Abstract
MX ⋯HN+ hydrogen bond synthons have been exploited in preparation of crystalline salts [4,4'-H2bipy][MX4] [X = Cl, M = Pd, Pt, Co, Zn, Hg, Mn, Cd and Pb; X = Br, M = Pd, Co, Zn and Mn]. In these salts three structural forms for the halometallate species are observed: mononuclear square planar (M = Pd, Pt) or tetrahedral (M = Co, Zn, Hg) and polymeric cis edge-sharing octahedral (M = Mn, Cd, Pb). These correspond to three structural motifs which form the basis of the crystal structures formed in their [4,4'-H2bipy]J+ salts: ribbon polymer (M = Pt, Pd); herring-bone packing of cyclic dimers (M = Co, Zn, Hg); layer cross-linked polymers [{MX,},]2"" (M = Mn, Cd, Pb). The factors controlling the structures adopted, the hierarchy of intermolecular interactions present in these crystals and the principles that may be inferred and exploited further are considered. © The Royal Society of Chemistry 2000.
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CITATION STYLE
Gillon, A. L., Lewis, G. R., Guy Orpen, A., Rotter, S., Starbuck, J., Wang, X. M., … Ruiz-Pérez, C. (2000). Organic-inorganic hybrid solids: Control of perhalometallate solid state structures t. Journal of the Chemical Society, Dalton Transactions, (21), 3897–3905. https://doi.org/10.1039/b005036i
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