Huber Lab @ RU Bochum
@shuberlab.bsky.social
Research in organic and supramolecular chemistry at Ruhr-University Bochum, Germany. Key interests are applications of halogen or chalcogen bonding in solution.
I was checking your work while you wrote and fully agree: beautiful examples that I'm ashamed to admit I mostly missed.
Which somewhat proves the point that having a common name helps keeping track and finding relevant work (at least from now on).
Which somewhat proves the point that having a common name helps keeping track and finding relevant work (at least from now on).
October 21, 2025 at 11:55 PM
I was checking your work while you wrote and fully agree: beautiful examples that I'm ashamed to admit I mostly missed.
Which somewhat proves the point that having a common name helps keeping track and finding relevant work (at least from now on).
Which somewhat proves the point that having a common name helps keeping track and finding relevant work (at least from now on).
If you meant that we shouldn't "rebrand" existing phenomena and pretend they weren't know before, I'm fully with you. But I don't think that was/is the intention. Or did I misunderstand your point?
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October 21, 2025 at 11:38 PM
If you meant that we shouldn't "rebrand" existing phenomena and pretend they weren't know before, I'm fully with you. But I don't think that was/is the intention. Or did I misunderstand your point?
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Does chalcogen bonding need a name? That's a philosophical question, but in my view it really helps to scan the literature (try finding chalcogen bonding adducts from earlier times...). Weakish Lewis acids, yes, but so are hydrogen bond donors... ;-)
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October 21, 2025 at 11:36 PM
Does chalcogen bonding need a name? That's a philosophical question, but in my view it really helps to scan the literature (try finding chalcogen bonding adducts from earlier times...). Weakish Lewis acids, yes, but so are hydrogen bond donors... ;-)
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(here is the link:) chemrxiv.org/engage/chemr...
Biaxial Recognition: Towards Chiral Resolution of Allene-Dicarbonyl Compounds by Iodolium-Based Halogen Bond Donors
The coordination of allene dicarbonyl compounds to cyclic iodonium salts is presented as a new biaxial halogen bonding recognition motif. 1H¬ NMR titrations and isothermal titration calorimetry (ITC) ...
chemrxiv.org
September 19, 2025 at 2:52 PM
(here is the link:) chemrxiv.org/engage/chemr...
Yes, I like how the viewing angles combine (by chance)
August 30, 2025 at 9:17 AM
Yes, I like how the viewing angles combine (by chance)
Thanks to Saber and Richard for the many measurements, to Christoph Held for the very nice cooperation and to our NMR department for their patience!
August 7, 2025 at 10:36 AM
Thanks to Saber and Richard for the many measurements, to Christoph Held for the very nice cooperation and to our NMR department for their patience!
Congrats - very useful method. And welcome to BlueSky!
April 29, 2025 at 6:54 PM
Congrats - very useful method. And welcome to BlueSky!