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An Evaluation of Harmonic Vibrational Frequency Scale Factors
2.6K
Citations
57
References
2007
Year
EngineeringMechanical EngineeringHarmonic FrequenciesComputational ChemistryChemistrySpectra-structure CorrelationModal AnalysisScale FactorsStructural VibrationPhysicsPhysical ChemistryQuantum ChemistryAb-initio MethodPhysicochemical AnalysisNatural SciencesSpectroscopyRandom VibrationStructural MechanicsVibration Control
The study evaluates harmonic vibrational frequency scale factors across many electronic‑structure methods and investigates how varying the exact exchange percentage in hybrid DFT affects those factors. Scale factors were obtained by least‑squares fitting of theoretical harmonic frequencies from a broad set of wave‑function and DFT methods (HF, MP2, QCISD, CCSD, etc.) with various basis sets to 1066 experimental fundamentals, and the influence of basis‑set size was also examined. A near‑linear correlation was found between the scale factor magnitude and the proportion of exact exchange in the functional.
Scale factors for obtaining fundamental vibrational frequencies, low-frequency vibrational frequencies, zero-point vibrational energies (ZPVEs), and thermal contributions to enthalpy and entropy have been derived through a least-squares approach from harmonic frequencies determined at more than 100 levels of theory. Wave function procedures (HF, MP2, QCISD, QCISD(T), CCSD, and CCSD(T)) and a large and representative range of density functional theory (DFT) approaches (B3-LYP, BMK, EDF2, M05-2X, MPWB1K, O3-LYP, PBE, TPSS, etc.) have been examined in conjunction with basis sets such as 6-31G(d), 6-31+G(d,p), 6-31G(2df,p), 6-311+G(d,p), and 6-311+G(2df,p). The vibrational frequency scale factors were determined by a comparison of theoretical harmonic frequencies with the corresponding experimental fundamentals utilizing a standard set of 1066 individual vibrations. ZPVE scale factors were generally obtained from a comparison of the computed ZPVEs with experimental ZPVEs for a smaller standard set of 39 molecules, though the effect of expansion to a 48 molecule data set was also examined. In addition to evaluating the scale factors for a wide range of levels of theory, we have also probed the effect on scale factors of varying the percentage of incorporated exact exchange in hybrid DFT calculations using a modified B3-LYP functional. This has revealed a near-linear relationship between the magnitude of the scale factor and the proportion of exact exchange. Finally, we have investigated the effect of basis set size on HF, MP2, B3-LYP, and BMK scale factors by deriving values with basis sets ranging from 6-31G(d) up to 6-311++G(3df,3pd) as well as with basis sets in the cc-pVnZ and aug-cc-pVnZ series and with the TZV2P basis.
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