Extended pseudochalcogenides such as the solid-state carbodiimides (incorporating complex À N = C = N À units with D 1h symmetry) or cyanamides (with a less symmetrical N C À N 2À unit) have been extensively investigated, and a large number including alkali [1] and alkaline-earth metals, [2] main-group elements, [3] d 10 transition metals, [4] and also rare-earth metals [5] have been reported. The synthesis of the complete set of MNCN (M = Mn-Cu) phases with only partially filled 3d orbitals, however, looked far more difficult, because firstprinciples calculations [6] had predicted them to be unstable in terms of formation enthalpy DH f and Gibbs formation energy DG f , with the instability continuously rising from MnNCN to CuNCN, thereby mirroring the gradual filling of antibonding levels from 3d 5 to 3d 9 . Nonetheless, we have succeeded in finding new routes to synthesize the MNCN series of the divalent 3d metals as a prerequisite to determine their crystal structures. MnNCN, the first carbodiimide of a magnetic transition metal ever realized, is made by a metathesis around 600 8C involving ZnNCN and MnCl 2 [7] but this method is unsuitable for the later, more unstable compounds. FeNCN, [8] CoNCN, and NiNCN [9] are synthesized, instead, by a two-step route via the corresponding hydrogencyanamides M(HNCN) 2 at about 400 8C.[10] Finally, the most delicate carbodiimide, CuNCN, is obtained by the oxidation of a copper(I) cyanamide precursor under aqueous conditions at room temperature. [11] The magnetic properties of the carbodiimides involving divalent transition metals are similar to those of the isolobal oxides, in particular by indicating antiferromagnetic interactions. For example, the magnetic structure of MnNCN based on spin-polarized neutron diffraction reveals frustration between the high-spin (S = 5/2) Mn 2+ ions as a function of temperature [12] but also shows that the carbodiimide unit ensures a strong magnetic communication. Likewise, experimental as well as theoretical studies on the magnetic structure of CuNCN have shown a fascinating interplay between geometrical packing and exchange couplings. [13] Finally, UV/Vis measurements on MnNCN [14] stress the importance of the more covalent MnÀN bond and higher ligand-field splitting compared to Mn-O chromophores but a smaller nephelauxetic ratio. Also, the Mn À N bond lacks significant p interaction.In light of this information, the design of a carbodiimide that is not antiferromagnetic requires an alternative composition, for example, by moving towards a different oxidation state. The hypothetical chromium(III) carbodiimide, Cr 2 -(NCN) 3 , is such a synthetic target although its isolobal oxide Cr 2 O 3 is, in fact, antiferromagnetic. Because the electron configuration (3d 3 ) is even lower than in the MnNCN case, theory [6] implies that the synthetic route for MnNCN should also be applicable for Cr 2 (NCN) 3 . In addition, there is related information with respect to existing rare-earth metal(III) carbodiimides. Recent research on such Ln 2 (NCN) 3 ...