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Dynamic covalent diblock copolymers: Instructed coupling, micellation and redox responsiveness

  • Qinglai Yang
  • , Ling Bai
  • , Yuanqing Zhang
  • , Fangxia Zhu
  • , Yuhong Xu
  • , Zhifeng Shao
  • , Yu Mei Shen
  • , Bing Gong
  • Shanghai Jiao Tong University
  • Chinese Academy of Sciences

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

Instructed by association units that allow reversible and unsymmetrical disulfide bond formation, hydrophilic (PEG) and hydrophobic (PLA) polymer chains are efficiently coupled into amphiphilic diblock copolymers. The desymmetrization of otherwise symmetrical reversible disulfide bond formation is achieved with amide association units that integrate both directional H-bonding and reversible disulfide bond formation, which ensure the connection of different polymer blocks while minimizing self-coupling. The resultant amphiphilic block copolymers self-assemble into long-lasting spherical micelles that are responsive to free thiols.

Original languageEnglish
Pages (from-to)7431-7441
Number of pages11
JournalMacromolecules
Volume47
Issue number21
DOIs
StatePublished - Nov 11 2014

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