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Rigid tetraarylene-bridged cavitands from reduced-symmetry resorcin[4]arene derivatives.

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Container molecules (cavitands) derived from resorcin[4]arene are of broad interest in supramolecular chemistry as hosts and fragments of larger constructs. Herein is presented a new class of rigid cavitand where… Click to show full abstract

Container molecules (cavitands) derived from resorcin[4]arene are of broad interest in supramolecular chemistry as hosts and fragments of larger constructs. Herein is presented a new class of rigid cavitand where the resorcin[4]arene carbon framework is extended with four bridging arylene rings. Two tenable, isomeric precursors of differing symmetry (C2v and C4) were prepared, of which only one afforded the desired fused bowl. X-ray crystallographic studies provide conformational insight, and show that the cavitand can bind small molecules in the solid state.

Keywords: resorcin arene; rigid tetraarylene; arene; symmetry; tetraarylene bridged

Journal Title: Chemical communications
Year Published: 2018

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