The title complex, ([Fe(C(4)H(4)O(4))(H(2)O)(4)])(n), is an infinite polymeric compound bridged by the succinate dianion. Two carboxylate groups coordinate in a monodentate manner to the Fe(II) atom, in a trans fashion, with an O-Fe-O bond angle of 175.72 (6) degrees and Fe-O distances of 2.0886 (14) and 2.1008 (15) A. One of the uncoordinated carboxylate O atom forms an intramolecular hydrogen bond with a coordinated water molecule. Extensive hydrogen bonding between parallel polymeric complex chains results in a three-dimensional supramolecular structure.
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http://dx.doi.org/10.1107/s0108270102020693 | DOI Listing |
Acta Crystallogr E Crystallogr Commun
December 2017
Department of Chemistry, Taras Shevchenko National University of Kyiv, Volodymyrska St. 64, Kyiv 01601, Ukraine.
In the title polymeric complex, {[Fe(CHN)(HO)](CHCHSO)·2CHOH} , the Fe cation, located on an inversion centre, is coordinated by four water mol-ecules in the equatorial positions and two 1,2-bis-(pyridin-4-yl)ethene mol-ecules in the axial positions. This results in a distorted octa-hedral geometry for the [NO] coordination polyhedron. The 1,2-bis-(pyridin-4-yl)ethene mol-ecules bridge the Fe cations, forming polymeric chains running along the axis direction.
View Article and Find Full Text PDFActa Crystallogr Sect E Struct Rep Online
October 2010
In the title compound, {[Fe(C(2)N(10))(H(2)O)(4)]·2H(2)O}(n), the coordin-ation geometry around the Fe(II) atom, which lies on a center of inversion, is distorted octa-hedral, with bonds to four O atoms and two N atoms. The azotetra-zolate ligand displays a bridging coordination mode, forming an infinite zigzag chain. Inter-molecular O-H⋯O and O-H⋯N hydrogen bonding and offset face-to-face π-π stacking inter-actions [centroid-centroid distance = 3.
View Article and Find Full Text PDFActa Crystallogr Sect E Struct Rep Online
January 2008
Department of Chemistry, Shangqiu Normal College, 476000 Shangqiu, Henan, People's Republic of China.
In the crystal structure of the title compound, {[Fe(2)(C(7)H(3)NO(4))(2)(H(2)O)(6)]·4H(2)O}(n), there are two types of coordination for the Fe(II) atoms. One Fe(II) atom is in a distorted octa-hedral N(2)O(4) environment, with two chelating rings from the pyridine-dicarboxyl-ate ligands and two O atoms from the water mol-ecules, while the other is in a distorted octa-hedral O(6) environment with two O atoms from the pyridine-dicarboxyl-ate ligands and four O atoms from the water mol-ecules. Both Fe(II) atoms lie on crystallographic centers of symmetry.
View Article and Find Full Text PDFActa Crystallogr C
December 2002
Department of Chemistry, Zhejiang University, Hangzhou Zhejiang, People's Republic of China.
The title complex, ([Fe(C(4)H(4)O(4))(H(2)O)(4)])(n), is an infinite polymeric compound bridged by the succinate dianion. Two carboxylate groups coordinate in a monodentate manner to the Fe(II) atom, in a trans fashion, with an O-Fe-O bond angle of 175.72 (6) degrees and Fe-O distances of 2.
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