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Cited by 238

The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

Clicking Pentafluorostyrene Copolymers: Synthesis, Nanoprecipitation, and Glycosylation

Becer, C. Remzi, Babiuch, Krzysztof, Pilz, David, Hornig, Stephanie, Heinze, Thomas, Gottschaldt, Michael, Schubert, Ulrich S.·2009·Macromolecules

Abstract

Glycopolymers consisting of styrene (St) and pentafluorostyrene (PFS) were synthesized by a combination of nitroxide-mediated polymerization and “click” chemistry. A series of well-defined homopolymers as well as block and random copolymers of St and PFS were obtained with different ratios by using Bloc Builder as an alkoxyamine initiator. Some copolymers showed self-assembly behavior into regular nanospheres with diameters ranging from 70 to 720 nm by applying the nanoprecipitation technique. In addition, a thiol−glycoside (2,3,4,6-tetra- O -acetyl-1-thio-β- d -glucopyranose) was reacted under ambient conditions with PFS moieties on the polymeric backbone utilizing a thiol− para fluoro “click” reaction. This nucleophilic substitution reaction was performed with high yields, and the reaction kinetic was monitored online with 19 F NMR spectroscopy. Finally, the deacetylation of the protected glucose moieties was carried out to yield well-defined glycopolymers. The polymers were characterized in detail by 1 H, 13 C, and 19 F NMR spectroscopy, size exclusion chromatography, and MALDI TOF-MS.

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Crossref · 10.1021/ma9000176

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Metadata

Authors
Becer, C. R., Babiuch, K., Pilz, D., Hornig, S., Heinze, T., Gottschaldt, M., & Schubert, U. S.
Venue
Macromolecules
Published
2009-03-12
Volume
42
Issue
7
Pages
2387-2394
ISSN
  • 0024-9297 (ISSN-L)
  • 1520-5835
OpenAlex
W2124502694
Cited by
238
References
4
FWCI
12.45
Type
journal article
Language
en
Open access
closed

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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