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Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
Published on: February 15, 2016
Two packing motifs based upon chains of edge-sharing PbI6 octahedra
Andreas Lemmerer1, David G Billing
1Molecular Sciences Institute, School of Chemistry, University of the Witwatersrand, Private Bag 3, PO Wits 2050, South Africa. andy@hobbes.gh.wits.ac.za
Abstract:
The compounds catena-poly[p-phenylenediammonium [[diiodolead(II)]-di-mu-iodo] dihydrate], {(C6H10N2)[PbI4].2H2O}n, (I), and catena-poly[bis(3,5-dimethylanilinium) [[diiodolead(II)]-di-mu-iodo]], {(C8H12N)2[PbI4]}n, (II), crystallize as organic-inorganic hybrids. As such, the structures consist of chains of [PbI2]- units extending along the c axis in (I) and along the b axis in (II). The asymmetric unit in (I) contains one Pb atom on a site of 2/m symmetry, two I atoms and a water molecule on mirror planes, and a p-phenylenediammonium molecule that sits around a site of 2/m symmetry with the C and N atoms on a mirror plane. In (II), the Pb atom is on a twofold axis and the two I atoms are on general positions. Each Pb atom is octahedrally coordinated to six I atoms, arranged as chains of edge-sharing octahedra. Both compounds undergo hydrogen-bonding interactions between the ammonium groups and the I atoms. In addition, there are hydrogen bonds between the water molecules and the ammonium groups and halides in (I), and between the ammonium groups and the ring systems in (II).
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