Macromolecular chemist @tugraz running the CD-lab for Organocatalysis in Polymerization #organocatalysis #olefinmetathesis #porouspolymers PI-run account

Austria
Joined July 2019
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Hard carbon derived from poly(dicyclopentadiene) under specific carbonization conditions offers superior rate capability and enhanced cyclability in carbonate electrolytes. doi.org/10.1002/advs.78311
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SURMOFs for opical oxygen sensing in organic solvents as one of the many outcomes of the "Porous Materials @ Work for Sustainability" lead-project @tugraz Congrats Theresa! doi.org/10.1039/d6tc02088g
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New @ChemRxiv, study on using hydroxyethyl acrylate to turn epoxy-amine thermosets into covalent adaptable networks. doi.org/10.26434/chemrxiv.15…
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New study: Lewis-base catalysed carbamate formation under coating-relevant conditions. The key point is that base catalysis is particularly effective in reacting with acidic alcohols, such as phenols. onlinelibrary.wiley.com/doi/…
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A novel approach to optically sensing oxygen in organic solvents based on phosphorescent SURMOFs is available to preview on @ChemRxiv see: doi.org/10.26434/chemrxiv.15…
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New @ChemRxiv - a very basic study on the influence of the alcohol's acidity on organo-base catalyzed carbamate formation from aliphatic isocyanates. doi.org/10.26434/chemrxiv.15…
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Preview @ChemRxiv: Polydicyclopentadien-Derived Turbostratic Hard Carbon for Long Cycle Life Sodium-Ion Battery Anodes. chemrxiv.org/doi/full/10.264…
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New work from @tugraz: Lewis base/oxirane combinations as catalysts for transesterification and ROP of caprolactone. is there carbenoid catalytic activity involved? doi.org/10.1007/s00706-026-0… follow up of doi.org/10.1002/adsc.70218
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MOFs as catalytic platform for covalent adaptable networks: catalysis meets reinforcement by @only_renner et al. read the new @angew_chem paper: doi.org/10.1002/anie.8126769
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We are happy to have contributed to the detailed studies led by the Resel group @tugraz on a transient, previously unknown chiral phase of 1,1'-biphenyl. doi.org/10.1021/acs.jpcc.5c0…
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We @tugraz disclosed a modular and inexpensive method of generating carbenoid reactivity in situ. Azoles & oxiranes catalyze benzoin condensation. O2 exclusion not needed. Utility is demonstrated by producing a thermoset from the glycidylether of vanillin. doi.org/10.1002/adsc.70218
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Mark your calendars! The next YPRA (Young Polymer Researchers Austria) meeting will be held in Leoben from June 29 to July 1, 2026. Visit the website for more information. ypra.at/frontend/index.php?s…
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you can find work @chemrixv on Lewis base/oxirane combinations acting as a catalytic system in the glycolysis of poly(ethylene terephthalate) and the ring-opening polymerization of ε-caprolactone doi.org/10.26434/chemrxiv-20…
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Replying to @ChemRxiv
@ChemRxiv you can find work on Lewis base/oxirane combinations acting as a catalytic system in the glycolysis of poly(ethylene terephthalate) and the ring-opening polymerization of ε-caprolactone doi.org/10.26434/chemrxiv-20…
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Replying to @jaimeojedas @tugraz
We have not done that. The lifetimes given in the paper were determined at the intensity plateau.
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Replying to @jaimeojedas
no idea - but interesting question!
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There's no need for thiols anymore! 😇 Hot lithography with formulations based on novel photobases, alcohols, and acrylates is disclosed in Mater. Horiz. doi.org/10.1039/D5MH01050K
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News from @TUGraz: Residual DMF compromises photostability of Zr MOFs – fluorination does not help! pubs.acs.org/doi/10.1021/acs…
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New @ChemRxiv: interested in an inexpensive way to take advantage of carbenoid reactivity without excluding humidity or oxygen? Take a look here: doi.org/10.26434/chemrxiv-20… #nhc #organocatalysis #polymerization
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Great study led by @_NinaStrasser_ @tugraz on changes in thermal expansion of a MOF upon de- and rehydration just released @JMaterChem! see: doi.org/10.1039/D5TC01746G
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