Abstract
By a mild modified Eglinton coupling a series of diynebridged macrobicyclic hosts capable of endocavital complexation were synthesized and their structures and complexation properties investigated by X‐ray analysis. The inclusion of DMSO in 7 suggests a direct correlation between steric fit and orientation of the guest. On the basis of this hypothesis, the orientation of acetone in an endocavital inclusion of 2 was predicted and verified by X‐ray analysis. Comparison of the single‐crystal X‐ray structures of the vacant macrobicycle 3 and of a family of macrobicycles showing endocavital or “pocket” complexation of neutral organic guests suggests that torsion of the cavities upon complexation results from induced fit. Hydrogenation of the triple bonds leads to the more flexible macrobicycles 10–12 with collapsable cavities. The absorption and emission spectra of the diynebridged macrobicyclic hosts 1 and 3, of their hydrogenated analogues 11 and 12, and of a hemicage parent compound of 2 (14) were investigated. The macrobicyclic compounds 3, 11, 12 and 14 exhibit a strong fluorescence in CH~2~Cl~2~ solution at room temperature. The lack of fluorescence of 2 under such conditions is attributed to the presence of low‐energy charge‐transfer excited states, as indicated by the charge‐transfer bands in the absorption spectrum. In a rigid CH~2~Cl~2~ matrix at 77 K all the examined compounds are fluorescent.