Abstract
We present an implementation of equation-of-motion oscillator strengths for the multilevel CCSD (MLCCSD) model where CCS is used as the lower level method (CCS/CCSD). In this model, the double excitations of the cluster operator are restricted to an active orbital space, whereas the single excitations are unrestricted. Calculated nitrogen K-edge spectra of adenosine, adenosine triphosphate (ATP), and an ATP-water system are used to demonstrate the performance of the model. Projected atomic orbitals (PAOs) are used to partition the virtual space into active and inactive orbital sets. Cholesky decomposition of the Hartree-Fock density is used to partition the occupied orbitals. This Cholesky-PAO partitioning is cheap, scaling as O(N3), and is suitable for the calculation of core excitations, which are localized in character. By restricting the single excitations of the cluster operator to the active space, as well as the double excitations, the CCSD-in-HF model is obtained. A comparison of the two models-MLCCSD and CCSD-in-HF-is presented for the core excitation spectra of the adenosine and ATP systems.