The absorption maximum of the orange-colored copper(II) complex of the cyclam derivative L, which has two 3,7-diazabicyclo[3.3.1]nonane units, occurs at 390 nm. This is the lowest value for a copper(II) tetraamine known so far, and indicates an extremely strong ligand field. This maximum is shifted by 110 nm (5740 cm , 68 kJ mol ) to lower wavelengths than that of the parent compound [Cu(cyclam)] ; cyclam=1,4,8,11-tetraazacyclotetradecane.
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http://dx.doi.org/10.1002/1521-3773(20010702)40:13<2465::AID-ANIE2465>3.0.CO;2-X | DOI Listing |
Org Lett
January 2025
State Key Laboratory of Antiviral Drugs, Pingyuan Laboratory, Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, Henan 453007, China.
Highly asymmetric (3+3) annulation of diaziridines with oxiranes via C-N bond cleavage in diaziridine was achieved under 10 mol % of chiral copper(II) complex as the catalyst under mild reaction conditions. With Cu(OTf) as the Lewis acid and C-symmetric imidazolidine-pyrroloimidazolone pyridine as the ligand, diverse tetrahydro-[1,3,4]-oxadiazines were obtained by stereospecific C-N/C-O bond formation in moderate to good yields (up to 93% yield) and high diastereo- (>20:1 dr) and enantioselectivities (up to 92% ee). The catalytic cycle and stereochemical model were proposed by DFT calculation.
View Article and Find Full Text PDFChem Biodivers
January 2025
Al-Azhar University - Assiut Branch, Pharmacology, Assiut, Cairo, EGYPT.
Herein, Schiff base was synthesized via reaction between 2-bromo-4-(trifluoromethoxy)aniline and 2-hydroxybenzaldehyde. The ligand was reacted with Cu(II) salt to obtain complex. The compounds were characterization using various techniques.
View Article and Find Full Text PDFSmall
January 2025
Analytical & Environmental Science Division and Centralized Instrument Facility, CSIR-CSMCRI, G. B. Marg, Bhavnagar, 364002, India.
The present work reports the synthesis, characterization, and excited state photo-physical studies of two copper(II) compounds, 1 & 2, which show interference-free emission with homocysteine (Hcy). Cu(II) complexes offer an orthogonal detection strategy involving fluorescence and electrochemical methods, paving the way for improved point-of-care diagnostics and early cardiovascular diseases intervention. The reduction-induced emission enhancement (RIEE) of Cu complexes facilitates the fluorescence measurement of Hcy at physiological pH.
View Article and Find Full Text PDFJ Trace Elem Med Biol
January 2025
Center for Global Health Research (CGHR), Saveetha Medical College, Saveetha Institute of Medical and Technical Sciences (SIMATS), Saveetha University, Chennai, India. Electronic address:
[CuL(tmen)] is a sequence of four ternary mononuclear Schiff base copper(II) complexes that are derived from L-valine, suitable 5'-substituted-2'-hydroxyacetophenones (where the substituents are -Cl for L, -Me for L, -OMe for L, and -H for L), and tmen (where tmen-N,N,N',N' tetramethyl ethylenediamine). Without isolating the Schiff base ligand or producing any other intermediate products, all of the complexes were synthesised. These compounds were identified using elemental analysis, molar conductance, UV-Vis, FTIR, EPR, VSM-RT, and CD spectra.
View Article and Find Full Text PDFJ Phys Chem A
January 2025
Novosibirsk State University, Pirogov str. 1, Novosibirsk 630090, Russian Federation.
Nine metal complexes formed by three symmetric β-diketonates (, acetylacetonate (), 1,1,1,3,3,3-hexafluoro-acetylacetonate (), and 2,2,6,6-tetramethylheptane-3,5-dionate ()) and three metal ions (with three different coordination geometries, , Be - tetrahedral, Cu - square planar, and Pb - "swing" square pyramidal) were investigated. The study combines structural analyses, vibrational spectroscopic techniques, and quantum chemical calculations with the aim of bridging crystal structure, electronic structure, molecular topology, and far-infrared (FIR) spectroscopic characteristics. The effect of intramolecular interactions on the structural, electronic, and spectroscopic features is the center of this study.
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