4.2 Article

Cleavage of Polystyrene-b-Poly(ethylene oxide) Block Copolymers with a Trithiocarbonate Linkage in Solutions

Journal

JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
Volume 48, Issue 17, Pages 3834-3840

Publisher

WILEY
DOI: 10.1002/pola.24169

Keywords

block copolymer; cleavage; living radical polymerization; photochemistry; RAFT; trithiocarbonate

Funding

  1. National Natural Science Foundation of China [20974099]
  2. Cao Guang-Biao High Technology Development Fund of Zhejiang University [2008RC006]
  3. Fundamental Research Funds for the Central Universities [2009QNA4038]
  4. State Key Laboratory of Chemical Engineering [SKL-ChE-10D04]

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In this work, the polystyrene-b-poly(ethylene oxide) (PS-b-PEO) block copolymers with a trithiocarbonate group between the blocks were prepared by polymerization of styrene in the presence of a trithiocarbonate reversible addition fragmentation chain transfer (RAFT) agent connected with PEO. Decomposition of the trithiocarbonate group by UV irradiation was investigated in three different types of solvent: tetrahydrofuran (THF, common solvent for both blocks), cyclohexane/dioxane mixture (selective solvent for the PS block) and N,N-dimethylformamide (DMF)/ethanol mixture (selective solvent for the PEO block). It is found that cleavage of the block copolymers can take place in all these three solvents and the cleavage ratio ranges from 76 to 86%. The micellar morphologies in selective solvents before and after cleavage were examined. It is observed that the size of the micelles is reduced after cleavage and sometimes aggregation of the micelles occurs due to removal of the corona of micelles. It shows that this work provides a facile and general method for synthesis of cleavable block copolymers. (C) 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3834-3840, 2010

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