Synthesis and coordinating properties of the anionic tridentate ligand, methyl tris(1-pyrazolyl)gallate, [MeGa(N2C3H3)3]−. X-ray crystal structure of [MeGa(N2C3H3)3]Mo(CO)2(η3-C3H5)

1978 ◽  
Vol 56 (16) ◽  
pp. 2099-2108 ◽  
Author(s):  
Kenneth R. Breakell ◽  
Steven J. Rettig ◽  
Douglas L. Singbeil ◽  
Alan Storr ◽  
James Trotter

The anionic tridentate ligand, [MeGa(N2C3H3)3]−, has been characterized and its coordinating properties studied. It acts as a six-electron chelating ligand to divalent transition metal ions giving complexes of the type, [MeGa(N2C3H3)3]2M (M = Mn, Fe, Co, Ni, Cu, Zn), believed to possess an octahedral MN6 core. The ligand also forms numerous carbonyl complexes and its coordinating ability in Mo, W, and Mn carbonyl derivatives is compared with that of similar boron ligands and the η5-C5H5 ligand. From ir measurements and bond length data it appears that the [MeGa(N2C3H3)3]− ligand is superior in creating an electron-rich transition metal centre, and it also affords greater steric protection for the central metal. The expected tridentate chelating nature of the new ligand has been demonstrated through a crystal structure determination of the complex [MeGa(N2C3H3)3]Mo(CO)2(η3-C3H5). Crystals of this complex are tetragonal, a = 26.217(3), c = 10.723(2) Å, Z = 16, space group I41/a. The structure was solved by Patterson and Fourier syntheses and was refined by full-matrix least-squares procedures to a final R of 0.030 and Rw of 0.031 for 2582 reflections with I ≥ 3σ(I).

2005 ◽  
Vol 358 (13) ◽  
pp. 3799-3806 ◽  
Author(s):  
Kalagouda Gudasi ◽  
Ramesh Vadavi ◽  
Rashmi Shenoy ◽  
Manjula Patil ◽  
Siddappa A. Patil ◽  
...  

1991 ◽  
Vol 44 (2) ◽  
pp. 303 ◽  
Author(s):  
R Bhula ◽  
DC Weatherburn

The crystal structure of [ Mn ( terpy )2](I3)2( terpy = 2,2°:6°,2°-terpyridene) has been determined by X-ray crystallography. The crystals are triclinic, space group Pī , a 9.357(4), b 8.600(2), c 24.531(8) Ǻ, α 93.64(2), B 95.58(3), γ 91.52(2)°, Z 2, V 1960(1)Ǻ3. The structure has been refined to a residual R of 0.065 (Rw 0.070). The coordination sphere of the metal ion is distorted octahedral with each terpy ligand coordinated in a meridional fashion. The structure is compared with those of other M( terpy )2n+ complexes formed by first-row transition metal ions.


1995 ◽  
Vol 50 (11) ◽  
pp. 1679-1684 ◽  
Author(s):  
Oliver Seidelmann ◽  
Lothar Beyer ◽  
Rainer Richter

N,N-diethyl-Nʹ-ferrocenoyl-thiourea and N-(morpholino-thiocarbonyl)ferrocenecarboxylic amide have been prepared by the reaction of ferrocenoyl chloride with potassium thiocyanate and the respective amine in dry acetone. These bidentate ligands yield neutral heterometalIic complexes with Ni(II), Cu(II), Mn(II) and Co(III). The dark brown air stable crystals of bis-(N,N-diethyl-Nʹ-ferrocenoylthioureato)nickel(II) were characterized by X-ray structure de­termination. Lattice dimensions: a = 1870.9(1), 6= 1161.5(1), c = 1491.4(1) pm; space group Pca21, Z = 4, R = 0.030 for 5707 observed reflections.


2017 ◽  
Vol 9 (2) ◽  
pp. 209-218 ◽  
Author(s):  
M. S. Hossain ◽  
C. M. Zakaria ◽  
M. K. Zahan

Metal complexes of Mn(II), Fe(II), Co(II) and Cd(II) ions with Schiff base ligand 4-{(pyridin-2-ylimino)methyl}phenol derived from condensation of 2-amino pyridine with 4-hydroxybenzaldehyde was prepared. The ligand and complexes were isolated from the reaction in the solid form  and characterized by conductivity, magnetic moment, TLC, IR, UV-Visible, thermal analysis and some physical measurements. During complexation reaction with transition metal ions Schiff base act as a deprotonated tridentate ligand and IR spectra showed that N and O atoms are coordinated to the central metal atom. The observed values confirmed that the complexes have octahedral geometry. The Schiff base and its metal complexes have been found to have moderate to strong antibacterial activity.


2018 ◽  
Vol 9 (4) ◽  
pp. 281-286
Author(s):  
Amadou Gueye ◽  
Farba Bouyagui Tamboura ◽  
Jean-Marc Planeix ◽  
Nathalie Gruber ◽  
Mohamed Gaye

The reactions of the Schiff base 2-((2-hydroxyphenylimino)methyl)-6-methoxyphenol (H2L), obtained by direct condensation of 2-aminophenol and 2-hydroxy-3-methoxybenzaldehyde, with some transition  metal ions (Mn(II), Co(II), Ni(II), Cu(II) and Zn(II)) afforded complexes of general formulae [M2(L)2(solvent)x] (M: Mn, Co, Ni, Cu or Zn; Solvent: DMSO or H2O). These compounds were characterized by elemental analysis, UV-Vis, IR, 1H- and 13C-NMR spectroscopies, molar conductivity and room temperature magnetic measurements. The structure of zinc(II) complex has been determined by X-ray crystallography. Crystal data for C32H34N2O8S2Zn2 (M =769.47 g/mol): Orthorhombic, space group Pbca (no. 61), a = 16.3176(7) Å, b = 9.1247(3) Å, c = 21.8274(10) Å, V = 3250.0(2) Å3, Z = 4, T = 173(2) K, μ(MoKα) = 1.658 mm-1, Dcalc = 1.573 g/cm3, 28116 reflections measured (4.5° ≤ 2Θ ≤ 60.3°), 4457 unique (Rint = 0.0409, Rsigma = 0.0371) which were used in all calculations. The final R1 was 0.0307(0.0466) and wR2 was 0.0649 (0.0701) (all data). The coordination sphere of the Zn center is best described as a trigonal bipyramid.


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