Lanthanide mixed halides

Lanthanides as components in non-oxide systems As halides With co-catalysts for olefin polymerization in mixed halides for oxychlorination as supports... 

Cyclooctatetraenyl lanthanide(III) halides of the type [(COT)Ln(/x-Cl)(THF)2]2 (Figure 77a) are the most important precursors for the preparation of other half-sandwich (see Half-sandwich Complexes) and mixed sandwich complexes with cyclooctatetraenyl ligands. These complexes are readily accessible by reacting anhydrons lanthanide trichlorides with K2[C0T] in a molar ratio of 1 1. The compounds consist of centrosyimnetric, chloro-bridged dimers with... 

RXH. The hydride halides RXH of the divalent rare earth metals have been known for a long time. All of them, EuXH, YbXH with X = Cl, Br, 1, and SmBrH (Beck and Limmer 1982) crystallize in the PbFCl-type structure, which is also adopted by the hydride halides of the alkaline earth metals MXH (Ehrlich et al. 1956), by the mixed halides RXX of divalent lanthanides, and many oxyhalides ROX of the trivalent metals. The colorless compounds RXH of R = Sm, Eu, Yb therefore have to be addressed as normal salts. The hydrogen content of these compounds is strictly stoichiometric. 

Additional areas of lanthanide halide chemistry that have been reviewed include the synthesis, phase studies, and structures of complex lanthanide halides - compounds formed between one or more group 1 cation and lanthanide element halides (Meyer 1982). Halides in combination with lanthanide elements in the II, III, and IV oxidation states were considered with the chemistry of the heavier halides being emphasized. More recently the reduced ternary lanthanide halides (Meyer 1983) and the reduced halides of the lanthanide elements were reviewed (Meyer 1988). The latter review considered lanthanides in which the formal oxidation state of the cation was 2 and included hydride halides, oxide halides, mixed-valence ternary halides, and reduced halide clusters. Corbett et al. (1987) discussed the structures and some bonding aspects of highly reduced lanthanide halides and compounds stabilized by a second-period element bound within each cluster, e.g., SC7CIJ2B, SC5CI5B, YjCljC. 

Numerous lanthanide (III) chloride-bromide systems have been characterized. Again, the changes observed can be understood from radius ratio considerations. Most of these studies have been effected by confining the mixed halides in quartz or... 

No, the editor didn t know what this name meant either.) It means salts of the triva-lent anions of Group V, restricted in [1] to arsenides, antimonides and bismuthides and prepared by reaction of sodium pnictides with anhydrous halides of transition and lanthanide metals. This violently exothermic reaction may initiate as low as 25°C. Avoidance of hydrated halides is cautioned since these are likely to react uncontrollably on mixing. Another paper includes a similar reaction of phosphides, initiated by grinding [2], Nitrides are reported made from the thermally initiated reaction of sodium azide with metal halides, a very large sealed ampoule is counselled to contain the nitrogen [3],... 

The study of coordination compounds of the lanthanides dates in any practical sense from around 1950, the period when ion-exchange methods were successfully applied to the problem of the separation of the individual lanthanides,131-133 a problem which had existed since 1794 when J. Gadolin prepared mixed rare earths from gadolinite, a lanthanide iron beryllium silicate. Until 1950, separation of the pure lanthanides had depended on tedious and inefficient multiple crystallizations or precipitations, which effectively prevented research on the chemical properties of the individual elements through lack of availability. However, well before 1950, many principal features of lanthanide chemistry were clearly recognized, such as the predominant trivalent state with some examples of divalency and tetravalency, ready formation of hydrated ions and their oxy salts, formation of complex halides,134 and the line-like nature of lanthanide spectra.135... 

The addition of a base, typically ammonia, to mixtures of transition metal halides and alcohols allows the synthesis of homoleptic alkoxides and phenoxides for a wide range of metals. Anhydrous ammonia was first used in the preparation of titanium alkoxides where the reaction is forced to completion by the precipitation of ammonium chloride.41 Although useful for the synthesis of simple alkoxides and phenoxides of Si, Ge, Ti, Zr, Hf, V, Nb, Ta and Fe, as well as a number of lanthanides,42-47 the method fails to produce pure /-butoxides of a number of metals.58 Presumably, secondary reactions between HC1 and Bu OH take place. However, mixing MC14(M = Ti, Zr) with the Bu OH in the presence of pyridine followed by addition of ammonia proves successful, giving excellent yields of the M(OBul)4 complexes.59... 

Synthetic routes leading to two series of (COT)lanthanide(III) scorpio-nate mixed sandwich complexes were reported. The early lanthanide derivatives (COT)Ln(Tp) and (COT)Ln(TpMe2) (Ln = Ce, Pr, Nd, Sm) were obtained by reacting the dimeric halide precursors [(COT)Ln(p-Cl)(THF)]2 with KTp or KTpMe2. For small lanthanide ions (COT)Ln(Tp) (Ln = Er,... 

Unusually, chloride is foimd in the first coordination sphere of lanthanum as well as nitrate in the serendipitously discovered mixed anion complexes [EaCl2(N03)(12-crown-4)]2 and [LaCl2(N03)(18-crown-6)]. A few complexes have been reported with other halides, such as [Sml3(dibenzo-18-crown-6)] (tricapped trigonal prismatic) and [LaBr3(12-crown-4)(acetone)] (distorted square antiprismatic). Lanthanide thiocyanate complexes of crown ethers are now starting to be studied. Several thiocyanate complexes of the... 

Hydrates of the oxoanion and halide complexes are numerous for Am and Cm and a few have also been reported for Bk and Cr . The hexahydrate trichlorides and tribromides, AnCl3 6H20 (An = Am or Bk) and AnBr3 6H20 (An = Am or Cf), are isostructural with the hydrated lanthanide chlorides and involve mixed ligand complexes, such as [AnCl2(H20)6]". ... 

In addition to this wide range of uses for yttrium, new applications of yttrium complexes are under continual development. Examples include hydrate with halide and other simple ligands, with oxygen donor ligands with lanthanides, or mixed (e.g., metal diyttrium-barium and yttrium-copper), with nitrogen donor ligands, with... 

The absence of reliable thermodynamic data for the tetrafluorides has contributed to difficulties in defining the chemistry of the rare earth elements. The fact that only Ce, Pr, and Tb form stable Rp4(s) phases has been established (see section 2.4) however, the thermochemistry of these fluorides has remained uncertain. Insight is provided by the work of Johansson (1978), who has correlated data for lanthanide and actinide oxides and halides and derived energy differences between the trivalent and tetravalent metal ions. The results, which have been used to estimate enthalpies of disproportionation of RF4 phases, agree with preparative observations and the stability order Prp4< TbP4 < CeP4. However, the results also indicate that tetravalent Nd and Dy have sufficient stability to occur in mixed metal systems like those described by Hoppe (1981). 

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. 

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