The homoleptic, square pyramidal organochromium(III) compound [NBu(4)](2)[Cr(C(6)F(5))(5)] (1) reacts with excess organic isocyanides, CNR [R = (t)Bu, 2,6-dimethylphenyl (Xy)], under dissociation of the apical C(6)F(5) ligand to give the more saturated, singly charged complexes [NBu(4)][trans-Cr(C(6)F(5))(4)(CNR)(2)] [R = (t)Bu (2), Xy (3)], containing six monodentate C-donor ligands. These compounds exhibit an axially distorted octahedral structure (single-crystal X-ray diffraction) with the four C(6)F(5) groups defining the equatorial positions and the CNR ligands occupying the axial ones. Compounds 2 and 3 both behave as spin quartet species (S = 3/2) at microscopic level (EPR spectroscopy), their macroscopic magnetic properties depending upon the nature of the terminal R group, as established by magnetisation measurements. When the R substituent is the saturated alkyl group (t)Bu, the compound (2) behaves as a simple paramagnet, with no magnetic interaction between individual Cr(III) centres along the whole temperature range measured (1.8-265 K). By contrast, a weak antiferromagnetic interaction is detected for compound 3 at low temperature with T(N) = 0.19(1) K. Since the closest intermetallic distances are similar in the crystals of 2·CH(2)Cl(2) and 3·1.75CH(2)Cl(2) (ca. 1.1 nm), we conclude that the insaturation of the aromatic Xy group together with the extended intermolecular π-π stacking interactions between Xy rings observed in the crystal lattice of 3·1.75CH(2)Cl(2) (centroid-to-centroid distance: 0.35 nm) favour magnetic interaction between the individual magnetic centres.