Abstract:The thiosemicarbazide and hydrazide Cu(II) complexes, [Cu 3 L 2 1 (py) 4 Cl 2 ] (1), [Cu(HL 2 )py] (2) and [Cu(HL 3 )py] (3), (H 2 L 1 = 1-picolinoylthiosemicarbazide, H 3 L 2 = N 0 -(2-hydroxybenzylidene)-3-hydroxy-2-naphthohydrazide, H 3 L 3 = 2-hydroxy-N 0 -((2-hydroxy-naphthalen-1-yl)methylene)benzohydrazide) have been prepared and characterized through physicochemical and spectroscopic methods as well as X-ray crystallography. Complex 1 has a centrosymmetric structure with -N-N-bridged Cu 3 skeleton. Neig… Show more
“…Unlike these, the spectrum of 3 contains five bands in the range characteristic for SO 4 2-group: three around 1000 cm -1 and two around 600 cm -1 , which supports the bridging role of sulfate ion [27]. Despite general similarity visualized in these figures, coordination geometry shows fine, but significant differences.…”
Section: Resultsmentioning
confidence: 68%
“…IR spectra of 1, 2, 2a and 4 possess one sharp band at 1114, 1112, 1057 and 1118 cm -1 , respectively, and other at 618, 616, 607 and 620 cm -1 , respectively, which correspond to uncoordinated SO 4 2-group [27]. Unlike these, the spectrum of 3 contains five bands in the range characteristic for SO 4 2-group: three around 1000 cm -1 and two around 600 cm -1 , which supports the bridging role of sulfate ion [27].…”
Section: Resultsmentioning
confidence: 99%
“…The thermal analysis of compounds with potential biological activity is a common part in their characterization [3,4] as offers valuable, sometimes essential data to develop new pharmaceutical forms [5] or to detect structural changes or polymorphism [6] in materials used in drug formulation or in their quality control [7]. In addition, with increasing sensitivity of thermal equipments by means of thermal methods, important structural details could be determined [8] that are sometimes difficult to obtain by other techniques.…”
The syntheses of complexes of Cu(II) with biological active ligand, pyridoxal thiosemicarbazone (PLTSC) and its derivative, pyridoxal S-methylisothiosemicarbazone, are described. All coordination compounds were characterized by elemental analysis, molar conductivity and infrared spectra. The crystal and molec-is determined by single-crystal X-ray crystallography, too. The thermal decomposition of all the ligands and complexes was determined by simultaneous TG/DSC measurements. The decomposition mechanisms were compared and analyzed from the aspects of the relationships between the structures of the compounds and their thermal decomposition pattern.
“…Unlike these, the spectrum of 3 contains five bands in the range characteristic for SO 4 2-group: three around 1000 cm -1 and two around 600 cm -1 , which supports the bridging role of sulfate ion [27]. Despite general similarity visualized in these figures, coordination geometry shows fine, but significant differences.…”
Section: Resultsmentioning
confidence: 68%
“…IR spectra of 1, 2, 2a and 4 possess one sharp band at 1114, 1112, 1057 and 1118 cm -1 , respectively, and other at 618, 616, 607 and 620 cm -1 , respectively, which correspond to uncoordinated SO 4 2-group [27]. Unlike these, the spectrum of 3 contains five bands in the range characteristic for SO 4 2-group: three around 1000 cm -1 and two around 600 cm -1 , which supports the bridging role of sulfate ion [27].…”
Section: Resultsmentioning
confidence: 99%
“…The thermal analysis of compounds with potential biological activity is a common part in their characterization [3,4] as offers valuable, sometimes essential data to develop new pharmaceutical forms [5] or to detect structural changes or polymorphism [6] in materials used in drug formulation or in their quality control [7]. In addition, with increasing sensitivity of thermal equipments by means of thermal methods, important structural details could be determined [8] that are sometimes difficult to obtain by other techniques.…”
The syntheses of complexes of Cu(II) with biological active ligand, pyridoxal thiosemicarbazone (PLTSC) and its derivative, pyridoxal S-methylisothiosemicarbazone, are described. All coordination compounds were characterized by elemental analysis, molar conductivity and infrared spectra. The crystal and molec-is determined by single-crystal X-ray crystallography, too. The thermal decomposition of all the ligands and complexes was determined by simultaneous TG/DSC measurements. The decomposition mechanisms were compared and analyzed from the aspects of the relationships between the structures of the compounds and their thermal decomposition pattern.
“…In addition, the catalytic properties of vanadium (Hosseini-Monfared et al, 2010, cerium (Jiao et al, 2014) and palladium complexes (Arumugam et al, 2015) have been explored. Further, structural data for copper (Liu et al, 2012), molybdenum (Miao, 2012) and vanadium (Kurup et al, 2010) complexes are available. As part of our ongoing work with these ONO tridentate ligands (Lee et al, ISSN 2056-9890 2013), we hereby describe the crystal and molecular structures of the title compound, (I), as well as a detailed analysis of the intermolecular associations through a Hirshfeld surface analysis.…”
A highly distorted pentacoordinated C2NO2 geometry is observed for the Sn atom owing to a tridentate mode of coordination of the Schiff base ligand and the restricted bite angles it subtends. In the crystal, supramolecular layers sustained by C—H⋯O, π–π, C—H⋯π(arene) and C—H⋯π(chelate ring) interactions are formed.
“…[3] The presence of additional donor atom(s) X in the acyl moiety enables bridging mode of the corresponding acyl thiosemicarbazides by the coordination with metal ions through both donor sets (O, N 2 ) and (X, S, N 1 ) (figure 1d). [4][5][6][7][8] In such cases, the obtained complexes are oligonuclear systems with complicated topologies. Herein, the present work reports the synthesis and structure determination of a new acyl thiosemicarbazide ligand H2L (figure 2) derived from Nmethylanthranilic acid.…”
The new ligand N‐methylanthraniloyl(4‐ethylthiosemicarbazide) H2L was synthesized by the treatment of anthranilic acid hydrazide and ethyl isothiocyanate in absolute ethanol. The composition and structure of H2L were characterized by spectroscopic methods such as ESI MS, IR, 1H and 13C{1H} NMR spectroscopy as well as SCXRD. Reaction of H2L and mixture of [Cu(MeCN)4](PF6) and o‐phenanthroline in methanol gave rise to a cationic Cu(II) trinuclear complex, which could be separated as PF6– salt with the composition of [Cu3(L)2(o‐phen)2](PF6)2. The spectroscopic and X‐ray crystallographic data analyses demonstrated that H2L deprotonates hydrazide protons and the resulting dianion {L2–} acts as bridging ligand of which most potential donor atoms form stable chelates with Cu(II) ions. In particular, the central Cu(II) ion coordinates with two dianions {L2–} via (O, N2) donor sets, thereby adopting a distorted square planar coordination mode with trans configuration. While each of two terminal Cu(II) ions is five‐coordinate with the coordination sphere composed of (S, N1, Namine) and (N,N) donor sets belonging {L2–} and o‐phenanthroline, respectively.
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