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N,N,N′,N′-tetramethylethylene diamine as a co-catalyst in the anionic polylymerization of methyl methacrylate

✍ Scribed by Bengt Wesslén; Gunnar Mattsson


Book ID
105337482
Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
530 KB
Volume
28
Category
Article
ISSN
0887-624X

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✦ Synopsis


Abstract

Anionic polymerization of methyl methacrylate in toluene solution has been studied. The polymerizations were initiated by fluorenyllithium as well as by butyl‐, benzyl‐, and phenylmagnesium halides, and carried out in the presence of polar additives. Especially the organomagnesium initiators gave generally rise to highly isotactic polymers (mm = 0.90‐0.95) in the absence of solvating additives. In the presence of the bidentate ligand N,N,N′,N′‐tetramethylethylene diamine (TMEDA) at molar ratios of 1–2 relative to magnesium, highly syndiotactic polymers were obtained at −78°C (rr = 0.8–0.9), while at higher temperatures stereoblock polymers or stereocomplexes were formed. It is proposed that at low temperatures the magnesium cations are strongly solvated under the influence of TMEDA, with the formation of monomeric ion pairs. The large solvated magnesium cations will not have any directional influence on the monomer in the propagation step, with syndiotactic propagation as a result.


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Radical polymerization of methyl methacr
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## Abstract The specific features of free‐radical polymerization of methyl methacrylate in the presence of a new initiating system, benzoyl peroxide‐__N,N__‐dimethyl‐__N__‐(methylferrocenyl)amine, are studied. Mutual influence of ferrocenyl‐ and amine groups on kinetic parameters of polymerization