## Abstract New amphiphilic oligomers ending at one side with a reactive function were synthesized by radical polymerization of a vinyl monomer, __N__‐acryloylmorpholine, in the presence of functionalized chain‐transfer agents (CTAs). The oligomers were characterized in terms of molecular weight an
Synthesis of end-functionalized low molecular weight poly(butyl acrylate) and its elongation using a diisocyanate
✍ Scribed by Yoshihide Kawaguchi; Hajime Yasuda
- Book ID
- 104425001
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 145 KB
- Volume
- 46
- Category
- Article
- ISSN
- 1381-5148
No coin nor oath required. For personal study only.
✦ Synopsis
Bifunctionalized poly(butyl acrylate) and poly(methyl methacrylate) were synthesized by the polymerization of butyl acrylate or methyl methacrylate using an organosamarium complex, [SmMe(C Me ) (CH -CH-CHCH )] , as an initiator 5 5 2 2 2 2 followed by the insertion of aldehydes. The polymerization proceeds quantitatively to afford the hydroxy-end functionalized polymer (M . 4120) with narrow molecular weight distributions (M /M , 1.13). The attempted chain elongation of the n w n resulting polymer with 4,49-methylenebis(phenylisocyanate) has however failed, while the chain extension was realized by the reaction of poly(e-caprolactone-co-butyl acrylate-co-e-caprolactone) (M . 15,200, M /M , 1.23) with a diisocyanate n w n
affording the desired high solid paint with M of 87,600 using a limited amount of THF as a solvent.
📜 SIMILAR VOLUMES
## Abstract Amphiphilic oligomers of poly(__N__‐acryloylmorpholine) terminated at one end by primary amino groups have been prepared by free radical polymerization of the corresponding monomer, __N__‐acryloylmorpholine, in the presence of cysteamine (2‐mercaptoethylamine) as chain‐transfer agent. T