Air and moisture stable covalently-bonded tin() coordination polymers

Four covalently-bonded tin( ii ) coordination polymers, (1)-(4) , were hydrothermally prepared in aqueous alkaline media by the reactions of SnSO 4 with 1,2,4,5-benzenetetracarboxylic acid (1) , 1,3,5-benzenetricarboxylic acid (2) , 4-hydroxypyridine-2,6-dicarboxylic acid (3) , and 1,3,5-cyclohexane...

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Veröffentlicht in:Dalton transactions : an international journal of inorganic chemistry 2018, Vol.47 (24), p.813-822
Hauptverfasser: de Lima, G. M, Walton, R. I, Clarkson, G. J, Bitzer, R. S, Ardisson, J. D
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Sprache:eng
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Zusammenfassung:Four covalently-bonded tin( ii ) coordination polymers, (1)-(4) , were hydrothermally prepared in aqueous alkaline media by the reactions of SnSO 4 with 1,2,4,5-benzenetetracarboxylic acid (1) , 1,3,5-benzenetricarboxylic acid (2) , 4-hydroxypyridine-2,6-dicarboxylic acid (3) , and 1,3,5-cyclohexanetricarboxylic acid (4) . All products were structurally authenticated by single-crystal X-ray diffraction, and the number of different tin centres and their oxidation states were confirmed by 119 Sn Mössbauer spectroscopy. In addition, the comparison between experimental and simulated X-ray powder diffraction patterns confirmed the authenticity of the samples. Our crystallographic results for (1)-(4) show that the Sn( ii ) centres are tetracoordinated and exhibit distorted disphenoidal geometries, corroborating the presence of one stereochemically active lone electron pair at each metal site. Products (1) and (2) display bi-dimensional polymeric structures, (3) exhibits a one-dimensional architecture, whereas (4) shows a remarkable three-dimensional coordination network. Hirshfeld surface and supramolecular analyses for the repeating units of (1)-(4) were also performed in order to identify structurally important non-covalent interactions. Compounds (1)-(4) display 1D, 2D or 3D coordination networks, in which the Sn( ii ) cations exhibit distorted disphenoidal geometries due to the stereochemically active electron lone pairs.
ISSN:1477-9226
1477-9234
DOI:10.1039/c8dt01370e