Quantitative quantum chemistry

被引:206
作者
Helgaker, Trygve [1 ]
Klopper, Wim [2 ]
Tew, David P. [2 ]
机构
[1] Univ Oslo, Ctr Theoret & Computat Chem, Dept Chem, Oslo, Norway
[2] Univ Karlsruhe, Inst Phys Chem, Lehrstuhl Theoret Chem, Karlsruhe, TH, Germany
关键词
electronic-structure theory; basis-set extrapolation; explicit correlation; coupled-cluster theory;
D O I
10.1080/00268970802258591
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
We review the current status of quantum chemistry as a predictive tool of chemistry and molecular physics, capable of providing highly accurate, quantitative data about molecular systems. We begin by reviewing wave-function based electronic-structure theory, emphasizing the N-electron hierarchy of coupled-cluster theory and the one-electron hierarchy of correlation-consistent basis sets. Following a discussion of the slow basis-set convergence of dynamical correlation and basis-set extrapolations, we consider the methods of explicit correlation, from the early work of Hylleraas in the 1920s to the latest developments in such methods, capable of yielding high-accuracy results in medium-sized basis sets. Next, we consider the small corrections to the electronic energy (high-order virtual excitations, vibrational, relativistic, and diagonal Born-Oppenheimer corrections) needed for high accuracy and conclude with a review of the composite methods and computational protocols of electronic-structure theory.
引用
收藏
页码:2107 / 2143
页数:37
相关论文
共 310 条
[31]   Gaussian geminals in explicitly correlated coupled cluster theory including single and double excitations [J].
Bukowski, R ;
Jeziorski, B ;
Szalewicz, K .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (09) :4165-4183
[32]   VARIATIONAL CALCULATION OF GROUND STATE OF LITHIUM ATOM [J].
BURKE, EA .
PHYSICAL REVIEW, 1963, 130 (05) :1871-&
[33]   Correlation energy extrapolation by intrinsic scaling. I. Method and application to the neon atom [J].
Bytautas, L ;
Ruedenberg, K .
JOURNAL OF CHEMICAL PHYSICS, 2004, 121 (22) :10905-10918
[34]   Correlation energy extrapolation by intrinsic scaling. V. Electronic energy, atomization energy, and enthalpy of formation of water [J].
Bytautas, L ;
Ruedenberg, K .
JOURNAL OF CHEMICAL PHYSICS, 2006, 124 (17)
[35]   PIECEWISE POLYNOMIAL CONFIGURATION INTERACTION NATURAL ORBITAL STUDY OF 1S2-HELIUM [J].
CARROLL, DP ;
SILVERSTONE, HJ ;
METZGER, RM .
JOURNAL OF CHEMICAL PHYSICS, 1979, 71 (10) :4142-4163
[36]   Accurate adiabatic correction for the hydrogen molecule using the Born-Handy formula [J].
Cencek, W ;
Kutzelnigg, W .
CHEMICAL PHYSICS LETTERS, 1997, 266 (3-4) :383-387
[37]   MANY-ELECTRON EXPLICITLY CORRELATED GAUSSIAN FUNCTIONS .2. GROUND-STATE OF THE HELIUM MOLECULAR ION HE-2(+) [J].
CENCEK, W ;
RYCHLEWSKI, J .
JOURNAL OF CHEMICAL PHYSICS, 1995, 102 (06) :2533-2538
[38]   MANY-ELECTRON EXPLICITLY CORRELATED GAUSSIAN FUNCTIONS .1. GENERAL-THEORY AND TEST-RESULTS [J].
CENCEK, W ;
RYCHLEWSKI, J .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (02) :1252-1261
[39]   Benchmark calculations for He2+ and LiH molecules using explicitly correlated Gaussian functions [J].
Cencek, W ;
Rychlewski, J .
CHEMICAL PHYSICS LETTERS, 2000, 320 (5-6) :549-552
[40]   Helium dimer interaction energies from Gaussian geminal and orbital calculations [J].
Cencek, W ;
Jeziorska, M ;
Bukowski, R ;
Jaszunski, M ;
Jeziorski, B ;
Szalewicz, K .
JOURNAL OF PHYSICAL CHEMISTRY A, 2004, 108 (15) :3211-3224