## 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
Metathesis polymerization of endo-5- and exo-5-chloromethylbicyclo[2.2.1]hept-2-ene and of 5,5-bis(chloromethyl)bicyclo[2.2.1]hept-2-ene; microstructure of the polymers
β Scribed by Kenneth J. Ivin; Luk-Mui Lam; John J. Rooney
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 494 KB
- Volume
- 195
- Category
- Article
- ISSN
- 1022-1352
No coin nor oath required. For personal study only.
β¦ Synopsis
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, head/tail and m/r microstructures. No headβtail bias was observed in any of the polymers.
π SIMILAR VOLUMES
13C NMR spectra of the three title polymers have been determined for polymers of different tacticities. Assignments to the various possible HWHT/TT and m/r dyad structures were made. These were facilitated by the use of optically active monomers in the case of 1 and 3. In the precursor polymers the
## Abstract For Abstract see ChemInform Abstract in Full Text.