10 research outputs found
Transition metal complexes with Girard reagents and their hydrazones
This is the first review dealing with the coordination chemistry of metal complexes with Girard's reagents and their hydrazones. The short introduction points out to chemical properties and significance of these organic compounds. The next section briefly describes synthetic methods for preparing complexes with Girard's reagents, as well as modes of coordination of these ligands. The last two extensive sections review the preparation, stereochemistry and structural characteristics of metal complexes with Girard's hydrazones, including some newer non-hydrazonic derivatives of Girard's reagents, also.[Acknowledgments. Projekat Ministarstva nauke Republike Srbije, br. 172014
Bis{N,N,N-trimethyl-2-oxo-2-[2-(2,3,4- trihydroxybenzylidene)hydrazinyl]ethanaminium} tetrachloridozincate(II) methanol solvate1
The asymmetric unit of the title compound, (C12H18N3O4)2[ZnCl4]·CH3OH, consists of two Girard reagent-based cations, a tetrachloridozincate anion and a molecule of methanol as solvate. These components are interconnected in the crystal structure by an extensive network of O—H⋯O, N—H⋯O, C—H⋯O, O—H⋯N, O—H⋯Cl, N—H⋯Cl and C—H⋯Cl hydrogen bonds. The shortest intermolecular interaction is realized between the cation and anion [H⋯Cl = 2.29 (5) Å; O—H⋯Cl = 167 (3)°]. C—H⋯O interactions also play a important role in the interconnection of the cations
Amino(5-{2-[amino(iminio)methyl]hydrazin-1-yl}-3,5-dimethyl-4,5-dihydro-1H-pyrazol-1-yl)methaniminium dinitrate
The reaction of aqueous solutions of aminoguanidine hydrogennitrate and acetylacetone produces the title pyrazole salt, C7H18N8
2+·2NO3
−. The crystal structure is stabilized by a complex N—H⋯O hydrogen-bonding network. The difference in the engagement of the two nitrate anions in hydrogen bonding is reflected in the variation of the corresponding N—O bond lengths
Transition metal complexes with Girard reagent-based ligands, Part I: Synthesis and crystal structure of the first cobalt(III) complexes with Schiff base derivative of Girard reagent
A new ligand, pyridoxilidene Girard-T hydrazone, [H3L]Cl-2 . 2H(2)O, and its octahedral cobalt(III) complexes [Co(HL) (NO2)(3)] . H2O (1) and [Co(HL)(2)](PF6)(3) (2) were synthesized. The X-ray analysis of (1) showed that the complex has a mer-octahedral configuration formed by coordination of the tridentate ONO neutral Schiff-base molecule and three monodentate N-bonded NO2 groups. Hydrogen bonds and intermolecular interactions for this complex are discussed. Complex (2) also has a mer-octahedral configuration. The ligand and complexes were characterized by elemental analysis, conductometric and magnetochemical measurements, IR and UV-Visible, H-1 and C-13 NMR spectra. (C) 2004 Published by Elsevier B.V
Dioxidovanadium(V) complexes with pyridoxalaminoguanidine: Synthesis, spectral and structural characterization
Three square-pyramidal complexes of dioxidovanadium(V) with pyridoxalaminoguanidine (PLAG), of the formulas NH4[VO2(PLAG−2H)]∙H2O (1), VO2(PLAG−H) (2) and K[VO2(PLAG−2H)]∙H2O (3) have been synthesized and characterized by IR and UV-Vis spectral analysis and in case of 1 and 3 by X-ray crystallography as well. The reaction of aqueous ammoniacal solution of NH4VO3 and PLAG resulted in formation of 1, which in MeOH undergoes spontaneous transformation into 2, which, in turn, in the reaction with KOH transforms into 3. In these complexes PLAG is coordinated in a common tridentate ONN mode, via phenoxide oxygen atom and nitrogen atoms of azomethine and imino groups of the aminoguanidine fragment. In all previously characterized complexes PLAG was coordinated in neutral form. However, here we have proven that this ligand can be coordinated in both mono- (2) and doubly deprotonated form (1 and 3) as well. [Projekat Ministarstva nauke Republike Srbije, br. 172014]
Transition metal complexes with thiosemicarbazide-based ligands. Part 58. Synthesis, spectral and structural characterization of dioxovanadium(V) complexes with salicylaldehyde thiosemicarbazone
The first two complexes of dioxovanadium(V) with salicylaldehyde thiosemicarbazone (SALTSC), of the coordination formulas [VO2(SALTSC––H)]∙H2O (1) and NH4[VO2(SALTSC–2H] (2), were synthesized and characterized by elemental analysis, conductometric measurements, IR and UV–Vis spectroscopy and X-ray analysis. The complexes were obtained in the reaction of an aqueous ammoniacal solution of NH4VO3 and SALTSC. The results of the characterization showed that SALTSC was coordinated in the usual ONS tridentate mode as monoanion in complex 1 and dianion in complex 2. In both complexes, the vanadium atom is in a deformed square-pyramidal environment and is slightly shifted towards the apical oxo-ligand (» 0.52 Å)
Original scientific paper
Transition metal complexes with thiosemicarbazide-based ligands. Part 57. Synthesis, spectral and structural characterization of dioxovanadium(V) and dioxomolybdenum(VI) complexes with pyridoxal S-methylisothiosemicarbazon