Dobrovetsky Group

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Dobrovetsky Group

Dobrovetsky Group

@DobrovetskyG

We do main group chemistry

Israel Katılım Ağustos 2018
400 Takip Edilen1.7K Takipçiler
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Dobrovetsky Group
Dobrovetsky Group@DobrovetskyG·
Freshly published in @InorgChemFront doi.org/10.1039/D6QI00… We show how substituents at the C vertices affect the reactivity of ortho-carboranes in reaction with cAAC. Huge congrats to the very talented Nardeen Safadi and Vladimir Kampel!!
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Josh Abbenseth
Josh Abbenseth@AbbensethJosh·
Only a couple of days left to submit abstracts for oral presentations at the ICCC 2026 (iccc2026.com)! I will be hosting a special symposium on P-block chemistry covering strained geometries and unusual electronic structures. See you there =)
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Eunsung Lee
Eunsung Lee@EunsungLee5·
We warmly invite researchers and students to submit their work. Oral abstract deadline: March 10, 2026 iccc2026.com
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Dobrovetsky Group
Dobrovetsky Group@DobrovetskyG·
Freshly published in @InorgChemFront doi.org/10.1039/D6QI00… We show how substituents at the C vertices affect the reactivity of ortho-carboranes in reaction with cAAC. Huge congrats to the very talented Nardeen Safadi and Vladimir Kampel!!
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The Ye Group
The Ye Group@The_Ye_Lab·
Check out our latest work. And yes, even in an air- and moisture-free lab, we occasionally like to play with water. Congrats to Julius and all contributors. Crystalline Water Adducts of a Dual-Site Lewis Superacidic Borane | Inorganic Chemistry pubs.acs.org/doi/full/10.10…
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Demyan 🇺🇦 Prokopchuk ⌬ (@dpro.bsky.social)
Deeply honored to have been selected as a 2026 Sloan Research Fellow! The tenacity and talent of my research group members, current and former, make this dream a reality. 😄 Thanks so much to my nominator and letter writers for your steadfast support! #SloanFellow
Sloan Foundation@SloanFoundation

Congrats to the 126 early-career scholars awarded a 2026 Sloan Research Fellowship, whose creativity and innovation set them apart as the next generation of scientific leaders! Our Fellows represent 7 fields and 44 institutions across the US and Canada. sloan.org/fellowships/20…

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Harder-Research
Harder-Research@harder_research·
Last week: homogeneous redox-catalysis with Al(I)-Al(III) @LLL_lab_SUSTech Now: heterogenous alkene hydrogenation with Al(0), earth’s most abundant metal. Observations and calculations point to reactivity at the metal surface. Preprint: shorturl.at/I9R0B Main group power 💪
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LLLiu Group
LLLiu Group@LLL_lab_SUSTech·
Aluminum: lightest p-block metal with very low electronegativity. Converting Al(III) to Al(I) in stoichiometric reactions is rare. But now, we've made Al redox catalysis a reality! Check it out @nature nature.com/articles/s4158…
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Alex Spokoyny
Alex Spokoyny@organomimetic·
Boron cluster with boron-centered redox activity?Check. Same cluster with boron-centered basic sites that can be reversibly protonated? Check. With these two unique properties established in the same system, we present the first manifestation of boron-centered PCET reactivity. For more, check out this preprint: lnkd.in/gg9wJ5jK Work led by Varun Tej in a collaboration with @ChemXin, Hannah Shafaat and their amazing teams!
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Mark Gandelman
Mark Gandelman@MarkGandelman·
Chemoselective catalytic C=O reduction of conjugated enones has been challenging and largely the domain of metal-based catalysts. We show that N-Heterocyclic Nitrenium can serve as an efficient organocatalyst for this transformation. The mechanism is quite complex :)
J. Am. Chem. Soc.@J_A_C_S

Organocatalytic Deoxygenative Reduction of α,β-Unsaturated Ketones | Journal of the American Chemical Society pubs.acs.org/doi/10.1021/ja…

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Ashraf Brik
Ashraf Brik@AshrafBrik·
I’m honored to share that I’ve received the Max Bergman Medal (2026). Grateful to the colleagues, collaborators, students, and mentors who made this work possible — and to the broader community for the inspiration and support along the way. max-bergmann-kreis.de/max-bergmann-m…
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