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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Griesser, Thomas
Montanuniversität Leoben
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (9/9 displayed)
- 2023Hydrogen Evolution Reaction on Ultra-Smooth Sputtered Nanocrystalline Ni Thin Films in Alkaline Media—From Intrinsic Activity to the Effects of Surface Oxidationcitations
- 2023Exploring Aromatic S-Thioformates as Photoinitiatorscitations
- 2023On‐Demand Activation of Transesterification by Chemical Amplification in Dynamic Thiol‐Ene Photopolymerscitations
- 2023Sustainable Bio-Based UV-Cured Epoxy Vitrimer from Castor Oilcitations
- 2023Sustainable Bio-Based UV-Cured Epoxy Vitrimer from Castor Oilcitations
- 2021High resolution additive manufacturing with acrylate based vitrimers using organic phosphates as transesterification catalystcitations
- 2020Tailored Interfaces in Fiber-Reinforced Elastomerscitations
- 2020Exploiting the Carbon and Oxa Michael Addition Reaction for the Synthesis of Yne Monomerscitations
- 2014Preparation of PDMS ultrathin films and patterned surface modification with cellulosecitations
Places of action
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article
Exploring Aromatic S-Thioformates as Photoinitiators
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>