The theory of electron correlation in excited states is used in evaluating spectroscopic quantities exemplified by the calculation of term level splittings among excited states of the carbonhyphen;I isoelectronic sequence. Agreement with experiment is generally better than 10percnt;, which is 4ndash;25 times better than that achieved by conventional Hartreehyphen;Fock (HF) calculations and 2ndash;10 times better than that achieved by standard multiconfigurational HF calculations.
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