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Synthesis of Diblock Codendrimer by Double Click Chemistry

  • Lee, Jae Wook (Department of Chemistry, Dong-A University) ;
  • Han, Seung Choul (Department of Chemistry, Dong-A University) ;
  • Ji, Won Ho (Department of Chemistry, Dong-A University) ;
  • Jin, Sung-Ho (Department of Chemistry Education, Pusan National University) ;
  • Kim, Ji Hyeon (Department of Chemical and Biological Engineering, Gachon University)
  • Received : 2012.09.09
  • Accepted : 2012.09.24
  • Published : 2012.12.20

Abstract

Efficient double click methods for the synthesis of diblock codendrimers were developed. The synthetic strategy involved the sequential click reactions between an alkyne and an azide. The short core building block, 1,4-diazidobutane, was chosen to serve as the azide functionalities for dendrimer growth via click reactions with the alkyne-functionalized PAMAM dendrons as hydrophilic dendron and alkyne-functionalized Fr$\acute{e}$chet-type dendrons as hydrophobic dendron. The structure of diblock codendrimers was confirmed by $^1H$ and $^{13}C$ NMR spectroscopy, IR spectroscopy, mass spectrometry, and GPC analysis.

Keywords

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