Tetrahalides actinide

The preparation and properties of numerous actinide haUdes have been described by D. Brown Although the oxidation numbers of actinides in halides can vary from II to VI, most solid state studies are limited to di-, tri- and tetrahalides. 

The compounds known are summarized in Table 10.1. The only compound of an early actinide in the -1-2 state is Thl2, a metallic conductor which is probably Th + (e )2 (D)2-Certain heavier actinides form MX2 (Am, Cf, Es), which usually have the structure of the corresponding EuX2 and are thus genuine M + compounds. All four trihalides exist for all the actinides as far as Es, except for thorium and protactinium. Tetrafluorides exist for Th-Cm and the other tetrahalides as far as NpX4 (and in the gas phase in the case of PuCE). Pentahalides are only known for Pa, U, and Np whilst there are a few MFe (M = U-Pu), uranium is the only actinide to form a hexachloride. The known actinide halides are generally stable compounds most are soluble in (and hydrolysed by) water. 

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. 

With the exception of thorium, the actinides form trihalides. For uranium and neptunium, reduction of the MX4 compounds with hydrogen is necessary, but for the elements from plutonium onwards the action of the carbon tetrahalide or aluminium halide on the dioxide is usually employed. The trifluorides are insoluble but the rest dissolve to give solutions containing ions. 

There are no experimental data for the heat capacity and therefore entropy of p-ThBr4 and we have selected the estimated valne of the entropy of Konings et al. [2006KON/MOR], based on the trends in the entropies of the actinide tetrahalides ... 

An analysis of vapour pressure measurements of a number of actinide tetrahalides is used to infer their molecular structure. The results offer no evidence for deviations from tetrahedral symmetry. 

Table 6 Heats and free energies offormation of actinide tetrahalides (solids)...

The lanthanide and actinide halides remain an exceedingly active area of research since 1980 they have been cited in well over 2500 Chemical Abstracts references, with the majority relating to the lanthanides. Lanthanide and actinide halide chemistry has also been reviewed numerous times. The binary lanthanide chlorides, bromides, and iodides were reviewed in this series (Haschke 1979). In that review, which included trihalides (RX3), tetrahalides (RX4), and reduced halides (RX , n < 3), preparative procedures, structural interrelationships, and thermodynamic properties were discussed. Hydrated halides and mixed metal halides were discussed to a lesser extent. The synthesis of scandium, yttrium and the lanthanide trihalides, RX3, where X = F, Cl, Br, and I, with emphasis on the halide hydrates, solution chemistry, and aspects related to enthalpies of solution, were reviewed by Burgess and Kijowski (1981). The binary lanthanide fluorides and mixed fluoride systems, AF — RF3 and AFj — RF3, where A represents the group 1 and group 2 cations, were reviewed in a subsequent Handbook (Greis and Haschke 1982). That review emphasized the close relationship of the structures of these compounds to that of fluorite. 

Comparable recent detailed reviews of the actinide halides could not be found. The structures of actinide fluorides, both binary fluorides and combinations of these with main-group elements with emphasis on lattice parameters and coordination poly-hedra, were reviewed by Penneman et al. (1973). The chemical thermodynamics of actinide binary halides, oxide halides, and alkali-metal mixed salts were reviewed by Fuger et al. (1983), and while the preparation of high-purity actinide metals and compounds was discussed by Muller and Spirlet (1985), actinide-halide compounds were hardly mentioned. Raman and absorption spectroscopy of actinide tri- and tetrahalides are discussed in a review by Wilmarth and Peterson (1991). Actinide halides, reviewed by element, are considered in detail in the two volume treatise by Katzet al. (1986). The thermochemical and oxidation-reduction properties of lanthanides and actinides are discussed elsewhere in this volume [in the chapter by Morss (ch. 122)]. 

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