CO2 in 1-Butyl-3-methylimidazolium Acetate. 2. NMR Investigation of Chemical Reactions

MARCEL BESNARD; ISABEL CABAÇO; FABIÁN VACA CHÁVEZ; NOËL PINAUD; PEDRO J. SEBASTIÃO; JOÃO A. P. COUTINHO; JOËLLE MASCETTI; YANN DANTEN

JOURNAL OF PHYSICAL CHEMISTRY A

AMER CHEMICAL SOC

Lugar: Washington; Año: 2012 vol. 116 p. 4890 - 4901

1089-5639

The solvation of CO2 in 1-butyl-3-methylimidazolium acetate (Bmim Ac) has been investigated by 1H, 13C, and 15N NMR spectroscopy at low CO2 molar fraction (mf) (xCO2 ca. 0.27) corresponding to the reactive regime described in part 1 of this study. It is shown that a carboxylation reaction occurs between CO2 and Bmim Ac, leading to the formation of a non-negligible amount (∼16%) of 1-butyl-3-methylimidazolium- 2-carboxylate. It is also found that acetic acid molecules are produced during this reaction and tend to form with elapsed time stable cyclic dimers existing in pure acid. A further series of experiments has been dedicated to characterize the influence of water traces on the carboxylation reaction. It is found that water, even at high ratio (0.15 mf), does not hamper the formation of the carboxylate species but lead to the formation of byproduct involving CO2. The evolution with temperature of the resonance lines associated with the products of the reactions confirms that they have a different origin. The main byproduct has been assigned to bicarbonate. All these results confirm the existence of a reactive regime in the CO2−Bmim Ac system but different from that reported in the literature on the formation of a reversible molecular complex possibly accompanied by a minor chemical reaction. Finally, the reactive scheme interpreting the carboxylation reaction and the formation of acetic acid proposed in the literature is discussed. We found that the triggering of the carboxylation reaction is necessarily connected with the introduction of carbon dioxide in the IL. We argue that a more refined scheme is still needed to understand in details the different steps of the chemical reaction in the dense phase.