Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (3/3 displayed)

  • 2015Photoreversible gelation of a triblock copolymer in an ionic liquid73citations
  • 2012Light-controlled reversible micellization of a diblock copolymer in an ionic liquid73citations
  • 2011UCST phase transition of azobenzene-containing random copolymer in an ionic liquid78citations

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Chart of shared publication
Watanabe, Masayoshi
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Kitazawa, Yuzo
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Ueki, Takeshi
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Usui, Ryoji
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So, Onyong
1 / 1 shared
Yamaguchi, Ayuko
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Niitsuma, Kazuyuki
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2015
2012
2011

Co-Authors (by relevance)

  • Watanabe, Masayoshi
  • Kitazawa, Yuzo
  • Ueki, Takeshi
  • Usui, Ryoji
  • So, Onyong
  • Yamaguchi, Ayuko
  • Niitsuma, Kazuyuki
OrganizationsLocationPeople

article

Light-controlled reversible micellization of a diblock copolymer in an ionic liquid

  • Watanabe, Masayoshi
  • Ueki, Takeshi
  • Nakamura, Yutaro
Abstract

<p>We report the reversible photoinduced self-assembly of a diblock copolymer in a typical hydrophobic ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate ([C <sub>4</sub>mim]PF <sub>6</sub>). A series of random copolymers consisting of 4-phenylazophenyl methacrylate and N- isopropylacrylamide (P(AzoMA-r-NIPAm)) show both photoresponsive solubility changes and upper critical solution temperature (UCST) phase transitions in [C <sub>4</sub>mim]PF <sub>6</sub>. The UCST phase transition temperature of the random copolymer depends strongly on the composition of AzoMA as well as on the photoisomerization state of the azobenzene moiety. The phase transition temperature of P(trans-AzoMA-r-NIPAm) in the dark is lower than that of P(cis-AzoMA-r-NIPAm) under UV-light irradiation. Reversible solubility changes by changing the wavelength of incident light were demonstrated by using the difference between the phase transition temperatures. On the basis of the results, we apply the thermo- and photoresponsive property of the random copolymer to a block copolymer system. A well-defined diblock copolymer (PEO-b-P(AzoMA-r-NIPAm)) was successfully prepared by combining anionic ring-opening polymerization of ethylene oxide (EO) and reversible addition-fragmentation chain transfer (RAFT) polymerization of AzoMA and NIPAm. A PEO-b-P(AzoMA-r-NIPAm) diblock copolymer is found to exhibit low-temperature micelle and high-temperature unimer (upper critical micellization temperature (UCMT)) transition in [C <sub>4</sub>mim]PF <sub>6</sub> from dynamic light scattering (DLS) measurements. The aggregation temperature of the diblock copolymer depends on the photoisomerization state of azobenzene, as expected. We demonstrated photoinduced self-assembly of the diblock copolymer in [C <sub>4</sub>mim]PF <sub>6</sub> at a "bistable" temperature. Reversibility of the micelle formation and dissolution into single polymer chains was also demonstrated.</p>

Topics
  • impedance spectroscopy
  • phase
  • phase transition
  • random
  • copolymer
  • block copolymer
  • chemical ionisation
  • dynamic light scattering
  • random copolymer
  • micelle formation