scholarly journals Diaquabis[4-(dimethylamino)pyridine-κN 1]bis[2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)acetato-κO 1]cobalt(II)

IUCrData ◽  
2019 ◽  
Vol 4 (1) ◽  
Author(s):  
Naouel Makouf ◽  
Aziza Chouiter ◽  
Henia Bouzidi Mousser ◽  
Amel Djedouani ◽  
Solenne Fleutot ◽  
...  

In the mononuclear title complex, [Co(C10H6NO4)2(C7H10N2)2(H2O)2], the CoII ion is located on an inversion centre and has a distorted octahedral coordination geometry of type CoN2O4 by two N atoms from the two 4-(dimethylamino)pyridine (DMAP) ligands, two carboxylate O atoms from the two deprotonated N-phthaloylglycine (Nphgly) ligands [systematic name: 2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)acetate] and two coordination water molecules. In the crystal, O—H...O, C—H...O hydrogen bonds and π–π stacking interactions link the molecules into the supramolecular structure.

2015 ◽  
Vol 71 (9) ◽  
pp. m162-m163
Author(s):  
Siddhartha S. Baisya ◽  
Baidyanath Ghosh ◽  
Parag S. Roy

In the title compound, [Zn(C8H5N5O3)(C12H8N2)(H2O)]·3H2O, a tridentate 2-amino-7-methyl-4-oxidopteridine-6-carboxylate ligand, a bidentate ancillary 1,10-phenanthroline (phen) ligand and a water molecule complete a distorted octahedral coordination geometry around the ZnIIatom. The pterin ligand forms two chelate rings. The phen and pterin ring systems are nearly perpendicular [dihedral angle = 85.16 (5)°]. Classical N—H...O, O—H...N and O—H...O hydrogen bonds and weak C—H...O hydrogen bonds link the complex molecules and lattice water molecules into a three-dimensional network. π–π stacking contacts are observed as well, with centroid-to-centroid distances of 3.5679 (14), 3.7004 (14), 3.6641 (15), 3.6974 (13) and 3.3412 (12) Å.


2007 ◽  
Vol 63 (3) ◽  
pp. m856-m856 ◽  
Author(s):  
William Clegg ◽  
Nicola C. Martin

The title compound, [CoCl2(C6H7N)2(C2H6O)2], was obtained unintentionally as the product of an attempted synthesis of a polycarboxylate-bridged network complex of cobalt(II) using aniline as a base to deprotonate the organic acid. The molecule is centrosymmetric, so pairs of equivalent ligands lie trans to each other in a slightly distorted octahedral coordination geometry. Molecules are linked by O—H...Cl and N—H...Cl hydrogen bonds involving all the potential donors, generating sheets parallel to (001). The phenyl rings protrude on both sides of these sheets and have normal hydrophobic contacts with each other, involving no intercalation or stacking interactions.


2012 ◽  
Vol 68 (4) ◽  
pp. m523-m524 ◽  
Author(s):  
Shao-Wei Tong ◽  
Shi-Jie Li ◽  
Wen-Dong Song ◽  
Dong-Liang Miao ◽  
Qi Deng

In the title complex polymer, [Sr(C10H7N6)2(H2O)2]n, the SrIIatom lies on an inversion centre and is coordinated by four N atoms from two bidentate bridgingtrans-related 5-[4-(1H-imidazol-1-yl)phenyl]tetrazolide ligands [Sr—N = 2.387 (4) Å for the tetrazolide moiety and Sr—N = 2.273 (5) Å for the imidazole moiety], and by two O atoms from water molecules [Sr—O = 2.464 (4) Å], giving a distorted octahedral coordination. Pairs of ligand bridges link the complex units, forming chains which extend along [111] and are inter-associated through Owater—H...N hydrogen bonds, giving a two-dimensional network structure parallel to (001). Weak π–π stacking interactions between the benzene and imidazole rings are also present [minimum ring centroid separation = 3.691 (4) Å].


2012 ◽  
Vol 68 (6) ◽  
pp. m777-m778 ◽  
Author(s):  
Ying Wang ◽  
Rui Jiao ◽  
Xiang-Lei Qiu ◽  
Jian Wang ◽  
Wei Huang

In the cation of the title compound, [Ru(C15H10ClN3)2]Cl2·2H2O, the metal atom exhibits a distorted octahedral coordination geometry provided by the N atoms of two tridentate terpyridine ligands. The ligands are approximately planar [maximum deviation = 0.156 (5) Å] and form a dihedral angle of 87.0 (3)°. In the crystal, the cations, anions and water molecules are linked into a three-dimensional network by C—H...Cl, C—H...O and O—H...Cl hydrogen bonds.


Author(s):  
Roman Doroschuk

The structure of the dinuclear title complex, [Cu2(C10H8N7)2(NO3)2(H2O)2]·2H2O, consists of centrosymmetric dimeric units with a copper–copper separation of 4.0408 (3) Å. The CuIIions in the dimer display a distorted octahedral coordination geometry and are bridged by two triazole rings, forming an approximately planar Cu2N4core (r.m.s. deviation = 0.049 Å). In the crystal, O—H...O, O—H...N and C—H...O hydrogen bonds and π–π interactions link the molecules into a three-dimensional network.


2012 ◽  
Vol 68 (4) ◽  
pp. m368-m368
Author(s):  
Chang-Ge Zheng ◽  
Peng Zhang ◽  
Ping Li ◽  
Pei-Pei Zhang

In the title compound, [Co(C8Cl4O4)(C3H4N2)2(H2O)2]n, the CoIIion displays a distorted octahedral coordination geometry with two O atoms from two monodentate tetrachloroterephthalate dianions, two N atoms from two imidazole molecules and two O atoms from two water molecules. The CoIIions are connectedviathe tetrachloroterephthalate dianions into a chain running along the crystallographic [110] direction. Adjacent chains are linked into a two-dimensional network arranged parallel to (010) by classical N—H...O and O—H...O hydrogen bonds.


2013 ◽  
Vol 69 (12) ◽  
pp. m645-m646
Author(s):  
Qian Liang ◽  
Yulin Wang ◽  
Yan Zhao ◽  
Gaojuan Cao

In the monomeric title complex, [Cd(C2O4)(CH3N5)2(H2O)2], the CdIIion exhibits a distorted octahedral coordination geometry, with the equatorial plane defined by two O atoms from an oxalate ligand and two N atoms from two 5-amino-1H-tetrazole ligands; the axial sites are occupied by two water molecules, with longer Cd—O bond lengths. An intramolecular N—H...O hydrogen bond occurs. In the crystal, N—H...O as well as O—H...O and O—H...N hydrogen bonds (some of which are bifurcated) link the complex molecules into a three-dimensional network.


2012 ◽  
Vol 68 (4) ◽  
pp. m388-m388 ◽  
Author(s):  
Zhao-Hui Meng ◽  
Hui Lian ◽  
Shu-Shen Zhang ◽  
Yu-Quan Feng

In the title compound, [Cr(C7H2N2O7)Cl(C12H8N2)(H2O)], the CrIIIatom displays a distorted octahedral coordination geometry, with the chelating phenantroline and 3,5-dinitrosalicylate ligands intranspositions. In the crystal, molecules are connectedviaO—H...O hydrogen bonds into a two-dimensional framework parallel to (100). In addition, there are π–π stacking interactions between phenanthroline ligands along thecaxis, with a mean interplanar distance of 3.456 (4) Å.


Author(s):  
Khatib Awni ◽  
Fatbi Aqrn ◽  
David Deamer ◽  
Allen Oliver

The title complex of formula [Ni(NH2CH3CHCOO)2(H20)2].2H2O has been prepared from nickel(II) chloride in an aqueous solution by adding D-alanine and potassium hydroxide. It has beett crystallized from an aqueous solution and its structure was determined by X-ray structure analysis. The nickel(II) atom adopts distorted octahedral coordination geometry with two bidentate alanine molecules and two water molecules. The complex is neutral and dihydrated. The network crystal structure shows hydrogen bonding between water and amide hydrogens within the lattice, and each fragment of the complex contains two water molecules as hydrated water.


2013 ◽  
Vol 69 (2) ◽  
pp. m101-m101
Author(s):  
Liang Wang

The dinuclear title complex, [Co2(C15H8O7)2(H2O)6], lies across an inversion center. The unique CoIIion is coordinated in a slightly distorted octahedral coordination geometry by two O atoms from a chelating 4-(carboxyphenoxy)phthalate ligand, three water O atoms and a further O atom from a bridging carboxylate group of a symmetry-related 4-(carboxyphenoxy)phthalate ligand. In the crystal, O—H...O hydrogen bonds link the molecules into a three-dimensional network.


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