Steric factors govern the formation of half-sandwich complexes (C5Me4R)Ln[N(SiHMe2)2]2 according to acid-base reactions utilising Ln[N(SiHMe2)2)3(thf)2 and substituted cyclopentadienes. Subsequent trimethylaluminium-promoted silylamide elimination produces the first half-sandwich bis(tetramethylaluminate) complexes (C5Me4R)Ln(AlMe4)2.

Download full-text PDF

Source
http://dx.doi.org/10.1039/b212754gDOI Listing

Publication Analysis

Top Keywords

half-sandwich complexes
8
high tetraalkylaluminate
4
tetraalkylaluminate fluxionality
4
fluxionality half-sandwich
4
complexes trivalent
4
trivalent rare-earth
4
rare-earth metals
4
metals steric
4
steric factors
4
factors govern
4

Similar Publications

Heterobimetallic complexes of an ambidentate deferiprone derivative, 3-hydroxy-2-methyl-1-(3-((pyridin-2-ylmethyl)amino)propyl)pyridin-4(1H)-one (PyPropHpH), incorporating an octahedral [Co(4N)] (4N = tris(2-aminoethyl)amine (tren) or tris(2-pyridylmethyl)amine (tpa)) and a half-sandwich type [(η--cym)Ru] (-cym = -cymene) entity have been synthesized and characterized by various analytical techniques. The reaction between PyPropHpH and [Co(4N)Cl]Cl resulted in the exclusive (O,O) coordination of the ligand to Co(III) yielding [Co(tren)PyPropHp](PF) () and [Co(tpa)PyPropHp](PF) (). This binding mode was further supported by the molecular structure of [Co(tpa)PyPropHp](ClO)(OH)·6HO () and [Co(tren)PyPropHpH]Cl(PF)·2HO·CHOH (), respectively, obtained via the slow evaporation of the appropriate reaction mixtures and analyzed using X-ray crystallography.

View Article and Find Full Text PDF
Article Synopsis
  • Control of individual atomic spins is essential for advancements in spintronics, quantum sensing, and quantum information processing, with scanning tunneling microscopy (STM) being a effective tool for manipulation.
  • The research presents a new method for self-assembling magnetic organometallic complexes using iron atoms and specific molecules (Cu(dbm) and FePc) on a silver substrate, effectively forming complexes that mimic metallocenes.
  • Magnetic properties of these complexes show a notable Kondo effect, which is explained through density functional theory calculations indicating that the interaction between Fe 3d-orbitals and benzene π-orbitals enhances Kondo screening, offering insights for designing hybrid organometallic systems.
View Article and Find Full Text PDF

Anilido-oxazoline-ligated iron complexes, including bis(anilido-oxazolinate) iron(II), mononuclear iron(II) alkyl and aryloxide, as well as the dinuclear analogues, were synthesized, and their catalytic performance on ring-opening polymerization (ROP) has been studied. Transmetalation of FeCl(THF) with in situ-generated anilido-oxazolinate lithium afforded the bis(anilido-oxazolinate) iron complexes and . Half-sandwich anilido-oxazolinate iron trimethylsilylalkyl complexes and could be synthesized in good yields via taking pyridine as an L-type ligand.

View Article and Find Full Text PDF

An artesunate-modified half-sandwich iridium(iii) complex inhibits colon cancer cell proliferation and metastasis through the STAT3 pathway.

RSC Chem Biol

December 2024

Jiangsu Collaborative Innovation Center of Biomedical Functional Materials/Nanjing Drum Tower Hospital, College of Chemistry and Materials Science, Nanjing Normal University Nanjing 210023 China

Colon cancer is one of the most commonly diagnosed cancers and is recognized as the most aggressive tumor of the digestive system. Aberrant activation of signal transducer and activator of transcription 3 (STAT3) is associated with proliferation, metastasis and immunosuppression of the tumor cells. Here, to inhibit the STAT3 pathway and suppress metastasis in colon cancer cells, the half-sandwich iridium complex Ir-ART containing an artesunate-derived ligand was synthesized.

View Article and Find Full Text PDF

Theoretical Prediction of Divalent Actinide Borozene Complexes.

Molecules

December 2024

Laboratory of Nuclear Energy Chemistry, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, China.

The aromatic boron cluster B () has similar π bonding to CH, which is named "borozene". The B ligand has been observed to stabilize monovalent Ln(+I) in -LnB (Ln = La, Pr, Tb, Tm, and Yb) borozene complexes. Low-valency actinide complexes have been reported more rarely, and B may be one of the potential ligands.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!