Reaction of [{Au(C6X5)2}Ag]n (X = Cl, F) with the crown thioethers 1,4,7-trithiacyclononane ([9]aneS3), 1,4,8,11-tetrathiacyclotetradecane ([14]aneS4), or 1,4,7,10,13,16,19,22-octathiacyclotetracosane ([24]aneS8) affords a series of heteronuclear Au(I)/Ag(I) compounds of stoichiometry [{Au(C6X5)2}Ag(L)x] (L = [9]aneS3, x = 2 (1, 4); L = [14]aneS4, x = 1 (2, 5); L = [24]aneS8, x = 0.5 (3, 6)) formed via Ag-S bonds and Au···Ag contacts. X-ray diffraction studies of some of these complexes reveal different structural arrangements and nuclearity depending on the nature of the crown thioether ligand and on the presence or absence of aurophilic interactions. All the complexes are luminescent in the solid state but not in solution. Density functional theory calculations on representative model systems of complexes 2-4 and 6 were carried out to determine the origin of the electronic transitions responsible for their optical properties, which strongly depend on the nature of the perhalophenyl groups bonded to gold.
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Anal Chim Acta
February 2025
CAS Key Laboratory of Separation Sciences for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, PR China. Electronic address:
Dimethoate (DIM) is one of the most extensively applied organophosphorus pesticides (OPs), which is used to boost farm productivity due to its high insecticidal efficacy. However, the excessive use of DIM can result in the extensive contamination of soil, groundwater and food. Monitoring of DIM in environmental and food samples is crucial in view of its potential health risks and environmental hazards from excessive residues.
View Article and Find Full Text PDFJ Am Chem Soc
August 2024
Department of Chemistry and Biochemistry, Materials Science Institute, Knight Campus for Accelerating Scientific Impact, and Institute of Molecular Biology, University of Oregon, Eugene, Oregon 97403-1253, United States.
Persulfides (RSS) are ubiquitous source of sulfides (S) in biology, and interactions between RSS and bioinorganic metal centers play critical roles in biological hydrogen sulfide (HS) biogenesis, signaling, and catabolism. Here, we report the use of contact-ion stabilized [Na(15-crown-5)][BuSS] () as a simple synthon to access rare metal alkyl persulfide complexes and to investigate the reactivity of RSS with transition metal centers to provide insights into metal thiolate persulfidation, including the fundamental difference between alkyl persulfides and alkyl thiolates. Reaction of with [Co(TPA)(OTf)] afforded the η-alkyl persulfide complex [Co(TPA)(SSBu)] (), which was characterized by X-ray crystallography, UV-vis spectroscopy, and Raman spectroscopy.
View Article and Find Full Text PDFACS Omega
June 2024
MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, Sun Yat-sen University, Guangzhou, Guangdong 510275, China.
The synthesis of metal macrocycle complexes holds paramount importance in coordination and supramolecular chemistry. Toward this end, we report a new, mild, and efficient protocol for the synthesis of cyclometalated macrocycle Ir(III) complexes: [Ir()](PF) (), [Ir()](PF) (), and [Ir()](PF) (), where presents 10,17-dioxa-3,6-diaza-2(2,8),7(8,2)-diquinolina-1,8(1,4)-dibenzenacyclooctadecaphane, is 10,13,16,19,22,25-hexaoxa-3,6-diaza-2(2,8),7(8,2)-diquinolina-1,8(1,4)-dibenzenacyclohexacosaphane, and is 4-methyl-10,13,16,19,22,25-hexaoxa-3,6-diaza-2(2,8),7(8,2)-diquinolina-1,8(1,4)-dibenzenacyclohexacosaphane. This synthesis involves the preassembly of two symmetric 2-phenylquinoline arms into C-shape complexes, followed by cyclization with diamine via in situ interligand C-N cross-coupling, employing a metal ion as a template.
View Article and Find Full Text PDFChemistry
June 2024
The Florey, The University of Melbourne, Victoria, Australia.
A relaxin-like gonad-stimulating peptide (RGP), Aso-RGP, featuring six cysteine residues, was identified in the Crown-of-Thorns Starfish (COTS, Acanthaster cf. solaris) and initially produced through recombinant yeast expression. This method yielded a single-chain peptide with an uncleaved C-peptide (His Tag) and suboptimal purity.
View Article and Find Full Text PDFDalton Trans
March 2024
Friedrich Schiller University Jena, Institute of Inorganic and Analytical Chemistry, Humboldtstraße 8, D-07743 Jena, Germany.
The reactions of dimesitylphosphane oxide MesP(O)H with Lawessons reagent and dimesitylphoshane with selenium yield MesP(E)H with E = S (1a) and E = Se (1b), respectively, with moderate yields. Metalation of dimesitylphosphane sulfide 1a with -butyllithium, sodium hydride or potassium hydride in THF allows the isolation of dinuclear dimesityl-thiophosphinites of the type [(thf)A-S-PMes] [A = Li (4), Na (5), K (2a)] with central four-membered AS rings. The weaker base THP leads to the very similar aggregate [(thp)K-S-PMes] (3a) as has also been observed for the homologous potassium dimesityl-selenophosphinites of the type [(L)K-Se-PMes] [L = thf (2b), thp (3b)].
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