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Crystal structure of poly[[di-aqua-tetra-μ 2 -cyanido-platinum(II)iron(II)] methanol 4/3-solvate]: a three-dimensional Hofmann clathrate analogue.

Authors :
Hiiuk VM
Mykhailovych V
Shova S
Golenya IA
Gural'skiy IA
Source :
Acta crystallographica. Section E, Crystallographic communications [Acta Crystallogr E Crystallogr Commun] 2022 Jan 25; Vol. 78 (Pt 2), pp. 216-219. Date of Electronic Publication: 2022 Jan 25 (Print Publication: 2022).
Publication Year :
2022

Abstract

In the title polymeric coordination compound, {[FePt(CN) <subscript>4</subscript> (H <subscript>2</subscript> O) <subscript>2</subscript> ]·1.33CH <subscript>3</subscript> OH} <subscript> n </subscript> , the Fe <superscript>II</superscript> cation (site symmetry 4/ mm.m ) is coordinated by the N atoms of four cyanide anions (CN <superscript>-</superscript> ) and the O atoms of two water mol-ecules, forming a nearly regular [FeN <subscript>4</subscript> O <subscript>2</subscript> ] octa-hedron. According the Fe-N and Fe-O bond lengths, the Fe <superscript>II</superscript> atom is in the high-spin state. The cyanide anions act in a bridging manner to connect the Fe <superscript>II</superscript> and Pt <superscript>II</superscript> atoms. The [Pt(CN) <subscript>4</subscript> ] <superscript>2-</superscript> moieties (Pt with site symmetry 4/ mm.m ) have a perfect square-planar shape. The latter anion is located perpendicular to the FeN <subscript>4</subscript> plane, thus ensuring the creation of a three-dimensional framework. The crystal structure features methanol solvent mol-ecules of which 4/3 were located per Fe <superscript>II</superscript> cation. These solvent mol-ecules are located in hexa-gonal pores; they inter-act with coordinating water mol-ecules through weak hydrogen bonds. Other guest mol-ecules could not be modelled in a satisfactory way and their contribution to the scattering was removed by a mask procedure.<br /> (© Hiiuk et al. 2022.)

Details

Language :
English
ISSN :
2056-9890
Volume :
78
Issue :
Pt 2
Database :
MEDLINE
Journal :
Acta crystallographica. Section E, Crystallographic communications
Publication Type :
Academic Journal
Accession number :
35145754
Full Text :
https://doi.org/10.1107/S2056989022000573