An adsorbent with multiple interaction sites for the adsorption of nitrogen-containing compounds (NCCs) has been realized in a silver ion functionalized Cr3+ based metal-organic framework (Cr)-MIL-101-SO3Ag. The adsorptive denitrogenation performance of (Cr)-MIL-101-SO3Ag was evaluated in a batch adsorption system in terms of both its adsorption capacity and selectivity, of which, quinoline and indole were selected as representative organonitrogen contaminants in liquid fuels. (Cr)-MIL-101-SO3Ag could interact with NCCs through multiple ways simultaneously, which exhibited about 50% higher adsorption capacity compared to (Cr)-MIL-101-SO3H, and a still high level of adsorption amount could be remained even in a model fuel where toluene (15% v) was added as a co-solvent and benzothiophene (BT) was added as a competitive adsorbate. The highly efficient and selective denitrogenation performance, we speculated was a combined results of these multiple interaction sites. The immobilized Ag(I) sites could strongly interact with NCCs through pi-complexation, which was thought to be responsible for its high adsorption capacity, meanwhile, the hard lewis acid site (Cr3+), which could preferentially interact with the hard nitrogen bases and the acid-base interaction between nitrogen bases and remaining -SO3H groups endowed (Cr)-MIL-101-SO3Ag with high selectivity over BT and other aromatic compounds. Futhermore, the enhanced interaction of (Cr)-MIL-101-SO3Ag with NCCs was also confirmed from the IR spectra with the significantly enhanced absorbance peak at 806 or 745 cm(-1) observed for QUI and IND, respectively when compared to BT. After five successive adsorption-desorption cycles, the adsorption capacity of (Cr)-MIL-101-SO3Ag was almost unchanged, and the structural stability was well maintained, making it a potential adsorbent for deep denitrogenation of liquid fuels. (C) 2018 Elsevier Inc. All rights reserved.