Synthesis of amphiphilic polystyrene–ionene diblock copolymers with controlled block lengths
✍ Scribed by Eugène T. W. M. Schipper; Jan C. M. van Hest; Alexander H. C. Roelofs; Pieter Piet; Anton L. German
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 517 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0959-8103
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Amphiphilic polystyrene‐ionene diblock copolymers with blocks of controlled molecular weights were synthesized by a new method. The preparation starts with the anionic polymerization of styrene with 3‐(dimethylamino)propyl‐lithium as initiator, yielding tertiary amino end‐functionalized polystyrenes of molecular weights that can be varied over a wide range from 1 to 100kg/mol, and a relatively low polydispersity (M̄~w~/M̄~n~ = 1.1–1.4). The crucial step in this method is the stepwise coupling of the reactive end‐group of the polystyrene with bromo‐ and tertiary‐amino‐terminated monodisperse oligomeric 2,4‐ionenes. The amphiphilic polymers with well‐defined block lengths were characterized by thin‐layer chromatography, end‐group titration and elemental analysis. Amphiphilic block copolymers with a monodisperse ionene block consisting of up to 10 quaternary ammonium groups could be derived.
📜 SIMILAR VOLUMES
Compatibilization of polystyrene/polypropylene (PS/PP) blends, by use of a series of butadiene-styrene block copolymers was studied by means of small-angle X-ray scattering (SAXS) and transmission electron microscopy (TEM). The compatibilizers used differ in molar mass and the number of blocks. It w
Amphiphilic block copolymers of vinyl ethers (VES) of the type -[CH2CH(OCH,CH,0 R)]. - [CH,CH(OiBu)]n -were synthesized by living cationic polymerization, where R is a I>-glucose residue, and m and n are the degrees of polymerization (m = 20-50; n = 11-89). To obtain them, sequential living block c