Gaussian-3 theory using reduced Moller-Plesset order

被引:1189
作者
Curtiss, LA
Redfern, PC
Raghavachari, K
Rassolov, V
Pople, JA
机构
[1] Argonne Natl Lab, Div Chem, Argonne, IL 60439 USA
[2] Argonne Natl Lab, Div Sci Mat, Argonne, IL 60439 USA
[3] AT&T Bell Labs, Lucent Technol, Murray Hill, NJ 07974 USA
[4] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
关键词
D O I
10.1063/1.478385
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 variation of Gaussian-3 (G3) theory is presented in which the basis set extensions are obtained at the second-order Moller-Plesset level. This method, referred to as G3(MP2) theory, is assessed on 299 energies from the G2/97 test set [J. Chem. Phys. 109, 42 (1998)]. The average absolute deviation from experiment of G3(MP2) theory for the 299 energies is 1.30 kcal/mol and for the subset of 148 neutral enthalpies it is 1.18 kcal/mol. This is a significant improvement over the related G2(MP2) theory [J. Chem. Phys. 98, 1293 (1993)], which has an average absolute deviation of 1.89 kcal/mol for all 299 energies and 2.03 kcal/mol for the 148 neutral enthalpies. The corresponding average absolute deviations for full G3 theory are 1.01 and 0.94 kcal/mol, respectively. The new method provides significant savings in computational time compared to G3 theory and, also, G2(MP2) theory. (C) 1999 American Institute of Physics. [S0021-9606(99)30309-3].
引用
收藏
页码:4703 / 4709
页数:7
相关论文
共 15 条
[1]  
BLAUDEAU JP, COMMUNICATION
[2]  
Cl L., 2023, GAUSSIAN94, V14, DOI [10.3389/fimmu, DOI 10.3389/FIMMU]
[3]  
Curtiss L. A., 1995, QUANTUM MECH ELECT S, P139
[4]   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
[5]   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
[6]   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
[7]   GAUSSIAN-2 THEORY USING REDUCED MOLLER-PLESSET ORDERS [J].
CURTISS, LA ;
RAGHAVACHARI, K ;
POPLE, JA .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (02) :1293-1298
[8]   Gaussian-2 (G2) theory: Reduced basis set requirements [J].
Curtiss, LA ;
Redfern, PC ;
Smith, BJ ;
Radom, L .
JOURNAL OF CHEMICAL PHYSICS, 1996, 104 (13) :5148-5152
[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]  
HEHRE WJ, 1987, AB INITIO MOL ORBITA