Abstract

Three simple colorimetric anion sensors ( 1, 2, and 3) containing anthrone, 1,3-indanedione, and malononitrile as signaling chromophores and an indole binding site have been designed and synthesized. The introduction of electron-withdrawing groups can not only provide chromogenic signal output, but also tune the sensitivity and selectivity of indole-based anion sensors by electron push–pull features. Their anion binding and sensing properties were investigated in detail by dramatic color changes, UV–vis absorption, and 1H NMR. As results revealed, sensor 1 showed high selectivity for F − over AcO − and H 2PO 4 − with a distinct change in color due to the deprotonation of indole NH group. The excellent selectivity of 1 for F − can be attributed to the fitness in the acidity of its NH-group, which is tuned to be able to distinguish the subtle difference in the affinity of F −, AcO −, and H 2PO 4 − to NH proton.

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