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 (5/5 displayed)

  • 2019Mechanical Thrombectomy in Ischemic Stroke Patients With Alberta Stroke Program Early Computed Tomography Score 0–5122citations
  • 2017Synthesis of acidic vinylcyclopropanes for dental applications7citations
  • 2017Development of low‐shrinkage composites based on novel crosslinking vinylcyclopropanes12citations
  • 2017Evaluation of Difunctional Vinylcyclopropanes as Reactive Diluents for the Development of Low‐Shrinkage Composites17citations
  • 2016Bis(4‐methoxybenzoyl)diethylgermane: A Highly Efficient Photoinitiator for the Polymerization of Vinylcyclopropanes25citations

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Chart of shared publication
Mordasini, Pasquale
1 / 1 shared
Michel, Patrik
1 / 1 shared
Chaloulos-Iakovidis, Panagiotis
1 / 1 shared
Hajdu, Steven D.
1 / 1 shared
Panos, Leonidas
1 / 1 shared
Gralla, Jan
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Friedrich, Benjamin
1 / 1 shared
Requena, Manuel
1 / 1 shared
Maegerlein, Christian
1 / 1 shared
Ribo, Marc
1 / 1 shared
Pierot, Laurent
1 / 1 shared
Gawlitza, Matthias
1 / 1 shared
Kaesmacher, Johannes
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Schaafsma, Joanna
1 / 1 shared
Pereira, Vitor Mendes
1 / 1 shared
Costalat, Vincent
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Benali, Amel
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Fässler, Pascal
4 / 7 shared
Catel, Yohann
4 / 12 shared
Pruvost, Chloé
1 / 1 shared
Moszner, Norbert
4 / 5 shared
Tauscher, Sven
3 / 3 shared
Pesch, Carmen
1 / 1 shared
Gorsche, Christian
1 / 3 shared
Schörpf, Sebastian
1 / 1 shared
Liska, Robert
1 / 13 shared
Chart of publication period
2019
2017
2016

Co-Authors (by relevance)

  • Mordasini, Pasquale
  • Michel, Patrik
  • Chaloulos-Iakovidis, Panagiotis
  • Hajdu, Steven D.
  • Panos, Leonidas
  • Gralla, Jan
  • Friedrich, Benjamin
  • Requena, Manuel
  • Maegerlein, Christian
  • Ribo, Marc
  • Pierot, Laurent
  • Gawlitza, Matthias
  • Kaesmacher, Johannes
  • Schaafsma, Joanna
  • Pereira, Vitor Mendes
  • Costalat, Vincent
  • Benali, Amel
  • Fässler, Pascal
  • Catel, Yohann
  • Pruvost, Chloé
  • Moszner, Norbert
  • Tauscher, Sven
  • Pesch, Carmen
  • Gorsche, Christian
  • Schörpf, Sebastian
  • Liska, Robert
OrganizationsLocationPeople

article

Bis(4‐methoxybenzoyl)diethylgermane: A Highly Efficient Photoinitiator for the Polymerization of Vinylcyclopropanes

  • Fässler, Pascal
  • Fischer, Urs
  • Catel, Yohann
  • Moszner, Norbert
Abstract

<jats:p>Bis(4‐methoxybenzoyl)diethylgermane (BMDG) is used for the photopolymerization of six 1,1‐disubstituted 2‐vinylcyclopropanes (VCPs). A significantly higher photopolymerization reactivity compared to the conventional camphorquinone (CQ)/amine or CQ/amine/iodonium salt photoinitiator systems is observed. Furthermore, the influence of the electron‐withdrawing substituents on the monomer reactivity is investigated. 1‐Ethoxycarbonyl‐1‐ethylcarbamoyl‐2‐vinylcyclopropane <jats:bold>5</jats:bold> and 1‐ethoxycarbonyl‐2‐vinylcyclopropanecarboxylic acid <jats:bold>2</jats:bold> are found to be the most reactive monomers. 1,1‐Disubstituted VCP‐based dental composites containing BMDG are formulated. Those materials exhibit good mechanical properties as well as a low polymerization shrinkage. <jats:boxed-text content-type="graphic" position="anchor"><jats:graphic xmlns:xlink="http://www.w3.org/1999/xlink" mimetype="image/png" position="anchor" specific-use="enlarged-web-image" xlink:href="graphic/macp201600463-abs-0001-m.png"><jats:alt-text>image</jats:alt-text></jats:graphic></jats:boxed-text></jats:p>

Topics
  • impedance spectroscopy
  • reactive
  • composite
  • amine