Although actinide (An) L 3 -edge x-ray absorption near-edge structure (XANES) spectroscopy has been very effective in determining An oxidation states in insulating, ionically-bonded materials, such as in certain coordination compounds and mineral systems, the technique fails in systems featuring more delocalized 5f orbitals, especially in metals. Recently, actinide L 3 -edge resonant x-ray emission spectroscopy (RXES) has been shown to be an effective alternative. This technique is further demonstrated here using a parametrized partial unoccupied density of states method to quantify both occupancy and delocalization of the 5f orbital in α-Pu, δ-Pu, PuCoGa 5 , PuCoIn 5 , and PuSb 2 . These new results, supported by FEFF calculations, highlight the effects of strong correlations on RXES spectra and the technique's ability to differentiate between f -orbital occupation and delocalization.