Malte Fischer

Excited to share that our Al/Cd platforms serve as tamed Al(II) surrogates. Thanks a lot to @lablichtenberg.bsky.social (&FW) for the great collaboration and effort on EPR! Read all about it in @chemicalscience.rsc.org 👩‍🔬👨‍🔬⬇️ #MyFirstChemSci @unikassel.bsky.social
pubs.rsc.org/en/content/a...

Untapped catalytic ability of aluminium has been unlocked Could the discovery of a catalyst in which aluminium shifts easily between oxidation states be the beginning of the end for costly transition-metal catalysts?

Could the discovery of a catalyst in which aluminium shifts easily between oxidation states be the beginning of the end for costly transition-metal catalysts?

go.nature.com/4rkI0AW

Hauptgruppen‐ und Molekülchemie Im Jahr 2025 waren aller guten Dinge der Hauptgruppenchemie drei: ein dreifach geladenes Triborattrianion, ein Molekül mit linearer Al3-Einheit, das dritte Erdalkalimetall, das Stickstoff bindet, ein ...

Great to see this out! @fabiandankert.bsky.social and I summarise some of our favourite papers in main group chemistry over the last year

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Ambiphilic Reactivity and Switchable Methyl Transfer at a T-Shaped Bi(NNN) Complex Enabled by a Redox-Active Pincer Ligand We report the transition-metal-like reactivity of a geometrically constrained, ambiphilic bismuth(III) trisamide. Planarization of the Bi(III) center unlocks Bi–C bond formation when reacted with mild...

📣Our new paper is out in @jacs.acspublications.org (our very first one)!🥳

We show how a redox-active ligand unlocks C–X bond scission at an ambiphilic T-shaped Bi(III) compound. A big collaborative effort with my brilliant colleagues from Berlin.

👉 pubs.acs.org/doi/10.1021/...

The group will soon be advertising a 3-year PDRA position @imperialchemistry.bsky.social. The successful candidate will research the synthesis and reactivity of complexes with alkaline earth-metal bonds. Start date: 03/26. Please get in touch for infomal inquries.

Just 4 weeks left to apply for the PhD position in our research group! Deadline: 31 January. Don’t miss out, apply today :)

What's my #CSDPacked @ccdc.cam.ac.uk? My publishing name is Malte Fischer.

Huge congratulations!🥳

TIRE CHANGE: First Mg(I) complex with a Cp* ligand enables facile ligand exchange. Reaction with RONa gives (BDI)Mg-MgOR and Cp*Na. This paves the way for syntheses of many new asymmetric Mg(I) complexes. @angew_chem onlinelibrary.wiley.com/doi/epdf/10....

https://onlinelibrary.wiley.com/doi/full/10.1002/anie.202515545#

Our group's very first ACIE paper is out!🥳

Awesome work by Soti and a great cooperation with the Bittl group and @franemmerling.bsky.social.

Dedicated to @christianlimberg.bsky.social and Franc Meyer

@humboldtuni.bsky.social @manchester.ac.uk

onlinelibrary.wiley.com/doi/full/10....

First post, first publication!
I’m over the moon to share the first publication from our small research group! 🚀 pubs.rsc.org/en/content/a... @chemcomm.rsc.org
Jan explored a funky P=P-containing heterocycle and its reversible! bond activation chemistry, with DFT insights from Francesco. #newPI

Functional Al/Cd Heterometallics─From Controlled Al(I) Transfer to Nucleophilic Transfer of Cadmium Ions Low-valent cadmium compounds have remained largely unexplored as electron reservoirs, with no precedent for their use in reduction or bond activation chemistry. Here, we address this gap by integratin...

Thrilled to share a first publication of the group! We report on cadmium aluminyls that find application as Cd-nucleophiles and(!) Al(I)-Transfer reagents. Now out in @jacs.acspublications.org ! 🥳👍
Thanks a lot to @chemieverband.bsky.social for the generous funding. pubs.acs.org/doi/10.1021/...

Honored to welcome guests from the prestigious Tsinghua University in Beijing tsinghuauniversity.bsky.social for a fruitful exchange with representatives of the Faculty of Chemistry and the CRC 1633 in Göttingen. Many thanks for the inspiring discussions and the successful collaboration!

π‐Complexes of Main‐Group Metal Cations: Exploration of Lewis Acid Reactivity A series of cationic main-group complexes was obtained using the neutral, zwitterionic ligand IDP. The Lewis acidity of these complexes is explored by catalytic hydrophosphinations and halide additio...

Our latest publication reports the successful isolation of π-stabilized tetryliumylidenes [E–X]+ starting from pyramidanes based on a biradicaloid ligand . This milestone was made possible thanks to David’s relentless efforts . Proud of the team!

Did you know that #stannylenes can shine orange and green?
Philipp elucidated the mechanism of the dual #emission, the #excited state #dynamics, #excimer formation and light-induced bond #homolysis. #Maingroup #tin #photophysics #photochemistry onlinelibrary.wiley.com/doi/10.1002/anie.202510044

Kinetic Stabilization in Diaryl-Substituted Stannylenes: N2O Reactivity, Intramolecular C–H Activation, and Crystalline (Eind)Li(THF)2 as a Versatile Precursor in Tin Chemistry The reactivity of the kinetically stabilized stannylene (MesTer)2Sn (1) (MesTer = –C6H3-2,6-(2,4,6-Me3-C6H2)2) toward N2O is revisited, yielding the terminal tin(IV) hydroxide 2 via formal intramolecular C(sp3)–H activation of a putative terminal stannanone intermediate. By switching to Eind ligation (Eind = 1,1,3,3,5,5,7,7-octaethyl-s-hydrindacen-4-yl) at the tin center, the synthesis and characterization of the crystalline lithium salt (Eind)Li(THF)2 (3) is reported, serving as a straightforward precursor for the clean generation of the corresponding stannylene (Eind)2Sn (4). Compound 4 can be further cleanly converted into the heteroleptic Eind/halide stannylene (Eind)SnCl (6). Both 4 and 6 serve as suitable precursors for the synthesis of the heteroleptic s-hydrindacene-/amido-substituted stannylene (Eind)Sn{N(SiMe3)2} (5).

Excited to share our contribution to the special issue "Organometallic Chemistry Beyond the Transition Metals: Fundamentals and Applications of the P-Block" – now published @Organometallics! Check it out 👉 @pubs.acs.org #ChemSky
pubs.acs.org/doi/10.1021/...

Check out Fabio's next paper on the Nature of the Heavy Formal Double Bonds As=Ch, Sb=Ch and Bi=Ch (Ch = S, Se, Te) in NCN-Pincer Supported Arsinidene, Stibinidene and Bismuthinidene Chalcogenides - now published in Chemical Science pubs.rsc.org/en/content/articlelanding/2025/sc/d5sc03320a

Intriguing Reactivity of a 1,2‐Dihydrodialumane Towards Organic Azides – From a Terminal Diazido–Dialumane to Pendulum‐Clock‐Like Azide Bridging The reaction of a dihydro-dialane supported by a hybrid ligand (DNI) with organic azides yields structurally diverse aluminium species, including the first example of low oxidation state aluminium az...

Thrilled of having contributed to this investigation of low-valent aluminium species and their unique reactivity with azides. Great collaboration with the Stalke and Krawczuk groups! onlinelibrary.wiley.com/doi/10.1002/...

Our manuscript on unlocking the ambiphilicity of boryl anions is now published in JACS @jacs.acspublications.org (pubs.acs.org/doi/full/10....)! Chonghe, Junyi, Xibao, and coworkers report the synthesis and reactivity of the first anionic diazoborane! #maingroup #boron @gilliardgroup.bsky.social

LOW-VALENT Si, Ge, Sn, Pb: HOW LOW CAN WE GO???
Hydrocarbon-soluble Mg(0) reduces Si all the way to Si(4-). Unfortunately not stable and decomposing to the HSi(3-) anion. However, Sn(4-) is stable and functions as 4-fold Nu or 8e reducing agent. Preprint: shorturl.at/4mH0O

Isolation of the parent triplet titanocene via NHC stabilisation We present the synthesis and characterization of the parent isolable monomeric triplet titanocene complex, stabilized by the N-heterocyclic carbene (NHC) IMe4. Investigated by SQUID magnetometry and…

🔓Explore recent #OpenAccess work by @maltefischer.bsky.social‬, @townrowresearch.bsky.social‬ and colleagues on the isolation of the parent triplet titanocene via NHC stabilisation🔥

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📍@unigoettingen.bsky.social‬ and @kit.edu‬
🧪

Rreactivity of Pnictaalumenes towards 1,3-Dipole Molecules fresh out in @angewandtechemie.bsky.social Tim, Edgar and Leonie uncover unique insertion chemsitry giving a plethora of Al,P,N-heterocycles! Again a fruitful collaboration with the Braunschweig Group!

doi.org/10.1002/anie...

Dalton Transactions promotional graphic for the HOT articles collection.

This year's HOT articles collection is now online🔥

This collection represents the top 10% of research published in our journal each quarter. Congratulations to all the authors whose articles are featured in this collection👏

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#Chemsky 🧪

A Fresh Twist on the Phospha-(Aza)-Wittig Reaction The reactivity of an unsupported phosphinidene oxide, BnArNP═O (Bn = benzyl; Ar = bulky aryl group), as the electrophilic partner in Wittig reactions with ylides is described. Reactions with methylene-triphenylphosphorane (H2C═PPh3) and ethylidene-triphenyl-phosphorane (HMeC═PPh3), proceed as expected, giving rise to the phosphaalkene metathesis products and triphenylphosphine oxide. This reaction can be extended to other ylides such as N-(triphenylphosphoranylidene)methanamine (MeN═PPh3), to afford an aminoiminophosphane BnArNP═NMe. In these reactions the phosphinidene oxide plays the role of an electrophile, which would typically be the remit of an organic carbonyl in classical Wittig reactions. Further mechanistic insight into such transformations can be gained by altering the nature of the phosphorus-ylide. Upon reacting BnArNP═O with H2C═PMe3 (which possesses a smaller, more Lewis basic, phosphine) an alternative product is formed. This transformation supports the formation of a betaine intermediate that subsequently undergoes hydrogen-migration to afford an oxidized phosphorus(V) compound related to phosphorus acid.

Fresh out of the oven. Check out Chenyang’s most recent work in JACS (@jacs.acspublications.org). We explore the reactivity of a phosphinidene oxide as the electrophilic partner in Wittig transformations. Hope you enjoy.

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Such beautiful chemistry, Ian!😊

Many thanks, Sakya!☺️

Huge congratulations to Jennifer and Navutheya, whose master’s and bachelor’s theses are summarized here, and to Christopher for his outstanding help with SCXRD! 2/2

Carbene-activated stannylenes to access selective C(sp3)–H bond scission at the steric limit - Nature Communications The ubiquity of N-heterocyclic carbenes (NHCs) in chemical research typically arises from their potent stabilizing capabilities and role as innocent spectators to stabilize otherwise non-bottleable co...

Thrilled to share our latest work from the lab, in collaboration with @townrowresearch.bsky.social , exploring the fusion of heteroleptic amido-substituted stannylenes and NHCs! #chemsky www.nature.com/articles/s41... 1/2

Flash Communication: Cyanophosphide Transfer Reactions Cyanophosphides of the general form [RPCN]− can be viewed as cyanide adducts of phosphinidenes and are phosphorus species in the (+1)-oxidation state. We have recently reported on the stable cyanophosphide [DippTerPCN]K (DippTer = 2,6-Dipp2C6H3, Dipp = 2,6-iPrC6H3) and now investigate its reactions with ECln (E = Ge, n = 2; E = P, As, n = 3) in either salt metathesis or base-assisted dehydrohalogenation reactions. In the case of GeCl2, salt metathesis with [DippTerPCN]K afforded the dimer of a chlorogermylene [DippTerP(CN)GeCl]2. When only 0.5 equiv of GeCl2 was used, the diphosphanylgermylene [DippTerP(CN)]2Ge was generated in solution. With ECl3 (E = P, As), facile cyanophosphide transfer was achieved from DippTerP(H)CN in NEt3-assisted dehydrohalogenation, giving diphosphanes or arsaphosphanes of the type DippTerP(CN)ECl2 (E = P, As), respectively.

Ayu is keeping it up! This piece is about ArPCN- transfer to give Germylenes and phosphapnictanes! Thanks @maltefischer.bsky.social and @fabiandankert.bsky.social for their help! Thanks Organomteallics for the smooth proceedings! #31p #phosphorus

pubs.acs.org/doi/10.1021/...

Some new fantastic chemistry from Christian and team!😊