Polymer synthesis: Facilitating functionality

Journal name:
Nature Chemistry
Volume:
2,
Pages:
164–165
Year published:
DOI:
doi:10.1038/nchem.563

Monomers that contain masked ketene groups provide new opportunities for facile crosslinking and post-synthetic modification of polymers in a wide variety of materials applications.

References

  1. Marimuthu, M. & Kim, S. Curr. Nanosci. 5, 189203 (2009).
  2. Place, E. S., George, J. H., Williams, C. K. & Stevens M. M. Chem. Soc. Rev. 38, 11391151 (2009).
  3. Perlin, L., MacNeil, S. & Rimmer, S. Soft Matter 4, 23312349 (2008).
  4. Jagur-Grodzinski, J. Polym. Adv. Technol. 21, 2747 (2010).
  5. Dhal, P. K., Polomoscanik, S. C., Avila, L. Z., Holmes-Farley, S. R. & Miller, R. J. Adv. Drug Deliv. Rev. 61, 11211130 (2009).
  6. Ghanbari, H. et al. Trends Biotechnol. 27, 359367 (2009).
  7. Leibfarth, F. A. et al. Nature Chem. 2, 207212 (2010).
  8. Meldrum, A. N. J. Chem. Soc. 93, 598601 (1908).
  9. Moad, G. & Solomon, D. H. The Chemistry of Radical Polymerization (Elsevier, 2005).
  10. Kosravi, E. & Szymanska-Buzar, T. (eds) Ring Opening Metathesis Polymerisation and Related Chemistry: State of the Art and Visions for the New Century (Kluwer Academic, 2002).

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Affiliations

  1. Steve Rimmer is in the Polymer Centre, Department of Chemistry at the University of Sheffield, Sheffield, S3 7HF, UK.
    s.rimmer@sheffield.ac.uk

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