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The M(PyDTC)(2) (M: Cu, Co, or Ni) and CuPyDTC complexes, prepared by reactions of ammonium pyrrolidinedithiocarbamate with metal nitrates, are examined for qualitative analysis, speciation, and mutual separation using thin-layer chromatography systems. These complexes and their mixtures are spotted to the activated and non-activated thin layers of silica gel 60GF(254) (Si-60GF(254)) with a 250-microm thickness. Toluene-dichloromethane mixtures (4:1, 1:1, 1:4 v/v) are used as mobile phases for running of the complexes. All of these chromatographic systems are successfully used for speciation of Cu(2+) and Cu(1+) cations. The best analytical separation for the qualitative analysis of corresponding metal cations and mutual separation of components in M(PyDTC)(2) and CuPyDTC complexes are obtained when using pure toluene-dichloromethane (1:1 v/v) on the activated layer. This study shows that it is possible to qualitatively analyze and satisfactorily separate a mixture of Cu(1+), Cu(2+), Ni(2+), and Co(2+) cations on cited chromatographic systems. These results may be also said for the adaptability or validity on column chromatography.
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http://dx.doi.org/10.1093/chromsci/48.6.473 | DOI Listing |
ACS Appl Mater Interfaces
September 2025
Leibniz-Institut für Katalyse e.V. (LIKAT), Albert-Einstein-Str. 29a, Rostock 18059, Germany.
Metal-organic frameworks (MOFs) are transformative platforms for heterogeneous catalysis, but distinguishing atomically dispersed metal sites from subnanometric clusters remains a major challenge. This often demands the integration of multiple characterization techniques, many of which either lack the resolving power to distinguish active sites from their surrounding environments (e.g.
View Article and Find Full Text PDFLangmuir
September 2025
College of Electrical Engineering, Guizhou University, Guiyang 550025, China.
Effective detection and timely resolution of internal faults in lithium-ion batteries (LIBs) are necessary prerequisites for the safe use of batteries. In this study, the adsorption properties of four lithium-ion battery thermal runaway characteristic gases (CO, CH, CH, and CH) on the surface of ReSSe monolayers modified with Cu ( = 1-3) clusters were systematically investigated based on first-principles calculations. The calculation results showed that the introduction of Cu, Cu, and Cu reduced the bandgap of the ReSSe monolayer to 0.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
State Key Laboratory of Bioinspired Interfacial Materials Science, Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, Suzhou, Jiangsu, 215123, P.R. China.
Modern catalysis science has traditionally viewed carbon monoxide (CO) poisoning negatively due to its detrimental effects, such as the deactivation of metal sites. Here, we demonstrate a transformative approach by converting CO poisoning into a beneficial strategy to achieve high activity and selectivity in urea electrosynthesis. We designed a multiscale and multisite nanoreactor composed of copper-carbon dots (Cu-CDs) and bornite (CuFeS), which exploits CO-poisoned iron sites as anchors to facilitate efficient multi-species integration.
View Article and Find Full Text PDFBiomol Biomed
August 2025
Department of Gastrointestinal Surgery, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Cuproptosis is a copper-dependent form of regulated cell death that begins when ferredoxin 1 (FDX1) reduces Cu²⁺ to Cu¹⁺, allowing the ion to bind lipoylated enzymes of the tricarboxylic-acid (TCA) cycle, drive protein aggregation, dismantle iron-sulphur clusters and trigger fatal proteotoxic stress. Most tumours, despite accumulating copper, evade this fate through glucose-metabolic rewiring. First, oncogenic stabilisation of hypoxia-inducible factor-1 alpha (HIF-1α) and MYC increases pyruvate dehydrogenase kinase (PDK) activity, which phosphorylates and inactivates the pyruvate dehydrogenase complex (PDC), shrinking the lipoylated target pool in mitochondria and cutting the feed into the TCA cycle.
View Article and Find Full Text PDFChem Sci
August 2025
School of Material Science and Engineering, University of Jinan Jinan 250024 China
Transition-metal sites with mixed valence often coexist in diverse catalysts, yet their precise roles remain elusive. Taking a thiadiazole-coordinated Cu nanozyme system as an example, we developed ligand side-group engineering to modulate adjacent dicopper sites with different mixed Cu/Cu states. Amino functionalization of the ligand induced the cleavage of the electron-communicating S-bridge connecting adjacent copper centers, allowing precise manipulation of the ratio of mixed Cu/Cu sites.
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