Acetylide-protected gold nanoclusters represent a recently described class of nanocluster compounds that are computationally predicted to be more stable than well-studied thiolate-protected clusters. Ligand exchange of thiolates-for-acetylides on these clusters as well as the reverse reaction are so-far unknown. Such reactions can inform a practical understanding of stability and other differences between thiolate- and acetylide-protected gold clusters. Here it is shown that acetylide-for-thiolate ligand exchange is facile when using either a lithium phenylacetylide or a gold(i)-phenylacetylide complex as incoming ligand to thiolate-protected gold clusters, whereas the reaction fails when using phenylacetylene. Both partial and full exchange are possible, as is the reverse reaction. While the overall reaction resembles ligand exchange, it may be better described as a metathesis reaction. Notably, while the simple thiolate-for-acetylide exchange reaction is enthalpically unfavorable, metathesis reactions between these ligands are enthalpically favorable. Intercluster exchange is also observed between thiolate-protected and acetylide-protected clusters.
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http://dx.doi.org/10.1039/d0nr00869a | DOI Listing |
Angew Chem Int Ed Engl
January 2025
TU Dortmund University, Faculty for Chemistry and Chemical Biology, Otto-Hahn-Str. 6, 44227, Dortmund, GERMANY.
Precise control over the catenation process in interlocked supramolecular systems remains a significant challenge. Here, we report a system in which a lantern-shaped Pd2L4 cage can dimerize to form two distinct Pd4L8 catenanes with different interlocking degree: a previously described quadruply interlocked double cage motif of D4 symmetry and an unprecedented triply interlocked structure of C2h symmetry. While the former structure features a linear arrangement of four Pd(II) centers, separated by three mechanically linked pockets, the new motif has a staggered shape.
View Article and Find Full Text PDFDalton Trans
January 2025
Department of Chemistry, University of Victoria, P.O. Box 3065, Victoria, BC V8W 3 V6, Canada.
A charge-tagged N-heterocyclic carbene (NHC) has been synthesized and its utility in allowing the dynamic behaviour of metal complexes to be monitored in real time using electrospray ionization mass spectrometry demonstrated. This compound was used to prepare different metal-NHC complexes, and the kinetic behaviour of complex formation and ligand exchange was monitored in real time through the use of pressurized sample infusion electrospray mass spectrometry (PSI-ESI-MS).
View Article and Find Full Text PDFIn motoneurons, spatiotemporal dendritic patterns are established in the ventral nerve cord. While many guidance cues have been identified, the mechanisms of temporal regulation remain unknown. Previously, we identified the actin modulator Cdc42 GTPase as a key factor in this process.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Institut für Anorganische Chemie, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 18, D-72076 Tübingen, Germany.
The homoleptic complex La(InMe) is obtained from the respective aluminium congener La(AlMe) a donor-assisted tetramethylaluminate/tetramethylindate exchange protocol. Compound La(InMe) exhibits interesting thermal lability as well as distinct cluster formation like LaIn(C)(CH)(CH)(CH) and LaIn(CH)(CH) upon addition of an excess of donor or thermal treatment. The neutral potentially tridentate ligand MeTACN (1,4,7-trimethyl-1,4,7-triazacyclononane) is used to investigate donor-triggered intermediates.
View Article and Find Full Text PDFJ Inorg Biochem
January 2025
Yusuf Hamied Department of Chemistry, Lensfield Rd, Cambridge CB2 1EW, UK.
By introducing new-to-nature transformations, artificial metalloenzymes hold great potential for expanding the biosynthetic toolbox. The chemistry of an active cofactor in these enzymes is highly dependent on how the holoprotein is assembled, potentially limiting the choice of organometallic complexes amenable to incorporation and ability of the protein structure to influence the metal centre. We have previously reported a method utilising ligand exchange as a means to introduce ruthenium-arene fragments into a four-helix bundle protein.
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