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Journal of molecular spectroscopy v.342, 2017년, pp.4 - 16   SCI SCIE
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Anharmonic, dynamic and functional level effects in far-infrared spectroscopy: Phenol derivatives

Bakker, Daniël J. (Radboud University, Institute for Molecules and Materials, FELIX Laboratory, Toernooiveld 7c, 6525 ED Nijmegen, The Netherlands ) ; Ong, Qin (Radboud University, Institute for Molecules and Materials, FELIX Laboratory, Toernooiveld 7c, 6525 ED Nijmegen, The Netherlands ) ; Dey, Arghya (Radboud University, Institute for Molecules and Materials, FELIX Laboratory, Toernooiveld 7c, 6525 ED Nijmegen, The Netherlands ) ; Mahé, Jérôme (LAMBE CNRS UMR8587, Université ) ; Gaigeot, Marie-Pierre (d'Evry val d'Essonne, Blvd F. Mitterrand, Bât Maupertuis, 91025 Evry, France ) ; Rijs, Anouk M. (LAMBE CNRS UMR8587, Université ) ;
  • 초록  

    Abstract The far-infrared (far-IR) spectra of phenol and four ortho-substituted phenol derivatives, including three deuterated analogs, are presented. These spectra, measured using the free electron laser FELIX, are used to compare the performance of Born-Oppenheimer Molecular Dynamics (BOMD) with several commonly used levels of static density functional theory in the far-IR region. The molecules studied here form intramolecular hydrogen bonds of different strengths (except phenol), display diverse degrees of flexibility, and the OH moieties of the molecules provide large amplitude, anharmonic OH torsional modes. Since several of the molecules contain two OH groups, strong anharmonic couplings can also be present. Moreover, the experimental far-IR spectra of phenol and saligenin show overtones and combination bands as proven by the measurements of their deuterated analogs. All these characteristics of the molecules enable us to test the performance of the applied levels of theory on different complicating factors. Briefly summarized, both the strength of the hydrogen bond and molecular rigidity do not significantly influence the agreement between theory and experiment. All applied theoretical methods have difficulties to consistently predict modes that include the anharmonic OH torsional motion, resulting in overestimated intensities and frequencies. Coupling between two OH functional groups provides an additional challenge for theories, as seen for catechol. The various employed theoretical methods are found to complement each other, showing good results for complex harmonic modes in the case of static B3LYP-D3, while improved results are observed for anharmonic modes, including the OH torsional modes and their couplings, in the case of BOMD. Additionally, BOMD calculates the relative intensities better than the other theories. VPT2 reproduces weak anharmonic modes well, but it overestimates shifts and intensities for strong anharmonic modes. Highlights Gas phase far-infrared spectra of phenol and phenol derivatives. Comparison of Born-Oppenheimer Molecular Dynamics and Static DFT. Calculations of hydrogen bonding, flexibility, couplings and anharmonicity. Coupling of functional groups and their influence on theories match to experiment. Graphical abstract [DISPLAY OMISSION]


  • 주제어

    Far-infrared spectroscopy .   Born-Oppenheimer Molecular Dynamics (BOMD) .   Hydrogen bonding .   Large amplitude motions .   Density functional theory .   Phenol derivatives.  

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