Actinide complexes tetrahalides

Actinide halides and oxyhalides are known to form numerous complexes with oxygen and nitrogen donor ligands and the preparation and properties of such compounds have recently been reviewed (12, 13). Relatively few protactinium halide complexes are known, but this situation reflects the lack of research rather than a tendency not to form complexes. However, there is sufficient information available for certain ligands to permit a comparison with the behavior of other actinide halides, and to illustrate the similarities and differences observed with the tetrahalides of thorium to plutonium inclusive and, to a lesser extent, with the protactinium and uranium pentahalides. 

Like other actinide tetrahalides, protactinium tetrachloride and tetrabromide form stable complexes with phosphine oxides (48, 55) and iV jAT -dimethylacetamide (24), but the tetrachloride-dimethyl sulfoxide... 

The actinide tetrachloride-DMSO complexes are particularly interesting (18). There is a pronounced change in stability proceeding along the actinide series with 1 5 complexes being the most stable for thorium and protactinium and the 1 3 complexes for the remaining actinides. The 1 7 complex could not be obtained pure with thorium tetrachloride and under the preparative conditions required, namely, recrystallization from hot dimethyl sulfoxide, protactinium(IV) was oxidized. The solid 1 5 and 1 3 protactinium tetrachloride compounds are, in fact, unstable in dry nitrogen, behavior which contrasts markedly with the stability of the tetrahalide-phosphine oxide and DMA complexes. 

Even fewer complexes with nitrogen donor ligands have been reported and all are methyl cyanide adducts (Tables X and XI). Protactinium pentabromide forms a soluble 1 3 complex in contrast to the 1 1 complexes formed by niobium and tantalum pentahalides (46). Other actinide pentahalide-methyl cyanide complexes are still unknown. Protactinium tetrachloride, tetrabromide, and tetraiodide react with anhydrous, oxygen-free methyl cyanide to form slightly soluble 1 4 complexes (44, 48) which are isostructural with their actinide tetrahalide analogs. 

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