scholarly journals Di-μ-thiosemicarbazide-κ4S:S-bis[chloridobis(triphenylphosphane-κP)silver(I)]

2013 ◽  
Vol 69 (2) ◽  
pp. m83-m84 ◽  
Author(s):  
Yupa Wattanakanjana ◽  
Chaveng Pakawatchai ◽  
Ruthairat Nimthong

The dinuclear title complex, [Ag2Cl2(CH5N3S)2(C18H15P)2], lies across an inversion center. The AgIion exhibits a slightly distorted tetrahedral coordination geometry formed by a P atom from a triphenylphosphane ligand, two metal-bridging S atoms from thiosemicabazide ligands and one chloride ion. The S atoms bridge two symmetry-related AgIions, forming a strictly planar Ag2S2core with an Ag...Ag separation of 2.7802 (7) Å. There is an intramolecular N—H...Cl hydrogen bond. In the crystal, N—H...Cl and N—H...S hydrogen bonds link complex molecules, forming layers parallel to (001). These layers are connected through π–π stacking interactions [centroid–centroid distance = 3.665 (2) Å], leading to the formation of a three-dimensional network.

2015 ◽  
Vol 71 (6) ◽  
pp. m133-m134 ◽  
Author(s):  
Arunpatcha Nimthong-Roldán ◽  
Janejira Ratthiwal ◽  
Yupa Wattanakanjana

In the dinuclear title complex, [Ag2Cl2(C7H8N2S)(C25H22P2)2]·0.5CH3CN, each AgIion displays a distorted tetrahedral coordination geometry with two P atoms from two bis(diphenylphosphanyl)methane (dppm) ligands, one bridging chloride ion, one terminal chloride ion and one terminal S atom from theN,N′-phenylthiourea (ptu) ligand. The dppm ligands and the bridging chloride ion force the two Ag atoms into close proximity, with a short Ag...Ag separation of 3.2064 (2) Å. In the crystal, complex molecules are linked by N—H...Cl hydrogen bonds forming a dimer. The dimers are linkedviaweak C— H...Cl hydrogen bonds forming a two-dimensional supramolecular architecture in theyzplane. In addition, an intramolecular N—H...Cl hydrogen bond is observed.


2012 ◽  
Vol 68 (8) ◽  
pp. m1114-m1114
Author(s):  
Jin-He Zhao ◽  
Yan-Xia Lin ◽  
Wei Wu ◽  
Zhong Zhang

In the centrosymmetric title compound, [Cu2(C10H8O4)Cl2(C10H8N2)2(H2O)2]·2H2O, the CuIIatom is five-coordinated in a distorted square-pyramidal geometry by two N atoms from a chelating 2,2′-bipyridine ligand, one O atom from a 1,4-phenylenediacetate ligand, one Cl atom and one water molecule. The 1,4-phenylenediacetate ligand, lying on an inversion center, bridges two CuIIatoms. In the crystal, O—H...O and O—H...Cl hydrogen bonds and π–π interactions between the pyridine rings [centroid–centroid distance = 3.740 (5) Å] link the complex molecules and uncoordinated water molecules into a three-dimensional network.


Author(s):  
Arunpatcha Nimthong-Roldán ◽  
Yupa Wattanakanjana ◽  
Jintana Rodkeaw

The title complex, [Ag3Br2(C25H22P2)3]Br·C7H8N2S, comprises a trinuclear [Ag3Br2(C25H22P2)3]+unit, a Br−anion and oneN,N′-dimethylthiourea molecule (ptu). Three AgIions are linkedviatwo μ3-bridging Br atoms, leading to a distorted triangular bipyramid with an Ag...Ag separation range of 3.1046 (6)–3.3556 (6) Å. The triangular Ag3arrangement is stabilized by six P atoms from three chelating bis(diphenylphosphanyl)methane (dppm) ligands. The AgIion presents a distorted tetrahedral coordination geometry. In the crystal, the bromide anion is connected to the ptu molecule through N—H...Br hydrogen bonds [graph-set motifR21(6)]. Each bromide/ptu aggregate links the complex ionviaC—H...S and C—H...Br hydrogen bonds, leading to the formation of a three-dimensional network. Two phenyl rings from two dppm ligands were modelled as disordered over two sites.


2016 ◽  
Vol 72 (12) ◽  
pp. 1845-1847
Author(s):  
Nada Al-Najjar ◽  
Gregory A. Solan ◽  
Kuldip Singh

In the mononuclear title complex, [CuI(C2H3N)(C26H24N2)], the CuIion has a distorted tetrahedral coordination environment, defined by two N atoms of the chelating 2-(naphthalen-1-yl)-6-[(2,4,6-trimethylphenyl)imino]pyridine ligand, one N atom of an acetonitrile ligand and one iodide ligand. Within the complex, there are weak intramolecular C—H...N hydrogen bonds, while weak intermolecular C—H...I interactions between complex molecules, help to facilitate a three-dimensional network.


2012 ◽  
Vol 68 (6) ◽  
pp. m773-m774 ◽  
Author(s):  
Chaveng Pakawatchai ◽  
Yupa Wattanakanjana ◽  
Patcharanan Choto ◽  
Ruthairat Nimthong

In the mononuclear title complex, [CuI(C6H8N2S)(C18H15P)2], the CuI ion is in a slightly distorted tetrahedral coordination geometry formed by two P atoms from two triphenylphosphane ligands, one S atom from a 4,6-dimethylpyrimidine-2(1H)-thione ligand and one iodide ion. There is an intramolecular N—H...I hydrogen bond. In the crystal, π–π stacking interactions [centroid–centroid distance = 3.594 (1) Å] are observed.


2009 ◽  
Vol 65 (6) ◽  
pp. m685-m686
Author(s):  
Xian-Ge Wu ◽  
Jun-Xia Xiao ◽  
Liang Qin

In the title complex, [Ag(NO3)(C5H5NO)]n, the AgIatom is coordinated by two O atoms from two different 4-pyridone ligands and two O atoms from one nitrate anion, displaying a nearly planar coordination geometry. The O atoms of two 4-pyridone ligands bridge two symmetrically related AgNO3units, forming a dimer, with an Ag...Ag separation of 3.680 (2) Å. Neighbouring dimers are linked into an infinite chain through weak Ag...O interactions [2.765 (2) Å], Ag...Ag interactions [3.1511 (4) Å] and π–π stacking interactions [centroid–centroid distance = 3.623 (4) Å]. N—H...O and C—H...O hydrogen bonds assemble these chains into a three-dimensional network.


2015 ◽  
Vol 71 (12) ◽  
pp. m230-m231
Author(s):  
B. Karpagam ◽  
G. Chakkaravarthi ◽  
G. Rajagopal

In the title complex, [Ni(C16H15N3O2S)(C18H15P)], the NiIIatom has a distorted tetrahedral coordination geometry, comprised of N, S, O and P atoms of the tridentate thiosemicarbazide ligand and the P atom of the triphenylphosphane ligand. The benzene ring makes a dihedral angle of 53.08 (11)° with the phenyl ring of the phenylthiosemicarbazide moiety and dihedral angles of 73.69 (11), 20.38 (11) and 71.30 (11)° with the phenyl rings of triphenylphosphane ligand. A pair of N—H...N hydrogen bonds generates anR22(8) ring graph-set motif. The ethoxy group is disordered over two positions, with site occupancies of 0.631 (9) and 0.369 (9). The molecular structure is stabilized by a weak intramolecular C—H...O hydrogen bond. In the crystal, weak N—H...N and C—H...π interactions connect the molecules, forming a three-dimensional network.


Author(s):  
Arunpatcha Nimthong-Roldán ◽  
Paramee Sripa ◽  
Yupa Wattanakanjana

In the title compound, [AgCl(C7H7N3O2S)(C18H15P)2], the AgIion is in a distorted tetrahedral coordination environment formed by P atoms from two triphenylphosphane ligands, one terminal S atom from the 1-(4-nitrophenyl)thiourea ligand and a chloride ion. In the crystal, bifurcated (N—H)2...Cl hydrogen bonds [with graph-set motifR21(6)] connect complex molecules, forming zigzag chains along [001]. These chains are linkedviaweak C—H...O hydrogen bonds, forming a two-dimensional network parallel to (100). An intramolecular N—H...Cl hydrogen bond forming anS(6) ring is also observed.


Author(s):  
Arunpatcha Nimthong-Roldán ◽  
Nichakan Promsuwhan ◽  
Walailak Puetpaiboon ◽  
Yupa Wattanakanjana

The mononuclear mixed-ligand title complex, [CuCl(C7H7N3O2S)(C18H15P)2], displays a distorted tetrahedral coordination sphere around the CuIatom, with two P atoms from two triphenylphosphane molecules, one terminal S atom from a 1-(4-nitrophenyl)thiourea molecule and a chloride ion as ligands. An intramolecular N—H...Cl hydrogen bond stabilizes the molecular conformation [graph-set motifR22(6)]. In the crystal, further N—H...Cl hydrogen bonds connect individual molecules into zigzag chains parallel to [001]. The chains are linked by weak C—H...O hydrogen-bonding interactions into a three-dimensional network.


2007 ◽  
Vol 63 (3) ◽  
pp. m800-m802 ◽  
Author(s):  
William T. Eckenhoff ◽  
Tomislav Pintauer

In the title compound, [Cu(C14H12N2)2]C24H20B·CH2Cl2, CuI is chelated by two 2,9-dimethyl-1,10-phenanthroline (2,9-Me2phen) ligands, in a distorted tetrahedral coordination geometry. The average Cu—N bond length is 2.032 Å, and the interligand dihedral angle is 77.60 (6)°. The complexes form π–π stacking interactions between 2,9-Me2phen ligands, with a perpendicular interplanar separation of 3.652 (5) Å.


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