Zinc(II) and copper(II) complexes of a tridentate Mannich base L1 derived from 2-hydroxy-1,4-naphthoquinone, pyridinecarboxyaldehyde and 2-aminomethylpyridine, [ZnL1Cl(2)]·H(2)O 1 and [CuL1Cl(2)]·2H(2)O 2, have been synthesized and fully characterized. The structure of complex 1 has been elucidated by a single crystal X-ray diffraction study: the zinc atom is pentacoordinate and the coordination geometry is a distorted square base pyramid, with a geometric structural parameter τ equal to 0.149. Vibrational spectroscopy and ab initio DFT calculations of both compounds have confirmed that the two complexes exhibit similar structures. Full assignment of the vibrational spectra was also supported by careful analysis of the distorted geometries generated by the normal modes.
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http://dx.doi.org/10.1016/j.saa.2012.03.048 | DOI Listing |
Acta Crystallogr E Crystallogr Commun
January 2025
Department of Chemistry, KU Leuven, Biomolecular Architecture, Celestijnenlaan 200F, Leuven (Heverlee), B-3001, Belgium.
Two novel complexes, [Cu()Cl] and [Zn()Cl], were synthesized from 1,1'-[(3-fluoro-phen-yl)methyl-ene]bis-[3-(3-fluoro-phen-yl)imidazo[1,5-]pyridine] (), and copper(II) and zinc(II) chloride, respectively. The structures of these complexes were confirmed using ESI-MS, IR and H NMR spectra. The results reveal mononuclear structures in which the central metal atoms are coordinated by two N atoms from the imidazole rings and two Cl ligands.
View Article and Find Full Text PDFACS Omega
December 2024
Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati, Assam 781 039, India.
In a quest to explore interconvertible assemblies of hydrates of cobalt(II), copper(II), and zinc(II) 2,6-pyridinedicarboxylate (), complexes having cation of a chloro-substituted analogue N-{(10-chloroanthracen-9-yl)methyl}-3-(1H-imidazol-1-yl)propan-1-amine were investigated. In the case of cobalt and copper complexes, a crystallized stable hydrate and a less stable methanol hydrate were guided by concentration-dependent crystallizations. The unit-cells of the crystals of the methanol hydrates of the two cobalt and copper complexes each belong to the P1̅ space group but have different stoichiometries as well as large differences in packing.
View Article and Find Full Text PDFJ Inorg Biochem
March 2025
Department of Inorganic Chemistry, Faculty of Science, Palacký University, 17. listopadu 12, CZ-779 00 Olomouc, Czech Republic. Electronic address:
The copper(II), cobalt(II), and zinc(II) complexes with 2-(1H-benzimidazol-2-ylmethylsulfanylmethyl)-1H-benzimidazole (tbb) and 2-[2-[2-(1H-benzimidazol-2-yl)ethylsulfanyl]ethyl]-1H-benzimidazole (tebb), [Cu(tbb)Cl] (1), [Co(tbb)Cl] (2), [Zn(tbb)Cl] (3), [Cu(tebb)Cl(HO)]Cl (4), [Co(tebb)Cl]·nCHOH (5) and [Zn(tebb)Cl(HO)]Cl (6), have been prepared and evaluated for antiproliferative activity. The structure of (4) was proved by X-ray diffraction crystallography. The coordination compounds were tested for their cytotoxic activities in cancer cell lines in vitro.
View Article and Find Full Text PDFJ Inorg Biochem
February 2025
Faculty of Chemistry, University of Wroclaw, F. Joliot-Curie 14, 50-383 Wroclaw, Poland; Chemistry and Biochemistry, Florida International University, 11200 SW 8th St, Miami, FL 33199, United States. Electronic address:
Metal ion coordination is crucial in bacterial metabolism, while divalent metal ions serve as essential cofactors for various enzymes involved in cellular processes. Therefore, bacteria have developed sophisticated regulatory mechanisms to maintain metal homeostasis. These involve protein interactions for metal ion uptake, efflux, intracellular transport, and storage.
View Article and Find Full Text PDFACS Catal
November 2024
Department of Chemistry, University of Rochester, Rochester, New York 14627, United States.
The air-stable copper(II) catalyst [Cu(FOX-L1)(MeCN)][OTf] () is prepared from a fused meso-dipyridylbisoxazolidine (FOX-L1) and CuBr, followed by treatment with AgOTf. The compound is a catalyst for the dehydration of 1-phenylethanol to styrene (+HO) in over 95% yield at 1 mol % catalyst loading. Other alcohols (benzylic, tertiary, or allylic) are also efficiently dehydrated by this catalyst.
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