Three new tetranuclear compounds of formula [Fe-4(mu-CN)(4)(phen)(4)(L)(2))](PF6)(4)center dot G where L = tris(pyridin-2-ylmethyl)amine (TPMA) [G = 0] (1), (6-methylpyrid-2-ylmethyl)-bis(pyrid-2-ylmethyl)amine (MeTPMA) [G = 0] (2), or bis(6-methylpyrid-2-ylmethyl)-(pyrid-2-ylmethyl)amine(Me(2)TPMA) [G = NH4PF6] (3) and phen = 1,10-phenanthroline) have been synthesized and characterized. The three compounds crystallize in the C2/c space group and consist of [Fe-4(mu-CN)(4)(phen)(4)(L)(2))](4+) square shaped cations with two distinct iron(II) sites. The sites, associated with [Fe(phen)(2)(CN)(2)] and [Fe(L)(NC)(2)] moieties, are connected by cyanide bridging ligands and reside in different [FeN4C2] and [FeN6] ligand field strength environments. For 1, the structural features of both sites at 100 and 293 K are those of an iron(II) atom in the low-spin state, according to the magnetic. properties. At 370 K the structure of the [FeN6] site is consistent with a quite complete change of spin state from the low-spin state to the high-spin state, a behavior confirmed by the magnetic study. Introduction of a methyl substituent in the sixth position of one or two pyridine groups to get MeTPMA or Me(2)TPMA derivatives, respectively, induce in 2 and 3 notable steric constraint in the [FeN6] site making longer the average Fe-N bond distances thereby weakening the ligand field strength and stabilizing the high-spin state. The [FeN4C2] site remains in the low-spin state in the three compounds.