Abstract
A halogen-bonded eight-fold interpenetrated diamondoid net was constructed employing a node generated in the solid state. Specifically, co-crystallization of a tetrahedral-like tecton, rctt-tetrakis(4-pyridyl)cyclobutane (4,4′-TPCB), combined with a rigid halogen-bond donor, 1,4-diiodoperchlorobenzene, achieved a diamondoid architecture. In the co-crystal, 4,4′-TPCB is found to form three types of linkages based on one cis- and two trans-orientations enabled by the intrinsic rctt-stereochemisty of the central cyclobutane ring. Thus, 4,4′-TPCB is able to adapt to the constraints of the diamondoid net owing to the flexibility of the pendant 4-pyridyl groups.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 4349-4352 |
| Number of pages | 4 |
| Journal | CrystEngComm |
| Volume | 22 |
| Issue number | 26 |
| DOIs | |
| State | Published - Jul 14 2020 |
All Science Journal Classification (ASJC) codes
- General Chemistry
- General Materials Science
- Condensed Matter Physics
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