Anion Recognition Based on a Combination of Double-Dentate Hydrogen Bond and Double-Side Anion-π Noncovalent Interactions.

Anion recognitions between common anions and a novel pincer-like receptor (N,N'-bis(5-fluorobenzoyloxyethyl)urea, BFUR) were theoretically explored, particularly on geometric features of the BFUR@X (X = F- , Cl- , Br- , I- , CO3 2- , NO3 - , and SO4 2- ) systems at a molecular level in this work. Complex structures show that two N-H groups as a claw and two -C6 F5 rings on BFUR as a pair of tweezers simultaneously interact with captured anions through cooperative double-dentate hydrogen bond and double-side anion-π interactions. The binding energies and thermodynamic information indicate that the recognitions of the seven anions by BFUR in vacuum are enthalpy-driven and entropy-opposed, which occur spontaneously. Although the binding energy ΔEcp between F- and BFUR is relatively high (289.30 kJ·mol-1 ), ΔEcp , ΔG, and ΔH of the recognition for CO3 2- and SO4 2- are much larger than the cases of F- , Cl- , Br- , I- , and NO3 - , suggesting that BFUR is an ideal selective anion receptor for CO3 2- and SO4 2- . Additionally, energy decomposition analysis based on localized molecular orbital energy decomposition analysis (LMO-EDA) was performed; electronic properties and behaviors of the present systems were further discussed according to calculations on frontier molecular orbital, UV-vis spectra, total electrostatic potential, and visualized weak interaction regions. The present theoretical exploration of BFUR@X (X = F- , Cl- , Br- , I- , CO3 2- , NO3 - , and SO4 2- ) systems is fundamentally crucial to establish an anion recognition structure-property relationship upon combination of different noncovalent interactions, that is, double-dentate hydrogen bond and double-side anion-π interactions.