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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University of Vienna

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2014Stimuli-Responsive Tertiary Amine Functional PEGs Based on N,N-Dialkylglycidylamines35citations
  • 2013Hydration Layer Coupling and Cooperativity in Phase Behavior of Stimulus Responsive Peptide Polymers37citations

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Herzberger, Jana
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Hinderberger, Dariush
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Werre, Mathias
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Fischer, Karl
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Jaumann, Eva A.
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Hassouneh, Wafa
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2014
2013

Co-Authors (by relevance)

  • Herzberger, Jana
  • Hinderberger, Dariush
  • Werre, Mathias
  • Frey, Holger
  • Fischer, Karl
  • Jaumann, Eva A.
  • Mcdaniel, Jonathan R.
  • Hassouneh, Wafa
  • Chilkoti, Ashutosh
OrganizationsLocationPeople

article

Stimuli-Responsive Tertiary Amine Functional PEGs Based on N,N-Dialkylglycidylamines

  • Kurzbach, Dennis
  • Herzberger, Jana
  • Hinderberger, Dariush
  • Werre, Mathias
  • Frey, Holger
  • Fischer, Karl
Abstract

<p>Amine-functional poly(ethylene glycol) (PEG) copolymers have been prepared that exhibit thermo- and pH- responsive behavior in aqueous solution. Three novel tertiary di(n-alkyl)glycidylamine monomers have been introduced for anionic ring-opening copolymerization (AROcP) with ethylene oxide (EO): N,N-di(n-butyl)glycidylamine (DButGA), N,N-di(n-hexyl)glycidylamine (DHexGA), and N,N-di(n-octyl)glycidylamine (DOctGA). Via controlled AROcP we synthesized well-defined (M<sub>w</sub>/M<sub>n</sub> = 1.05-1.14), water-soluble block- and gradient-type PEG copolymers, containing up to 25 mol % of the respective dialkylglycidylamine comonomer. Molecular weights ranged from 4900 to 12-000 g mol<sup>-1</sup>. Detailed in-situ<sup>1</sup>H NMR kinetics and<sup>13</sup>C triad analyses elucidate the microstructures of the copolymers and the relative reactivity of the novel comonomers. Notably, the n-alkyl chain length had no significant influence on the relative reactivity of the glycidylamine comonomers. Calculated reactivity ratios ranged from r<sub>EO</sub> = 1.84, r<sub>DButGA</sub> = 0.49 to r<sub>EO</sub> = 1.78, r<sub>DOctGA</sub> = 0.42, manifesting the formation of gradient copolymers. Thermo- and pH-responsive properties of these copolymers are precisely tunable by the comonomer ratio, and cloud points in aqueous solution can be adjusted between 21 and 93 °C. Electron paramagnetic resonance (EPR) spectroscopic studies with TEMPO as a spin probe were conducted to elucidate host-guest interactions of the copolymers. Unexpectedly, the n-alkyl chain length of the different glycidylamine comonomers only influences the inverse phase transition of the gradient copolymers, but not of the block copolymers on the nanoscale. Self-assembly of the block- and gradient-type copolymers in aqueous alkaline solution by both static and dynamic light scattering has also been investigated after confirming the existence of pure unimers in methanol.</p>

Topics
  • microstructure
  • phase
  • phase transition
  • electron spin resonance spectroscopy
  • molecular weight
  • copolymer
  • Nuclear Magnetic Resonance spectroscopy
  • block copolymer
  • amine
  • self-assembly
  • dynamic light scattering
  • gradient copolymer