Journal
JOURNAL OF CHEMICAL PHYSICS
Volume 121, Issue 22, Pages 10852-10862Publisher
AMER INST PHYSICS
DOI: 10.1063/1.1814937
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The information gained in the context of extrapolating the correlation energy by intrinsic scaling is used to shorten the full configurational expansions of electronic wave function without compromising their chemical accuracy. The truncations are accomplished by judiciously limiting the participation of the ranges of predetermined approximate sets of natural orbitals in the various excitation categories. (C) 2004 American Institute of Physics.
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