Weix Group at UW-Madison. Primarily student run, with the occasional DJW tweet. Mostly group news. @weixgroup.bsky.social

Joined November 2017
105 Photos and videos
24 Jul 2025
Perhaps belatedly, we are shutting down on twitter - thank you to all the chemists out there who participated. It was pretty awesome while it lasted! Times change and so must we. Check out our website for the latest news as we change up how we share things. -DJW
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21 May 2025
Congratulations Dr. Lauren Ehehalt on a fantastic thesis defense! We're so excited to see all your future work at @EastmanChemCo 🥳🎉🎓
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Weix Group retweeted
Honoring Excellence in Chemistry Teaching! Congratulations to our 2025 Chemistry Teaching Award winners! Thank you for all of your hard work! Learn more here loom.ly/J00JlKM
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14 Mar 2025
Congrats to Julianna for receiving an Outstanding Chemistry Teaching Assistant Award for your work with Chem 636 and the NMR facilities! Well deserved! 🎉
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Our work on Ni- and Co-catalyzed Cross-Electrophile Coupling to Form Sterically Hindered C(sp2)–C(sp3) Bonds is now online at @J_A_C_S! Congrats to Tianrui, Anthony, Kasturi, and our collaborators Madeline (@KozlowskiMarisa) and @NovartisScience doi.org/10.1021/jacs.4c16912
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24 Jan 2025
Our work on in-situ generation of alkyl chlorides using Ghosez’s reagent and coupling with aryl chlorides is now online at @JOC_OL Congrats Ben! Check it out! doi.org/10.1021/acs.orglett.…
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Welcome to Abi! We're excited to see all your awesome work in the group! 🥳✌️
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26 Nov 2024
Wondering "What is XEC"? Want to use XEC but don't know where to start? Check out our guide to XEC, which includes a flowchart comprised of all the data we compiled during the writing of our Chemical Reviews publication! weixgroup.chem.wisc.edu/xec-…
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26 Nov 2024
We're incredibly proud to say that our review of Cross-Electrophile Coupling: Principles, Methods, and Applications in Synthesis is now online and open access at @ACSChemRev! Congrats to the team for this labor of love (and data!) pubs.acs.org/doi/10.1021/acs…
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28 Oct 2024
Question 5: What Organic Additive is most commonly used across all XEC?
47% TMSCl
11% Pyridine
9% Trifluoroacetic Acid
33% nBu4Br
66 votes • Final results
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28 Oct 2024
The wide variety of organic additives used means that TMSCl represents the largest portion with only 12% of all organic additives used. Silane reagents like TMSCl can activate metal powder reductants or by playing a direct role in the reaction mechanism.
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26 Oct 2024
Question 4: What Cation is most commonly employed when Inorganic Additives are used in XEC?
32% Mg 2
21% Li 1
14% Na 1
33% Zn 2
81 votes • Final results
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26 Oct 2024
While Zn salts can be generated in situ over the course of an XEC reaction, alkali and alkaline earth metal salts predominate by one to two orders of magnitude over other salt additives. Among all salt additives, Mg Salts (eg. MgCl2 and MgBr2) are the most common (27%)
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22 Oct 2024
Question 3: What percent of XEC reports form Csp2-Csp3 Bonds?
16% 40
36% 55
24% 63
24% 85
25 votes • Final results
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22 Oct 2024
While Csp2-Csp3 bonds do make up 55% of all XEC publications reported, the remaining 45% is comprised of a wide variety of other coupling types, from Csp2-Csp2 and Csp3-Csp3 to alkene and alkyne difunctionalization, among many others!
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