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Straightforward Synthesis of Cysteine-Reactive Telechelic Polystyrene
- Source :
- Macromolecules. 41:599-606
- Publication Year :
- 2007
- Publisher :
- American Chemical Society (ACS), 2007.
-
Abstract
- Synthesis of a thiol-reactive telechelic polystyrene and conjugation of cysteine is reported. A dimethylfulvene-protected maleimide-functionalized atom transfer radical polymerization (ATRP) initiator (3) was synthesized, and the thermostability was compared to the analogous furan-protected initiator (1) by thermogravometric analysis (TGA). The former protecting group was stable to a higher temperature than the latter in the bulk phase (143 °C vs 125 °C) and thus was investigated as an initiator for the ATRP of styrene. Kinetic studies of the polymerization of styrene mediated by copper(I)/N,N,N‘,N‘ ‘,N‘ ‘-pentamethyldiethylenetriamine (PMDETA) indicated that the reaction proceeded in a controlled manner with high initiator efficiency (92%). Polystyrene with a number-average molecular weight (Mn) of 2530 Da and a narrow polydispersity index (PDI) of 1.15 was then synthesized and subjected to atom transfer radical (ATR) coupling to form the bis-functionalized polymer. Gel permeation chromatography (GPC) an...
- Subjects :
- chemistry.chemical_classification
Telechelic polymer
Polymers and Plastics
Bulk polymerization
Atom-transfer radical-polymerization
Organic Chemistry
Polymer
Styrene
Inorganic Chemistry
Gel permeation chromatography
chemistry.chemical_compound
chemistry
Polymerization
Polymer chemistry
Materials Chemistry
Polystyrene
Subjects
Details
- ISSN :
- 15205835 and 00249297
- Volume :
- 41
- Database :
- OpenAIRE
- Journal :
- Macromolecules
- Accession number :
- edsair.doi...........e8b4d04aa520c5db692224100520b661
- Full Text :
- https://doi.org/10.1021/ma702161q