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 (2/2 displayed)

  • 2008Carbanions on tap - Living anionic polymerization in a microstructured reactor56citations
  • 2008Ionic polymerizations in microstructured reactorscitations

Places of action

Chart of shared publication
Wurm, Frederik R.
2 / 42 shared
Wilms, Daniel
2 / 2 shared
Klos, Johannes
2 / 2 shared
Frey, Holger
2 / 29 shared
Chart of publication period
2008

Co-Authors (by relevance)

  • Wurm, Frederik R.
  • Wilms, Daniel
  • Klos, Johannes
  • Frey, Holger
OrganizationsLocationPeople

article

Carbanions on tap - Living anionic polymerization in a microstructured reactor

  • Wurm, Frederik R.
  • Löwe, Holger
  • Wilms, Daniel
  • Klos, Johannes
  • Frey, Holger
Abstract

<p>The paper describes the living anionic polymerization of styrenes to homo- and diblock copolymers in continuous flow, using a microstructured mixing set-up ("microreactor"). Reaction times and experimental effort are significantly reduced compared to classical batch methods that often require stringent reaction conditions and strict drying of the apparatus by "break-seal" and "high vacuum" techniques. In continuous flow, residual impurities can be removed by purging the reactor with monomer and initiator solution before polymer samples are collected at the device outlet on a scale of up to 200 g · h<sup>-1</sup>. Facile molecular weight adjustment is achieved by variation of the flow rates of initiator or monomer solutions. The polymerization of styrene in THF and cyclohexane was studied with respect to control of molecular weight and polydispersity. Furthermore, diblock copolymers with different block lengths and low polydispersities, consisting of styrene- and 4-tert-butoxystyrene blocks were synthesized, employing a second micromixer for a delayed introduction of the additional monomer. All materials were investigated by NMR-spectroscopy, SEC/MALLS, and MALDI-TOF mass spectrometry, confirming narrow molecular weight distributions (MWDs; M̄<sub>w</sub>/M̄<sub>n</sub> 1.09-1.25), molecular weights in the range of 500-70000 g · mol<sup>-1</sup>, and complete end-functionalization. No dimerization due to side reactions that would occur in the presence of oxygen was observed, evidencing efficient shielding of the apparatus from environmental influences.</p>

Topics
  • impedance spectroscopy
  • Oxygen
  • mass spectrometry
  • molecular weight
  • copolymer
  • size-exclusion chromatography
  • Nuclear Magnetic Resonance spectroscopy
  • functionalization
  • matrix-assisted laser desorption–ionisation
  • spectrometry
  • drying
  • polydispersity