We explore the possibility of calculating electronic excited states by using perturbation theory along a range separated adiabatic connection. Starting from the energies of a partially interacting Hamiltonian, a first order correction is defined with two variants of perturbation theory: a straightforward perturbation theory, and an extension of the Grling Levy one that has the advantage of keeping the ground state density constant at each order in the perturbation. Only the first steroids, simpler, variant is tested here on the helium and beryllium atoms and on the hydrogen molecule.
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