693.932 PEOPLE
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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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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
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article
Exploiting the Carbon and Oxa Michael Addition Reaction for the Synthesis of Yne Monomers
Abstract
<p>Herein, we demonstrated the synthesis of multifunctional alkyne building blocks from commercially available acrylate monomers exploiting the carbon and oxa Michael addition reaction. These compounds were obtained in decent yields and show similar or even higher photoreactivity than the initial acrylates. Importantly, selected thiol-yne formulations can be processed by stereolithography and significantly outperform the corresponding acrylate in terms of modulus and toughness. The high compatibility of such cured materials with osteosarcoma cells makes these photopolymers interesting for hard tissue engineering.</p>