scholarly journals Dibromido(di-2-pyridylamine-κ2N2,N2′)platinum(II)

2012 ◽  
Vol 68 (4) ◽  
pp. m453-m453 ◽  
Author(s):  
Kwang Ha

The PtIIion in the title complex, [PtBr2(C10H9N3)], is four-coordinated in an essentially square-planar environment by two N atoms from a chelating di-2-pyridylamine (dpa) ligand and two Br−anions. The dpa ligand is not planar, with the dihedral angle between the pyridine rings being 40.8 (2)°. The complex molecules are stacked in columns along [001] through π–π interactions between the pyridine rings [centroid–centroid distances = 3.437 (3) and 3.520 (3) Å]. Intermolecular N—H...Br hydrogen bonds connect the molecules into chains running along [010]. Intramolecular C—H...Br interactions are also observed.

2012 ◽  
Vol 68 (4) ◽  
pp. m479-m479 ◽  
Author(s):  
Kwang Ha

The PtIIion in the title complex, [PtI2(C10H9N3)], is four-coordinated in a distorted square-planar environment defined by the two pyridine N atoms of the chelating di-2-pyridylamine (dpa) ligand and by two I−anions. The dpa ligand is not planar, the dihedral angle between the pyridine rings being 52.8 (3)°. Pairs of complex molecules are assembled through intermolecular N—H...I hydrogen bonds, forming a dimer-type species. The complexes are stacked in columns along thebaxis and display several intermolecular π–π interactions between the pyridine rings, with a shortest ring centroid–centroid distance of 3.997 (5) Å.


2012 ◽  
Vol 68 (4) ◽  
pp. m440-m440
Author(s):  
Kwang Ha

In the title complex, [Pt(NCS)2(C10H9N3)], the PtIIion is four-coordinated in a distorted square-planar environment by the two pyridine N atoms of the chelating di-2-pyridylamine (dpa) ligand and two mutuallycisS atoms from two linear thiocyanate anions. The dpa ligand is not planar, the dihedral angle between the pyridine rings being 30.8 (4)°. In the crystal, the complex molecules are stacked in columns along theaaxis and are connected by intermolecular N—H...N hydrogen bonds, forming supramolecular chains along thebaxis.


2012 ◽  
Vol 68 (6) ◽  
pp. m834-m834 ◽  
Author(s):  
Kwang Ha

The PtII ion in the title complex, [PtI2(C14H10N4)], exists in a distorted square-planar environment defined by the two pyridine N atoms of the chelating 2,3-di-2-pyridylpyrazine ligand and two iodide anions. The pyridine rings are inclined to the least-squares plane of the PtI2N2 unit [maximum deviation = 0.070 (3) Å] at 66.1 (2) and 65.9 (2)°; the pyrazine ring is perpendicular to this plane [dihedral angle = 89.7 (2)°]. Two intermolecular C—H...I hydrogen bonds, both involving the same I atom as hydrogen-bond acceptor, generate a layer structure extending parallel to (001). Molecules are stacked in columns along the a axis. Along the b axis, successive molecules stack in opposite directions.


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.


2009 ◽  
Vol 65 (6) ◽  
pp. m615-m616 ◽  
Author(s):  
Nam-Ho Kim ◽  
In-Chul Hwang ◽  
Kwang Ha

In the title compound, [PdCl2(C10H8N2)]·CH2Cl2, the Pd2+ion is four-coordinated in a slightly distorted square-planar environment by two N atoms of the 2,2′-bipyridine (bipy) ligand and two chloride ions. The compound displays intramolecular C—H...Cl hydrogen bonds and pairs of complex molecules are connected by intermolecular C—H...Cl hydrogen bonds. Intermolecular π–π interactions are present between the pyridine rings of the ligand, the shortest centroid–centroid distance being 4.096 (3) Å. As a result of the electronic nature of the chelate ring, it is possible to create π–π interactions to its symmetry-related counterpart [3.720 (2) Å] and also with a pyridine ring [3.570 (3) Å] of the bipy unit. The present structure is a redetermination of a previous structure [Vicenteet al.(1997). Private communication (refcode PYCXMN02). CCDC, Cambridge, England]. In the new structure refinement all H atoms were located in a difference Fourier synthesis. Their coordinates were refined freely, together with isotropic displacement parameters.


2006 ◽  
Vol 62 (4) ◽  
pp. m870-m872
Author(s):  
Chang-Qing Li ◽  
Li-Na Zhu ◽  
Xiao-Zeng Li ◽  
Rong Li

A new polymorph of the title complex, [Ni(C22H18N4O6)], has been synthesized and structurally characterized. Ni(II) is coordinated by the four nitrogen donors of the macrocyclic ligand with a distorted square-planar geometry. C—H...O hydrogen bonds and π...π stacking interactions link the complex molecules, forming an infinite three-dimensional supramolecular network.


2012 ◽  
Vol 68 (8) ◽  
pp. m1135-m1135 ◽  
Author(s):  
Hadi Kargar ◽  
Reza Kia ◽  
Fatemeh Ganji ◽  
Valiollah Mirkhani

In the title Schiff base complex, [Cu(C19H18Cl2N2O2)], the CuIIion is coordinated in a distorted square-planar environment by two N atoms and two O atoms of the tetradentate ligand. The dihedral angle between the benzene rings is 36.86 (14)°. In the crystal, molecules are linked into inversion dimers by pairs of weak C—H...O hydrogen bonds. In addition, π–π [centroid–centroid distance = 3.7279 (16) Å] and weak C—H...π interactions are observed.


2007 ◽  
Vol 63 (11) ◽  
pp. m2821-m2821
Author(s):  
He-Dong Bian ◽  
Fu-Ping Huang ◽  
Qing Yu ◽  
Hong Liang

In the title complex, [Cu(C9H6NO2S2)2(C3H4N2)2], the CuII atom, lying on an inversion centre, is coordinated by two O atoms and two N atoms in a geometry deviating slightly from square planar. Intermolecular hydrogen bonds link the complex molecules into a layer structure.


2012 ◽  
Vol 68 (4) ◽  
pp. m519-m519
Author(s):  
Kwang Ha

In the title complex, [Pd(N3)2(C10H9N3)], the PdIIion is in a slightly distorted square-planar coordination environment. The ligator atoms comprise the two pyridine N atoms of the chelating di-2-pyridylamine (dpa) ligand and two N atoms from two azide anions. The dpa ligand coordinates the Pd atom in a boat conformation, the dihedral angle between the pyridine rings being 24.4 (1)°. The pyridine rings are somewhat inclined to the least-squares plane of the PdN4unit, making dihedral angles of 29.02 (9) and 26.47 (9)°. The azide ligands are slightly bent, with N—N—N angles of 173.0 (4) and 174.2 (4)°. In the crystal, molecules are connected by N—H...N and C—H...N hydrogen bonds, forming chains along thecaxis. When viewed down thebaxis, successive chains are stacked in opposite directions. Intramolecular C—H...N hydrogen bonds are also observed.


IUCrData ◽  
2016 ◽  
Vol 1 (4) ◽  
Author(s):  
Assia Mili ◽  
Souheyla Chetioui ◽  
Djamil-Azzeddine Rouag ◽  
Jean-Pierre Djukic ◽  
Corinne Bailly

In the title complex, [Pd(C17H13N2O2)Cl], the PdIIatom is tetracoordinated by an N and two O atoms of an (E)-1-[(2-methoxyphenyl)diazenyl]naphthalen-2-olate ligand and by a Cl atom, and has a square-planar coordination. In the crystal, molecules are linked by pairs of C—H...Cl hydrogen bonds, forming inversion dimers. The dimers are linkedviaoffset π–π interactions [intercentroid distance = 3.546 (3) Å], forming chains running parallel to [100].


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