MoVI complexes with novel ditopic diaminotetraphenol ligands have been prepared by using a one-pot procedure in methanol or DMSO with [MoO 2 (acac) 2 ] (acac = acetylacetonate) as the molybdenum source. The complexes were characterised with X-ray diffraction, NMR spectroscopic studies, elemental analysis and IR spectroscopy. In the solid state, the compounds represent either a rodlike molecular or oxido-
Six new tetranuclear copper(II) complexes were prepared exploiting novel ditopic alkylenediamine‐N,N,N′,N′‐tetraphenolate ligands. The geometrical parameters of the compounds can be varied by introducing different solvents of crystallization into the lattice. The structures of all six complexes were determined from single‐crystal X‐ray diffraction analyses and the magnetic properties of the complexes were estimated by computational DFT calculations. The relationship between the magnetic exchange coupling constant (J) and the Cu–O–Cu angle (θ) in these bis(phenoxido)‐bridged complexes was investigated and a magnetostructural correlation was established between J and the θ angle. All studied complexes showed strong antiferromagnetic behaviour.
The coordination chemistry of uranyl ions was studied using long n-alkyl chain (n = 5-8) bridged by N,N,N',N'-tetrakis(2-hydroxy-3-methyl-5-tert-butylbenzyl)diaminoalkanes (H4L1-H4L4) as ligands. All ligands formed 2:1 (U-to-L ratio) complexes with uranyl ions, but in addition 1:1 complexes could be characterized using ligands H4L2 and H4L3. The complexes were characterized by elemental analysis, spectroscopy (IR and NMR), and X-ray diffraction. The 2:1 complexes are of two types: [(UO2)2(H2Lm)(NO3)2(solvent)2] (m = 1 and 2; solvent = ethanol or propanol) or (cation)2[(UO2)2(H2Lm)(NO3)2(anion)2]·xsolvent (m = 2 and 4; cation = triethylammonium, anion = nitrate or thiocyanate, and solvent = dichloromethane and acetonitrile; x = 1 or 2). The 1:1 complexes have the formula [(UO2)2(H2Lm)2] (m = 2 and 3). In the solid state, 2:1 complexes are almost in a linear conformation with the uranyl ion at both ends of the ligand. The 1:1 complexes are cyclic dinuclear molecules. Preliminary studies of the ligands as uranyl ion extractors from water to dichloromethane were also performed. A high extraction efficiency was observed with H4L3 for uranyl ions, and in the presence of Cu(II), Ni(II), Co(II), and Zn(II) ions, a good extraction selectivity for uranyl ions was found with H4L1.
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