The mol-ecular structure of the title compound, trans-[Cu(C2H)Cl(C26H24P2)2], consists of an Ru(II) cation, located on an inversion centre, in an octa-hedral environment defined by two chelating phosphines, one acetyl-ide and one chloride ligand. The -C CH and the chlorine ligands are disordered over two equivalent positions (0.5 occupancy each). The coordination geometry is distorted octa-hedral, with the -C CH fragment and the Cl ligand in trans positions. The four P atoms occupy the equatorial plane of the octa-hedron and the chloride and acetyl-ide ligands the axial positions.
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http://dx.doi.org/10.1107/S1600536812044558 | DOI Listing |
Acta Crystallogr E Crystallogr Commun
December 2020
Department of Chemistry, University of Iowa, 305 Chemistry Building, Iowa City, IA 52242-1290, USA.
The mol-ecular structure of -bis-(pyridin-3-yl)ethyl-ene (), CHN, as determined by single-crystal X-ray diffraction is reported. The mol-ecule self-assembles into two dimensional arrays by a combination of C-H⋯N hydrogen bonds and edge-to-face C-H⋯ inter-actions that stack in a herringbone arrangement perpendicular to the crystallographic -axis. The supra-molecular forces that direct the packing of as well as its packing assembly within the crystal are also compared to those observed within the structures of the other symmetrical isomers -1,2-bis-(-pyrid-yl)ethyl-ene ( , , where = ' = 2 or 4).
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
June 2018
Department of Chemistry, University of Rochester, Rochester, NY 14627, USA.
Structural characterization of the ionic complexes [FeCl(CHP)][FeCl]·0.59CHCl or [(dppen)FeCl][FeCl]·0.59CHCl (dppen = -1,2-bis-(di-phenyl-phosphane)ethyl-ene, PCH) and [FeCl(CHP)][FeCl]·CHCl or [(dpbz)FeCl][FeCl]·CHCl (dpbz = 1,2-bis-(di-phenyl-phosphane)benzene, PCH) demonstrates coordination of two bidentate phosphane ligands (bis-phosphanes) to a single iron(III) center, resulting in six-coordinate cationic complexes that are balanced in charge by tetra-chlorido-ferrate(III) monoanions.
View Article and Find Full Text PDFActa Crystallogr Sect E Struct Rep Online
December 2012
Departamento de Ciencias Quimicas, Facultad de Ciencias Exactas, Universidad Andres Bello, Avenida Republica 275, Santiago, Chile.
The mol-ecular structure of the title compound, trans-[Cu(C2H)Cl(C26H24P2)2], consists of an Ru(II) cation, located on an inversion centre, in an octa-hedral environment defined by two chelating phosphines, one acetyl-ide and one chloride ligand. The -C CH and the chlorine ligands are disordered over two equivalent positions (0.5 occupancy each).
View Article and Find Full Text PDFActa Crystallogr Sect E Struct Rep Online
January 2012
In the crystal structure of the title compound, [Cu(C(4)H(4)NO(4)S)(2)(C(2)H(8)N(2))(2)], the Cu(2+) ion resides on a centre of symmetry. The environment of Cu(2+) ion is a distorted octa-hedron. The axial bond lengths between the Cu(II) ion and the N atoms are considerably longer than the equatorial bond distances between the Cu(II) ion and the N atoms of the ethyl-enediamine ligand as a consequence of the Jahn-Teller effect.
View Article and Find Full Text PDFActa Crystallogr Sect E Struct Rep Online
November 2010
Institute of General and Inorganic Chemistry, NAS Ukraine, prosp. Palladina 32/34, Kyiv 03680, Ukraine.
In the title compound, [Cu(C(5)H(14)NO(6)P(2))(2)(H(2)O)(2)], the Cu(II) atom occupies a special position on an inversion centre. It exhibits a distorted octa-hedral coordination environment consisting of two O,O'-bidentate (1-ammonio-pentane-1,1-di-yl)diphospho-nate anions in the equatorial plane and two trans water mol-ecules located in axial positions. The ligand mol-ecules are coordinated to the Cu(II) atom in their zwitterionic form via two O atoms from different phospho-nate groups, creating two six-membered chelate rings with a screw-boat conformation.
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