π–π Dimerization of a mono(pyridyl–imine) platinum(II) chelate

2012 ◽  
Vol 68 (7) ◽  
pp. m189-m193
Author(s):  
Rosanne C. Salmond ◽  
Orde Q. Munro

The cation of the title complex salt, chlorido{2,2-dimethyl-N-[(E)-1-(pyridin-2-yl)ethylidene]propane-1,3-diamine}platinum(II) tetrafluoridoborate, [PtCl(C12H19N3)]BF4, exhibits a nominally square-planar PtIIion coordinated to a chloride ion [Pt—Cl = 2.3046 (9) Å] and three unique N-atom types,viz.pyridine, imine and amine, of the tridentate Schiff base ligand formed by the 1:1 condensation of 1-(pyridin-2-yl)ethanone and 2,2-dimethylpropane-1,3-diamine. The cations are π-stacked in inversion-related pairs (dimers), with a mean plane separation of 3.426 Å, an intradimer Pt...Pt separation of 5.0785 (6) Å and a lateral shift of 3.676 Å. The centroid (Cg) of the pyridine ring is positioned approximately over the PtIIion of the neighbouring cation (Pt...Cg= 3.503 Å).

2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
Ramadan M. El-mehdawi ◽  
Abdussalam N. EL-dewik ◽  
Mufida M. Ben-Younes ◽  
Fathia A. Treish ◽  
Ramadan G. Abuhmaiera ◽  
...  

The title complex was isolated as a red solid from the reaction of 4-(salicylaldiminato)antipyrine, HL, and cobalt (II) acetate in ethanol. The complex has been characterized by elemental analysis, FTIR, UV-Vis, and X-ray single crystal diffraction. Two crystallographically different cationic units, A and B, of the title complex are found. Both units are essentially isostructural; nevertheless, small differences exist between them. Both units contain four cobalt atoms arranged at the corners of distorted cubane-like core alternatively with phenoxy oxygen of the Schiff base. In both cases, one cobalt binds to three coordinated sites from the corresponding tridentate Schiff base ligand, and the fourth one was bonded by the acetate oxygen, and the fifth and the sixth donor sites come from the phenolate oxygen of another Schiff base ligand.


2004 ◽  
Vol 59 (6) ◽  
pp. 655-660 ◽  
Author(s):  
Pritha Talukder ◽  
Amitabha Datta ◽  
Samiran Mitra ◽  
Georgina Rosair

The title compounds, [Cu(C16H23N2O)SCN] (1) and [Cu(C16H23N2O)N3] (2), containing a tridentate Schiff base ligand, which is the 1:1 condensation product of benzoylacetone and 2- diethylaminoethylamine, have been synthesised and their crystal structures determined. The structure of 1 is based on a four coordinate copper centre with square-planar geometry formed by the N2O donor set of the Schiff base and an N atom of the thiocyanate anion. A similar arrangement occurs in 2 with the N2O donor set of the Schiff base and an N atom of the azide anion. The Cu-N and Cu-O distances are 1.924(8), 2.073(8), 1.927(9) and 1.910(6)Å , for 1 and 1.960(4), 2.050(4), 1.935(4) and 1.907(3) for 2, respectively.


1978 ◽  
Vol 56 (15) ◽  
pp. 2000-2002 ◽  
Author(s):  
M. T. H. Tarafder ◽  
M. Akbar Ali

New complexes with the Schiff base ligand derived from S-benzyldithiocarbazate (NH2—NH—CSSCH2C6H5) have been prepared and characterized by elemental analyses, magnetic, conductometric, ir, and electronic spectral studies. The tridentate ONS Schiff base S-benzyl-β-N-(phenyl, phenylhydroxymethyl)methylenedithiocarbazate gave mono-ligand complexes with Ni(II) and Cu(II) having the general formula [MligandX] (M = Ni(II) and Cu(II); X = NO3, Cl, Br, NCS). A proposed square-planar structure for the nickel complexes is supported by magnetic and spectral data. A square-planar structure is also suggested for Cu(II) complexes. The ir results give evidence of the different bondings present in the complexes.


RSC Advances ◽  
2016 ◽  
Vol 6 (66) ◽  
pp. 61214-61220 ◽  
Author(s):  
Samim Khan ◽  
Subrata Jana ◽  
Michael G. B. Drew ◽  
Antonio Bauza ◽  
Antonio Frontera ◽  
...  

A square planar copper(ii) complex has been synthesized using a tridentate Schiff base ligand H2L and characterized. During complex formation, bromination at the 4 position of the aromatic ring of the Schiff base ligand has taken place.


Author(s):  
Fumiya Kobayashi ◽  
Atsushi Koga ◽  
Ryo Ohtani ◽  
Shinya Hayami ◽  
Masaaki Nakamura

The title complex, [Ni(C20H14ClN3O)], with an asymmetrically chloride-appended Schiff base ligand has been synthesized and structurally characterized at 100 K. In the compound, the central nickel(II) ion has a square-planar coordination geometry with N3O donors of the π-conjugated tetradentate Schiff base ligand. In the crystal, the complexes are connected into an inversion dimerviaan Ni...Ni interaction [3.1753 (5) Å] and a pair of π–π interactions [centroid–centroid distance = 3.8416 (16) Å]. The dimers are linkedviaa C—H...Cl hydrogen bond, forming a chain along thec-axis direction. The dimer chains interact with each other through π–π interactions [centroid–centroid distance = 3.8736 (16) Å], forming a layer expanding parallel to theacplane.


2007 ◽  
Vol 63 (11) ◽  
pp. m2854-m2854 ◽  
Author(s):  
Yin-Qiu Liu ◽  
Xi-Rui Zeng ◽  
Qiu-Yan Luo ◽  
Ya-Ping Xu

The title complex, [Mn(C20H14N2O2)], is a mononuclear manganese(II) compound. The manganese(II) ion is four-coordinated in a square-planar geometry by two imine N and two phenolate O atoms from one 2,2′-[o-phenylenebis(nitrilomethylidyne)]diphenolate Schiff base ligand. No strong hydrogen bonds were found in the crystal structure.


Author(s):  
Sibel Demir Kanmazalp ◽  
Seher Meral ◽  
Necmi Dege ◽  
Aysen Alaman Agar ◽  
Igor O. Fritsky

In the title complex, (6,6′-{(1E,1′E)-[ethane-1,2-diylbis(azanylylidene)]bis(methanylylidene)}bis[2-(trifluoromethoxy)phenol]-κ4 O,N,N′,O′)nickel(II), [Ni(C18H12F6N2O4)], the nickel(II) ion has a square-planar coordination sphere, being ligated by two N and two O atoms of the Schiff base ligand 6,6′-{(1E,1′E)-[ethane-1,2-diylbis(azanylylidene)]bis(methanylylidene)}bis[2-(trifluoromethoxy)phenol] (L). Inversion-related molecules are linked by a short Ni...Ni interaction of 3.2945 (6) Å forming a dimer. In the crystal, the dimers stack up the a axis, with a closest Ni...Ni separation of ca 3.791 Å. There are no other significant intermolecular interactions present. However, the Hirshfeld surface analysis and the two-dimensional fingerprint plots indicate that the packing is dominated by H...F/F...H, H...H, O...H/H...O and C...H/H...C contacts.


2006 ◽  
Vol 62 (7) ◽  
pp. m1533-m1534 ◽  
Author(s):  
Han-Na Hou

The title compound, [Cu(C14H15N2O)(NCS)], is a mononuclear copper(II) complex, with two molecules in the asymmetric unit. The CuII ion is coordinated by one O and two N atoms of a Schiff base ligand, and by one N atom of a thiocyanate anion, forming a square-planar geometry.


Author(s):  
Amalina Mohd Tajuddin ◽  
Hadariah Bahron ◽  
Hamizah Mohd Zaki ◽  
Karimah Kassim ◽  
Suchada Chantrapromma

The asymmetric unit of the title complex, [Pd(C15H13FNO)2], contains one half of the molecule with the PdIIcation lying on an inversion centre and is coordinated by the bidentate Schiff base anion. The geometry around the cationic PdIIcentre is distorted square planar, chelated by the imine N- and phenolate O-donor atoms of the two Schiff base ligands. The N- and O-donor atoms of the two ligands are mutuallytrans, with Pd—N and Pd—O bond lengths of 2.028 (2) and 1.9770 (18) Å, respectively. The fluorophenyl ring is tilted away from the coordination plane and makes a dihedral angle of 66.2 (2)° with the phenolate ring. In the crystal, molecules are linked into chains along the [101] direction by weak C—H...O hydrogen bonds. Weak π–π interactions with centroid–centroid distances of 4.079 (2) Å stack the molecules alongc.


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