Sandwich compounds examples

Although the chemistry of zirconium in its lower oxidation states is still relatively unexplored, it is developing. Examples which offer the possibility of further exploitation include the blue, paramagnetic zirconium(III) compound 32) [L2Zr(/r-Cl)2ZrL2] L = C5H3(SiMe3)2-l,3, and the sandwich and half-sandwich compounds derived from cycloheptatriene red... 

Many other shapes are possible for complexes. The simplest are linear, with coordination number 2. An example is dimethylmercury(O), Hg(CI l,)2 (4), which is a toxic compound formed by bacterial action on aqueous solutions of I Ig ions. Coordination numbers as high as 12 are found for members of the / block, but they are rare in the d block. One interesting type of d-mctal compound in which there are 10 links between the ligands and the central metal ion is ferrocene, dicyciopentadi-enyliron(O), [Fe(C5H5)2] (5). Ferrocene is an aptly named sandwich compound, with the two planar cyclopentadienyl ligands the bread and the metal atom the filling. The formal name for a sandwich compound is a metallocene. 

The ability of the crown ether ligand, 12-crown-4, to separate the lithium cation from the organic moiety, thus stabilizing the SSIP structure, was also observed in the study dealing with cyclopentadienyllithium systems . As described in Section II.C.3, SSIP structures of these compounds are characterized by low x( Li) values. However, it is important to reahze that the variation found for x( Li) is basically caused by the local symmetry around the lithium cation and other highly symmetric situations will also lead to small x( Li) values. Examples are the sandwich compounds mentioned in Section n.C.3. It is thus necessary to consider also / Li and C chemical shift data in order to classify a certain complex as SSIP or CIP. 

A metal sandwich compound does not strictly fit our previous concept of an ABfl-type molecule, since the ligand atoms interact strongly with each other as well as with the central atom. It is desirable to extend the discussion to these molecules, however, since they provide clear and important examples of how to treat the situation in which the ligands in a complex are themselves polyatomic entities with an internal set of MOs perturbed by interaction with the AOs of the central atom. 

One of the most important carbon 7i-donors are the cyclopentadienes and their heteroanalogues, for instance 15 and 16. In general, cyclopentadiene itself forms three general types of mononuclear Cp transition metal complexes Cp2M 3 (symmetric molecules with mutually parallel Cp rings examples M = Fe, Cr, Ni), Cp2ML 124 [bent metallocenes, L = H, R, CO, etc. (n=l-3)], and half-sandwich compounds CpML 125 (n — 1 4) [21b], In the bent sandwich complexes... 

While the mercury compound shows localized N—Hg bonds, the TADB-system (which is isoelectronic with cyclopentadiene) forms a low-spin complex with iron. This was the first identified example of a sandwich-compounds of a boron-nitrogen ring. The complex is prepared by adding an etheric solution of TADBLi to a suspension of FeCl2 in tetra-hydrofuran. 

Recent advances in the techniques of photoelectron spectroscopy (7) are making it possible to observe ionization from incompletely filled shells of valence elctrons, such as the 3d shell in compounds of first-transition-series elements (2—4) and the 4/ shell in lanthanides (5, 6). It is certain that the study of such ionisations will give much information of interest to chemists. Unfortunately, however, the interpretation of spectra from open-shell molecules is more difficult than for closed-shell species, since, even in the simple one-electron approach to photoelectron spectra, each orbital shell may give rise to several states on ionisation (7). This phenomenon has been particularly studied in the ionisation of core electrons, where for example a molecule (or complex ion in the solid state) with initial spin Si can generate two distinct states, with spin S2=Si — or Si + on ionisation from a non-degenerate core level (8). The analogous effect in valence-shell ionisation was seen by Wertheim et al. in the 4/ band of lanthanide tri-fluorides, LnF3 (9). More recent spectra of lanthanide elements and compounds (6, 9), show a partial resolution of different orbital states, in addition to spin-multiplicity effects. Different orbital states have also been resolved in gas-phase photoelectron spectra of transition-metal sandwich compounds, such as bis-(rr-cyclo-pentadienyl) complexes (3, 4). 

Work directed at preparing and characterizing stacked complexes has been developed since the late 1980s, and the syntheses are carefully controlled. The principles of the approach are outhned below, but may be summarized as an example of the method. The archetypal sandwich compound is ferrocene. 

The compound (C5Et5)2Co (CP2C0) (38) was one of the earhest examples of transition metal sandwich compounds to... 

Mixed valency is not limited to consideration of individual ions in different oxidation states. Delocahzed systems also exist that exhibit properties of mixed valency, as in many organometalhc mixed valence compounds. For example, phthalocyanine, Pc (1), sandwich compounds of the lanthanides, Ln(Pc)2, are best described as containing the two Pc anionic ligands in mixed valent charge states of —2 and — 1 with the metal ion Ln +. 

The very rich structural chemistry of organometallic compounds also provides many examples of conformational polymorphism. For instance, cyclic ligands often have low barriers to rotation so that conformational variations between polymorphs might not be unexpected. Riley and Davis (1976) reported the structures of the dimorphic sandwich compound 5-VII, a system in which the molecular geometry is determined by the crystallographic site symmetry for both polymorphs (Fig. 5.8). In the triclinic form, the molecular site symmetry is C, requiring the trans orientation... 

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