In the crystal structure of the centrosymmetric binuclear title complex, [Ni(2)(C(12)H(8)N(2)O(2)S)(2)(CH(3)OH)(4)], there are inter-molecular O-H⋯O, O-H⋯N and O-H⋯S hydrogen bonds. These help to stabilize the structure and link the mol-ecules, forming a three-dimensional network structure. The Ni(2+) cation exists in a slightly distorted octahedral NiNO(5) coordination environment. The thio-phene rings are disordered over two equivalent conformations with occupancies of 0.881 (3) and 0.119 (3).
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http://dx.doi.org/10.1107/S160053681102143X | DOI Listing |
Acta Crystallogr C Struct Chem
September 2024
Laboratorio de Síntesis y Caracterización de Nuevos Materiales, Centro de Química, Instituto Venezolano de Investigaciones Científicas (IVIC), Apto. 21827, Caracas 1020-A, Venezuela.
The synthesis and structural characterization of four novel supramolecular hydrogen-bonded arrangements based on self-assembly from molecular `[Cu(2,2'-biimidazole)]' modules and malonate anions are presented, namely, tetrakis(2,2'-biimidazole)di-μ-chlorido-dimalonatotricopper(II) pentahydrate, [Cu(CHO)Cl(CHN)]·5HO or [Cu(Hbiim)(μ-Cl)Cu(mal)]·5HO, aqua(2,2'-biimidazole)malonatocopper(II) dihydrate, [Cu(CHO)(CHN)(HO)]·2HO or [Cu(Hbiim)(mal)(HO)]·2HO, bis[aquabis(2,2'-biimidazole)copper(II)] dimalonatodiperchloratocopper(II) 2.2-hydrate, [Cu(CHN)(HO)][Cu(CHO)(ClO)]·2.2HO or [Cu(Hbiim)(HO)][Cu(mal)(ClO)]·2.
View Article and Find Full Text PDFJ Am Chem Soc
August 2024
Department of Chemistry, Johns Hopkins University, Baltimore, Maryland 21218, United States.
The chemistry of copper-dioxygen complexes is relevant to copper enzymes in biology as well as in (ligand)Cu-O (or Cu-O) species utilized in oxidative transformations. For overall energy considerations, as applicable in chemical synthesis, it is beneficial to have an appropriate atom economy; both O-atoms of O are transferred to the product(s). However, examples of such dioxygenase-type chemistry are extremely rare or not well documented.
View Article and Find Full Text PDFJ Inorg Biochem
August 2024
School of Chemistry, Trinity College Dublin, The University of Dublin, College Green, Dublin 2, Ireland. Electronic address:
IUCrdata
November 2023
Department of Chemical Sciences, University of Johannesburg, 2006, South Africa.
The title compound, [RuCl(CHP)] or [RuCl(dppm)] (dppm = bis-(di-phenyl-phosphan-yl)methane, CHP) crystallizes as two half-mol-ecules (completed by inversion symmetry) in space group ( = 2), with the Ru atoms occupying inversion centers at 0,0,0 and 1/2, 1/2, 1/2, respectively. The bidentate phosphane ligands occupy equatorial positions while the chlorido ligands complete the distorted octa-hedral coordination spheres at axial positions. The bite angles of the phosphane chelates are similar for the two mol-ecules [(P-Ru-P) = 71.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
October 2023
School of Chemistry, University of St Andrews, St Andrews, Fife KY16 9ST, United Kingdom.
The title compound, [Fe(CN)(CHN)]·2HO, has been synthesized solvothermally and characterized by single-crystal X-ray diffraction. The octa-hedral iron coordination polyhedron contains two di(pyrimidin-2-yl)amine ligands coordinated in a bidentate fashion, and two monodentate dicyanimido ligands, each coordinated a terminal N atom, with the latter in a orientation. The ligand configuration about the iron atom is chiral, although the compound crystallizes as a racemic mixture: the Fe-N distances (> 2.
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