It is known that some non-dynamic effects of electron correlation can be included in coupled cluster theory using a tailoring technique that separates the effects of non-dynamic and dynamic correlations. Recently, the simple pCCD (pair coupled cluster doubles) wavefunction was shown to provide good results for some non-dynamic correlation problems, such as bond-breaking, in a spin-adapted way with no active space selection. In this paper, we report a study of excited states using "tailored coupled cluster singles and doubles," to attempt to use pCCD as a kernel for more complete coupled-cluster singles and doubles (CCSD) results for excited states. Several excited states are explored from those primarily due to single excitations to those dominated by doubly excited states and from singlet-triplet splittings for some diradical states. For the first two situations, tailored pCCD-TCCSD offers no improvement over equation of motion-CCSD. However, when we explore the singlet-triplet gap of diradical molecules that are manifestly multi-reference, a pCCD kernel provides improved results, particularly with generalized valence bond orbitals.
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