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Synthetic,structural and spectroscopic studies of complexes derived from the copper(II) perchlorate/fumaric acid/N,N′-chelates tertiary reaction systems
Authors:Katerina N Lazarou  Aris Terzis  Spyros P Perlepes  Catherine P Raptopoulou
Institution:1. Institute of Materials Science, NCSR “Demokritos”, 153 10 Aghia Paraskevi, Attikis, Greece;2. Department of Chemistry, University of Patras, 265 04 Patras, Greece
Abstract:The synthetic investigation of the Cu(ClO4)2·6H2O/fumaric acid (H2fum)/N,N’-chelates (1,10-phen, 2,2′-bpy) tertiary reaction systems has yielded mononuclear, dinuclear and tetranuclear complexes, and three coordination polymers. The chemical and structural identity of the products depends on the solvent, the absence or presence of external hydroxides in the reaction mixtures and the N,N’-donor. Three fumarato(−2) complexes, i.e. compounds Cu2(fum)(phen)4](ClO4)2·2H2O (1·2H2O), Cu(fum)(phen)(H2O)]n (3) and Cu2(fum)(bpy)2(H2O)2]n(ClO4)2n (6), were isolated and structurally characterized, and four non-fumarato complexes, i.e. compounds Cu43-ΟΗ)22-ΟΗ)2(phen)4(H2O)2](ClO4)4·2H2O (2·2H2O), Cu(ClO4)(phen) (MeCN)2(H2O)](ClO4) (4), Cu(ClO4)(phen)(MeCN)2]n(ClO4)n (5) and Cu(ClO4)2(bpy)(MeCN)2] (7), were simultaneously obtained from the reaction systems investigated. The coordination versatility of the fumarato(−2) ligand is reflected to the three different coordination modes observed in 1·2H2O, 3 and 6; the monodentate bridging μ2OO′ mode in 3, the asymmetric chelating bridging μ2OO′:κO′′:κO′′′ mode in 1·2H2O and 3, and the syn,syn bridging μ4OO′:κO′′:κO′′′ mode in 6. The crystal structures of the complexes are stabilized by intra- and inter-molecular hydrogen bonding and π–π stacking interactions leading to interesting supramolecular architectures. Characteristic IR bands of the complexes are discussed in terms of the known structures, and the coordination modes of the fum2− ligands.
Keywords:Copper(II) complexes  Fumarato(&minus  2) complexes  N  N&prime  -chelates  IR spectra
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