Electronic interactions between polycyclic arenes in cyclophanes

Abstract

The π-π interaction between polycyclic arenes and the effects of orientation were studied in [2.2]-, [3.3]-, and [3.2]naphthalenophanes, [2]naphthaleno[2]paracyclophanes, and syn- and anti[2.2](2,7)fluorenophane by electron absorption and emission spectroscopy as well as by optically detected magnetic resonance (ODMR) of the excited triplet state. The π-π interaction in the excited singlet and triplet state was found to be highest if a maximal number of sixmembered rings of the interacting arenes in a parallel orientation are completely eclipsed. Similarly, the π-π interaction between the nonbonding nitrogen electron pair and the aromatic π electrons was investigated in isomeric etheno-bridged naphthalenopyridinophanes and an anthracenopyridinophane; in these pyridinophanes, the pyridine rings are fixed perpendicularly above different sites of the naphthalene and anthracene units, respectively.