In the title compound, (C(3)H(12)N(2))[Cu(C(7)H(3)NO(4))(2)]·4H(2)O, the Cu(II) atom is six-coordinated in a distorted octa-hedral geometry by two tridentate pyridine-2,6-dicarboxyl-ate (pydc) ligands. In the crystal, inter-molecular O-H⋯O, N-H⋯O and weak C-H⋯O hydrogen bonds, as well as π-π stacking inter-actions between the pyridine rings of the pydc ligands [centroid-centroid distance = 3.4714 (14) Å] are present. C=O⋯π inter-actions between the carbonyl groups and pyridine rings [O⋯centroid distances = 3.150 (2) and 3.2233 (19) Å] are also observed.
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http://dx.doi.org/10.1107/S1600536811024378 | DOI Listing |
Acta Crystallogr E Crystallogr Commun
September 2024
Institute of Bioorganic Chemistry, Academy of Sciences of Uzbekistan, 100125, M. Ulugbek Str. 83, Tashkent, 700125, Uzbekistan.
The title compound, (CHNO)[CuCl(CHNO)]·2HO, was prepared by reacting Cu acetate dihydrate, solid 8-hy-droxy-quinoline (8-HQ), and solid pyridine-2,6-di-carb-oxy-lic acid (Hpydc), in a 1:1:1 molar ratio, in an aqueous solution of dilute hydro-chloric acid. The Cu atom exhibits a distorted CuONCl octa-hedral geometry, coordinating two oxygen atoms and one nitro-gen atom from the tridentate Hpydc ligand and three chloride atoms; the nitro-gen atom and one chloride atom occupy the axial positions with Cu-N and Cu-Cl bond lengths of 2.011 (2) Å and 2.
View Article and Find Full Text PDFNanoscale
May 2024
School of Chemical Sciences, National Institute of Science Education and Research (NISER), Bhubaneswar-752050, Orissa, India.
Electrochemical carbon dioxide (CO) conversion has enormous potential for reducing high atmospheric CO levels and producing valuable products simultaneously; however the development of inexpensive catalysts remains a great challenge. In this work, we successfully synthesised a 1D Cu-based metal-organic framework [Cu(PyDC)(HO)], which crystallizes in an orthorhombic system with the space group, by the hydrothermal method. Among the different catalysts utilized, the heterostructures of cathodized Cu-CuO@CC demonstrate increased efficiency in producing CHOH and CH, achieving maximum FE values of 37.
View Article and Find Full Text PDFRSC Adv
January 2024
Department of Electrical Engineering, College of Engineering, King Saud University Riyadh 11421 Saudi Arabia.
Efficient energy storage and conversion is crucial for a sustainable society. Battery-supercapacitor hybrid energy storage devices offer a promising solution, bridging the gap between traditional batteries and supercapacitors. In this regard, metal-organic frameworks (MOFs) have emerged as the most versatile functional compounds owing to their captivating structural features, unique properties, and extensive diversity of applications in energy storage.
View Article and Find Full Text PDFDalton Trans
August 2023
Institute of Engineering Thermophysics, Chinese Academy of Sciences, Beijing 100190, China.
Post-synthetic modification can be used for structural replacement or functional modification of materials after they have been formed or assembled. It can effectively combine various modification methods for metal-organic frameworks (MOFs) such as defect control, replacement of metal sites, or functionalization of ligands. In this work, organic ligands that incorporate N-functionalities or amino groups were introduced into defective UiO-66 through post-synthetic ligand exchange (PSE) to improve its water adsorption performance.
View Article and Find Full Text PDFInorg Chem
March 2023
Université Paris-Saclay, CEA, CNRS, NIMBE, 91191 Gif-sur-Yvette, France.
''-Tetramethylethane-1,2-diammonioacetate (L1) and ''-tetramethylpropane-1,3-diammonioacetate (L2) are two flexible zwitterionic dicarboxylates which have been used as ligands for the uranyl ion, 12 complexes having been obtained from their coupling to diverse anions, mostly anionic polycarboxylates, or oxo, hydroxo and chlorido donors. The protonated zwitterion is a simple counterion in [HL1][UO(2,6-pydc)] (), where 2,6-pydc is 2,6-pyridinedicarboxylate, but it is deprotonated and coordinated in all the other complexes. [(UO)(L2)(2,4-pydcH)] (), where 2,4-pydc is 2,4-pyridinedicarboxylate, is a discrete, binuclear complex due to the terminal nature of the partially deprotonated anionic ligands.
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