Gaussian-3 theory using scaled energies

被引:113
作者
Curtiss, LA
Raghavachari, K
Redfern, PC
Pople, JA
机构
[1] Argonne Natl Lab, Div Mat Sci, Argonne, IL 60439 USA
[2] Lucent Technol, Bell Labs, Murray Hill, NJ 07974 USA
[3] Argonne Natl Lab, Div Chem, Argonne, IL 60439 USA
[4] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
关键词
D O I
10.1063/1.480668
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 modification of Guassian-3 (G3) theory using multiplicative scale factors, instead of the additive higher level correction, is presented. In this method, referred to as G3S, the correlation energy is scaled by five parameters and the Hartree-Fock energy by one parameter. The six parameters are fitted to the G2/97 test set of 299 energies and the resulting mean absolute deviation from experiment is 0.99 kcal/mol compared to 1.01 kcal/mol for G3 theory. The G3S method has the advantage compared to G3 theory in that it can be used for studying potential energy surfaces where the products and reactants have a different number of paired electrons. In addition, versions of the computationally less intensive G3(MP3) and G3(MP2) methods that use scaled energies are also presented. These methods, referred to as G3S(MP3) and G3S(MP2), have mean absolute deviations of 1.16 and 1.35 kcal/mol, respectively. (C) 2000 American Institute of Physics. [S0021-9606(00)30902-3].
引用
收藏
页码:1125 / 1132
页数:8
相关论文
共 28 条
[1]   QUANTUM-MECHANICAL CALCULATIONS TO CHEMICAL ACCURACY [J].
BAUSCHLICHER, CW ;
LANGHOFF, SR .
SCIENCE, 1991, 254 (5030) :394-398
[2]   Comparison of results from parametrized configuration interaction (PCI-80) and from hybrid density functional theory with experiments for first row transition metal compounds [J].
Blomberg, MRA ;
Siegbahn, PEM ;
Svensson, M .
JOURNAL OF CHEMICAL PHYSICS, 1996, 104 (23) :9546-9554
[3]   A NEW SEMI-EMPIRICAL METHOD OF CORRECTING LARGE-SCALE CONFIGURATION-INTERACTION CALCULATIONS FOR INCOMPLETE DYNAMIC CORRELATION OF ELECTRONS [J].
BROWN, FB ;
TRUHLAR, DG .
CHEMICAL PHYSICS LETTERS, 1985, 117 (04) :307-313
[4]   Gaussian-3 theory: a variation based on third-order perturbation theory and an assessment of the contribution of core-related correlation [J].
Curtiss, LA ;
Redfern, PC ;
Raghavachari, K ;
Pople, JA .
CHEMICAL PHYSICS LETTERS, 1999, 313 (3-4) :600-607
[5]   Gaussian-3 (G3) theory for molecules containing first and second-row atoms [J].
Curtiss, LA ;
Raghavachari, K ;
Redfern, PC ;
Rassolov, V ;
Pople, JA .
JOURNAL OF CHEMICAL PHYSICS, 1998, 109 (18) :7764-7776
[6]   Assessment of Gaussian-2 and density functional theories for the computation of enthalpies of formation [J].
Curtiss, LA ;
Raghavachari, K ;
Redfern, PC ;
Pople, JA .
JOURNAL OF CHEMICAL PHYSICS, 1997, 106 (03) :1063-1079
[7]   Assessment of Gaussian-2 and density functional theories for the computation of ionization potentials and electron affinities [J].
Curtiss, LA ;
Redfern, PC ;
Raghavachari, K ;
Pople, JA .
JOURNAL OF CHEMICAL PHYSICS, 1998, 109 (01) :42-55
[8]   Gaussian-3 theory using reduced Moller-Plesset order [J].
Curtiss, LA ;
Redfern, PC ;
Raghavachari, K ;
Rassolov, V ;
Pople, JA .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (10) :4703-4709
[9]   GAUSSIAN-2 THEORY FOR MOLECULAR-ENERGIES OF 1ST-ROW AND 2ND-ROW COMPOUNDS [J].
CURTISS, LA ;
RAGHAVACHARI, K ;
TRUCKS, GW ;
POPLE, JA .
JOURNAL OF CHEMICAL PHYSICS, 1991, 94 (11) :7221-7230
[10]  
CURTISS LA, 1998, ENCY COMPUTATIONAL C