## Abstract Tetraarylsuccinonitriles 1 show an atypical “stepwise” initiation mechanism in freeradical polymerization, particularly in the case of methyl methacrylate (MMA) as monomer. In the prior phase of the polymerization reaction very high concentrations of primary radicals lead to the formati
Initiation of polymerization with substituted ethanes—12. Free radical polymerization of methyl methacrylate and styrene initiated with 3-methoxycarbonyl-3-methyl-2,2,5,5-tetraphenylhexanedinitrile
✍ Scribed by Dietrich Braun; Hans Jörg Lindner; Hartmut Tretner
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 353 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0014-3057
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✦ Synopsis
The title compound, the first member of a homologous series of oligomers formed by free radical polymerization of methyl methacrylate initiated by tetraphenylbutanedinitrile, was synthesized and its structure was determined by X-ray diffraction. The longest C--C bond of this molecule measures 1.628 A and can be thermally split to give radicals. The activation energy of this dissociation was found to be 150 kJ/mol. The kinetics of the free radical polymerization of methyl methacrylate and styrene initiated with the title compound shows remarkable deviations from the ideal polymerization kinetics, indicating that primary radical termination might be the main chain termination reaction.
📜 SIMILAR VOLUMES
## Abstract Tetraarylsuccinonitriles 2 were synthesized via oxidative dimerization of diarylacetonitriles 1 in basic media. The thermal decomposition of 2 results in two identical diarylcyanomethyl semi‐radicals 3. The dissociation energy (__E__~a~) measured using the thiophenol radical scavenging
## Abstract The triazoline derivative 1 was used as an additive in the chain‐growth controlled radical polymerization of vinylic monomers to afford narrowly distributed polymers. This new system is applicable to styrene as well as to methacrylates. The monomer consumption and the variation of the m