We show a marked tendency of Fe(II) to form heteroleptic [Fe(L)(L')](ClO4)(2) complexes from pairs of chelating tris-imine 3bpp, tpy, or 2bbp ligands. New synthetic avenues for spin crossover research become thus available, here illustrated with three new heteroleptic compounds with differing magnetic behaviors: [Fe(H(4)L1)(Cl-tpy)](ClO4)(2)center dot C3H6O (1), [Fe(H2L3)(Me3bpp)](ClO4)(2)center dot C3H6O (2), [Fe(H(4)L1)(2bbp)](ClO4)(2)center dot 3C(3)H(6)O (3). Structural studies demonstrate that 1 is in the low-spin (LS) state up to 350 K, while complexes 2 and 3 are, by contrast, in the high-spin (HS) state down to 2 K, as corroborated through magnetic susceptibility measurements. Upon exposure to the atmosphere, the latter exhibits the release of three molecules of acetone per complex, turning into the solvent-free analogue [Fe(H(4)L1)(2bbp)](ClO4)(2) (3a), through a single-crystal-to-single-crystal transformation. This guest extrusion process is accompanied by a spin switch, from HS to LS.