scholarly journals Crystal structure oftrans-(1,8-dibutyl-1,3,6,8,10,13-hexaazacyclotetradecane-κ4N3,N6,N10,N13)bis(isonicotinato-κO)nickel(II) determined from synchrotron data

2016 ◽  
Vol 72 (2) ◽  
pp. 223-225 ◽  
Author(s):  
Jong Won Shin ◽  
Dae-Woong Kim ◽  
Dohyun Moon
Keyword(s):  
Molecular Structure ◽  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Equatorial Plane ◽  
Self Assembly ◽  
Title Compound ◽  
Isonicotinic Acid ◽  
Inversion Center ◽  
Coordination Environment ◽  
Distorted Octahedral

The title compound, [Ni(C6H4NO2)2(C16H38N6)], was prepared through self-assembly of a nickel(II) azamacrocyclic complex with isonicotinic acid. The NiIIatom is located on an inversion center and exhibits a distorted octahedral N4O2coordination environment, with the four secondary N atoms of the azamacrocyclic ligand in the equatorial plane [average Ni—Neq= 2.064 (11) Å] and two O atoms of monodentate isonicotinate anions in axial positions [Ni—Oax= 2.137 (1) Å]. Intramolecular N—H...O hydrogen bonds between one of the secondary amine N atoms of the azamacrocyclic ligand and the non-coordinating carboxylate O atom of the anion stabilize the molecular structure. Intermolecular N—H...N hydrogen bonds, as well as π–π interactions between neighbouring pyridine rings, give rise to the formations of supramolecular ribbons extending parallel to [001].

Dibromido-2κ2 Br-bis(4-methylpyridine-1κN){μ-2,2′-[propane-1,3-diylbis(nitrilomethylidyne)]diphenolato-1κ4 O,N,N′,O′:2κ2 O,O′}nickel(II)zinc(II)

2007 ◽  
Vol 63 (11) ◽  
pp. m2676-m2677 ◽  
Author(s):  
Leyla Tatar Yıldırım ◽  
Orhan Atakol
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Equatorial Plane ◽  
Title Compound ◽  
Tetrahedral Coordination ◽  
Coordination Environment ◽  
Distorted Octahedral Coordination ◽  
Distorted Octahedral ◽  
Distorted Tetrahedral Coordination ◽  
Distorted Octahedral Coordination Environment

The molecule of the title compound, [NiZnBr2(C17H16N2O2)(C6H7N)2], contains a heterodinuclear arrangement. The two metal ions are bridged via phenol O atoms of the propane-1,3-diylbis(nitrilomethylidyne)]diphenolate (salpd2−) ligand. The two bridging O atoms of salpd2− and two Br atoms constitute a distorted tetrahedral coordination environment around the ZnII ion, while the NiII ion has a distorted octahedral coordination environment formed by two O and two N atoms of salpd2− in the equatorial plane and two N atoms of two 4-methylpyridine ligands in the axial positions. In the crystal structure, weak intermolecular C—H...Br hydrogen bonds link the molecules into chains along the c axis. Weak intramolecular C—H...O and C—H...N hydrogen bonds are also present.

scholarly journals cis-Bromidobis(ethylene-1,2-diamine)(2-methylpropan-1-amine)cobalt(III) dibromide

IUCrData ◽  
2018 ◽  
Vol 3 (9) ◽  
Author(s):  
M. Manjunathan ◽  
K. Anbalagan ◽  
K. Sambathkumar ◽  
E. Govindan
Keyword(s):  
Hydrogen Bonds ◽  
Equatorial Plane ◽  
Title Compound ◽  
Complex Cation ◽  
Octahedral Coordination ◽  
Supramolecular Framework ◽  
Coordination Environment ◽  
Distorted Octahedral Coordination ◽  
Distorted Octahedral ◽  
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 ligated by three N atoms and a bromine ion in the equatorial plane, and by two N atoms occupying the axial positions. In the crystal, the complex cation and the two Br− counter-anions are linked by N—H...Br hydrogen bonds, forming a supramolecular framework.

scholarly journals Crystal structure ofcatena-poly[[bis(acetato-κO)copper(II)]-bis[μ-4-(1H-imidazol-1-yl)phenol]-κ2N3:O;κ2O:N3]

2017 ◽  
Vol 73 (2) ◽  
pp. 209-212
Author(s):  
Mehmet Poyraz ◽  
Musa Sarı
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Title Compound ◽  
Octahedral Coordination ◽  
Stacking Interactions ◽  
Coordination Environment ◽  
Heterocyclic Ligand ◽  
Distorted Octahedral Coordination ◽  
Distorted Octahedral ◽  
Distorted Octahedral Coordination Environment

In the title compound, [Cu(CH3COO)2(C9H8N2O)2]n, the CuIIion resides on a centre of inversion, displaying a tetragonally distorted octahedral coordination environment defined by two pairs of N and O atoms of symmetry-related 4-(1H-imidazol-1-yl)phenol ligands and the O atoms of two symmetry-related acetate ligands. The bridging mode of the 4-(1H-imidazol-1-yl)phenol ligands is associated with a very long Cu...O interactions involving the phenol O atom of the heterocyclic ligand, which creates chains extending parallel to [100]. In the crystal, the chains are arranged in a distorted hexagonal rod packing and are linkedviaC—H...O hydrogen bonds and by π–π stacking interactions involving centrosymmetrically related pairs of imidazole and phenol rings.

scholarly journals cis-Bromidobis(ethylene-1,2-diamine)(methylamine)cobalt(III) dibromide

IUCrData ◽  
2018 ◽  
Vol 3 (6) ◽  
Author(s):  
S. Manimaran ◽  
E. Govindan ◽  
M. Manjunathan ◽  
K. Sambathkumar ◽  
K. Anbalagan
Keyword(s):  
Hydrogen Bonds ◽  
Equatorial Plane ◽  
Title Compound ◽  
Complex Cation ◽  
Octahedral Coordination ◽  
Supramolecular Framework ◽  
Coordination Environment ◽  
Distorted Octahedral Coordination ◽  
Distorted Octahedral ◽  
Distorted Octahedral Coordination Environment

In the title compound, [CoBr(CH5N)(C2H8N2)2]Br2, the cobalt(III) ion has a distorted octahedral coordination environment and is ligated by four N atoms in the equatorial plane, with an additional N atom and a Br− ion 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 supramolecular framework.

scholarly journals Bis{N-[2-hydroxy-1,1-bis(hydroxymethyl)ethyl]glycinato-κ3O,N,O′}iron(II)

2014 ◽  
Vol 70 (7) ◽  
pp. m274-m274
Author(s):  
Ning Jiang ◽  
Juan-Juan Hou
Keyword(s):  
Hydrogen Bonds ◽  
Title Compound ◽  
Three Dimensional ◽  
Octahedral Coordination ◽  
Inversion Center ◽  
Coordination Environment ◽  
Distorted Octahedral Coordination ◽  
Dimensional Network ◽  
Distorted Octahedral ◽  
Distorted Octahedral Coordination Environment

In the title compound, [Fe(C6H12NO5)2], the FeIIion lies on an inversion center and is coordinated by two N atoms and four O atoms from two tridentateN-[2-hydroxy-1,1-bis(hydroxymethyl)ethyl]glycine ligands, forming a slightly distorted octahedral coordination environment. In the crystal, O—H...O, O—H...N and weak C—H...O hydrogen bonds link molecules, forming a three-dimensional network.

scholarly journals Crystal structure oftrans-aqua(perchlorato-κO)bis(propane-1,3-diamine-κ2N,N′)copper(II) perchlorate

2014 ◽  
Vol 70 (11) ◽  
pp. 438-440
Author(s):  
J. Govindaraj ◽  
K. Rajkumar ◽  
A. S. Ganeshraja ◽  
K. Anbalagan ◽  
A. SubbiahPandi
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Coordination Sphere ◽  
Equatorial Plane ◽  
Title Compound ◽  
Octahedral Coordination ◽  
Distorted Octahedral Coordination ◽  
Distorted Octahedral ◽  
Diamine Ligands

In the title compound, [Cu(ClO4)(C3H10N2)2(H2O)]ClO4, the CuIIatom has a distorted octahedral coordination sphere and is coordinated by the N atoms of two propane-1,3-diamine ligands in the equatorial plane. The axial positions are occupied by a water O atom and an O atom of a disordered perchlorate anion [occupancy ratio 0.631 (9):0.369 (9)]. In the crystal, the various components are linkedviaO—H...O, N—H...O and C—H...O hydrogen bonds, forming sheets lying parallel to (001).

scholarly journals Crystal structure and DFT study of bis{(S)-2-[(2-hydroxybenzyl)amino]-4-methylpentanoato-κ2N,O}(1,10-phenanthroline-κ2N,N′)nickel(II)

2017 ◽  
Vol 73 (9) ◽  
pp. 1393-1397 ◽  
Author(s):  
Md. Serajul Haque Faizi ◽  
Necmi Dege ◽  
Sergey Malinkin
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Title Compound ◽  
Three Dimensional ◽  
Complex Molecules ◽  
Coordination Environment ◽  
Distorted Octahedral Coordination ◽  
Distorted Octahedral ◽  
Phenanthroline Ligand ◽  
Distorted Octahedral Coordination Environment

In the title compound, [Ni(C13H18NO3)2(C12H8N2)], the NiIIcation shows a distorted octahedral coordination environment. It is formed by two N atoms from the phenanthroline ligand, as well as two N and two O atoms belonging to two 2-[(2-hydroxybenzyl)amino]-4-methylpentanoate ligands. Complex molecules are connected into layers propagating along theabplaneviahydrogen bonds formed by O atoms of carboxylate and phenoxide groups, which are further connected into a three-dimensional motif.

scholarly journals trans-Dichloridobis(4-methoxyaniline-κN)palladium(II)

2009 ◽  
Vol 65 (6) ◽  
pp. m673-m673 ◽  
Author(s):  
Volodimir Bon ◽  
Svitlana Orysyk ◽  
Vasyl Pekhnyo
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Title Compound ◽  
Planar Geometry ◽  
Coordination Environment ◽  
Square Planar ◽  
A Chain

In the title compound, [PdCl2(C7H9NO)2], the Pd atom is situated on a crystallographic centre of inversion. The coordination environment of the Pd atom shows a slightly distorted square-planar geometry. The crystal structure exhibits weak intermolecular Pd...Cl interactions, with Pd...Cl distances of 3.6912 (6) Å. A chain-like arrangement of molecules realized by intermolecular N—H...Cl hydrogen bonds is observed along [010].

scholarly journals Bis(1-dodecyl-4-aza-1-azoniabicyclo[2.2.2]octane)tetraisothiocyanatocobalt(II)

IUCrData ◽  
2020 ◽  
Vol 5 (1) ◽  
Author(s):  
Niels Ole Giltzau ◽  
Martin Köckerling
Keyword(s):  
Hydrogen Bonding ◽  
Equatorial Plane ◽  
Title Compound ◽  
Unit Cell ◽  
Octahedral Coordination ◽  
Coordination Environment ◽  
Distorted Octahedral Coordination ◽  
Distorted Octahedral ◽  
Triclinic Unit Cell ◽  
Distorted Octahedral Coordination Environment

The title compound, [Co(C18H37N2)2(NCS)4], consists of a cobalt(II) ion positioned on the origin of the triclinic unit cell. It is coordinated by the N atoms of two trans-oriented 1-dodecyl-4-aza-1-azoniabicyclo[2.2.2]octane (DABCO+) cations, which carry n-dodecyl chains at the non-coordinating N atoms. The distorted octahedral coordination environment of the CoII ion is completed through four N atoms of isothiocyanate ions, which are arranged within the equatorial plane. Non-classical hydrogen bonding of the types C—H...N and C—H...S between the filamentous molecules lead to the formation of layers parallel to (001).

scholarly journals Crystal structure of aquatris{μ-N-[bis(diethylamino)phosphoryl]-2,2,2-trichloroacetamidato-κ3O,O′:O}calciumsodium

2016 ◽  
Vol 72 (12) ◽  
pp. 1683-1686 ◽  
Author(s):  
Iuliia Shatrava ◽  
Kateryna Gubina ◽  
Vladimir Ovchynnikov ◽  
Viktoriya Dyakonenko ◽  
Vladimir Amirkhanov
Keyword(s):  
Molecular Structure ◽  
Crystal Structure ◽  
Water Molecules ◽  
Carbonyl Groups ◽  
Coordination Environment ◽  
Distorted Octahedral Coordination ◽  
Distorted Octahedral ◽  
Phosphoryl Groups ◽  
Cl Atoms ◽  
Distorted Octahedral Coordination Environment

In the molecular structure of the title compound, [CaNa(C10H20Cl3N3O2P)3(H2O)], the Ca2+ion has a slightly distorted octahedral coordination environment defined by six O atoms which belong to the carbonyl and phosphoryl groups of the three coordinating ligands. Two Cl atoms of CCl3groups and four O atoms form the coordination environment of the Na+ion: three from the carbonyl groups of ligands and one O atom from a coordinating water molecule. In the crystal, the bimetallic complexes are assembled into chains along thec-axis directionviaO—H...O hydrogen bonds that involve the coordinating water molecules and the phosphoryl groups.

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