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The method of frozen natural orbital (FNO) basis set truncation for coupled-cluster theory is described. Numerical comparisons of the FNO potential energy surfaces of a group of small molecules at the CCSD(T) level in DZP, cc-pVTZ, cc-pVQZ bases show that truncation of up to 50% of the virtual space yields CC correlation energies that are accurate to 90 or 95% when added to the full MBPT(2) basis result. The FNO truncation method is also applied to dimethylnitramine (DMNA): both the equilibrium structure and dimer interactions, yielding results at the CCSD(T) level in both a DZP and cc-pVTZ basis set that agree with literature values. CCSD(T) calculations at two possible equilibrium structures of 1,3,5-trinitrohexahydro-1,3,5-triazine (RDX) in a truncated DZP basis are also reported.
Taube et al. (Sat,) studied this question.