CLUSTERS halide valency

Very important from the chemical viewpoint are cluster halides of lanthanide metals (Ln) with the formal valence v<3 (Table 3.17). Thus, the structure and physical properties of LnE type compounds correspond in fact to the formula Ln + (I )2e, while the halides with v < 2 have typically cluster structures based on chains (single or double) of Me octahedra, surrounded by halogen atoms. The LnX type compounds constitute a peculiar class of 2-dimensional metals the Ln-Ln bond distance in them depends on the size of the anion (compare Tb-Tb distances of 3.79... 

Solid-state cluster chemistry is dominated by octahedral (M 5L8)L6 and (MsLi2)L units which are the focus of this paper. These two cluster types are different in the way the metal octahedral core is surrounded by the ligands. In (MsLg)L6-type clusters (Fig. 6.1a), typical for molybdenum and rhenium halides, chalcogenides, and chalcohalides, eight innei hgands (L ) cap the octahedron faces and six outer ligands (L ) are located in the apical positions [9]. For metals with a smaller number of valence electrons, the (M6L i2)L -type clusters... 

Of course, valence electron concentration is not only related to the metal atoms but also to the number and valence of the ligands. Ligand deficiency creates vacant coordination sites at metal atoms and results in cluster condensation, which is the fusion of clusters via short M-M contacts into larger units ranging from zero- to three-dimensional. The chemistry of metal-rich halides of rare earth metals comprises both principles, incorporation of interstitial atoms and cluster condensation, with a vast number of examples [22, 23]. 

There are several interesting families of inorganic mixed-valence compounds that we have not discussed here (see Yvon, 1979 McCarley, 1982). For example, there are metal-cluster compounds such as the Chevrel phases, M,jMo6X8(X = S or Se) and condensed metal-cluster chain compounds such as TlMojScj, TijTe, NaMo O and M PtjO. TTF halides and TTF-TCNQ complexes (Section 1.9) constitute molecular mixed-valent systems in which the mixed valency is associated with an entire molecule the charge on TTF in such compounds is nonintegral. The structure of TTF-Br(, 79 and... 

The lower halides of niobium and tantalum consist of tightly bound clusters of metal atoms, with metal-metal distances close to those found in the metal. They contain ions with average oxidation numbers between +III and +1 (Table 43). Their size depends on the valence electron concentrations (VEC) that are available on the metal atoms for M—M bonding, and on the halide-metal ratio.644 Several reviews have been devoted to the clusters of early transition metals.3,643... 

Technetium(II) complexes are paramagnetic with the d5 low-spin configuration. A characteristic feature is the considerable number of mixed-valence halide clusters containing Tc in oxidation states of +1.5 to + 3. This area has been reviewed (42). For convenience, all complexes, except those of [Tc2]6+, are treated together here. EPR spectroscopy is particularly useful in both the detection of species in this oxidation state and the study of exchange reactions in solution. The nuclear spin of "Tc (1 = f) results in spectra of 10 lines with superimposed hyperfine splitting. The d5 low-spin system is treated as a d1 system in the hole formalism (40). 

Little is known about the oxidative addition of organohaUdes to early transition metal atoms. Nevertheless, macroscale amounts of solvated transition metal halides in lower valency states have been obtained. Re yields interesting clusters in reactions with 1,2-dibromoethane and oxalyl chloride... 

Although the above mentioned face- and edge-halide-bridged clusters are characterised by 84 and 76 valence electrons respectively, it was apparent by the early 1970 s that the great majority of octahedral transition metal clusters possess 86 electrons. Braterman rationalised the 86 cluster valence electron count for octahedral metal carbonyl clusters, such as [Co6(CO)i6]75), [Ru6C(CO)17]76) and [Co6(CO)i4]4- 77) in terms of localised M-CO... 

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