Journal
JOURNAL OF CHEMICAL PHYSICS
Volume 135, Issue 9, Pages -Publisher
AMER INST PHYSICS
DOI: 10.1063/1.3629780
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Funding
- National Science Foundation (NSF) [CHE-1050405]
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [1050405] Funding Source: National Science Foundation
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Conventional natural and Brueckner orbitals (BOs) are rather frequently used for improving active orbital spaces in various configuration interaction (CI) approaches. However, the natural and Brueckner single-determinant models per se fail to give an adequate picture of highly correlated and quasidegenerate states such as open-shell singlet and dissociative states. We suggest the use of the spin-polarized extended BOs formally defining them in the same manner as in Lowdin's spin-extended Hartree-Fock method. Such BO orbitals turn out to be quite flexible and particularly useful for analyzing highly correlated electronic states. It is shown that the extended BOs always exist, unlike the usual unrestricted BOs. We discuss difficulties related to violation of size-consistency for spin projected determinant models. The working algorithm is proposed for computing BOs within the full CI and related complete active space methodology. The extended BOs are analyzed in terms of the special density-like matrices associated with spin-up and spin-down BO orbitals. From these density matrices, the corresponding spin-polarization diagrams are produced for effectively unpaired (essentially correlated) electrons. We illustrate the approach by calculations on cyclic hydrogen clusters (H-4, H-6, and H-8), certain carbene diradicals and monoradicals, and low-lying excited states. The computations show that the BO spin-projected determinant provides a strong overlap with the multi-configurational state even for quasidegenerate states and bond breaking processes. (C) 2011 American Institute of Physics. [doi:10.1063/1.3629780]
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