期刊
JOURNAL OF CHEMICAL PHYSICS
卷 121, 期 22, 页码 10852-10862出版社
AMER INST PHYSICS
DOI: 10.1063/1.1814937
关键词
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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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