Metathesis ring opening polymerization of 5,6-bis(chloromethyl)bicyclo[2.2.1]hepta-2-ene
β Scribed by Lamies A. Shahada; W.James Feast
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- English
- Weight
- 254 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0014-3057
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β¦ Synopsis
Abstraet--5,6-Bis(chloromethyl)bicyclo[2.2.1]hepta-2-ene undergoes ring opening metathesis polymerization to give poly{1,4-[2,3-bis(chloromethyl)-cyclopentylene] vinylene}. Initiation with MoCIs/MeaSn derived catalyst gives atactic polymer with predominantly trans vinylenes, whereas initiation with the WC16/Me4Sn system gives atactic polymer with predominantly cis vinylenes.
π SIMILAR VOLUMES
## Abstract The three title monomers were polymerized using a variety of Ruβ, Irβ, Moβ, Wβ and Reβbased metathesis catalyst systems to yield polymers having a wide range of __cis__ double bond contents in each case. The ^13^C NMR spectra of the polymers were interpreted in terms of __cis/trans__, h
## Abstract The title monomers 1 and 2 were polymerized by Ruβ, Irβ, Moβ, Wβ and Reβbased metathesis catalysts to yield polymers with __cis__ contents ranging from 10% to at least 90% for 1 and 23β60% for 2. Assignments of the ^13^C NMR spectra were made. No significant headβtail bias was observed