## Abstract The kinetics of the anionic ring‐opening polymerization of several cyclodisilazanes substituted with different groups on silicon atoms has been investigated in toluene/tetrahydrofuran (THF) using benzyllithium as initiator. Two different behaviours were observed: for hindered substituen
Anionic ring-opening polymerization of cyclodisilazanes, 2. Influence of additives on the kinetics of polymerization
✍ Scribed by Stéphane Bruzaud; Anne-Françoise Mingotaud; Alain Soum
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 693 KB
- Volume
- 198
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
The kinetics of the anionic ring‐opening polymerization of the DD~NMe~ cyclodisilazane, initiated by benzyllithium, has been investigated in different experimental conditions. In non‐polar solvents, the active centers are aggregated ion pairs which are in equilibrium with a small amount of monomeric species. In the presence of additives such as THF, dioxane or tetramethyl‐ethylenediamine, there is only one type of active center. The aggregates are dissociated into light ion pairs externally solvated by the additive. The paper demonstrates also that the kinetics of the polymerization (i.e., rate constant of propagation k~p~) is a function of both the nature and the amount of additives.
📜 SIMILAR VOLUMES
## Abstract The anionic ring‐opening polymerization of a model monomer of cyclodisilazanes 1, initiated with both organosodium and organolithium initiators, was investigated. Under specific conditions, this polymerization exhibits all the characteristics of a living process. Indeed, whatever the ex