Complexation dynamics of CH3SCN and Li(+) in acetonitrile studied by two-dimensional infrared spectroscopy.

Ion-molecule complexation dynamics were studied with CH3SCN and Li(+) in acetonitrile by vibrationally probing the nitrile stretching vibration of CH3SCN. The nitrile stretching vibration of CH3SCN has a long lifetime (T1 = ∼90 ps) and its frequency is significantly blue-shifted when CH3SCN is bound with Li(+) ions to form a CH3SCNLi(+) complex in acetonitrile. Such spectral properties enable us to distinguish free CH3SCN and the CH3SCNLi(+) complex in solutions and measure their dynamics occurring on hundred picosecond timescales. For the complexation between CH3SCN and Li(+) in acetonitrile, the change in enthalpy (ΔH = -7.17 kJ mol(-1)) and the change in entropy (ΔS = -34.4 J K(-1) mol(-1)) were determined by temperature-dependent FTIR experiments. Polarization-controlled infrared pump-probe (IR PP) spectroscopy was used to measure the population decay and orientational dynamics of free CH3SCN and the CH3SCNLi(+) complex. Especially, the orientational relaxation of the CH3SCNLi(+) complex was found to be almost 3 times slower than those of free CH3SCN because Li(+) ions strongly interact with the neighboring solvents. Most importantly, the complexation dynamics of CH3SCN and Li(+) in acetonitrile were successfully measured in real time by 2DIR spectroscopy for the first time and the dissociation and association time constants were directly determined by using the two-species exchange kinetic model. Our experimental results provide a comprehensive overview of the ion-molecule complexation dynamics in solutions occurring under thermal equilibrium conditions.