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)

  • 2013Reverse Iodine Transfer Polymerization (RITP) of 1,1,2,2‐Tetrahydroperfluorodecyl Acrylate in Supercritical Carbon Dioxide6citations

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Bouilhac, Cécile
1 / 3 shared
Chirat, Mathieu
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Jolyduhamel, Christine
1 / 4 shared
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2013

Co-Authors (by relevance)

  • Bouilhac, Cécile
  • Chirat, Mathieu
  • Jolyduhamel, Christine
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article

Reverse Iodine Transfer Polymerization (RITP) of 1,1,2,2‐Tetrahydroperfluorodecyl Acrylate in Supercritical Carbon Dioxide

  • Bouilhac, Cécile
  • Chirat, Mathieu
  • Lacroixdesmazes, Patrick
  • Jolyduhamel, Christine
Abstract

<jats:p>Reverse iodine transfer polymerization (RITP) of 1,1,2,2‐tetrahydroperfluorodecyl acrylate (FDA) is successfully performed in supercritical carbon dioxide (scCO<jats:sub>2</jats:sub>) at 70 °C under a CO<jats:sub>2</jats:sub> pressure of 300 bar. PolyFDA (PFDA) of increasing molecular weights (from 10 000 to 100 000 g mol<jats:sup>−1</jats:sup>) is synthesized with good agreement between theoretical, <jats:sup>1</jats:sup>H NMR spectroscopy and and size exclusion chromatography/refractive index/right‐angle laser‐light scattering/differential viscometer (SEC/RI/RALLS/DV)‐estimated molecular weights (<jats:inline-graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="graphic/macp201300385-math-0001.png" xlink:title="urn:x-wiley:10221352:macp201300385:equation:macp201300385-math-0001" />). Furthermore, the increase of <jats:inline-graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="graphic/macp201300385-math-0002.png" xlink:title="urn:x-wiley:10221352:macp201300385:equation:macp201300385-math-0002" /> goes with a decrease of the dispersity of the polymers (<jats:italic>Đ</jats:italic> from 2.06 to 1.33), which is consistent with a controlled radical polymerization (CRP). Lastly, the structure of final PFDA and therefore the RITP process are confirmed by matrix‐assisted laser desorption ionization time‐of‐flight mass spectrometry (MALDI‐TOF MS) analyses. <jats:boxed-text content-type="graphic" position="anchor"><jats:graphic xmlns:xlink="http://www.w3.org/1999/xlink" mimetype="image/jpg" position="anchor" specific-use="enlarged-web-image" xlink:href="graphic/macp201300385-abs-0001-m.jpg"><jats:alt-text>image</jats:alt-text></jats:graphic></jats:boxed-text></jats:p>

Topics
  • impedance spectroscopy
  • polymer
  • Carbon
  • mass spectrometry
  • molecular weight
  • size-exclusion chromatography
  • Nuclear Magnetic Resonance spectroscopy
  • matrix-assisted laser desorption–ionisation
  • spectrometry
  • light scattering