𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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

✍ 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.

✦ Synopsis


Abstract

The three title monomers were polymerized using a variety of Ru‐, Ir‐, Mo‐, W‐ and Re‐based 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 head‐tail bias was observed in any of the polymers.


πŸ“œ SIMILAR VOLUMES


Ring-opening metathesis polymerization o
✍ Kenneth J. Ivin; Luk-Mui Lam; John J. Rooney πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 361 KB

## Abstract The title monomers 1 and 2 were polymerized by Ru‐, Ir‐, Mo‐, W‐ and Re‐based metathesis catalysts to yield polymers with __cis__ contents ranging from 10% to at least 90% for 1 and 23–60% for 2. Assignments of the ^13^C NMR spectra were made. No significant head‐tail bias was observed

13C NMR spectra of hydrogenated polymers
✍ Andrew G. Carvill; Ruth M. E. Greene; James G. Hamilton; Kenneth J. Ivin; Alan M πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 489 KB

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