The Ye Group

Boron and organometallic chemistry @Uni_Wue

[The Ye Group @The_Ye_Lab]

@SRDChem @ChemicalScience Thanks Soumya!

[The Ye Group @The_Ye_Lab]

Check out our latest work on constructing a carboranyl-substituted 3-azaborole dianion by B≡N triple-bond cleavage, now online in @ChemicalScience
Thanks to Zhenyang Lin and his team for computational support, and congrats to Libo and all co-authors!
https://t.co/GtVYO99YGk

[Boron-Chem-Research @Boron_Chemistry]

Stepwise B[triple bond, length as m-dash]N bond cleavage by isocyanides: access to the 3-azaborole structural motif ( @chemicalscience ): https://t.co/dDpeowMKcK ( @The_Ye_Lab ).

[The Ye Group @The_Ye_Lab]

Big congratulations to our alumnus Chonghe Zhang! @Chonghe10

[MIT Chemistry @ChemistryMIT]

Congratulations to Chonghe Zhang, who was named the winner of a 2026 Young Investigator Award by the @AmerChemSociety’s (ACS) Division of Inorganic Chemistry.

https://t.co/p7a2M2ukpy

[The Ye Group @The_Ye_Lab]

@LLL_lab_SUSTech @libo_xiang @Uni_WUE @GHierlmeier @DelordWencel 谢谢刘老师！

[The Ye Group @The_Ye_Lab]

Congrats to @libo_xiang, the first PhD student from AK-Ye at @Uni_WUE, on successfully defending her thesis today! Many thanks also to the other two examiners, @GHierlmeier and @DelordWencel. We wish Libo all the best and a bright future ahead!

[The Ye Group @The_Ye_Lab]

Please check out our recent review paper on boron-containing three-membered rings, published in the Special Issue in Honor of T. Don Tilley at 70 in Coord. Chem. Rev.
https://t.co/05U3WN6b8x

[The Ye Group @The_Ye_Lab]

@DeepakP11301175 Thanks Deepak!

[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 https://t.co/upS716uysX

[The Ye Group @The_Ye_Lab]

@weisu2223 Thanks Wei!

[The Ye Group @The_Ye_Lab]

Thrilled to share how we amplify the BN-ketenimine character of an amino-substituted iminoborane using ortho-carborane, now online in @InorgChem . Congrats to @libo_xiang and all contributors!
https://t.co/cIvTP0UfGg

[The Ye Group @The_Ye_Lab]

@DobrovetskyG @InorgChem Thanks Roman!

[The Ye Group @The_Ye_Lab]

Thrilled to share our latest work on a superacidic borirane derivative featuring a tris(carboranyl)borane environment, now online in @InorgChem
https://t.co/YqXVaokIv3
Thanks to all contributors!

[The Ye Group @The_Ye_Lab]

Thrilled to share our first paper in Organometallics! @Orgmet_ACS Flash Communication: An Inorganic Version of Alkyne–Azide Cycloaddition: Click-Like Reactions of an o-Carboranyl Iminoborane with Organic Azides https://t.co/ZCoz2fIeAw

[The Ye Group @The_Ye_Lab]

Please check out our latest collaborative work with Prof. Maron on bis(alkynyl)boranes and bond activation @angew_chem. Congrats to Chenchang and Alex @Uni_WUE. This work is dedicated to Prof. Wagner’s 60th birthday @MWagnerLab
https://t.co/V47BMEiT2A

[The Ye Group @The_Ye_Lab]

Thrilled to share that our article on borirenes and boriranes has been recognized as a Top Viewed Article. Check it out if you haven’t already https://t.co/I1CkyoXUr1 #TopViewedArticle

[The Ye Group @The_Ye_Lab]

@DrTodd_Hudnall @Uni_WUE @angew_chem @TDTilleyGroup Thanks Todd!

[The Ye Group @The_Ye_Lab]

How to make a carbophosphinocarbene with a carborane backbone?
Check out our latest work @Uni_WUE in @angew_chem, which is dedicated to Prof. Don Tilley @TDTilleyGroup on the occasion of his 70th birthday.
https://t.co/gD41MOi2wV

[ChemistryViews @ChemistryViews]

An ortho-carboranyl carbophosphinocarbene (CPC) has been synthesized, showing strong electron-donating ability and unique reactivity
https://t.co/0qjhS24eIp

[The Ye Group @The_Ye_Lab]

@DobrovetskyG Thanks Roman!