Conversion of a Re(IV) tetrahedral cluster to a Re(III) octahedral cluster: synthesis of [(CH3)C(NH2)(2)](4)[Re(6)Se(8)(CN)(6)] by a solvothermal route.

The compound [(CH(3))C(NH(2))(2)](4)[Re(6)Se(8)(CN)(6)] has been synthesized by the reaction at 200 degrees C for 3 days of Re(4)Te(4)(TeCl(2))(4)Cl(8), KSeCN, and NH(4)Cl in superheated acetonitrile. This compound crystallizes in the space group C2/c of the monoclinic system with four formula units in a cell of dimensions a = 20.3113(14) A, b = 10.1332(7) A, c = 19.9981(14) A, beta = 106.754(1) degrees, V = 3941.3(5) A(3) (T = 153 K). The [Re(6)Se(8)(CN)(6)](4-) anion comprises an Re(6) octahedron face capped by mu(3)-Se atoms, with each Re atom liganded by a CN group. The anions and cations are connected by an extensive network of hydrogen bonds. The conversion of a Re(IV) tetrahedral cluster to a Re(III) octahedral cluster appears to be unprecedented.