Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Synthesis of Phosphinodiselenoic Acid Ester Derivatives and their Application in the Controlled Radical Polymerization of Styrene

  • Song, Eun-Jin (Department of Chemistry, Chonnam National University) ;
  • Jo, Young-Shin (Department of Chemistry, Chonnam National University) ;
  • Bae, Go-Un (Department of Chemistry, Chonnam National University) ;
  • Oh, Il-Kwon (School of Mechanical Systems Engineering, Chonnam National University) ;
  • Jung, Hyun-Min (Advanced Materials Division, Korea Research Institute of Chemical Technology) ;
  • Lee, Sun-Woo (Department of Chemistry, Chonnam National University)
  • Published : 2009.09.20
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References

  1. Cunningham, M. F. Prog. Polym. Sci. 2002, 27, 1039 https://doi.org/10.1016/S0079-6700(02)00008-4
  2. Braunecker, W. A.; Matyjaszewski, K. Prog. Polym. Sci. 2007, 32, 93 https://doi.org/10.1016/j.progpolymsci.2006.11.002
  3. Hawker, C. J.; Bosman, A. W.; Harth, E. Chem. Rev. 2001, 101, 3661 https://doi.org/10.1021/cr990119u
  4. Wayland, B. B.; Poszmik, G.; Mukerjee, S. L.; Fryd, M. J. Am. Chem. Soc. 1994, 116, 7943 https://doi.org/10.1021/ja00096a080
  5. Kato, M.; Kamigaito, M.; Sawamoto, M.; Higashimura, T. Macromolecules 1995, 28, 1721 https://doi.org/10.1021/ma00109a056
  6. J. S. Wang, Matyjaszewski, K. Macromolecules 1995, 28, 7901 https://doi.org/10.1021/ma00127a042
  7. Wang, J. S.; Matyjaszewski, K. J. Am. Chem. Soc. 1995, 117, 5614 https://doi.org/10.1021/ja00125a035
  8. Matyjaszewski, K.; Xia, J. Chem. Rev. 2001, 101, 2921 https://doi.org/10.1021/cr940534g
  9. Chiefari, J.; Chong,Y. K.; Ercole, F.; Krstina, J.; Jeffery, J.; Le, T. P. T.; Mayadunne, R. T. A.; Meijs, G. F.; Moad, C. L.; Moad, G.; Rizzardo, E.; Thang, S. H. Macromolecules 1998, 31, 5559 https://doi.org/10.1021/ma9804951
  10. Destarac, M.; Charmot, D.; Franck, X.; Zard, S. Z. Macromol Rapid Comm 2000, 21, 1035 https://doi.org/10.1002/1521-3927(20001001)21:15<1035::AID-MARC1035>3.0.CO;2-5
  11. Wood, M. R.; Duncalf, D. J.; Rannard, S. P.; Perrier, S. Org. Lett. 2006, 8, 553 https://doi.org/10.1021/ol0525617
  12. Moad, G.; Rizzardo, E.; Thang, S. H. Polymer 2008, 49, 1079 https://doi.org/10.1016/j.polymer.2007.11.020
  13. Kim, S. S.; Cheong, W. J. Bull. Korean Chem. Soc. 2009, 30, 722 https://doi.org/10.5012/bkcs.2009.30.3.722
  14. Gigmes, D.; Berin, D.; Marque, S.; Guerret, O.; Tordo, P. Tetrahedron Lett. 2003, 44, 1227 https://doi.org/10.1016/S0040-4039(02)02848-4
  15. Moon, J.; Nam, H.; Kim, S.; Ryu, J.; Han, C.; Lee, C.; Lee, S. Tetrahedron Lett. 2008, 49, 5137 https://doi.org/10.1016/j.tetlet.2008.06.098
  16. Kimura, T.; Murai, T. J. Org. Chem. 2005, 70, 952 https://doi.org/10.1021/jo0484979

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