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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Materials Map under construction

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)

  • 2023Synthesis and Characterization of 3-Aminopropyl-phenyl Germanes2citations
  • 2023The Nanostructured Self-Assembly and Thermoresponsiveness in Water of Amphiphilic Copolymers Carrying Oligoethylene Glycol and Polysiloxane Side Chains1citations
  • 2014Thermal aging of electrolytes used in lithium-ion batteries – An investigation of the impact of protic impurities and different housing materials94citations

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Chart of shared publication
Torvisco, Ana
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Fischer, Roland C.
2 / 36 shared
Garstenauer, Christoph
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Pisano, Giuseppe
1 / 1 shared
Guazzelli, Elisa
1 / 10 shared
Turriani, Marco
1 / 1 shared
Martinelli, Elisa
1 / 17 shared
Biver, Tarita
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Galli, Giancarlo
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Kriechbaum, Manfred
1 / 16 shared
Fauler, Gisela
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Kapper, Katja
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Handel, Patricia
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Schmuck, Martin
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Koller, Stefan
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Stangl, Christoph
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Chart of publication period
2023
2014

Co-Authors (by relevance)

  • Torvisco, Ana
  • Fischer, Roland C.
  • Garstenauer, Christoph
  • Pisano, Giuseppe
  • Guazzelli, Elisa
  • Turriani, Marco
  • Martinelli, Elisa
  • Biver, Tarita
  • Galli, Giancarlo
  • Kriechbaum, Manfred
  • Fauler, Gisela
  • Kapper, Katja
  • Handel, Patricia
  • Schmuck, Martin
  • Koller, Stefan
  • Stangl, Christoph
OrganizationsLocationPeople

article

The Nanostructured Self-Assembly and Thermoresponsiveness in Water of Amphiphilic Copolymers Carrying Oligoethylene Glycol and Polysiloxane Side Chains

  • Pisano, Giuseppe
  • Guazzelli, Elisa
  • Turriani, Marco
  • Martinelli, Elisa
  • Biver, Tarita
  • Galli, Giancarlo
  • Uhlig, Frank
  • Kriechbaum, Manfred
Abstract

<p>Amphiphilic copolymer self-assembly is a straightforward approach to obtain responsive micelles, nanoparticles, and vesicles that are particularly attractive for biomedicine, i.e., for the delivery of functional molecules. Here, amphiphilic copolymers of hydrophobic polysiloxane methacrylate and hydrophilic oligo (ethylene glycol) methyl ether methacrylate with different lengths of oxyethylenic side chains were synthesized via controlled RAFT radical polymerization and characterized both thermally and in solution. In particular, the thermoresponsive and self-assembling behavior of the water-soluble copolymers in water was investigated via complementary techniques such as light transmittance, dynamic light scattering (DLS), and small-angle X-ray scattering (SAXS) measurements. All the copolymers synthesized were thermoresponsive, displaying a cloud point temperature (T<sub>cp</sub>) strongly dependent on macromolecular parameters such as the length of the oligo(ethylene glycol) side chains and the content of the SiMA counits, as well as the concentration of the copolymer in water, which is consistent with a lower critical solution temperature (LCST)-type behavior. SAXS analysis revealed that the copolymers formed nanostructures in water below T<sub>cp</sub>, whose dimension and shape depended on the content of the hydrophobic components in the copolymer. The hydrodynamic diameter (D<sub>h</sub>) determined by DLS increased with the amount of SiMA and the associated morphology at higher SiMA contents was found to be pearl-necklace-micelle-like, composed of connected hydrophobic cores. These novel amphiphilic copolymers were able to modulate thermoresponsiveness in water in a wide range of temperatures, including the physiological temperature, as well as the dimension and shape of their nanostructured assemblies, simply by varying their chemical composition and the length of the hydrophilic side chains.</p>

Topics
  • nanoparticle
  • impedance spectroscopy
  • chemical composition
  • copolymer
  • small angle x-ray scattering
  • self-assembly
  • dynamic light scattering