Abstract

Anion recognition is widely used in several biological fields. Squaramide derived compounds appear as potential structures to recognize anions. Here, the bond mechanisms between the chloride (Cl-), bromide (Br-) and nitrate (NO3-) anions and anthracene-squaramide conjugated compounds are elucidated considering the influence of the: (i) number, (ii) nature, and (iii) position of the substituents: trifluoromethyl (-CF3) and nitro (-NO2). Energy decomposition analysis (EDA) shows that the interactions between Cl-, Br- and NO3- and anthracene-squaramide have an attractive interaction energy supported predominantly by electrostatic energy followed by orbital contribution. Molecular electrostatic potential (MEP) surfaces imply electrostatic interactions between Cl-, Br- and the oxygen atom from NO3- and the hydrogen atoms from N-H and C-H bonds present in the squaramide structure, and an aryl group, respectively. Cl- interacts with the receptors more strongly than Br-. The NO3- recognition is less attractive than those presented by Cl- and Br-, in agreement with the hardness-softness features of these anions. Importantly, one and, mostly, two group substitutions,-H →-CF3 or-NO2, favor the recognition of Cl-, Br- and NO3- due to the increase of the polarization in the receptor-NH⋯anion interaction. The-NO2 group promotes a larger effect relative to the-CF3 ligand. The-NO2 ligand positioned at the largest distance conceivable to the benzene-NH group promotes the lowest interference in the N-H⋯Cl- interaction. These results provide information to design receptors with a larger capability to recognize anions. This journal is