General Perturbative Approach for Spectroscopy, Thermodynamics, and Kinetics: Methodological Background and Benchmark Studies

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• 作者：Julien Bloino ; Malgorzata Biczysko ; Vincenzo Barone
• 刊名：Journal of Chemical Theory and Computation
• 出版年：2012
• 出版时间：March 13, 2012
• 年：2012
• 卷：8
• 期：3
• 页码：1015-1036
• 全文大小：565K
• 年卷期：v.8,no.3(March 13, 2012)
• ISSN：1549-9626

文摘

A general second-order perturbative approach based on resonance- and threshold-free computations of vibrational properties is introduced and validated. It starts from the evaluation of accurate anharmonic zero-point vibrational energies for semirigid molecular systems, in a way that avoids any singularity. Next, the degeneracy corrected second-order perturbation theory (DCPT2) is extended to a hybrid version (HDCPT2), allowing for reliable computations even in cases where the original formulation faces against severe problems, including also an automatic treatment of internal rotations through the hindered-rotor model. These approaches, in conjunction with the so-called simple perturbation theory (SPT) reformulated to treat consistently both energy minima and transition states, allow one to evaluate degeneracy-corrected partition functions further used to obtain vibrational contributions to properties like enthalpy, entropy, or specific heat. The spectroscopic accuracy of the HDCPT2 model has been also validated by computing anharmonic vibrational frequencies for a number of small-to-medium size, closed- and open-shell, molecular systems, within an accuracy close to that of well established but threshold-dependent perturbative-variational models. The reliability of the B3LYP/aug-N07D model for anharmonic computations is also highlighted, with possible improvements provided by the B2PLYP/aug-cc-pVTZ models or by hybrid schemes. On a general grounds, the overall approach proposed in the present work is able to provide the proper accuracy to support experimental investigations even for large molecular systems of biotechnological interest in a fully automated manner, without any ad hoc scaling procedure. This means a fully ab initio evaluation of thermodynamic and spectroscopic properties with an overall accuracy of about, or better than, 1 kJ mol^鈥?, 1 J mol^鈥? K^鈥? and 10 cm^鈥? for enthalpies, entropies, and vibrational frequencies, respectively.