Investigation of the mechanism of polymerization of butadiene by π-allylic nickel complexes
✍ Scribed by Bourdauducq, P. ;Dawans, F.
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1972
- Tongue
- English
- Weight
- 842 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0449-296X
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✦ Synopsis
Abstract
Various π‐allylic nickel complexes were synthesized by reacting bis(1,5‐cyclooctadiene)‐nickel with an allylic ester of trifluoroacetic acid. A study of the stereospecific polymerization of 1,3‐butadiene initiated by these catalysts showed the strong influence of the initial substitution in the π‐allylic ligand as well as of the solvent used for synthesis of the catalysts on the course of the reaction, i.e., on both the polymerization rate and the stereospecificity. Moreover, new catalytic species were isolated by adding electron‐accepting or electron‐donating ligands to some of the π‐allylic complexes. In that way, we were able to modify the behavior of the catalysts and, in some cases, to enhance catalytic activity considerably.
📜 SIMILAR VOLUMES
## Abstract The π‐allyl nickel halide‐oxygen system was found to be active as catalyst for stereospecific polymerization of butadiene. The catalyst from π‐allyl nickel chloride or π‐allyl nickel bromide yields the polymer of 90% __cis__‐1,4 content with high activity, whereas the catalyst from π‐al