Triple excitation effects in coupled-cluster calculations of indirect spin-spin coupling constants

被引:96
作者
Auer, AA [1 ]
Gauss, J [1 ]
机构
[1] Univ Mainz, Inst Phys Chem, D-55099 Mainz, Germany
关键词
D O I
10.1063/1.1386698
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 effect of triple excitations in coupled-cluster calculations of indirect spin-spin coupling constants is investigated in coupled-cluster singles and doubles (CCSD) calculations augmented by a perturbative treatment of triples [CCSD(T)], in calculations based on the CC3 model as well as in coupled-cluster singles, doubles, and triples (CCSDT) calculations. Though triple excitation effects are in most cases not particularly pronounced, it is demonstrated that among the approximate schemes for handling triples only the CC3 model with no orbital relaxation included (unrelaxed CC3) provides an adequate description. The otherwise successful CCSD(T) aproach appears to either significantly overestimate triple excitation effects or to yield corrections with the wrong sign in comparison to CCSDT. (C) 2001 American Institute of Physics.
引用
收藏
页码:1619 / 1622
页数:4
相关论文
共 37 条
[1]  
Auer A.A., UNPUB
[2]   The accurate determination of molecular equilibrium structures [J].
Bak, KL ;
Gauss, J ;
Jorgensen, P ;
Olsen, J ;
Helgaker, T ;
Stanton, JF .
JOURNAL OF CHEMICAL PHYSICS, 2001, 114 (15) :6548-6556
[3]   STARK, ZEEMAN, AND HYPERFINE PROPERTIES OF V=0, V=1, AND THE EQUILIBRIUM CONFIGURATION OF HYDROGEN-FLUORIDE [J].
BASS, SM ;
DELEON, RL ;
MUENTER, JS .
JOURNAL OF CHEMICAL PHYSICS, 1987, 86 (08) :4305-4312
[4]   Polarizabilities of CO, N2, HF, Ne, BH, and CH+ from ab initio calculations:: Systematic studies of electron correlation, basis set errors, and vibrational contributions [J].
Christiansen, O ;
Hättig, C ;
Gauss, J .
JOURNAL OF CHEMICAL PHYSICS, 1998, 109 (12) :4745-4757
[5]   The effect of triple excitations in coupled cluster calculations of frequency-dependent polarizabilities [J].
Christiansen, O ;
Gauss, J ;
Stanton, JF .
CHEMICAL PHYSICS LETTERS, 1998, 292 (4-6) :437-446
[6]   THE 2ND-ORDER APPROXIMATE COUPLED-CLUSTER SINGLES AND DOUBLES MODEL CC2 [J].
CHRISTIANSEN, O ;
KOCH, H ;
JORGENSEN, P .
CHEMICAL PHYSICS LETTERS, 1995, 243 (5-6) :409-418
[7]  
Christiansen O, 1998, INT J QUANTUM CHEM, V68, P1, DOI 10.1002/(SICI)1097-461X(1998)68:1<1::AID-QUA1>3.0.CO
[8]  
2-Z
[9]   SOLVENT DEPENDENCE OF THE MOLECULAR-STRUCTURE OF HYDROGEN-CYANIDE DETERMINED BY NMR OF PARTIALLY ORIENTED MOLECULES [J].
DOMBI, G ;
DIEHL, P ;
LOUNILA, J ;
WASSER, R .
ORGANIC MAGNETIC RESONANCE, 1984, 22 (09) :573-575
[10]   THE NUCLEAR SHIELDING DERIVATIVE AND SPIN SPIN COUPLING IN NITROGEN [J].
FRIEDRICH, JO ;
WASYLISHEN, RE .
JOURNAL OF CHEMICAL PHYSICS, 1985, 83 (07) :3707-3708