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Bis(1-phenylethylammonium) hexachloridostannate(IV) and bis(2-phenylethylammonium) hexachloridostannate(IV).
David G Billing1, Andreas Lemmerer, Melanie Rademeyer
1Molecular Sciences Institute, School of Chemistry, University of the Witwatersrand, Private Bag 3, PO Wits 2050, South Africa.
Crystal structures of two phenylethylammonium hexachloridostannate(IV) isomers reveal alternating organic-inorganic layers. These layers interact through N-H...Cl hydrogen bonding, forming a 2D sheet in the inorganic layer.
Area of Science:
- Crystal engineering
- Coordination chemistry
- Supramolecular chemistry
Background:
- Hexachloridostannate(IV) compounds are known for their diverse structural motifs.
- Organic ammonium cations can influence the assembly of inorganic anions in crystal structures.
- Hydrogen bonding plays a crucial role in directing the formation of extended networks.
Purpose of the Study:
- To elucidate the crystal structures of bis(1-phenylethylammonium) hexachloridostannate(IV) and bis(2-phenylethylammonium) hexachloridostannate(IV).
- To investigate the role of N-H...Cl hydrogen bonding in the assembly of these compounds.
- To characterize the layered structures formed by the organic and inorganic components.
Main Methods:
- Single-crystal X-ray diffraction analysis.
- Structural comparison of the two isomers.
- Analysis of hydrogen bonding interactions.
Main Results:
- Both compounds, (C(8)H(12)N)(2)[SnCl(6)], exhibit alternating layers of organic cations and inorganic [SnCl(6)](2-) anions.
- An extended two-dimensional hydrogen-bonded sheet is present within the inorganic layer.
- N-H...Cl hydrogen bonds mediate the interactions between the organic and inorganic layers.
- The tin atom in the 1-phenylethylammonium salt is located on an inversion center.
Conclusions:
- The crystal structures demonstrate a clear layered arrangement driven by hydrogen bonding.
- The phenylethylammonium cation isomers dictate specific packing arrangements and hydrogen bonding networks.
- These findings contribute to understanding the structure-property relationships in metal-organic hybrid materials.
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