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Crystal structure of bis[trans-dichloridobis-(propane-1,3-diamine-κ2N,N'chromium(III)] dichromate from synchrotron data.

Authors :
Dohyun Moon
Keon Sang Ryoo
Jong-Ha Choi
Source :
Acta Crystallographica Section E: Crystallographic Communications; Nov2016, Vol. 72 Issue 9, following p1293-1296, 9p
Publication Year :
2016

Abstract

The structure of the title compound, [CrCl<subscript>2</subscript>(tn)<subscript>2</subscript>]<subscript>2</subscript>[Cr<subscript>2</subscript>O<subscript>7</subscript>] (tn = propane-1,3-diamine; C<subscript>3</subscript>H<subscript>10</subscript>N<subscript>2</subscript>), has been determined from synchrotron data. The asymmetric unit contains one Cr<superscript>III</superscript> complex cation and half a [Cr<subscript>2</subscript>O<subscript>7</subscript>]<superscript>2-</superscript> anion. In the complex cation, the Cr<superscript>III</superscript> ion is coordinated by the four N atoms of two propane-1,3-diamine (tn) ligands in the equatorial plane and by two Cl atoms in a trans configuration, displaying a distorted octahedral coordination sphere. The two six-membered rings in the complex cation have an anti chair-chair conformation with respect to each other. The mean Cr-N(tn) and Cr-Cl bond lengths are 2.09 (1) and 2.320 (2) Å, respectively. The slightly bent dichromate anion is disordered over two sets of sites (occupancy ratio = 0.7:0.3) and has a staggered conformation. The crystal structure is stabilized by intermolecular hydrogen bonds involving the NH<subscript>2</subscript> groups of the tn ligands as donors and the O atoms of the [Cr<subscript>2</subscript>O<subscript>7</subscript>]<superscript>2-</superscript> anion and chlorido ligands as acceptors. [ABSTRACT FROM AUTHOR]

Subjects

Subjects :
CRYSTAL structure
PROPANE
CHROMIUM

Details

Language :
English
ISSN :
20569890
Volume :
72
Issue :
9
Database :
Complementary Index
Journal :
Acta Crystallographica Section E: Crystallographic Communications
Publication Type :
Academic Journal
Accession number :
119727499
Full Text :
https://doi.org/10.1107/S2056989016012755