New coupled cluster approaches based on the unrestricted Hartree–Fock reference for treating molecules with multireference character

2011 ◽  
Vol 13 (19) ◽  
pp. 8795 ◽  
Author(s):  
Jun Shen ◽  
Enhua Xu ◽  
Zhuangfei Kou ◽  
Shuhua Li
Keyword(s):  
Coupled Cluster ◽  
Hartree Fock

Coupled-cluster method in Fock space. II. Brueckner-Hartree-Fock method

1985 ◽  
Vol 32 (2) ◽  
pp. 743-747 ◽  
Author(s):  
Leszek Z. Stolarczyk ◽  
Hendrik J. Monkhorst
Keyword(s):  
Fock Space ◽  
Cluster Method ◽  
Coupled Cluster ◽  
Coupled Cluster Method ◽  
Hartree Fock

Analytic energy gradients for open-shell coupled-cluster singles and doubles (CCSD) calculations using restricted open-shell Hartree—Fock (ROHF) reference functions

1991 ◽  
Vol 182 (3-4) ◽  
pp. 207-215 ◽  
Author(s):  
Jürgen Gauss ◽  
Walter J. Lauderdale ◽  
John F. Stanton ◽  
John D. Watts ◽  
Rodney J. Bartlett
Keyword(s):  
Open Shell ◽  
Coupled Cluster ◽  
Hartree Fock ◽  
Reference Functions

Spin adapted restricted Hartree–Fock reference coupled cluster theory for open shell systems

1994 ◽  
Vol 100 (5) ◽  
pp. 3706-3716 ◽  
Author(s):  
Pavel Neogrády ◽  
Miroslav Urban ◽  
Ivan Hubac̆
Keyword(s):  
Open Shell ◽  
Coupled Cluster ◽  
Coupled Cluster Theory ◽  
Cluster Theory ◽  
Hartree Fock

Accuracy Assessment of the ROHF-CCSD(T) Calculationsof Dipole Moments of Small Radicals

1998 ◽  
Vol 63 (9) ◽  
pp. 1409-1430 ◽  
Author(s):  
Miroslav Urban ◽  
Pavel Neogrády ◽  
Juraj Raab ◽  
Geerd H. F. Diercksen
Keyword(s):  
Large Deviation ◽  
Theoretical Calculations ◽  
Dipole Moments ◽  
Accuracy Assessment ◽  
Open Shell ◽  
Basis Set ◽  
Coupled Cluster ◽  
Hartree Fock ◽  
Experimental Values

Dipole moments of a series of radicals, OH, NO, NS, SF, SO, PO, ClO, CN, LiO, NO2, and ClO2 were calculated by the Coupled Cluster CCSD(T) method with the single determinant restricted open shell Hartree-Fock (ROHF) reference. For all molecules theoretical dipole moments were carefully compared to experimental values. The size and the quality of the basis set were systematically improved. Spin adaptation in the ROHF-CCSD(T) method, largest single and double excitation amplitudes and the T1 diagnostics were considered as indicators in the quality assessment of calculated dipole moments. For most molecules the accuracy within 0.01-0.03 D was readily obtained. For ClO and CN the spin adaptation was necessary - its contribution was as large as 0.03-0.045 D. Large deviation from experiment is observed for OH in its A2Σ+ excited state (0.135 D) and especially for LiO in its 2Π ground state (0.22 D). No indication of the failure of theoretical calculations was found which leads to the conclusion that, even if there is still a space for the improvement of theoretical calculations, experimental values should be reconsidered.

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