Four dinuclear bismuth(III) Schiff-base complexes bearing Schiff-base ligands have been synthesized and structurally characterized by single-crystal X-ray diffraction, elemental analysis, and spectral techniques (FT-IR, NMR and MS). The analytical data reveal the bismuth(III) complexes possess 1:1 metal-ligand ratios. In vitro biological studies have revealed that bismuth(III) complexes displayed much higher antibacterial and antitumor activities than their parent ligands, which involves two gram-negative (S. aureus, B. subtili) and two gram-positive (E. coli, P. aeruginosa) bacteria, and human gastric cancer SNU-16 cells. The power-time curves of S. pombe exposed to tested compounds were detected by bio-microcalorimetry. Some thermokinetic parameters (k, Pt and Q) were derived based on the metabolic power-time curves, and their quantitative relationships with the concentrations (c) were further discussed.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.jinorgbio.2022.111931 | DOI Listing |
Int J Mol Sci
October 2024
Faculty of Chemistry, Adam Mickiewicz University, 61-614 Poznań, Poland.
New bismuth (III) complexes with acetophenone-4-methyl-3-thiosemicarbazone (L) and halogens (Cl and Br) in both bridging and terminal positions have been synthesized and structurally characterized using single-crystal X-ray diffraction. The pure complexes (Cl or Br) were found to be highly isostructural, which motivated our attempts to create solid solutions of these complexes. A series of such compounds was prepared using various procedures and stoichiometries.
View Article and Find Full Text PDFChem Commun (Camb)
October 2024
Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY-14853, USA.
Org Lett
September 2024
Department of Chemistry, Indian Institute of Technology Madras, Chennai 600036, Tamil Nadu, India.
Here we demonstrate the hydrohalogenation reactions of HDDA benzynes promoted by BiX reagents for the generation of complex aryl halides. All three bismuth(III) halides can act as the source for their respective halides, i.e.
View Article and Find Full Text PDFJ Am Chem Soc
August 2024
Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, United States.
The discovery and utilization of main-group element catalysts that behave similarly to transition metal (TM) complexes have become increasingly active areas of investigation in recent years. Here, we report a series of Lewis acidic bismuth(III) complexes that allow for the catalytic allylic C(sp)-H functionalization of olefins via an organometallic complexation-assisted deprotonation mechanism to generate products containing new C-C bonds. This heretofore unexplored mode of main-group reactivity was applied to the regioselective functionalization of 1,4-dienes and allylbenzene substrates.
View Article and Find Full Text PDFDalton Trans
June 2024
Department of Chemistry "G. Ciamician", University of Bologna, Via Selmi 2, 40126 Bologna, Italy.
Bismuth(III) complexes have been reported to act as inhibitors of the enzyme urease, ubiquitously present in soils and implicated in the pathogenesis of several microorganisms. The general insolubility of Bi(III) complexes in water at neutral pH, however, is an obstacle to their utilization. In our quest to improve the solubility of Bi(III) complexes, we selected a compound reported to inhibit urease, namely [Bi(HEDTA)]·2HO, and co-crystallized it with (i) racemic DL-histidine to obtain the conglomerate [Bi(HEDTA)(μ-D-His)]·6HO + [Bi(HEDTA)(μ-L-His)]·6HO, (ii) enantiopure L-histidine to yield [Bi(HEDTA)(μ-L-His)]·6HO, and (iii) cytosine to obtain [Bi(HEDTA)]·Cyt·2HO.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!