4.6 Article

Tuning the morphologies of amphiphilic metallo-supramolecular triblock terpolymers: from spherical micelles to switchable vesicles

期刊

SOFT MATTER
卷 5, 期 1, 页码 84-91

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/b813161a

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资金

  1. Dutch Counsel for Scientific Research
  2. Fonds der Chemischen Industrie
  3. Soft Matter cryo-TEM Research Unit
  4. Department of Chemical Engineering and Chemistry
  5. Eindhoven University of Technology
  6. STIPOMAT ESF Programme
  7. Politique Scientifique Federale [PAI VI/27]

向作者/读者索取更多资源

A well-defined poly(styrene)-block-poly(para-trifluoromethylstyrene)-[Ru]- poly(ethylene glycol) (PS-b-PTFMS-[Ru]-PEG) amphiphilic metallo-supramolecular triblock terpolymer containing a bis(2,2':6',2-terpyridine) ruthenium(II) complex (-[Ru] -) as a connection between the PS-b-PTFMS and the PEG block was successfully synthesized using the concepts of controlled radical polymerization and supramolecular chemistry. Spherical micelles, wormlike micelles, vesicles and hollow tubes were all accessed from this copolymer by varying the polarity of the solvent which provokes a change in the solvophilic to solvophilic ratio within the same macromolecule by dissolution or precipitation of the PTFMS-block. The self-assembled structures with both PS and PTFMS as insoluble blocks are presumed to be multicompartmentalized based on the incompatibility of these blocks. Furthermore, the thermoresponsive behavior of PTFMS allows reversible control over the size and morphology of the self-assembled structures.

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