SYNTHESIS AND CHARACTERIZATION OF TI (III), V (III),VO (IV), MOO (V),FE (II) AND FE (III) COMPLEXES OF BENZIL- 2,4-DINITROPHENYL HYDRAZONE P-BROMO ANILINE

2016 ◽  
Vol 2 (4) ◽  
pp. 177
Author(s):  
Raj Kamal Rastogi ◽  
Sonu Sharma ◽  
Gulshan Rastogi ◽  
Alok K. Singh
Keyword(s):  
Elemental Analysis ◽  
Magnetic Measurement ◽  
Measurement Data ◽  
Molar Conductance ◽  
Octahedral Geometry ◽  
Synthesis And Characterization ◽  
Distorted Octahedral Geometry ◽  
Distorted Octahedral ◽  
Uv Visible

The complexes of Benzil-2, 4-dinitrophenyl hydrazone-p- bromo aniline with Ti(III),V(III), VO(IV),MoO (V), Fe(II), Fe(III) have synthesized and characterized by elemental analysis, magnetic measurement data, molar conductance, TGA,UV-visible and IR spectra data. The complexes of Ti (III), V (III), Fe (II) and Fe (III) have octahedral geometry while VO (IV) and MoO(V) have distorted octahedral geometry due to the presence of M=O moiety.

Synthesis and Characterization of Some Transition Metal Complexes of Arylidene Salicyloyl and Benzoyl Hydrazones

1984 ◽  
Vol 39 (6) ◽  
pp. 812-816 ◽  
Author(s):  
Y. M. Temerk ◽  
S. A. Ibrahim ◽  
M. M. Kamal
Keyword(s):  
Transition Metal Complexes ◽  
Metal Ion ◽  
Octahedral Geometry ◽  
Molar Conductivity ◽  
Synthesis And Characterization ◽  
Distorted Octahedral Geometry ◽  
Bidentate Ligands ◽  
Conductivity Measurements ◽  
Distorted Octahedral

AbstractComplexes of arylidene salicyloyl- and benzoyl-hydrazones with the 3d metal ions, Cr(III), Mn(II), Fe(III), Co(II), Ni(II) and Cu(II), have been prepared using 2:1 ligand to metal ion ratio. Characterization of the isolated solids was accomplished by IR and electronic spectra, elemental analysis, and molar conductivity measurements. It is concluded that the two Schiff bases function as neutral bidentate ligands and the complexes formed assume a distorted octahedral geometry.

scholarly journals Crystal structure of a mononuclear RuIIcomplex with a back-to-back terpyridine ligand: [RuCl(bpy)(tpy–tpy)]+

2015 ◽  
Vol 71 (9) ◽  
pp. 1017-1021 ◽  
Author(s):  
Francisca N. Rein ◽  
Weizhong Chen ◽  
Brian L. Scott ◽  
Reginaldo C. Rocha
Keyword(s):  
Crystal Structure ◽  
Crystal Packing ◽  
Bidentate Ligand ◽  
Octahedral Geometry ◽  
Distorted Octahedral Geometry ◽  
Stacking Interactions ◽  
Bite Angle ◽  
Distorted Octahedral ◽  
The Mean

We report the structural characterization of [6′,6′′-bis(pyridin-2-yl)-2,2′:4′,4′′:2′′,2′′′-quaterpyridine](2,2′-bipyridine)chloridoruthenium(II) hexafluoridophosphate, [RuCl(C10H8N2)(C30H20N6)]PF6, which contains the bidentate ligand 2,2′-bipyridine (bpy) and the tridendate ligand 6′,6′′-bis(pyridin-2-yl)-2,2′:4′,4′′:2′′,2′′′-quaterpyridine (tpy–tpy). The [RuCl(bpy)(tpy–tpy)]+monocation has a distorted octahedral geometry at the central RuIIion due to the restricted bite angle [159.32 (16)°] of the tridendate ligand. The Ru-bound tpy and bpy moieties are nearly planar and essentially perpendicular to each other with a dihedral angle of 89.78 (11)° between the least-squares planes. The lengths of the two Ru—N bonds for bpy are 2.028 (4) and 2.075 (4) Å, with the shorter bond being opposite to Ru—Cl. For tpy–tpy, the mean Ru—N distance involving the outer N atomstransto each other is 2.053 (8) Å, whereas the length of the much shorter bond involving the central N atom is 1.936 (4) Å. The Ru—Cl distance is 2.3982 (16) Å. The free uncoordinated moiety of tpy–tpy adopts atrans,transconformation about the interannular C—C bonds, with adjacent pyridyl rings being only approximately coplanar. The crystal packing shows significant π–π stacking interactions based on tpy–tpy. The crystal structure reported here is the first for a tpy–tpy complex of ruthenium.

scholarly journals Synthesis and characterization of new complexes of Co+2 , Ni+2 , Cu+2 and Zn+2 with (Sodium acetate thio ) ethylene ligands

2013 ◽  
Vol 10 (3) ◽  
pp. 650-657
Author(s):  
Baghdad Science Journal
Keyword(s):  
Content Analysis ◽  
General Formula ◽  
Metal Content ◽  
Sodium Acetate ◽  
Magnetic Measurement ◽  
Synthesis And Characterization ◽  
Square Planar ◽  
Square Planar Complexes ◽  
Uv Visible

This research involves the preparation of new ligands 1,1,2,2- tetrakis (sodium acetate thio)ethylene(L1) and 1,1,2- tris(sodiumacetatethio) ethylene(L2), through the reaction of disodium thioglycolate) with tetra chloro ethylene or tri chloro ethylene in (1:4) or (1:3) moler ratio . Homodinucliar complexes of general formlu [M2(L1)] and [M2(L2)ClH2O] , when M= Co(II), Ni(II), Cu (II) and Zn(II) also mono nuclear complexes of general formula [M(L2)] . The prepared complexes were characterized using spectral method (UV/Visible/ IR) , metal content analysis , magnetic and atomic measurements . The spectral and magnetic measurement indicats that some complexes have tetrahedral or square planar complexes environtment .

scholarly journals Synthesis, Characterization and Antifungal Studies of Adducts of p- Ethylphenyldithiocarbonates of Copper(II)

2019 ◽  
Vol 31 (8) ◽  
pp. 1819-1824
Author(s):  
Shivangi Sharma ◽  
Renu Sachar ◽  
G.D. Bajju ◽  
Vikas Sharma
Keyword(s):  
Magnetic Susceptibility ◽  
Electron Spin Resonance ◽  
Room Temperature ◽  
Molar Conductance ◽  
Octahedral Geometry ◽  
Molar Ratio ◽  
Spectral Studies ◽  
Distorted Octahedral Geometry ◽  
Distorted Octahedral ◽  
Spin Resonance

A series of adducts of p-ethylphenyldithiocarbonates of copper(II) [(p-C2H5C6H4OCS2)2Cu] with ethyl pyridines and chloro pyridines have been synthesized in 1:2 molar ratio. They were characterized by elemental analysis, magnetic susceptibility and molar conductance measurements, infrared, electronic, electron spin resonance and mass spectroscopy, NMR and thermogravimetric analysis. In addition, antifungal studies of these adducts were also performed. The results revealed that the adducts have 1:2 stoichiometry, non-electrolytic and paramagnetic at room temperature. On the basis of spectral studies, a distorted octahedral geometry is proposed around copper(II) ion. ESR studies depicted elongated axial symmetry of Cu(II)adducts with nitrogen donors. Moreover, the adducts also showed potential antifungal activity against Fusarium oxysporium.

Synthesis and Structure of cis-Dioxobis(pyrimidine-2-thiolato-N,S)molybdenum(VI)

1992 ◽  
Vol 45 (11) ◽  
pp. 1933 ◽  
Author(s):  
PR Traill ◽  
AG Wedd ◽  
ERT Tiekink
Keyword(s):  
Least Squares ◽  
Octahedral Geometry ◽  
Distorted Octahedral Geometry ◽  
Monoclinic Space Group ◽  
Full Matrix ◽  
X Ray ◽  
Distorted Octahedral ◽  
Cell Dimensions ◽  
Unit Cell Dimensions

The characterization of two MoVI complexes, cis -[MoO2(2-pymS)2] and cis -[MoO2(2-pyS)2] (where 2-pymSH is pyrimidine-2-thiol and 2-pySH is pyridine-2-thiol), and their reaction with Ph3P are reported. The X-ray structure of cis -[MoO2(2-pymS)2] shows the molybdenum atom to exist in a distorted octahedral geometry defined by two mutually cis oxygen atoms and two chelating 2-pymS ligands so that the two sulfur atoms occupy approximate trans positions. Crystals of cis -[MoO2(2-pymS)2] are monoclinic, space group P 21/n, with unit cell dimensions: a 9.301(3), b 12.121(2), c 11.303(3) �, β 112.62(3)�, V 1176.3 �3, Z 4. The structure was refined by a full-matrix least-squares procedure to R 0.067 for 1858 reflections with I ≥ 2.5 (I).

scholarly journals Synthesis and characterization of μ-hydroxido- and μ-polycarboxylato-bridged iron(III) complexes with 2,2’-bipyridine

2014 ◽  
Vol 79 (8) ◽  
pp. 941-952
Author(s):  
Nikola Tasic ◽  
Jelena Rogan ◽  
Dejan Poleti ◽  
Lidija Radovanovic ◽  
Goran Brankovic
Keyword(s):  
Ligand Exchange ◽  
Diffuse Reflectance ◽  
Nir Spectroscopy ◽  
Octahedral Geometry ◽  
Distorted Octahedral Geometry ◽  
Dsc Analysis ◽  
Ligand Exchange Reaction ◽  
Distorted Octahedral ◽  
Structural Formulae

Four novel polymeric iron(III) complexes with 2,2?-bipyridine (bipy) and different aromatic polycarboxylato ligands as anions of phthalic (pht), isophthalic (ipht), terephthalic (tpht) and pyromellitic (pyr) acid were synthesized by ligand exchange reaction. The complexes were characterized by elemental and TG/DSC analysis, FTIR and diffuse reflectance UV-VIS-NIR spectroscopy and magnetic susceptibility measurements. Based on analytical and spectral data the formulae of the complexes are {[Fe4(bipy)2 (H2O)2(OH)6(pht)3]?2H2O}n (1), {[Fe4(bipy)2(Hipht)2(ipht)2(OH)6]?4H2O}n (2), {[Fe4(bipy)2(Htpht)2(OH)6(tpht)2]?4H2O}n (3) and {[Fe4(bipy)(H2O)8(OH)4 (pyr)2]?H2O}n (4). All complexes are red brown and low-spin with a distorted octahedral geometry and FeO6 or FeN2O4 chromophore. Polycarboxylato ligands have a bridging role in all cases, whereas monodentate COO groups are present in 2 and 3, bridging and chelate COO groups are established in 1 and 4. The thermal behaviour of 1-4 was investigated in detail and the molar dehydration enthalpies were calculated. According to the all those results, the structural formulae of the complexes 1-4 were proposed.

scholarly journals Synthesis and characterization of cis-dioxomolybdenum(VI) complexes having furil as precursor molecule

2012 ◽  
Vol 77 (9) ◽  
pp. 1205-1210
Author(s):  
Devendra Rao ◽  
Hardeo Yadav ◽  
Ashok Yadava ◽  
Sanjay Singh ◽  
Uma Yadav
Keyword(s):  
Oxygen Transfer ◽  
Chelating Agent ◽  
Molar Conductance ◽  
Octahedral Geometry ◽  
Transfer Reactions ◽  
Synthesis And Characterization ◽  
Precursor Molecule ◽  
Elemental Analyses ◽  
Tetraazamacrocyclic Ligands

Synthesis of some new dioxomolybdenum(VI) complexes having general formula [MoO2(mac)](acac)2, (where mac = tetraazamacrocyclic ligands derived from condensation of furil with 1,2-diaminobenzene or 2,3-diaminopyridine and their reaction with ?-diketones) using dioxometal ion as kinetic template are reported. The prepared complexes have been characterized by molar conductance, elemental analyses, infrared and electronic data. The spectral data indicate that ligands act as tetradentate chelating agent. Due to their biological relevance, molybdenum catalyzed oxygen transfer reactions have great interest. All the dioxomolybdenum(VI) complexes have octahedral geometry with six coordination.

scholarly journals Antitumor Activity of 6-(cyclohexylamino)-1,3-dimethyl-5(2-pyridyl)furo[2,3-d]pyrimidine-2,4(1H,3H)-dione and Its Ti(IV), Zn(II), Fe(III), and Pd(II) Complexes on K562 and Jurkat Cell Lines

2008 ◽  
Vol 2008 ◽  
pp. 1-5 ◽  
Author(s):  
Fahmideh Shabani ◽  
Shahriar Ghammamy ◽  
Khayroallah Mehrani ◽  
Mohammad Bagher Teimouri ◽  
Masoud Soleimani ◽  
...  
Keyword(s):  
Antitumor Activity ◽  
Elemental Analysis ◽  
Analysis Data ◽  
Molar Conductance ◽  
Carcinoma Cells ◽  
Elemental Analysis Data ◽  
Human T Lymphocyte ◽  
Ft Ir ◽  
Uv Visible

(6-(cyclohexylamino)-1,3-dimethyl-5(2-pyridyl)furo[2,3-d]pyrimidine-2,4(1H,3H)-dione) abbreviated as CDP was synthesized and characterized. Ti(IV), Zn(II), Fe(III), and Pd(II) metal complexes of this ligand are prepared by the reaction of salts of Ti(IV), Zn(II), Fe(III), and Pd(II) with CDP in acetonitrile. Characterization of the ligand and its complexes was made by microanalyses, FT-IR,1HNMR,13CNMR, and UV-Visible spectroscopy. All complexes were characterized by several techniques using elemental analysis (C, H, N), FT-IR, electronic spectra, and molar conductance measurements. The elemental analysis data suggest the stoichiometry to be 1:1 [M:L] ratio formation. The molar conductance measurements reveal the presence of 1:1 electrolytic nature complexes. These new complexes showed excellent antitumor activity against two kinds of cancer cells that are K562 (human chronic myeloid leukemia) cells and Jurkat (human T lymphocyte carcinoma) cells.

scholarly journals Synthesis and Spectral Characterization of Mn(II) and Co(II) Complexes with Tetradentate Macrocyclic Ligand

2021 ◽  
Vol 33 (9) ◽  
pp. 2207-2211
Author(s):  
Usha Bansal ◽  
Samta Goyal ◽  
Swati Agrawal
Keyword(s):  
Metal Complexes ◽  
Infrared Spectra ◽  
Elemental Analysis ◽  
Magnetic Moment ◽  
Macrocyclic Ligand ◽  
Molar Conductance ◽  
Octahedral Geometry ◽  
Metal Salts ◽  
Spectral Studies

Manganese(II) and cobalt(II) complexes were synthesized with [N4] tetradentate macrocyclic ligand using different metal salts i.e. MnCl2, Mn(NO3)2, CoCl2 and Co(NCS)2. The ligand was prepared by condensation of glyoxal and carbahydrazide. All these were characterized by elemental analysis, molar conductance measurements, magnetic moment, IR, mass, electronic and EPR spectral studies. Elemental analysis indicates that the complexes have composition MLX2 where (X = Cl–, NO3 –,NCS–). All the complexes were found to be non-electrolytic in nature so can be formulated as [MLX2]. Infrared spectra of metal complexes suggest that the ligand behaves as tetradentate. On the basis of magnetic moment, electronic and EPR spectral data, all the metal complexes were found to be high spin with octahedral geometry.

scholarly journals Synthesis and Characterization of 1-phenyl-3-methyl-4-stearoylpyrazol-5-one and Its Lanthanum(III) and Tungsten(VI) Complexes

2020 ◽  
pp. 140-151
Author(s):  
A. I. C. Ehirim ◽  
C. K. Enenebeaku ◽  
C. Asimole ◽  
M. O. C. Ogwuegbu ◽  
E. N. O. Ejike
Keyword(s):  
Elemental Analysis ◽  
13C Nmr ◽  
Synthesis And Characterization ◽  
Conductivity Measurements ◽  
Melting Points ◽  
1H And 13C Nmr ◽  
Solubility Profile ◽  
Uv Visible ◽  
Metal Ligand

The ligand, 1-phenyl-3-methyl-4-stearoylpyrazol-5-one (HSPy), and its La(III) and W(VI) complexes were synthesized and characterized spectroscopically using elemental analysis, UV-visible, IR, 1H and 13C NMR. Physical properties such as colour, melting points, conductivity measurements and solubility profile were also investigated. La(III) and W(VI) reacted with the ligand in the metal-ligand mole ratios of 1:3 and 1:2 to form neutral complexes of diaquo-trischelate La(SPy)3.2H2O and dioxoaquo-bischelate, WO2(SPy)2.H2O respectively.

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