Calibration sets and the accuracy of vibrational scaling factors: A case study with the X3LYP hybrid functional

被引:35
|
作者
Teixeira, Filipe [2 ]
Melo, Andre [2 ]
Cordeiro, M. Natalia D. S. [1 ]
机构
[1] Univ Vigo, Dept Quim Fis, Vigo 36310, Spain
[2] Univ Porto, Fac Ciencias, REQUIMTE, Dept Quim & Bioquim, P-4169007 Oporto, Portugal
来源
JOURNAL OF CHEMICAL PHYSICS | 2010年 / 133卷 / 11期
关键词
calibration; density functional theory; least squares approximations; vibrational states; LASER-INDUCED FLUORESCENCE; SMALL-RING COMPOUNDS; INFRARED-SPECTRUM; NONBOND INTERACTIONS; RAMAN-SPECTROSCOPY; NU-3; BANDS; FREQUENCIES; DENSITY; MOLECULES; HNCO;
D O I
10.1063/1.3493630
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A linear least-squares methodology was used to determine the vibrational scaling factors for the X3LYP density functional. Uncertainties for these scaling factors were calculated according to the method devised by Irikura [J. Phys. Chem. A 109, 8430 (2005)]. The calibration set was systematically partitioned according to several of its descriptors and the scaling factors for X3LYP were recalculated for each subset. The results show that the scaling factors are only significant up to the second digit, irrespective of the calibration set used. Furthermore, multivariate statistical analysis allowed us to conclude that the scaling factors and the associated uncertainties are independent of the size of the calibration set and strongly suggest the practical impossibility of obtaining vibrational scaling factors with more than two significant digits. (c) 2010 American Institute of Physics. [doi:10.1063/1.3493630]
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页数:7
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