Actinide elements complexes

Ion-exchange separations can also be made by the use of a polymer with exchangeable anions in this case, the lanthanide or actinide elements must be initially present as complex ions (11,12). The anion-exchange resins Dowex-1 (a copolymer of styrene and divinylben2ene with quaternary ammonium groups) and Amherlite IRA-400 (a quaternary ammonium polystyrene) have been used successfully. The order of elution is often the reverse of that from cationic-exchange resins. 

Special techniques for experimentation with the actinide elements other than Th and U have been devised because of the potential health ha2ard to the experimenter and the small amounts available (15). In addition, iavestigations are frequently carried out with the substance present ia very low coaceatratioa as a radioactive tracer. Such procedures coatiaue to be used to some exteat with the heaviest actinide elements, where only a few score atoms may be available they were used ia the earHest work for all the transuranium elements. Tracer studies offer a method for obtaining knowledge of oxidation states, formation of complex ions, and the solubiHty of various compounds. These techniques are not appHcable to crystallography, metallurgy, and spectroscopic studies. 

Actinides Elements 89 (Ac) through 102 (No) in the periodic table, 147 Activated complex A species formed by... 

Treatment of UCI4 with the lithium complex obtained from dicyclohexylcar-bodiimide followed by crystallization from pyridine afforded a dinuclear uranium(rV) oxalamidinate complex in the form of dark green crystals in 94% yield (Scheme 191). The same compound could also be obtained by first reducing UCI4 to LiUCli (or UQs+LiCl) followed by reductive dimerization of di(cyclo-hexyl)carbodiimide as shown in Scheme 191. The molecular structure of this first oxalamidinato complex of an actinide element is depicted in Figure 31. ° ... 

In terms of gross features of mechanism, a redox reaction between transition metal complexes, having adjacent stable oxidation states, generally takes place in a simple one-equivalent change. For the post-transition and actinide elements, where there is usually a difference of two between the stable oxidation states, both single two-equivalent and consecutive one-equivalent changes are possible. 

The redox reactions of the actinide elements have been the subject of a recent and authoritative review by Newton and Baker . The net activation process concept is used to interpret the experimental data. Empirical correlations shown to exist include those between the entropies of the activated complexes and their charges, and, for a set of similar reactions, between AG and AG , and and A/f . The present state of the evidence for binuclear species is discussed. 

Thirdly, some obvious applications of coordination chemistry are omitted from this volume if they are better treated elsewhere. This is the case when a specific application is heavily associated with one particular element or group of elements, to the extent that the application is more appropriately discussed in the section on that element. Essentially all of the coordination chemistry of technetium, for example, relates to its use in radioimmunoimaging inclusion of this in Chapter 20 of this volume would have left the chapter on technetium in Volume 5 almost empty. For the same reason, the applications of actinide coordination complexes to purification, recovery,... 

Studies of sulfoxide complexes of other actinide elements have appeared, (38, 40), but insufficient data are available to make any meaningful comparisons along the series. Work on the solvent extraction of actinide elements by sulfoxides has been reported (423). 

Osmium(VI) forms irons-0s02(malt)2 (98), while dioxouranium(VI) forms irons-U02(malt)2 (98) and many hydroxypyridinonate complexes, with bidentate and with tetradentate (177) ligands - trans-UO2L2 and UO2L, respectively. Several actinide elements form complexes with hexa- and octa-dentate hydrox5rpyridinonates (see Section IV.C.7 later). 

The HSAB principle is useful in solvent extraction, as it provides a guide to choosing ligands that react strongly (high log P) to give extractable complexes. For example, the actinide elements would be expected to, and do, complex strongly with the P-diketonates, R3C—CO—CHj—CO—CR3 (where R = H... 

The first and thus far only silsesquioxane complex of an actinide element is [Cy7Si70i2]2U (100). This colorless, nicely crystalline uranium(VI) compound is formed upon reaction of 3 with any uranium precursor, e.g., UCI4 in the presence of NEt3. In all cases oxidation of uranium to the hexavalent oxidation state is observed. The best synthetic route leading to 100 in ca. 80% yield is the reaction of 3 with uranocene as outlined in Scheme 33. 

The effects of tetracycline injection following injection of thorium-228 were not reported. Studies with a similar actinide element, plutonium, suggest that a thorium-tetracycline complex may be formed, which is excreted rapidly through the kidneys. Similarly, chelating agents such as EDTA... 

F. T. Edelmann, Scandium, yttrium and the lanthanide and actinide elements, excluding their zero oxidation state complexes in Comprehensive Organometallic Chemistry II (eds. E. W. Abel, EG. A. Stone and G. Wilkinson), Elsevier, Oxford, 1995, vol. 4 (ed.M.F. Lappert), ch. 2. 

Thorium forms one series of halides, another one of oxyhalides, and also a series of double or complex halides. In general, stability of these compounds toward heat decreases as die atomic weight of die halogen increases. These compounds are often isostructural with the corresponding compounds of other actinide elements in the (IV) oxidation state. 

The redox chemistry of the actinide elements, especially plutonium, is complex (Katz et al., 1980). Disproportionation reactions are especially important for the +4 and +5 oxidation states. Some of the equilibria are kinetically slow and irreversible. All transuranium elements undergo extensive hydrolysis with the +4 cations reacting most readily due to their large charge/radius ratio. Pu (IV) hydrolyzes extensively in acid solution and forms polymers. The polymers are of colloidal dimensions and are a serious problem in nuclear fuel reprocessing. 

Despite the extremely low concentrations of the transuranium elements in water, most of the environmental chemistry of these elements has been focused on their behavior in the aquatic environment. One notes that the neutrality of natural water (pH = 5-9) results in extensive hydrolysis of the highly charged ions except for Pu(V) and a very low solubility. In addition, natural waters contain organics as well as micro- and macroscopic concentrations of various inorganic species such as metals and anions that can compete with, complex, or react with the transuranium species. The final concentrations of the actinide elements in the environment are thus the result of a complex set of competing chemical reactions such as hydrolysis, complexation, redox reactions, and colloid formation. As a consequence, the aqueous environmental chemistry of the transuranium elements is significantly different from their ordinary solution chemistry in the laboratory. 

The most widely used neutral extractants, however, are the organophosphoms compounds, of which the ester, TBP, is the most important. TBP forms complexes with the actinide elements thorium, uranium, neptunium, and plutonium by bonding to the central metal atom via the phosphoryl oxygen in the structure... 

The actinide element, thorium, also forms a porphyrin complex, ThIV(Por)(acac)2, in the same way as the lanthanide derivatives (Scheme 8).l7a The acetylacetonato groups most likely coordinate to the thorium atom on the same side of the porphyrin (Scheme 8). Thlv and Ulv(OEP)Cl2L2 (L = PhCN, THF, py) are prepared from H2(OEP) and MC14.35... 

---