## Abstract Acrolein was polymerized in a polar solvent in the presence of __terc__‐ and __sec__‐butyl lithium as initiators. Using a low monomer to initiator molar ratio and 1‐h reaction time, cyclic structures were shown to be formed in the main chain of the resulting oligomers. The influence of
Synthesis and molecular weight characterization of low molecular weight end-functionalized poly(4-acryloylmorpholine)
✍ Scribed by Elisabetta Ranucci; Gloria Spagnoli; Luciana Sartore; Paolo Ferruti; Paolo Caliceti; Oddone Schiavon; Francesco M. Veronese
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 530 KB
- Volume
- 195
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
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 and molecular weight distribution, by means of analytical size‐exclusion chromatography (SEC) working in buffered aqueous media. This has been accomplished by determining a calibration curve for a set of SEC columns, with poly(N‐acryloylmorpholine) standards purposely obtained by means of preparative SEC. The transfer constant C~T~ of some CTAs towards N‐acryloylmorpholine has been estimated to be approximately 1.
📜 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
## Abstract New oligomers of __N__‐vinyl‐2‐pyrrolidone, functionalized at one end with hydroxy functions, were obtained by radical polymerization in the presence of a hydroxylated compound, namely 2‐isopropoxyethanol, acting as chain‐transfer agent. The oligomeric samples obtained were characterize
## Abstract __N__‐Carboxy‐(__N__^ϵ^‐benzyloxycarbonyl)‐L‐lysine anhydride (Z‐L‐lysine NCA) was polymerized in dimethylformamide with triethylamine, diethylamine or hexylamine as initiator, at varying molar ratios of NCA to initiator (M/I ratio). After removal of the protecting Z‐group the resulting