A Naphthalene Diimide Based Macrocycle Containing Quaternary Ammonium Groups: An Electron-Deficient Host for Aromatic Carboxylate Derivatives.

Naphthalene diimide (NDI) compounds are widely used as electron acceptors in various applications. Herein, we combine NDI with quaternary ammonium groups for the synthesis of a highly electron-deficient linear compound 2 and macrocycle 3. The complexation studies of the water-soluble macrocycle 3 with aromatic di- and tetra- carboxylate anions in water were done using absorption, emission, 1 H NMR and NOESY spectroscopic titrations. The NDI incorporated macrocycle 3 showed high binding affinities towards linear aromatic tetracarboxylate anions owing to the size and charge complementarity of the host-guest complex. Macrocycle 3 binds tetracarboxylate anion much better than dicarboxylate anions. Furthermore, the macrocycle 3 is solvated differently in acetonitrile and in water or dimethyl sulfoxide, which induces changes in conformation and photophysical properties. Such electron-deficient optically active macrocycles are useful for developing useful sensor materials.