On the weakly C–H⋯π hydrogen bonded complexes of sevoflurane and benzene
Dom, Johan J. J. ; van der Veken, Benjamin J. ; Michielsen, Bart ; Jacobs, Sam ; Xue, Zhifeng ; Hesse, Susanne ; Loritz, Hans-Martin ; Suhm, Martin A. et al.
Zitierfähiger Link (URL): http://resolver.sub.uni-goettingen.de/purl?gs-1/8712
A vibrational assignment of the anaesthetic sevoflurane, (CF3)2CHOCH2F, is proposed and its interaction with the aromatic model compound benzene is studied using vibrational spectroscopy of supersonic jet expansions and of cryosolutions in liquid xenon. Ab initio calculations, at the MP2/cc-pVDZ and MP2/aug-cc-pVDZ levels, predict two isomers for the 1 : 1 complex, one in which the near-cis, gauche conformer of sevoflurane is hydrogen bonded through its isopropylhydrogen atom, the other in which the same conformer is bonded through a bifurcated hydrogen bond with the fluoromethyl hydrogen atoms. From the experiments it is shown that the two isomers are formed, however with a strong population dominance of the isopropyl-bonded species, both in the jet and liquid phase spectra. The experimental complexation enthalpy in liquid xenon, DHo(LXe), of this species equals 10.9(2) kJ mol 1, as derived from the temperature dependent behaviour of the cryosolution spectra. Theoretical complexation enthalpies in liquid xenon were obtained by combining the complete basis set extrapolated complexation energies at the MP2/aug-cc-pVXZ (X = D,T) level with corrections derived from statistical thermodynamics and Monte Carlo Free Energy Perturbation calculations, resulting in a complexation enthalpy of 11.2(3) kJ mol 1 for the isopropyl-bonded complex, in very good agreement with the experimental value, and of 11.4(4) kJ mol 1, for the fluoromethyl-bonded complex. The Monte Carlo calculations show that the solvation entropy of the isopropyl-bonded species is considerably higher than that of the fluoromethyl-bonded complex, which assists in explaining its dominance in the liquid phase spectra.
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