14523-25-2Relevant articles and documents
Syntheses, structures and electrochemical properties of two co-crystal copper(II) melamine complexes
Xu, Li-Feng,Chen, Xiao-Li,Hu, Huai-Ming,Wang, Bao-Cheng
, p. 163 - 167 (2008)
Two new co-crystal copper(II) melamine complexes, [Cu(HBA)2(MA)2] [Cu(HBA)2] (1) and [Cu2(OAc)4(MA)·(H2O)]2[Cu(HPE)2] (2), MA, melamine; HBA, 2-hydroxybenzaldehyde; HPE, 1-(2-hydroxyphenyl)ethanone, have been synthesized and characterized by elemental analysis, IR and single crystal X-ray diffraction. Crystal structural analysis reveals that 1 and 2 all are co-crystal complexes and composed of two neutral coordination units. In 1, two mononuclear units adopt square planar and distorted octahedral coordination environments, respectively. In 2, one is a mononuclear unit with a square planar geometry and the other is a dinuclear unit with a paddle wheel structure in which the apical positions are rarely occupied by two different donor ligands. The 2D supramolecular structures are formed through strong hydrogen bonds with different modes. The electrochemical behaviors of complexes 1 and 2 were investigated.
Copper(II)-salicylaldehydate/-methoxy(pyridine-2-yl)methanolate complexes via in-situ hydrolysis of Schiff bases
Enamullah, Mohammed,Chamayou, Anne-Christine,Banu, Kazi Saima,Kautz, Anna Christin,Janiak, Christoph
, p. 186 - 194 (2017)
Reaction of copper(II) nitrate with N-2-(R-pyridyl)salicylaldimine affords the mononuclear bis[salicylaldehydato-κO,O′]copper(II) (1) via acidic hydrolysis of the aldimine ligand back to the salicylaldehyde. Similarly, reaction with (R)-N-1-(p-BrC6H4)ethyl-salicylaldimine or (R)-1-(p-BrC6H4)-N-((pyridin-2-yl)methylene)ethanamine in presence of 2,2′-bipyridine (bipy) provides the mixed-ligated dinuclear bis[(μ-salicylaldehydato-κO,O′:O′)(2,2′-bipyridine)nitrato-copper(II)] (2) or bis[{μ-methoxy(pyridine-2-yl)methanolato-κN,O:O}(methanol)nitrato-copper(II)] (3). The structures of 2 and 3 consist of a dinuclear unit involving two (bipy)(salicylaldehydate)- or {methoxy(pyridine-2-yl)methanolate}(methanol)-coordinated copper(II) cations and two nitrate anions. The coordination sphere of copper is of N2O4-type with an elongated octahedron due to the Jahn-Teller effect in 2. The axial positions of the square bipyramid are occupied by the oxygen atoms from NO3? and the phenoxo group of the nearest salicylaldehydate molecule. The coordination sphere of copper is of NO4-type in 3, with the alkoxido group of methoxy(pyridine-2-yl)methanolate bridging between the Cu atoms. Cyclic voltammograms for 1 demonstrate two quasi-reversible one electron charge transfer processes for [Cu(L)2]2?/[Cu(L)2]? and [Cu(L)2]?/[Cu(L)2] (L?=?salicylaldehydato), respectively in acetonitrile. DSC analyses reveal an irreversible phase transformation from solid to solid-liquid mixture phase, and then to an isotropic liquid phase for 1. The excited state properties of 1 studied by DFT/TDDFT are comparable to the experimental electronic spectrum.
Kinetics of Complex Formation of Inner-Complex Salts of Copper(II) with Porphyrins in Propanol
Berezin, B. D.,Trofimenko, G. M.,Semeikin, A. S.,Berezin, M. B.
, p. 478 - 483 (2008/10/08)
The kinetics of complex formation of the inner-complex salts of copper(II), CuL2 (HL is acetylacetone, 3-butyl-2,4-pentanedione, 3-benzyl-2,4-pentanedione, salicylaldehyde, and 3-formyl-5-tert-butylsalicylaldehyde), with (1-8)-alkylporphyrins are studied. The activation parameters for this reaction are calculated. It is shown that the reaction rate for the coordination of porphyrins with the Cu(2+) ion substantially depends on the nature of the anion in the case of organic salts.
