scholarly journals Di-μ3-chlorido-tetra-μ2-chlorido-dichloridotetrakis(N,N-diethylethane-1,2-diamine-κ2 N,N′)tetracadmium(II)

IUCrData ◽  
2019 ◽  
Vol 4 (12) ◽  
Author(s):  
Abdul-Razak H. Al-Sudani ◽  
Myasim Qasim Abdulridha ◽  
Benson M. Kariuki

In the title compound, [Cd4Cl8(C6H16N2)4], the Cd2+ cations and Cl− anions form M 4Cl8 clusters with six of the Cl− ions bridging Cd2+ cations and two being pendant. Each Cd2+ cation has distorted octahedral coordination completed by four Cl− ions and two N atoms of the asymmetrical bidentate amino ligand. The cluster consists of pairs of face-sharing hexahedra linked by a shared edge.

IUCrData ◽  
2020 ◽  
Vol 5 (1) ◽  
Author(s):  
Niels Ole Giltzau ◽  
Martin Köckerling

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).


2007 ◽  
Vol 63 (11) ◽  
pp. m2722-m2722 ◽  
Author(s):  
Ying Liu ◽  
Jianmin Dou ◽  
Dacheng Li ◽  
Xianxi Zhang

The dinuclear FeIII complex in the title compound, [Fe2Cl2O(C18H18N4)2](PF6)2, lies on a center of inversion. The FeIII atom is chelated by a tetradentate tris(2-pyridylmethyl)amine ligand via four N atoms and further coordinated by one chloride ion and one bridging oxide O atom, giving a distorted octahedral coordination geometry.


2014 ◽  
Vol 70 (8) ◽  
pp. m304-m304 ◽  
Author(s):  
Cassandra T. Eagle ◽  
Fredricka Quarshie ◽  
Kevin M. Cook

The complex molecule of the title compound, [Rh2{N(C6H5)COCH3}4(NCC7H7)], has crystallographically-imposed mirror symmetry. The four acetamide ligands bridging the dirhodium core are arranged in a 2,2-cismanner with two N atoms and two O atoms coordinating to the unique RhIIatomcisto one another. The Neq—Rh—Rh—Oeqtorsion angles on the acetamide bridge are 0.75 (7) and 1.99 (9)°. The axial nitrile ligand completes the distorted octahedral coordination sphere of one RhIIatom and shows a nonlinear coordination, with an Rh—N—C bond angle of 162.8 (5)°; the N—C bond length is 1.154 (7) Å.


2000 ◽  
Vol 57 (1) ◽  
pp. m12-m13 ◽  
Author(s):  
Shigeru Ohba ◽  
Naoki Yamada ◽  
Makoto Eishima

In the title compound,trans-[Co(NO2)2(cyclam)]ClO4, (I), where cyclam is 1,4,8,11-tetraazacyclotetradecane (C10H24N4), the CoIIIcomplex has a distorted octahedral coordination. The O atoms of each nitro ligand are disordered over two sites with 65:35% occupancy.


2017 ◽  
Vol 73 (9) ◽  
pp. 1279-1281 ◽  
Author(s):  
Andrew J. Peloquin ◽  
Madelyn B. Smith ◽  
Gary J. Balaich ◽  
Scott T. Iacono

The title compound, [IrCl(C12H8NO)2{(CH3)2SO}]·H3CCN or [IrCl(fppy)2(DMSO)]·H3CCN [where fppy is 4-(pyridin-2-yl)benzaldehyde and DMSO is dimethyl sulfoxide], is a mononuclear iridium(III) complex including two fppy ligands, a sulfur-coordinating DMSO ligand, and one terminal chloride ligand that define a distorted octahedral coordination sphere. The complex crystallizes from 1:1 DMSO–acetonitrile as an acetonitrile solvate. In the crystal, weak C—H...O and C—H...N hydrogen-bonding interactions between adjacent complexes and between the acetonitrile solvent and the complex consolidate the packing.


2006 ◽  
Vol 62 (7) ◽  
pp. m1553-m1554 ◽  
Author(s):  
Radoslava Ivaniková ◽  
Ingrid Svoboda ◽  
Hartmut Fuess ◽  
Anna Mašlejová

In the structure of the title compound, [CoCl2(C10H24N4)]Cl, the CoIII atom has a six-coordinate arrangement displaying distorted octahedral coordination geometry with the four N atoms from the 1,4,8,11-tetraazacyclotetradecane ring in the equatorial plane and two chloride anions in axial positions. The Co atom is located on a centre of inversion; the two Cl ions not bonded to Co are located on special positions of site symmetry \overline{4}.


IUCrData ◽  
2017 ◽  
Vol 2 (1) ◽  
Author(s):  
Takumi Tominaga ◽  
Tomoyuki Mochida

The CoIIatom in the mononuclear title compound, [Co(C5HF6O2)2(H2O)2]·2H2O, is situated on an inversion centre and exhibits a slightly distorted octahedral coordination sphere. In the crystal, molecules are arranged in layers parallel to (100), held together by O—H...O and O—H...F hydrogen bonds.


2014 ◽  
Vol 70 (11) ◽  
pp. m385-m386
Author(s):  
Rachel L. Nicholls ◽  
Christopher M. Pask ◽  
Bao Nguyen

The title compound [Na3(C11H6NO3)2(C2H3O2)]n, crystallized through diffusion of diethyl ether into methanol as needles. There are three crystallographically independent Na+cations present, each exhibiting a distorted octahedral coordination geometry, two through coordination by five O atoms and one N atom, and one through coordination by six O atoms. A series of intermolecular O...Na and N...Na contacts leads to the formation of chains along thea-axis direction.


2012 ◽  
Vol 68 (6) ◽  
pp. m775-m775
Author(s):  
Aphiwat Kaewthong ◽  
Mongkol Sukwattanasinitt ◽  
Nongnuj Muangsin

In the title compound, [Cu(C2H3O2)2(C12H12N2)2]·H2O, the CuII atom exhibits a distorted octahedral coordination geometry, defined by two N atoms from one 4,4′-dimethyl-2,2′-bipyridine ligand and four O atoms from two acetate ligands. In the crystal, O—H...O hydrogen bonds are observed between the coordinated carboxylate O atoms and the solvent water molecule.


2009 ◽  
Vol 65 (6) ◽  
pp. m612-m612
Author(s):  
Rüdiger W. Seidel

In the title compound, [Ni(NO3)2(C6H15OP)2], the NiIIion, lying on a crystallographic twofold axis, adopts a distorted octahedral coordination, consisting ofO-donor atoms of two symmetry-related triethylphospine oxide and two bidentate nitrate ligands.


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