## Radical copolymerizabilities of poly(ethylene glycol) allenyl methyl ether (2a and 2b, the number average molecular weight (M,) = 390 and 590, receptively) were evaluated by the copolymerization with styrene monomer (St). The relative reactivities of macromonomers have been decreased as the len
Synthesis and radical polymerization of end-allenoxy polyoxyethylene macromonomer
β Scribed by Yassin A. Aggour; Ikuyoshi Tomita; Takeshi Endo
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 488 KB
- Volume
- 28
- Category
- Article
- ISSN
- 1381-5148
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β¦ Synopsis
Poly(ethylene glycol) allenyl methyl ether (2) was prepared by the reaction of poly(ethylene glycol) monomethyl ether (the number average molecular weight (M,) = 550) with propargyl bromide, followed by the base-catalyzed isomerization reaction. Functionality of end-allenyl groups in the obtained macromonomer was determined as 92%
(from 'H-NMR). The radical polymerization of 2 was carried out in bulk and in benzene at 60 or 120Β°C to yield a polymer with poly(ethylene glycol) side chains. For instance, a polymer (3, 1!4, = 3900) was obtained in 39% yield by the polymerization of 2 in bulk at 60Β°C for 48 h using 6 mol% of or&-azobisisobutyronitrile (AIBN). The obtained polymer was soluble in organic solvents as well as water.
π SIMILAR VOLUMES
β£-(Methacrylyoxylethyloxycarbonylmethyl)--(N,N-diethyldithiocarbamyl)polystyrene macromonomers with different molecular weights were prepared by radical polymerization of styrene (St) using β€-methacryloxylethyl 2-N,N-diethyldithiocarbamylacetate (MAEDCA) as a polymerizable photoiniferter in toluene