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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1.080 Topics available

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (5/5 displayed)

  • 2024Synthesis and Characterization of Alkali Metal Hypersilyl Boratescitations
  • 2023Silicon and Germanium Functionalized Perylene Diimides – Synthesis, Optoelectronic Properties, and their Application as Non-Fullerene Acceptors in Organic Solar Cells2citations
  • 2023Exploring Aromatic S-Thioformates as Photoinitiators2citations
  • 2014Stable Silenolates and Brook-Type Silenes with Exocyclic Structures22citations
  • 2014Photoinduced Brook-type Rearrangement of Acylcyclopolysilanes18citations

Places of action

Chart of shared publication
Torvisco, Ana
3 / 15 shared
Fischer, Roland C.
4 / 36 shared
Walkner, Christoph
1 / 7 shared
Lainer, Thomas
1 / 1 shared
Tasch, Nina M.
1 / 1 shared
Stueger, Harald
1 / 1 shared
Sauermoser, Aileen
1 / 1 shared
Schlemmer, Bettina
1 / 1 shared
Ehmann, Birgit
1 / 1 shared
Zuccala, Elena
1 / 1 shared
Amenitsch, Heinz
1 / 46 shared
Trimmel, Gregor
1 / 19 shared
Holler, Sarah
1 / 2 shared
Reinfelds, Matiss
1 / 3 shared
Ludvíková, Lucie
1 / 1 shared
Marin-Beloqui, Jose Manuel
1 / 1 shared
Slanina, Tomáš
1 / 1 shared
Rath, Thomas
1 / 15 shared
Cruz, Gema Guedes De La
1 / 2 shared
Pueschmann, Sabrina
1 / 1 shared
Griesser, Thomas
1 / 9 shared
Rieger, Paul
1 / 1 shared
Schmallegger, Max
1 / 5 shared
Müller, Stefan
1 / 16 shared
Rausch, Martin
2 / 2 shared
Stüger, Harald
2 / 3 shared
Flock, Michaela
1 / 1 shared
Saf, Robert
1 / 5 shared
Hasken, Bernd
1 / 2 shared
Chart of publication period
2024
2023
2014

Co-Authors (by relevance)

  • Torvisco, Ana
  • Fischer, Roland C.
  • Walkner, Christoph
  • Lainer, Thomas
  • Tasch, Nina M.
  • Stueger, Harald
  • Sauermoser, Aileen
  • Schlemmer, Bettina
  • Ehmann, Birgit
  • Zuccala, Elena
  • Amenitsch, Heinz
  • Trimmel, Gregor
  • Holler, Sarah
  • Reinfelds, Matiss
  • Ludvíková, Lucie
  • Marin-Beloqui, Jose Manuel
  • Slanina, Tomáš
  • Rath, Thomas
  • Cruz, Gema Guedes De La
  • Pueschmann, Sabrina
  • Griesser, Thomas
  • Rieger, Paul
  • Schmallegger, Max
  • Müller, Stefan
  • Rausch, Martin
  • Stüger, Harald
  • Flock, Michaela
  • Saf, Robert
  • Hasken, Bernd
OrganizationsLocationPeople

article

Exploring Aromatic S-Thioformates as Photoinitiators

  • Cruz, Gema Guedes De La
  • Haas, Michael
  • Pueschmann, Sabrina
  • Griesser, Thomas
  • Rieger, Paul
  • Schmallegger, Max
Abstract

<p>Thiyl radicals were generated from aromatic S-thioformates by photolysis. The corresponding photo-initiated decarbonylation allows initiating polymerization reactions in both acrylate- and thiol-acrylate-based resin systems. Compared to aromatic thiols, the introduction of the photolabile formyl group prevents undesired reactions with acrylate monomers allowing photoinitiators (PIs) with constant reactivity over storage. To demonstrate the potential of S-thioformates as PIs, the bifunctional molecule S,S′-(thiobis(4,1-phenylene))dimethanethioate (2b) was synthesized, providing reactivity under visible light excitation. Consequently, acrylate-based formulations could successfully be processed by digital light processing (DLP)-based stereolithography at 405 nm in high resolution.</p>

Topics
  • resin