Terminal Molecular Isomer-Effect on Supramolecular Self-Assembly System Based on Naphthalimide Derivative and Its Sensing Application for Mercury(II) and Iron(III) Ions.

A series of naphthalimide derivative gelators (G-o, G-m, and G-p) with three molecular isomers as their terminal groups were designed and synthesized. Only G-m and G-p could form stable organogels in some solvents including methanol, acetonitrile, n-hexane, toluene, ethanol, DMSO, DMF, and mixed solvents of acetonitrile/HO (1/1, v/v). The different self-assembly structures were obtained from the self-assembly process of G-o, G-m, and G-p such as structures like a Chinese chestnut formed by irregular micrometer pieces, microbelts, and microbelt structures mingled with the bird's nest structures which exhibited different surface hydrophobicity with water contact angles of 121-139° due to their different intermolecular noncovalent interactions. To our surprise, G-p acetonitrile solution emitted 492 nm light with a red-shift of 72 nm compared with that emitted from G-o and G-m acetonitrile solution under 350 nm light excitation. Three gelators showed different detection abilities toward metal ions. G-o did not have any ability for sensitive and selective detection toward any ion. In contrast, G-m and G-p could sensitively and selectively detect Hg and Fe. The detection limits for Fe and Hg by G-m were 4.76 × 10 M and 7.01 × 10 M with the corresponding association constants ( K) of 1.64 × 10 and 3.79 × 10 M, respectively. The detection limits for Fe and Hg by G-p were 3.26 × 10 and 1.77 × 10 M with the corresponding K of 1.44 × 10 and 1.99 × 10 M, respectively. More interestingly, the back-titration of SCN could distinguish Hg from Fe. At the same time, xerogels G-m and G-p also exhibited responsiveness toward Fe and Hg through fluorescence changes. The photophysical properties, gel formation, hierarchical structures, surface wettability, and their function in this self-assembly system could be tuned through the molecular isomer effect. This work provides a new research paradigm for molecular isomer tuned supramolecular self-assembly materials from noncovalent interaction to molecular function.