Abstract

The title compound, {(C8H20N2)[PbCl4]}n, crystallizes as an layered inorganic–organic hybrid perovskite-type structure. Corner-sharing PbCl6 octa­hedra extend parallel to the ac plane. Adjacent layers are staggered relative to one another, with diammonium cations separating these layers. The cations exhibit symmetry and inter­act with the inorganic sheets via N—H⋯Cl hydrogen bonding in the right-angled halogen sub-type of the terminal halide hydrogen-bonding motif.

Highlights

  • Molecular Sciences Institute, School of Chemistry, University of the Witwatersrand, Private Bag 3, PO Wits 2050, South Africa

  • Similar structures have been reported by Billing & Lemmerer

  • Structure–properties relation experiments have been performed by Mitzi et al

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Summary

Matthew Kyle Rayner and David Gordon Billing*

Molecular Sciences Institute, School of Chemistry, University of the Witwatersrand, Private Bag 3, PO Wits 2050, South Africa. Symmetry codes: (i) x 12; y; z þ 32; (ii) x; y þ 32; z; (iii) x þ 12; y; z þ 52. R factor = 0.031; wR factor = 0.067; data-to-parameter ratio = 25.3. The title compound, {(C8H20N2)[PbCl4]}n, crystallizes as an layered inorganic–organic hybrid perovskite-type structure. Corner-sharing PbCl6 octahedra extend parallel to the ac plane. Adjacent layers are staggered relative to one another, with diammonium cations separating these layers. The cations exhibit 1 symmetry and interact with the inorganic sheets via. N—H Cl hydrogen bonding in the right-angled halogen subtype of the terminal halide hydrogen-bonding motif

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Mo K radiation
Matthew Kyle Rayner and David Gordon Billing
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