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 (1/1 displayed)

  • 2012Engineering a sharp physiological transition state for poly(<i>n</i>‐isopropylacrylamide) through structural control13citations

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Chang, Kai
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2012

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  • Chang, Kai
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article

Engineering a sharp physiological transition state for poly(<i>n</i>‐isopropylacrylamide) through structural control

  • Chang, Kai
  • Dicke, Zachary T.
Abstract

<jats:title>Abstract</jats:title><jats:p>Poly(<jats:italic>N</jats:italic>‐isopropylacrylamide) (pNIPAAm), a well‐studied, biologically inert polymer that undergoes a sharp aqueous thermal transition at 32 °C, has been a subject of widespread interest for possible biological applications. A major hindrance to its successful application is due to the difficulty of maintaining a sharp transition when the polymer is modified for a physiological transition temperature, especially in isotonic solutions. Current copolymer blends raise the transition temperature but also make the transition significantly broader. We have combined the use of reversible addition‐fragmentation chain transfer (RAFT) polymerization with tacticity control to synthesize well‐defined pNIPAAm that demonstrates sharp transitions under physiological conditions. By selecting a RAFT agent with appropriate end groups, controlling molecular weight, and increasing the racemo diad content, we were able to increase the thermal transition temperature of pure pNIPAAm to a sharp transition at 37.6 °C under isotonic conditions. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012</jats:p>

Topics
  • impedance spectroscopy
  • molecular weight
  • copolymer
  • tacticity