -HΓ Γ Γ phenyl interactions.
The photoohemical reaction of g&,EQS";yoloocta-lr5-diene (I) yielded the cross-bonded tricycle [3.3.0.02'6] octane (II) (1) and that of the cyclohexa-1,4-diene III led to the rearranged bicyclic product IV (2). We wish to report the p$toohemical reaction of the &&&-cyclodeca-1,6-diene system (3), (
The recent communication by Shani (1) in which the photolysis of cis, cis-cyclodeca---3,8-diene-1, 6-dione (I) is reported to give cis,\*, cis-tricyclo[5. 3. 0. 0 2, (+d ecane-4,9--dione prompts us to report results we had obtained independently which lead to the cis, -anti, cis (IIa) stereochemical