Inclusion of the (T) triples correction into the linear-r12 corrected coupled-cluster model CCSD(R12)

被引:62
作者
Fliegl, Heike
Hattig, Christof
Klopper, Wim [1 ]
机构
[1] Univ Karlsruhe TH, Inst Phys Chem, Lehrstuhl Theoret Chem, D-76128 Karlsruhe, Germany
[2] Forschungszentrum Karlsruhe, Inst Nanotechnol, D-76021 Karlsruhe, Germany
关键词
coupled-cluster theory; triples correction; linear-r(12) method;
D O I
10.1002/qua.20991
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
The recently developed singles-and-cloubles linear-r(12) corrected coupled-cluster model CCSD(R12) has been extended by inclusion of triples corrections in exactly the same manner as in the popular CCSD(T) model. The resulting model is denoted CCSD(T)(R12). An orthonormal auxiliary basis set is used for the resolution-of-the-identity approximation to calculate the three- and four-electron integrals needed in the linear-r12 Ansatz. CCSD(T)(R12) reaction energies are calculated for a test set of 15 chemical reactions involving 23 small molecules. The CCSD(T)(R12), CCSD(R12), and MP2-R12 results are compared with experimental data obtained by correcting experimental enthalpies of reaction for zero-point vibrational energies and finite temperature contributions. Conventional MP2, CCSD, and CCSD(T) results are presented for comparison. An estimate of the basis set limit is obtained by an aug-cc-pV(Q + d)Z/aug-cc-pV(5 + d)Z CCSD(T) extrapolation for a subset of 12 reactions. All CCSD(T) results are compared with the extrapolated values, and the errors are analyzed for the CCSD(T) and CCSD(T)(R12) models in various basis sets. (C) 2006 Wiley Periodicals, Inc.
引用
收藏
页码:2306 / 2317
页数:12
相关论文
共 30 条
[1]  
*ACS AIP, 1998, J PHYS CHEM REF DATA, V9
[2]   ELECTRONIC-STRUCTURE CALCULATIONS ON WORKSTATION COMPUTERS - THE PROGRAM SYSTEM TURBOMOLE [J].
AHLRICHS, R ;
BAR, M ;
HASER, M ;
HORN, H ;
KOLMEL, C .
CHEMICAL PHYSICS LETTERS, 1989, 162 (03) :165-169
[3]   THERMODYNAMISCHE EIGENSCHAFTEN VON FORMAMID [J].
BAUDER, A ;
GUNTHARD, HH .
HELVETICA CHIMICA ACTA, 1958, 41 (03) :670-673
[4]   An efficient implementation of second analytical derivatives for density functional methods [J].
Deglmann, P ;
Furche, F ;
Ahlrichs, R .
CHEMICAL PHYSICS LETTERS, 2002, 362 (5-6) :511-518
[5]   Gaussian basis sets for use in correlated molecular calculations. X. The atoms aluminum through argon revisited [J].
Dunning, TH ;
Peterson, KA ;
Wilson, AK .
JOURNAL OF CHEMICAL PHYSICS, 2001, 114 (21) :9244-9253
[6]   MEASUREMENTS OF HEATS OF COMBUSTION BY FLAME CALORIMETRY .6. FORMALDEHYDE, GLYOXAL [J].
FLETCHER, RA ;
PILCHER, G .
TRANSACTIONS OF THE FARADAY SOCIETY, 1970, 66 (568) :794-&
[7]   Coupled-cluster theory with simplified linear-r12 corrections:: The CCSD(R12) model -: art. no. 084107 [J].
Fliegl, H ;
Klopper, W ;
Hättig, C .
JOURNAL OF CHEMICAL PHYSICS, 2005, 122 (08)
[8]   Implementation of electronic ground states and singlet and triplet excitation energies in coupled cluster theory with approximate triples corrections [J].
Hald, K ;
Jorgensen, P ;
Christiansen, O ;
Koch, H .
JOURNAL OF CHEMICAL PHYSICS, 2002, 116 (14) :5963-5970
[9]   IMPROVEMENTS ON THE DIRECT SCF METHOD [J].
HASER, M ;
AHLRICHS, R .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 1989, 10 (01) :104-111
[10]   Basis-set convergence of correlated calculations on water [J].
Helgaker, T ;
Klopper, W ;
Koch, H ;
Noga, J .
JOURNAL OF CHEMICAL PHYSICS, 1997, 106 (23) :9639-9646