Reactions of laser-ablated U atoms with N-2 molecules upon code-position in excess argon or neon at 4 K gave intense NUN and weak UN absorptions. Annealing produced progressions of new absorptions for the UN2(N-2)(1,2,3,4,5) and UN(N-2)(1,2,3,4,5,6) complexes. The neon-to-argon matrix shift decreases with increasing NN ligation and therefore the number of noble gas atoms left in the primary coordination sphere around the NUN molecule. Small matrix shifts are observed when the secondary coordination layers around the primary UN2(N-2)(1,2,3,4,5) and UN(N-2)(1,2,3,4,5,6) complexes are changed from neon-to-argon to nitrogen. Electronic structure, energy, and frequency calculations provide support for the identification of these complexes and the characterization of the N U N and U N core molecules as terminal uranium nitrides. Code-position of U with pure nitrogen produced the saturated U(NN)(7) complex, which UV irradiation converted to the NUN(NN)(5) complex with slightly lower frequencies than found in solid argon.