SYNTHESIS AND CRYSTAL STRUCTURE OF [Ta6Cl12(PrCN)6][(Ta6Cl12)Cl6]·2PrCN - Compound with mixed-charge cluster units

S. Širac1, N. Brnicevic1, I. Bašic1, P. Planinia1 and R. McCarley2

1Ruder Boškovia Institute, 10001 Zagreb, Croatia
2Ames Laboratory and Iowa State University, Ames, Iowa, USA

Keywords: hexanuclear cluster, tantalum chloro cluster, mixed-charge cluster, crystal structure, butyronitrile complex

The title compound has been prepared by the reaction of [Ta6Cl12(EtOH)6]Cl2 with butyronitrile molecules in the presence of limited amount of air [1]. The cluster crystallizes in the triclinic space group P1- (No. 2) with Z = 1 and the unit cell parameters: a = 12.618(8) A, b = 13.189(2) A, c = 12.216(2) A, a = 93.31(2)o, b = 94.14(3)o, g = 93.95(3)o, R = 0.0894.

Two homonuclear mixed-charge cluster units: [Ta6Cl12]2+ in the [Ta6Cl12(PrCN)6]2+ cation and [Ta6Cl12]4+ in the [(Ta6Cl12)Cl6]2- anion are the main structural features of [Ta6Cl12(PrCN)6][(Ta6Cl12)Cl6]·2PrCN cluster. Based on this phenomenon this compound represents the first example of coexistence of differently charged [M6X12]n+ (n = 2, 4) units in the solid state chemistry of the hexanuclear halide clusters of niobium and tantalum. The average Ta-Ta bond distance in [Ta6Cl12(PrCN)6]2+ (2.868 A) cluster cation is considerably shorter than in [(Ta6Cl12)Cl6]2- (2.973 A) cluster anion. The former value is closely related to those found in [Ta6Cl12(EtOH)6][(Mo6Cl8)Cl6]·6EtOH (2.872 A) [2], or trans-[(Ta6Cl12)Cl2(PEt3)4]·CHCl3 (2.901 A) [3] with [Ta6Cl12]2+ unit, while the latter is related to the value of 2.962 A found in the cluster H2[(Ta6Cl12)Cl6]·6H2O containing [Ta6Cl12]4+ unit [4]. Consequently, the mean value of the Ta-Cl bond distance in [Ta6Cl12(PrCN)6]2+ cation of 2.459 A is longer than the corresponding mean value of bond distance (2.425 A) in [(Ta6Cl12)Cl6]2- anion. The other interatomic distances, angles and some properties of the cluster will be discussed in terms of the simultaneous presence of mixed-charge cluster units.

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  3. H. Imoto, S Hayakawa, N. Morita, T. Saito, Inorg. Chem. 29 (1990) 2007.
  4. C. B. Thaxton, R. A. Jacobson, Inorg. Chem. 10 (1971) 1460.