The distribution of metal aqua and chloro complexes is fundamental information for analysis of a chemical reaction involving these complexes. The present study investigated the speciation and structures of chromium aqua and chloro complexes using the thermodynamic model fitting analysis of UV-vis/X-ray absorption spectra. The existence of a negatively charged species was examined by adsorbability of chromium species on a strong base anion exchanger. In the results, a planar square [Cr(HO)], a planar square or distorted tetrahedral [CrCl(HO)], a trigonal bipyramidal [CrCl(HO)], and a distorted octahedral [CrCl(HO)] were confirmed and the thermodynamic parameters of complexation reactions were quantitatively determined. Investigation of the evolution of speciation of chromium aqua and chloro complexes in a pH 1 solution suggested the existence of [CrCl(HO) ] ( = 2 or 3) during the hydration process, which diminished in the equilibrium state. The kinetic analysis deserves further investigation to understand the speciation process quantitatively.
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http://dx.doi.org/10.1039/d2ra06279h | DOI Listing |
Talanta
April 2025
National Centre for Compositional Characterization of Materials (NCCCM), Bhabha Atomic Research Centre, Department of Atomic Energy, Hyderabad, 500 062, India.
A new and high performance polytetrafluoroethylene (PTFE) digestor was designed and fabricated in-house for the total dissolution of granite samples for the determination of technology-critical elements (TCEs) by inductively coupled plasma optical emission spectrometry (ICP-OES). Initially, the granite sample (∼0.25 g) was placed in the PTFE digestor and added 8 mL(v/v) of 20%HF+40%HCl+10%HNO acid mixture.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
October 2024
NMR Centre, Ruđer Bošković Institute, Zagreb, Croatia. Electronic address:
The need for a systematic approach in developing new metal-based drugs with dual anticancer-antimicrobial properties is emphasized by the vulnerability of cancer patients to bacterial infections. In this context, a novel organometallic assembly was designed, featuring ruthenium(II) coordination with p-cymene, one chlorido ligand, and a bidentate neutral Schiff base derived from 4-methoxybenzaldehyde and N,N-dimethylethylenediamine. The compound was extensively characterized in both solid-state and solution, employing single crystal X-ray diffraction, nuclear magnetic resonance, infrared, ultraviolet-visible spectroscopy, and density functional theory, alongside Hirshfeld surface analysis.
View Article and Find Full Text PDFInorg Chem
September 2023
Department of Chemistry, University of Iowa, Iowa City, Iowa 52242, United States.
A significant number of solid-state [UOCl] coordination compounds have been synthesized and structurally characterized. Yet, despite their purposive relative abundance in aqueous solutions, characterization of aquachlorouranium(VI) complexes remain rare. In the current study, a solid-state uranyl aqua chloro complex ((CHN)[UOCl(HO)]Cl) was synthesized using piperazinium as a charge-balancing ligand, and the structure was determined using single-crystal X-ray diffraction.
View Article and Find Full Text PDFInorg Chem
March 2023
Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99354, United States.
A novel actinide-containing coordination polymer, [Am(CO)(HO)Cl] (), has been synthesized and structurally characterized. The crystallographic analysis reveals that the structure is two-dimensional and comprised of pseudo-dimeric Am nodes that are bridged by oxalate ligands to form sheets. Each metal center is nine-coordinate, forming a distorted capped square antiprism geometry with a symmetry, and features bound oxalate, aqua, and chloro ligands.
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