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Chirality Generation in Supramolecular Clusters: Analogues of Octacoordinated Polyhedrons
Metal-free supramolecular clusters, comprising organic salts of triphenylacetic acid and primary amines, were characterized for the first time as the analogues of octacoordinated polyhedrons with a novel supramolecular chirality in the crystalline state. A ternary system yields triangular dodecahedr...
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Published in: | Crystal growth & design 2015-02, Vol.15 (2), p.658-665 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Metal-free supramolecular clusters, comprising organic salts of triphenylacetic acid and primary amines, were characterized for the first time as the analogues of octacoordinated polyhedrons with a novel supramolecular chirality in the crystalline state. A ternary system yields triangular dodecahedrons with chiral belts composed of four triphenylmethyl (trityl) groups involving right- or left-handed twist combinations (Δ:Λ = 4:0 or 0:4). The 12 benzene rings are divided into three layers along a 2-fold axis of symmetry, affording a structure that is similar to a censer (a traditional vessel for fragrance) comprising three parts: a head, body, and foot. A binary system with t-butylammonium or t-amylammonium provides different chiral triangular dodecahedrons, while the system with isobutylammonium provides a trans-bicapped octahedron with a 3-fold rotational axis of symmetry to yield a chiral belt of four trityl groups (Δ:Λ = 3:1 or 1:3). |
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ISSN: | 1528-7483 1528-7505 |
DOI: | 10.1021/cg5013445 |