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
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