Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5227022 | Tetrahedron | 2009 | 8 Pages |
A series of triangle-shaped polycyclic aromatics have been developed according to a facile synthetic protocol with high yields. As revealed by X-ray single crystal data, their molecular conformation and packing arrangement are significantly influenced by the electronic properties and steric bulk of peripheral subunits. The ‘saddle’-shaped hexahalotribenzocoronenes (ClTBC and FTBC) possess C2 symmetric structures and can self-assemble into well-defined columnar structures, dramatically different from hexabutyoxytribenzocoronene (TBC), which adopts a C3 symmetric ‘double-concave’ structure and less efficient packing arrangement. In the compound trithiophenocoronene (TTC), the five-membered corner rings produce a more open bay-region periphery alleviating intramolecular steric congestion. As a result, the molecule adopts an almost planar conformation.
Graphical abstract A series of triangle-shaped polycyclic aromatics have been developed. Their molecular conformation and packing arrangement are significantly dependent upon the electronic properties and steric bulk of peripheral subunits.Figure optionsDownload full-size imageDownload as PowerPoint slide