Ludwig Ralf
Universität Rostock, Institut für Chemie, Abteilung für Physikalische Chemie, Dr.-Lorenz-Weg 1, 18059 Rostock, Germany.
Phys Chem Chem Phys. 2015 Jun 7;17(21):13790-3. doi: 10.1039/c5cp00885a. Epub 2015 Apr 10.
We could show by means of dispersion-corrected DFT calculations that the interaction energy in protic ionic liquids can be dissected into Coulomb interaction, hydrogen bonding and dispersion interaction. The H-bond energy as well as the dispersion energy can be quantified to be 50 kJ mol(-1) each representing ten percent of the overall interaction energy. The dispersion interaction could be dissected into two portions. One third could be related to the dispersion interaction within an ion-pair enhancing the H-bond strength, two thirds stem from dispersion interaction between the ion-pairs. This distribution of dispersion interaction is reflected in the far infrared (FIR) spectra. The H-bond band is shifted weaker than the low frequency band where the latter indicates diffuse cation-anion interaction and H-bond bending motions. Finally, we can dissect the different types of interaction energies indicating their characteristic influence on vibrational modes in the FIR.
我们可以通过色散校正的密度泛函理论(DFT)计算表明,质子离子液体中的相互作用能可分解为库仑相互作用、氢键作用和色散相互作用。氢键能和色散能均可量化为50 kJ·mol⁻¹,各自占总相互作用能的10%。色散相互作用可分解为两部分。三分之一与离子对内部的色散相互作用有关,增强了氢键强度;三分之二则源于离子对之间的色散相互作用。这种色散相互作用的分布反映在远红外(FIR)光谱中。氢键带的位移比低频带弱,后者表明弥散的阳离子 - 阴离子相互作用和氢键弯曲运动。最后,我们可以剖析不同类型的相互作用能,表明它们对FIR中振动模式的特征影响。