Abstract

The synthesis of cationic binuclear palladium complexes of the type {(μ-X)[Pd(C 6F 5)L 2][Pd(C 6F 5)L′]}ClO 4 (L = N or P donors) is described. X can be a pseudohalide, such as CN, SCN or N 3, or a halide when L 2 is a bidentate N-ligand, such as bipy. Trinuclear complexes of the type {[(PPh 3) 2Pd](μ-X) 2[Pd(C 6F 5)L 2] 2}ClO 4 have only been obtained for X = CN. For X = other pseudohalide or halide, rearrangement reactions render binuclear double-bridged species along with binuclear single-bridged species of the above-mentioned type. The preparation of a pentanuclear complex {[Pd(μ-CN) 4][Pd(C 6F 5)(PPh 3) 2] 4}(ClO 4) 2 is also described.

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