Abstract
Abstract The coupled‐pair many‐electron theory, its linear approximation, and various other approximate coupled‐pair approaches based on the orthogonally spin‐adapted coupled‐pair theory are applied to simple model systems in which the degree of quasidegeneracy can be continuously varied over a wide range. The four‐electron models studied are three ab initio minimum basis set models involving four hydrogen atoms in various spatial arrangements as well as the semiempirical Pariser–Parr–Pople π‐electron model of cis ‐butadiene. The results are compared with the exact full configuration interaction results as well as with those obtained with other approximate limited configuration interaction approaches and Davidson's formula estimate, and the effect of quasidegeneracy on various approaches is discussed. We also examine the difference between the correlation energies obtained with the coupled‐pair many‐electron theory and its linear version and discuss the source of these differences and of the breakdown of the latter approximation in the case of very strong quasidegeneracies.
Keywords
Affiliated Institutions
Related Publications
An electron pair operator approach to coupled cluster wave functions. Application to He2, Be2, and Mg2 and comparison with CEPA methods
A method for obtaining coupled cluster expansions with double substitutions (CCD) utilizing the electron pair operator approach of self-consistent electron pair (SCEP) theory is...
Gaussian-1 theory: A general procedure for prediction of molecular energies
A general procedure is developed for the computation of the total energies of molecules at their equilibrium geometries. Ab initio molecular orbital theory is used to calculate ...
Correlation Problems in Atomic and Molecular Systems. IV. Extended Coupled-Pair Many-Electron Theory and Its Application to the B<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" display="inline"><mml:mrow><mml:msub><mml:mrow><mml:mi mathvariant="normal">H</mml:mi></mml:mrow><mml:mrow><mml:mn>3</mml:mn></mml:mrow></mml:msub></mml:mrow></mml:math>Molecule
The equations of the coupled-pair many-electron theory (CPMET) are extended to incorporate the effect of both unlinked and linked triexcited clusters. The minimal basis correlat...
The performance of a family of density functional methods
The results of a systematic study of molecular properties by density functional theory (DFT) are presented and discussed. Equilibrium geometries, dipole moments, harmonic vibrat...
A global, high accuracy <i>ab initio</i> dipole moment surface for the electronic ground state of the water molecule
A highly accurate, global dipole moment surface (DMS) is calculated for the water molecule using ab initio quantum chemistry methods. The new surface is named LTP2011 and is bas...
Publication Info
- Year
- 1980
- Type
- article
- Volume
- 18
- Issue
- 5
- Pages
- 1243-1269
- Citations
- 335
- Access
- Closed
External Links
Social Impact
Social media, news, blog, policy document mentions
Citation Metrics
Cite This
Identifiers
- DOI
- 10.1002/qua.560180511