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.
All Science Journal Classification (ASJC) codes
- Materials Science(all)
- Condensed Matter Physics