ABSTRACT
The fine and dynamic structure of the copper(II) ion solvated in a protic ionic liquid (PIL) comprising monoprotonated N-hexylethylenediaminium (HHexen(+)) and bis(trifluoromethanesulfonyl)amide (Tf2N(-)) [or trifluoroacetate (TFA(-))] was determined using NMR, visible electronic, and extended X-ray absorption fine structure (EXAFS) spectroscopy. The chelate-diamine group in the cationic unit facilitates advantageous dissolution of transition-metal salts in the present PIL. The interaction of the copper(II) ion with the chelate-diamine PIL was explored by the addition of copper(II) salts to the PIL, demonstrating competitive complexation between the ligand of the added copper(II) salt and the components of the ionic liquid to the copper(II) ion. The favorable mode of interaction of the present chelating PIL with the copper(II) ion was clarified based on a comparison of the interactions with analogous liquids, including the monoprotonated hexylaminium HHexam(Tf2N)-PIL, neat N-hexylethylenediamine (Hexen), and neat ethylenediamine (En). The coordination modes of the bis-Hexen and tris-Hexen copper(II) complexes in molecular liquids and in solids were also studied for comparison of the coordination structures around the copper(II) ion with those in the present PILs. The paramagnetic-induced relaxations derived from (13)C (ΔT(1p)(-1)) and (15)N (ΔT(2p)(-1)) NMR, the visible electronic spectra, and EXAFS analysis showed that the copper(II) ion tends to form a bis-Hexen complex in the HHexen-PIL despite the electrostatic repulsion and the fact that the counteranions are located at the axial sites, whereas in the HHexam(Tf2N)-PIL, the copper(II) ion exhibits affinity for the Tf2N anion over the protonated amines. The lifetime of the copper(II) complex formed in the PIL was determined to be ≈10(-4) s based on (13)C (ΔT(1p)(-1)) and (14)N (ΔT(2p)(-1)) NMR, which is appreciably longer than that in conventional molecular solvents.
