Raman and DFT Study on N-H+…Cl- Hydrogen Bonding in 1,1,3,3-Tetra-Methylguanidinium Chloride forming an Ion-pair Molecule in the Vapor Phase
Publication: Research - peer-review › Poster – Annual report year: 2009
The chemistry of 1,1,3,3-tetramethylguanidinium ([TMGH]+) chloride, a low temperature (molten) ionic liquid, is discussed, based on its Raman spectra associated with ab initio molecular orbital DFT-type quantum mechanical calculations (with 6-311+G(d,p) basis sets) on “molecules” in isolated gaseous free states without any assumed symmetry. The calculations on the monomeric [TMGH]+ ion and the dimeric ion pair converged to give geometries near the established crystal structure of the [TMGH]Cl salt. This salt is known to contain dimeric ion pairs of the kind [TMGH]ClCl[TMGH](Fig.1).Experimentally obtained Raman scattering spectra of the compound (as the solid, as solutes in ethanolic and aqueous solutions and as a vapor at 225 ºC) are presented and assigned, by comparing to the ab initio vibrational analyses (calculated IR and Raman band positions and intensities). It is concluded that dimeric molecular ion pairs with four N-H+…Cl- hydrogen bonds seem to exist also in the solutions, and probably are responsible for the relatively high solubility of the “salt” in ethanol. The “salt” can be easily sublimed at about 200-230 oC. The Raman spectrum of the vapor at 225 ºC has a characteristic strong band at 2229 cm-1 that shows that the gas phase consists of monomeric ion pair “molecules” (Fig.2) held together by one N-H+…Cl- hydrogen bond, the stretching band of which is causing the band (Fig.3).
|Conference||Conference on Molten Salts and Ionic Liquids|
|Period||24/08/08 → 29/08/08|
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