scholarly journals catena-Poly[[diaqua(1H-imidazo[4,5-f][1,10]phenanthroline)cobalt(II)]-μ-sulfato]

2009 ◽  
Vol 65 (6) ◽  
pp. m618-m618 ◽  
Author(s):  
Jian Yu

The CoIIion in the title complex, [Co(SO4)(C13H8N4)(H2O)2]n, has a slightly distorted octahedral coordination environment formed by two O atoms from two symmetry-related bridging sulfate ligands, two N atoms from a bis-chelating 1H-imidazo[4,5-f][1,10]phenanthroline (IPL) ligand and two O atoms from coordinated water molecules. The bridging sulfate ligands connect CoIIions to form a one-dimensional chain along theb-axis direction. In the crystal structure, intermolecular O—H...O, O—H...N and N—H...O hydrogen bonds link the chains into a three-dimensional network.

2017 ◽  
Vol 73 (9) ◽  
pp. 1302-1304 ◽  
Author(s):  
Hicham El Hamdani ◽  
Mohammed El Amane ◽  
Carine Duhayon

The title complex, [Co(C7H7N4O2)2(H2O)4], comprises mononuclear molecules consisting of a CoIIion, two deprotonated theophylline ligands (systematic name: 1,3-dimethyl-7H-purine-2,6-dione) and four coordinating water molecules. The CoIIatom lies on an inversion centre and has a slightly distorted octahedral coordination environment, with two N atoms of twotrans-oriented theophylline ligands and the O atoms of four water molecules. An intramolecular hydrogen bond stabilizes this conformation. A three-dimensional supramolecular network structure is formed by intermolecular O—H...O and O—H...N hydrogen bonds.


2012 ◽  
Vol 68 (6) ◽  
pp. m711-m712
Author(s):  
Jing Zhao ◽  
Heng Zhang ◽  
Guoyi Zhu

In the title compound, [Co(NO3)(C9H11N3)2]Cl·3H2O, the CoII atom is coordinated by four N atoms from two chelating 2-(2-aminoethyl)-1H-benzimidazole ligands and two O atoms from one nitrate anion in a distorted octahedral coordination environment. In the crystal, N—H...Cl, N—H...O, O—H...Cl and O—H...O hydrogen bonds link the complex cations, chloride anions and solvent water molecules into a three-dimensional network. π–π interactions between the imidazole and benzene rings and between the benzene rings are observed [centroid–centroid distances = 3.903 (3), 3.720 (3), 3.774 (3) and 3.926 (3) Å].


IUCrData ◽  
2018 ◽  
Vol 3 (6) ◽  
Author(s):  
S. Manimaran ◽  
M. Manjunathan ◽  
E. Govindan ◽  
K. Sambathkumar ◽  
K. Anbalagan

In the title complex, [CoBr(C2H7N)(C2H8N2)2]Br2, the CoIII centre has a distorted octahedral coordination environment, and is surrounded by four N atoms in the equatorial plane, with an additional N atom and the Br atom occupying the axial positions. The complex is isostructural with the Cl compound for which the X-ray structure has also been reported [Anbalagan, Mahalakshmi & Ganeshraja (2011). J. Mol. Struct. 1005, 45–52]. In the crystal, the complex cation and the two counter-anions are linked via N—H...Br hydrogen bonds, forming a three-dimensional network.


2015 ◽  
Vol 71 (6) ◽  
pp. m135-m136
Author(s):  
Jung-Su Son ◽  
Sung-Chul Lim ◽  
Hochun Lee ◽  
Seung-Tae Hong

In the structure of the title salt, [Co(C6H6N2)2(H2O)2](BF4)2, the CoIIatom is located on an inversion centre. The transition metal is in a slightly distorted octahedral coordination environment, defined by the cyano N atoms of four hex-3-enedinitrile ligands in equatorial positions and the O atoms of two water molecules in axial positions. The bridging mode of the hex-3-enedinitrile ligands leads to the formation of cationic chains extending parallel to [1-10]. The BF4−counter-anion is disordered over two sets of sites [occupancy ratio = 0.512 (19):0.489 (19)]. It is located in the voids between the cationic chains and is connected to the aqua ligands of the latter through O—H...F hydrogen bonds. One methylene H atom of the hex-3-enedinitrile ligand forms another and weak C—H...O hydrogen bond with a water O atom of a neighbouring chain, thus consolidating the three-dimensional network structure.


Author(s):  
Md. Serajul Haque Faizi ◽  
Natalia O. Sharkina

In the title compound, [Ni(C13H17NO3)(C12H8N2)(H2O)]·5H2O, the NiIIatom is in a distorted octahedral coordination environment provided by the two N atoms of one bidentate phenanthroline ligand and two O atoms and one N atom from a tridentate 2-[(2-hydroxybenzyl)amino]-4-methylpentanoic acid (HAMA) ligand and one water molecule. The complex was prepared by the reaction of nickel(II) nitrate with HAMA in the presence of 1,10-phenanthroline in a 1:1:1 ratio. In the crystal, the complex molecules and solvate water molecules are associatedviaO—H...O hydrogen bonds into a three-dimensional network.


2006 ◽  
Vol 62 (4) ◽  
pp. m830-m832 ◽  
Author(s):  
Zahra Aghajani ◽  
Mahboubeh A. Sharif ◽  
Hossein Aghabozorg ◽  
Azam Naderpour

The reaction of zinc(II) nitrate tetrahydrate with the proton-transfer compound LH2 [LH2 is (tataH)2(pydc), where tata is 2,4,6-triamino-1,3,5-triazine (melamine) and pydcH2 is pyridine-2,6-dicarboxylic acid] in aqueous solution leads to the formation of the title compound, (tataH)2[Zn(pydc)2].10H2O or (C3H7N6)2[Zn(C7H3O4)2].10H2O. The ZnII atom has a distorted octahedral coordination environment. Extensive intermolecular N—H...O and O—H...O hydrogen bonding involving the tataH and pydc ligands and the water molecules forms an extended three-dimensional network.


Author(s):  
Andrei I. Fischer ◽  
Vladislav V. Gurzhiy ◽  
Julia V. Aleksandrova ◽  
Maria I. Pakina

In the title cobalt(II) coordination polymer with isobutyrate ligands, {[Co{CH(CH3)2CO2}2(H2O)]·H2O}n, the Co2+ion is hexacoordinated in a slightly distorted octahedral coordination environment defined by two O atoms from two bridging water molecules and four O atoms from four bridging carboxylate ligands. The carboxylates adopt two different coordination modes, μ-(κ2O:O′) and μ-(κ2O:O), forming a one-dimensional polymeric chain extending along [010]. The intra-chain cobalt...cobalt separation is 3.2029 (2) Å. The polymeric chains are linked by hydrogen bonds involving the water molecules of solvation, giving a two-dimensional network structure lying parallel to (100).


Author(s):  
Edith Dimitri Djomo ◽  
Frédéric Capet ◽  
Justin Nenwa ◽  
Michel M. Bélombé ◽  
Michel Foulon

The FeIIIions in the hybrid title salt, (C7H11N2)[Fe(C2O4)2(H2O)2]·0.5H2O, show a distorted octahedral coordination environment, with four O atoms from two chelating oxalate dianions and two O atoms from twocisaqua ligands. The average Fe—O(oxalate) bond length [2.00 (2) Å] is shorter than the average Fe—O(water) bond length [2.027 (19) Å]. The ionic components are connectedviaintermolecular N—H...O and O—H...O hydrogen bonds into a three-dimensional network.


Author(s):  
Dohyun Moon ◽  
Jong-Ha Choi

The structure of the title double salt, [Cr(rac-chxn)3][ZnCl4]Cl·3H2O (chxn istrans-1,2-cyclohexanediamine; C6H14N2), has been determined from synchrotron data. The CrIIIion is coordinated by six N atoms of three chelating chxn ligands, displaying a slightly distorted octahedral coordination environment. The distorted tetrahedral [ZnCl4]2−anion, the isolated Cl−anion and three lattice water molecules remain outside the coordination sphere. The Cr—N(chxn) bond lengths are in a narrow range between 2.0737 (12) and 2.0928 (12) Å; the mean N—Cr—N bite angle is 82.1 (4)°. The crystal packing is stabilized by hydrogen-bonding interactions between the amino groups of the chxn ligands and the water molecules as donor groups, and O atoms of the water molecules, chloride anions and Cl atoms of the [ZnCl4]2−anions as acceptor groups, leading to the formation of a three-dimensional network. The [ZnCl4]2−anion is disordered over two sets of sites with an occupancy ratio of 0.94:0.06.


Author(s):  
Dohyun Moon ◽  
Jong-Ha Choi

The structure of the title compound, [CrCl(C12H8N2)2(H2O)][ZnCl4]·H2O, has been determined from synchrotron data. The CrIIIion is bonded to four N atoms from two 1,10-phenanthroline (phen) ligands, one water molecule and a Cl atom in acisarrangement, displaying an overall distorted octahedral coordination environment. The Cr—N(phen) bond lengths are in the range of 2.0495 (18) to 2.0831 (18) Å, while the Cr—Cl and Cr—(OH2) bond lengths are 2.2734 (7) and 1.9986 (17) Å, respectively. The tetrahedral [ZnCl4]2−anion is slightly distorted owing to its involvement in O—H...Cl hydrogen bonding with coordinating and non-coordinating water molecules. The two types of water molecules also interact through O—H...O hydrogen bonds. The observed hydrogen-bonding pattern leads to the formation of a three-dimensional network structure.


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