Sign in

Malte Fischer

@maltefischer.bsky.social
261 followers 259 following 19 posts

"Fishing" around in early transition metal and main group chemistry // TT Ass. Prof. @ Georg-August-Universität Göttingen // Liebig fellow // www.uni-goettingen.de/de/674212.html

PostsRepliesMedia
Reposted by Malte Fischer
Philipp Dabringhaus @pdabringhaus.bsky.social · 06/08/2026
Excited to share our first paper, just published in @angewandtechemie.bsky.social! 🥳 A first in Aluminum(I) chemistry!🔥 Charlotte reports the trapping of Aluminum(I) fragments within an ambiphilic ligand framework. (1/3) onlinelibrary.wiley.com/doi/10.1002/...
onlinelibrary.wiley.com
Ambiphilic Ligand Stabilization of Aluminum(I) Fragments: Halides, Cations, and a Hydride
Stabilization of elusive aluminum(I) halides in the framework of an ambiphilic ligand is reported. The unique bonding situation at the trigonal-bipyramidal aluminum center is analyzed, and the coordi....
3258
Reposted by Malte Fischer
coburgerpeter.bsky.social @coburgerpeter.bsky.social · 28/07/2026
Interested in multimetallic complexes? In our latest paper, we show how the hapticity in indenyl systems can be used as a switch to access different multimetallic coordination modes, including a rare Cr-Ag motif. Congratulations to everyone involved :) pubs.rsc.org/dt/article/d...
pubs.rsc.org
Submit This Form
094
Reposted by Malte Fischer
Oliver Townrow @townrowresearch.bsky.social · 11/06/2026
In this paper, we revisit one of the earliest reported bis(arene) sandwich complexes, [Fe(C6Me6)2], to finally solve a classic textbook question. As one of the reviewers mentioned, this is one for the organometallics purists! @chemieverband.bsky.social @kit.edu pubs.acs.org/doi/full/10....
pubs.acs.org
Revisiting the Fe(0) Sandwich Complex [Fe(C6Me6)2], Structural Solution to a 64-Year-Old Mystery
In this communication, we revisit one of E. O. Fischer’s seminal discoveries to solve a textbook question: is the iron(0) complex [Fe(C6Me6)2] an 18-valence-electron complex with a ‘ring-slip’ (η6,η4)...
1203
Reposted by Malte Fischer
Connie Lu @cluchem.bsky.social · 18/05/2026
#NewPI #Openings Dr. Hanna Cramer @h2cramer.bsky.social recently started her independent group at the Ruhr University Bochum. Check out her website below. She's looking to hire BS, MS and PhD students.
forschung.ruhr-uni-bochum.de
Hanna Hinrika Cramer Research Group
ResearchA more sustainable chemical industry must move away from fossil-based carbon sources and instead utilize renewable feedstocks, such as CO2 or…
065
Reposted by Malte Fischer
Josh Abbenseth @joshabbenseth.bsky.social · 01/05/2026
We explored the photophysics of heavy T‑shaped Pn trisamides and uncovered unique behaviour✨ A fantastic collaboration with the Winter and Coburger groups, combining synthesis, spectroscopy, and theory. Stellar work by Katharina and Soti 👏 chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/...
chemistry-europe.onlinelibrary.wiley.com
Phosphorescence of Heavy, T‐Shaped Pnictogen Trisamides in Solution at Room Temperature in the Near‐Infrared II Region
The unique photophysical properties of heavy T-shaped Sb and Bi trisamides are reported. A ligand-to-pnictogen charge-transfer excitation from a redox-active NNN pincer to a vacant pnictogen p-orbita...
1228
Reposted by Malte Fischer
Gilliard Group @gilliardgroup.bsky.social · 24/04/2026
The latest from the Gilliard and Cummins Labs....on the synthesis and reactivity of dioxaboriranes is now online in @natchem.nature.com (www.nature.com/articles/s41...)! Chonghe synthesized a series of unusual boron-O2 compounds, formed by N2 exchange from diazoboranes! @gilliardgroup.bsky.social
nature.com
Reactions of diazoboranes with oxygen enables the synthesis and isolation of dioxaboriranes - Nature Chemistry
Cyclic peroxides are highly reactive oxygen-containing species that play important roles in chemical synthesis. Now, the reaction between diazoboranes and triplet oxygen affords a family of cyclic dio...
1307
Malte Fischer @maltefischer.bsky.social · 09/04/2026
Excited to share our first publication of 2026 and our first foray into silicon chemistry now out in @angewandtechemie.bsky.social. Huge thanks to everyone involved for their hard work! onlinelibrary.wiley.com/doi/10.1002/...
onlinelibrary.wiley.com
Isolation and Reactivity of a Square‐Planar Trisamido Silane
We report the synthesis and comprehensive characterisation of a square-planar Si(+IV) hydride supported by an unsymmetric, trianionic and dearomatised N,N,N-pincer ligand. This system enables element...
1277
Reposted by Malte Fischer
Oliver Townrow @townrowresearch.bsky.social · 08/04/2026
Incredibly proud to share our group's latest publication, now out in JACS! Thanks to MSc student Luise and collaborator Robert for making this happen. pubs.acs.org/doi/10.1021/...
pubs.acs.org
A Simple, Air Stable Single-Ion Source of Iron(I)
Molecular complexes of iron in the rare +1 oxidation state have been shown to be efficient catalysts for industrially relevant chemical transformations, typically associated with the increasingly unsu...
93512
Reposted by Malte Fischer
Kay Severin @kay-severin.bsky.social · 02/04/2026
N-Heterocyclic allenes can be made using a Ti vinylidene complex. Work by Bastiaan Kooij with support from Damien Chen (computations), Rosario Scopelliti (XRD) & Farzaneh Fadaei-Tirani (XRD). Out in @angewandtechemie.bsky.social : onlinelibrary.wiley.com/doi/10.1002/...
1196
Reposted by Malte Fischer
Fabian Dankert @fabiandankert.bsky.social · 23/02/2026
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...
pubs.rsc.org
Al(II) Transfer Harnessing a Well-Defined Cadmium Precursor
Low-valent aluminum chemistry continues to expand the boundaries of main-group reactivity, yet the selective generation and transfer of Al(II) fragments remain underexplored. Controlled Al(II) transfe...
4348
Reposted by Malte Fischer
Nature @nature.com · 18/02/2026
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
go.nature.com
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?
0234
Reposted by Malte Fischer
Oliver Townrow @townrowresearch.bsky.social · 04/02/2026
Great to see this out! @fabiandankert.bsky.social and I summarise some of our favourite papers in main group chemistry over the last year gdch.app/article/haup...
gdch.app
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 ...
0185
Reposted by Malte Fischer
Josh Abbenseth @joshabbenseth.bsky.social · 07/01/2026
📣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/...
pubs.acs.org
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...
03912
Reposted by Malte Fischer
Josef Boronski @josefboronski.bsky.social · 08/01/2026
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.
01818
Reposted by Malte Fischer
Josh Abbenseth @joshabbenseth.bsky.social · 05/01/2026
Just 4 weeks left to apply for the PhD position in our research group! Deadline: 31 January. Don’t miss out, apply today :)
059
Reposted by Malte Fischer
Harder Research Group @harder-research.bsky.social · 17/10/2025
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....
0349
Reposted by Malte Fischer
Josh Abbenseth @joshabbenseth.bsky.social · 14/10/2025
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....
https://onlinelibrary.wiley.com/doi/full/10.1002/anie.202515545#
8376
Reposted by Malte Fischer
Marcel Schorpp @m-schorpp.bsky.social · 29/09/2025
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
2294
Reposted by Malte Fischer
Fabian Dankert @fabiandankert.bsky.social · 25/08/2025
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/...
pubs.acs.org
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...
24214
Reposted by Malte Fischer
SFB1633_unigoe @sfb1633-goe-sci.bsky.social · 31/07/2025
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!
081
Reposted by Malte Fischer
coburgerpeter.bsky.social @coburgerpeter.bsky.social · 26/07/2025
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!
chemistry-europe.onlinelibrary.wiley.com
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...
1152
Reposted by Malte Fischer
Katja Heinze's research group University of Mainz @labheinze.bsky.social · 22/07/2025
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
0201
Malte Fischer @maltefischer.bsky.social · 22/07/2025
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/...
pubs.acs.org
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).
1387
Reposted by Malte Fischer
Jens Beckmann @jensbeckmann.bsky.social · 18/07/2025
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
0164
Malte Fischer @maltefischer.bsky.social · 08/07/2025
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/...
onlinelibrary.wiley.com
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...
0122
Reposted by Malte Fischer
Robert J. Gilliard, Jr. @rjgilliard.bsky.social · 10/06/2025
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
0335
Reposted by Malte Fischer
Harder Research Group @harder-research.bsky.social · 28/05/2025
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
2328
Reposted by Malte Fischer
Dalton Transactions @daltontrans.rsc.org · 26/05/2025
🔓Explore recent #OpenAccess work by @maltefischer.bsky.social‬, @townrowresearch.bsky.social‬ and colleagues on the isolation of the parent triplet titanocene via NHC stabilisation🔥 pubs.rsc.org/en/content/a... 📍@unigoettingen.bsky.social‬ and @kit.edu‬ 🧪
pubs.rsc.org
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…
0125
Reposted by Malte Fischer
Hering-Junghans Lab @hering-lab.bsky.social · 10/04/2025
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...
0202
Reposted by Malte Fischer
Dalton Transactions @daltontrans.rsc.org · 03/04/2025
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👏 pubs.rsc.org/en/journals/... #Chemsky 🧪
Dalton Transactions promotional graphic for the HOT articles collection.
032
Reposted by Malte Fischer
GoicoecheaGroup @goicoecheagroup.bsky.social · 31/03/2025
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. pubs.acs.org/doi/full/10....
pubs.acs.org
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.
04610
Malte Fischer @maltefischer.bsky.social · 19/03/2025
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
nature.com
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...
2245
Reposted by Malte Fischer
Hering-Junghans Lab @hering-lab.bsky.social · 17/03/2025
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/...
pubs.acs.org
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.
0216
Malte Fischer @maltefischer.bsky.social · 13/03/2025
Some new fantastic chemistry from Christian and team!😊
030
Reposted by Malte Fischer
Josef Boronski @josefboronski.bsky.social · 11/03/2025
Catalytic methane functionalization and all it takes is... beryllium! We also compare the mechanisms of methane beryllation and borylation to reveal why Be finds it so easy @pubs.acs.org pubs.acs.org/doi/10.1021/...
pubs.acs.org
Methane Beryllation Catalyzed by a Base Metal Complex
The homogeneous catalytic functionalization of methane is extremely challenging due to the relative nonpolarity and high C–H bond strength of this hydrocarbon. Here, using catalytic quantities (10 mol...
26511
Reposted by Malte Fischer
Saurabh Chitnis @sschitnis.bsky.social · 10/03/2025
🚨Two projects out from our lab today (links fixed!) First up @angewandtechemie.bsky.social Macro/molecular chemistry of cis/trans P2N4 rings. Congrats @michaelland.bsky.social w/ @jasonmasuda.bsky.social for Xray onlinelibrary.wiley.com/doi/10.1002/... cc @dalchemistry.bsky.social
2164
Malte Fischer @maltefischer.bsky.social · 06/03/2025
Our story on stabilizing the parent triplet titanocene with an NHC is out! Congratulations to the entire team – it's great to be back with some Group 4 chemistry!☺️ @daltontrans.rsc.org @townrowresearch.bsky.social #chemsky pubs.rsc.org/en/content/a...
pubs.rsc.org
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 q...
0343
Reposted by Malte Fischer
mmhansmann.bsky.social @mmhansmann.bsky.social · 20/02/2025
We start our first post on Bluesky with a firework! Very proud of a brilliant team to publish our work on C(sp3)-atom transfer @science.org. www.science.org/doi/10.1126/... It has been a very exciting journey. Thanks @erc.europa.eu
612128
Reposted by Malte Fischer
Josef Boronski @josefboronski.bsky.social · 17/02/2025
Fully funded 3.5-year PhD studentship! Come and work on alkaline earth metal organometallic chemistry and metal-metal bonding @imperialcollegeldn.bsky.social! More details via the link: www.imperial.ac.uk/chemistry/po...
10423113
Reposted by Malte Fischer
Hering-Junghans Lab @hering-lab.bsky.social · 13/02/2025
Our first post here. Tim’s newest work on the reactivity of phosphaalumenes is out. When P=Al meets it’s smaller sibling a unique B,N,Al,P-heterocycle is formed. Congrats Tim and Leonie! #chemsky @chemcomm.bsky.social @likat.bsky.social #31p pubs.rsc.org/en/content/a...
pubs.rsc.org
A BNAlP-heterocycle
We report the [2+2]-cyclization reaction of a phosphaalumene with its lighter analog, an iminoborane, to give a species with a four-membered BNAlP-heterocycle with alternating Lewis basic and acidic c...
0438
Reposted by Malte Fischer
wolflab.bsky.social @wolflab.bsky.social · 12/02/2025
Pleased to share our latest work on a reactive iron-tin complex. Congrats to first author Yang Liu and thanks to our collaborators at the Gschwind and Meyer groups @Uni Regensburg and Göttingen! #iron #tin #119Sn #main_group_chemistry pubs.acs.org/doi/10.1021/...
pubs.acs.org
Synthesis and Reactivity of an Iron–Tin Complex with Adjacent Stannylidyne and Ferriostannylene Units
Heavier transition metal carbyne analogs hold significant potential for cooperative activation of small molecules. However, complexes containing more than one heavier tetrylidyne ligand RE (E = Si, Ge...
0194
Malte Fischer @maltefischer.bsky.social · 05/02/2025
Excited to share our debut paper of 2025! Just published in Inorganic Chemistry, this work, in fantastic collaboration with the Beckmann group, explores our foray into boron chemistry, highlighting the isolation and reactivity of a BO ketone analogue. pubs.acs.org/doi/10.1021/... #chemsky
pubs.acs.org
Structural Snapshots on Stepwise Anionic Oxoborane Formation: Access to an Acyclic BO Ketone Analogue and Its Metathesis Chemistry with CO2 and CS2
In this work, we disclose the synthesis and characterization of non-acid/base-stabilized anionic oxoboranes [MesTer2BO][K(L)] (MesTer = –C6H3-2,6-(2,4,6-Me3-C6H2)2, L = [2.2.2]-cryptand or 18-crown-6)...
3327
Reposted by Malte Fischer
Schneider Lab @schneider-lab.bsky.social · 29/01/2025
Our paper on triplet pnictinidenes (P, As, Sb) with transition metal substituents is out; congrats to Marc, Nils, Tarek and Rich and thanks to all that have contributed to get a comprehensive electronic structure picture @haenisch-group.bsky.social pubs.acs.org/doi/10.1021/...
pubs.acs.org
Transient Triplet Metallopnictinidenes M–Pn (M = PdII, PtII; Pn = P, As, Sb): Characterization and Dimerization
Nitrenes (R–N) have been subject to a large body of experimental and theoretical studies. The fundamental reactivity of this important class of transient intermediates has been attributed to their electronic structures, particularly the accessibility of triplet vs singlet states. In contrast, electronic structure trends along the heavier pnictinidene analogues (R–Pn; Pn = P–Bi) are much less systematically explored. We here report the synthesis of a series of metallodipnictenes, {M–Pn═Pn–M} (M = PdII, PtII; Pn = P, As, Sb, Bi) and the characterization of the transient metallopnictinidene intermediates, {M–Pn} for Pn = P, As, Sb. Structural, spectroscopic, and computational analysis revealed spin triplet ground states for the metallopnictinidenes with characteristic electronic structure trends along the series. In comparison to the nitrene, the heavier pnictinidenes exhibit lower-lying ground state SOMOs and singlet excited states, thus suggesting increased electrophilic reactivity. Furthermore, the splitting of the triplet magnetic microstates is beyond the phosphinidenes {M–P} dominated by heavy pnictogen atom induced spin–orbit coupling.
4299
Reposted by Malte Fischer
Josh Abbenseth @joshabbenseth.bsky.social · 23/01/2025
Excited to share our first paper of 2025 in Organometallics! 🥳 We showcase the reactivity of a geometrically constrained phosphine ligand in small molecule activation reactions. Great work by Soti! @humboldtuni.bsky.social Check it out here: 🔗 pubs.acs.org/doi/10.1021/... #chemsky #NewPI
pubs.acs.org
Flash Communication: Ligand Centered Cooperative O–H Bond Splitting by a Mo(CO)5(phosphine) Complex
The synthesis and reactivity of a molybdenum carbonyl complex ligated by geometrically constrained phosphorus trisamide are reported. Reaction with potassium tert-butoxide or methanol triggers ligand...
2294