scholarly journals Crystal structure of hexakis(urea-κO)chromium(III) dichromate bromide monohydrate from synchrotron X-ray data

2015 ◽  
Vol 71 (11) ◽  
pp. 1336-1339 ◽  
Author(s):  
Dohyun Moon ◽  
Shinnosuke Tanaka ◽  
Takashiro Akitsu ◽  
Jong-Ha Choi
Keyword(s):  
Hydrogen Bonding ◽  
Complex Cation ◽  
Three Dimensional ◽  
Chloride Salt ◽  
Coordination Environment ◽  
Hydrogen Bonding Interactions ◽  
Dimensional Network ◽  
Distorted Octahedral ◽  
The Individual ◽  
Distorted Octahedral Coordination Environment

The title bromide salt, [Cr{CO(NH2)2}6](Cr2O7)Br·H2O, is isotypic to the corresponding chloride salt. Within the complex cation, the CrIIIatom is coordinated by six O atoms of six urea ligands, displaying a slightly distorted octahedral coordination environment. The Cr—O bond lengths involving the urea ligands are in the range 1.9534 (13)–1.9776 (12) Å. The Cr2O72−anion has a nearly staggered conformation, with a bridging angle of 130.26 (10)°. The individual components are arranged in rows extending parallel to [100]. The Br−anion links the complex cation, as well as the solvent water molecule, through N—H...Br and O—H...Br hydrogen-bonding interactions. The supramolecular architecture also includes N—H...O and O—H...O hydrogen bonding between urea N—H and water O—H donor groups and the O atoms of the Cr2O72−anion as acceptor atoms, leading to a three-dimensional network structure.

scholarly journals cis-Bromidobis(1,2-diaminoethane-κ2 N,N′)(ethylamine-κN)cobalt(III) dibromide

IUCrData ◽  
2018 ◽  
Vol 3 (6) ◽  
Author(s):  
S. Manimaran ◽  
M. Manjunathan ◽  
E. Govindan ◽  
K. Sambathkumar ◽  
K. Anbalagan
Keyword(s):  
Hydrogen Bonds ◽  
Complex Cation ◽  
Three Dimensional ◽  
Title Complex ◽  
Coordination Environment ◽  
X Ray ◽  
Distorted Octahedral Coordination ◽  
Dimensional Network ◽  
Distorted Octahedral ◽  
Distorted Octahedral Coordination Environment

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.

scholarly journals Crystal structure ofcis-aquachloridobis(1,10-phenanthroline-κ2N,N′)chromium(III) tetrachloridozincate monohydrate from synchrotron data

2015 ◽  
Vol 71 (3) ◽  
pp. 288-290 ◽  
Author(s):  
Dohyun Moon ◽  
Jong-Ha Choi
Keyword(s):  
Hydrogen Bonding ◽  
Three Dimensional ◽  
Water Molecules ◽  
Coordination Environment ◽  
Bond Lengths ◽  
Hydrogen Bonding Pattern ◽  
Dimensional Network ◽  
Distorted Octahedral ◽  
Cl Atom ◽  
Distorted Octahedral Coordination Environment

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.

scholarly journals (2,2′-Bipyrazine-κ2N1,N1′)[1,2-bis(diphenylphosphanyl)methane-κP]tricarbonylrhenium(I) trifluoromethanesulfonate monohydrate

IUCrData ◽  
2017 ◽  
Vol 2 (6) ◽  
Author(s):  
D. Paul Rillema ◽  
Venugopal Komreddy ◽  
Nilmini K. Senaratne ◽  
David M. Eichhorn
Keyword(s):  
Water Molecule ◽  
Three Dimensional ◽  
Phenyl Group ◽  
Carbonyl Groups ◽  
Coordination Environment ◽  
Distorted Octahedral Coordination ◽  
Hydrogen Bonding Interactions ◽  
Dimensional Network ◽  
Distorted Octahedral ◽  
Distorted Octahedral Coordination Environment

The title compound, [Re(C8H6N4)(C25H22P2)(CO)3]CF3SO3·H2O, crystallizes with one [Re(C8N4H6){P(Ph)2CH2P(Ph)2}(CO)3]+cation, where Ph is a phenyl group, one CF3SO3−anion and one water molecule of hydration. The three C atoms of thefacialoriented carbonyl groups, two N atoms from the bipyrazine ligand and one P atom from the (bis)diphenylphosphanylmethane ligand define a distorted octahedral coordination environment about the central ReIatom. The Re—Ccarbonylbond lengthtransto the P atom is longer than the the two Re—Ccarbonylbond lengths in the plane with the bipyrazine ligand. Hydrogen-bonding interactions between the solvent water molecule and the cation, as well as weak C—H...O interactions, consolidate a three-dimensional network structure.

scholarly journals Crystal structure oftrans-bis{4-bromo-N-[(pyridin-2-yl)methylidene]aniline-κ2N,N′}dichloridoruthenium(II)

2015 ◽  
Vol 71 (9) ◽  
pp. 1067-1069
Author(s):  
Kittipong Chainok ◽  
Filip Kielar
Keyword(s):  
Hydrogen Bonding ◽  
Benzene Ring ◽  
Three Dimensional ◽  
Supramolecular Network ◽  
Complex Molecules ◽  
Coordination Environment ◽  
Hydrogen Bonding Interactions ◽  
Distorted Octahedral ◽  
Cl Atoms ◽  
Distorted Octahedral Coordination Environment

In the title complex, [RuCl2(C12H9BrN2)2] or [RuCl2(PM-BrA)2] (PM-BrA = 4-bromo-N-(2′-pyridylmethylene)aniline), the RuIIcation is located on a centre of inversion and is surrounded by four N atoms of two PM-BrA ligands in the equatorial plane and by two Cl atoms in atransaxial arrangement, displaying a distorted octahedral coordination environment. Two C atoms in the benzene ring of the PM-BrA ligand are equally disordered over two sets of sites. The benzene and pyridine rings of the PM-BrA ligand are oriented at dihedral angles of 62.1 (10) and 73.7 (11)° under consideration of the two orientations of the disordered benzene ring. In the crystal, the complex molecules are connectedviaC—H...Cl hydrogen-bonding interactions into a layered arrangement parallel (100). C—H...Br hydrogen bonding and weak aromatic π–π stacking interactions complete a three-dimensional supramolecular network.

scholarly journals cis-Bromido(n-butylamine-κN)bis(ethene-1,2-diamine-κ2 N,N′)cobalt(III) dibromide

IUCrData ◽  
2018 ◽  
Vol 3 (7) ◽  
Author(s):  
M. Manjunathan ◽  
S. Manimaran ◽  
K. Anbalagan ◽  
K. Sambathkumar ◽  
E. Govindan
Keyword(s):  
Complex Cation ◽  
Three Dimensional ◽  
The Other ◽  
Coordination Environment ◽  
Distorted Octahedral Coordination ◽  
Dimensional Network ◽  
Distorted Octahedral ◽  
Two Component ◽  
Ethylenediamine Ligand ◽  
Distorted Octahedral Coordination Environment

In the title compound, [CoBr(C2H8N2)2(C4H11N)]Br2, the cobalt(III) ion has a distorted octahedral coordination environment and is surrounded by four N atoms in the equatorial plane made up of three N atoms from the two ethylenediamine ligands and the remaining N from the n-butyl substituent, with the other N atom from the ethylenediamine ligand and the Br atom occupying the axial positions. In the crystal, the complex cation and the two counter-anions are linked via N—H...Br and C—H...Br hydrogen bonds, forming a three-dimensional network. The crystal studied was refined as a two-component inversion twin.

[Tris(2-aminoethyl)amine-κ3 N,N′,N′′,N′′′](L-tyrosinato-κ2 N,O)nickel(II) iodide dihydrate

2006 ◽  
Vol 62 (7) ◽  
pp. m1668-m1670 ◽  
Author(s):  
Yamei Pei ◽  
Li Wang
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonding ◽  
Title Compound ◽  
Three Dimensional ◽  
Octahedral Coordination ◽  
Coordination Environment ◽  
Distorted Octahedral Coordination ◽  
Dimensional Network ◽  
Distorted Octahedral ◽  
Distorted Octahedral Coordination Environment

In the title compound, [Ni(C9H10NO3)(C6H18N4)]I·2H2O, the NiII atom is in a slightly distorted octahedral coordination environment. In the crystal structure, extensive hydrogen bonding links molecules into a three-dimensional network.

scholarly journals Crystal structure of 2-methyl-1H-imidazol-3-ium aquatrichlorido(oxalato-κ2O,O′)stannate(IV)

2015 ◽  
Vol 71 (5) ◽  
pp. 520-522 ◽  
Author(s):  
Mouhamadou Birame Diop ◽  
Libasse Diop ◽  
Laurent Plasseraud ◽  
Thierry Maris
Keyword(s):  
Hydrogen Bonds ◽  
Water Molecule ◽  
Three Dimensional ◽  
Free Oxygen ◽  
Coordination Environment ◽  
Dimensional Network ◽  
Oxalate Ligand ◽  
Distorted Octahedral ◽  
Distorted Octahedral Coordination Environment ◽  
Oxygen Atoms

The tin(IV) atom in the complex anion of the title salt, (C4H7N2)[Sn(C2O4)Cl3(H2O)], is in a distorted octahedral coordination environment defined by three chlorido ligands, an oxygen atom from a water molecule and two oxygen atoms from a chelating oxalate anion. The organic cation is linked through a bifurcated N—H...O hydrogen bond to the free oxygen atoms of the oxalate ligand of the complex [Sn(H2O)Cl3(C2O4)]−anion. Neighbouring stannate(IV) anions are linked through O—H...O hydrogen bonds involving the water molecule and the two non-coordinating oxalate oxygen atoms. In combination with additional N—H...Cl hydrogen bonds between cations and anions, a three-dimensional network is spanned.

Redetermination of trans-diaquabis(picolinato-κ2 N,O)cobalt(II) dihydrate

2006 ◽  
Vol 62 (4) ◽  
pp. m796-m798 ◽  
Author(s):  
Zerrin Heren ◽  
Cem Cüneyt Ersanlı ◽  
Cem Keser ◽  
Nazan Ocak Ískeleli
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonding ◽  
Title Compound ◽  
Three Dimensional ◽  
Water Molecules ◽  
Inversion Center ◽  
Hydrogen Bonding Interactions ◽  
Dimensional Network ◽  
Distorted Octahedral

The crystal structure of the title compound, [Co(C6H4NO2)2(H2O)2]·2H2O, has been reinvestigated with improved precision [previous reports: Chang et al. (1972). J. Coord. Chem. 2, 31–34; Lumme et al. (1969). Suom. Kemistil. B, 42, 270]. In the title compound, the Co atom is located on an inversion center and its coordination can be described as slightly distorted octahedral, equatorially trans-coordinated by two N and O atoms of two picolinate ligands and axially coordinated by two O atoms of the water molecules. Intermolecular O—H...O and C—H...O hydrogen-bonding interactions result in the formation of an intricate three-dimensional network.

scholarly journals Bis[2-(2-aminoethyl)-1H-benzimidazole-κ2 N 2,N 3](nitrato-κ2 O,O′)cobalt(II) chloride trihydrate

2012 ◽  
Vol 68 (6) ◽  
pp. m711-m712
Author(s):  
Jing Zhao ◽  
Heng Zhang ◽  
Guoyi Zhu
Keyword(s):  
Three Dimensional ◽  
Water Molecules ◽  
Nitrate Anion ◽  
Coordination Environment ◽  
Distorted Octahedral Coordination ◽  
Dimensional Network ◽  
Distorted Octahedral ◽  
Benzene Rings ◽  
Chloride Trihydrate ◽  
Distorted Octahedral Coordination Environment

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].

scholarly journals Crystal structure of 4-(dimethylamino)pyridiniumcis-diaquabis(oxalato-κ2O,O′)ferrate(III) hemihydrate

2015 ◽  
Vol 71 (8) ◽  
pp. 934-936 ◽  
Author(s):  
Edith Dimitri Djomo ◽  
Frédéric Capet ◽  
Justin Nenwa ◽  
Michel M. Bélombé ◽  
Michel Foulon
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Bond Length ◽  
Three Dimensional ◽  
Coordination Environment ◽  
Distorted Octahedral Coordination ◽  
Dimensional Network ◽  
Distorted Octahedral ◽  
Ionic Components ◽  
Distorted Octahedral Coordination Environment

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.

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