The present work is aimed to investigate the catalytic activities of various Mn-based MOFs for carbon dioxide coupling with epoxides. The metal organic frameworks, [(CH3NH3][Mn(COOH)(3)] (MA-MnF), [(CH3CH2NH3][Mn(COOH)(3)] (EA-MnF), and [C3H5N2][Mn(COOH)(3)] (Im-MnF) were studied via several characterizations such as XRD, FT-IR, XPS, N-2-adsorption, TG-DSC, CO2 -adsorption and NH3-TPD. Interestingly, Im-MnF compound was observed to possess the highest catalytic activity among the studied compounds, which is associated not only with the amounts of basic sites, but also related to the nitrogen-containing species. 97.27% conversion of allyl-glycidyl ether (AGE, TOF: 36.78 h(-1)) and 97.66% selectivity to allyl-glycidyl carbonate (AGC) were obtained under the explored optimized conditions (100 degrees C, 15 bar, 6 h, 1.0 wt% of AGE). In addition, only a slight downward in catalytic activity was found when the sample was reused twice. Furthermore, coupling reactions of CO2 with various epoxides were also performed, of which, the yield of the cyclic carbonates followed the order: Epichlorohydrin > Allyl glycidyl ether > Styrene oxide > Cyclohexene oxide > Propylene oxide. Finally, a mechanism was proposed, which is in good agreement with the DFT calculation. (C) 2019 Elsevier Ltd. All rights reserved.