| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5225488 | Tetrahedron | 2008 | 11 Pages |
Abstract
Three new lacunar-type derivatives of β-unsubstituted dibenzotetraaza[14]annulene have been synthesized along with a range of their open-chain pendant group containing counterparts. The crystal structures of two representative products have been determined and the noncovalent interactions explored. A number of C–H⋯π and π⋯π interactions involving aliphatic chains and aromatic regions of the macrocycle have been evidenced. The relative ease and high yield of lacunization are suggested to be largely due to self-assembly processes, driven by favorable noncovalent interactions between reacting units.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
![First Page Preview: New lacunar-type and pendant groups containing derivatives of β-unsubstituted dibenzotetraaza[14]annulenes—syntheses and crystal structures New lacunar-type and pendant groups containing derivatives of β-unsubstituted dibenzotetraaza[14]annulenes—syntheses and crystal structures](/preview/png/5225488.png)