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 |
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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. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/c8dt01370e |