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Alkaline earth metal clusters

Note that the structures depicted in Fig. 5 are not self-similar because the angle of rotation of the faces differs for each layer. The layers should, therefore, not be called shells as they are called in the case of pure alkaline earth-metal clusters. With increasing size, the shape of the cluster will converge asymptotically to that of a perfect icosahedron. [Pg.174]

K.M. Fromm and E.D. Gueneau (2004) Polyhedron, vol. 23, p. 1479 - Structures of alkali and alkaline earth metal clusters with oxygen donor ligands (a review that includes comments on CVD). [Pg.323]

Thus a simple question arises Based on this model, at which size can we expect a stable alkaline-earth metal cluster As each alkaline-earth metal has two itinerant valence s electrons, stable clusters are expected for clusters constituting 4, 10, 20,... atoms, which was indeed confirmed by experiments. Although the configuration IS IP 1D ° corresponds to a closed electronic structure, 18 was not observed as a magic number in homogeneous clusters. This is because both ID and 2S levels... [Pg.274]

Abstract—Clusters of and C70 coated with alkali or alkaline earth metals are investigated using photo-... [Pg.169]

When building clusters by coating the fullerenes with metal, features similar to the electronic and geometric shells found in pure metal clusters[9] are observed in the mass spectra. In the case of fullerene molecules coated with alkaline earth metals (section 3), we find that a particularly stable structure is formed... [Pg.169]

In this section, we will investigate the structure of clusters produced when the metal oven is filled with one of the alkaline earth metals Ca, Sr, or Ba. [Pg.170]

The structures observed in the mass spectra of fullerene molecules covered with alkaline earth metals, as described in the previous section, all seem to have a geometric origin, resulting in particularly stable cluster configurations every time a highly symmetrical layer of metal atoms around a central fullerene molecule was completed. When replacing the alkaline earth metals by an alkali metal (i.e., Li, Na, K, Rb, or Cs), a quite different situation arises. [Pg.174]

Of course, the chemistry of zirconium cluster phases has been well described and reviewed in the literature [1-4]. Apart from a very few examples, mostly in the binary halides, almost all reduced zirconium halides contain octahedra of zirconium atoms centred on an interstitial atom Z. Several possible and experimentally realized Z include H, Be-N, K, Al-P, and the transition metals Mn-Ni. All these compounds have the general formula Ax"[(Zr6Z)Xi2X[J], with a " = alkali or alkaline earth metal cation, X=C1 Br or I, X =inner edge-bridging halide [5], X =outer exo-bonded halide, and 0[Pg.61]

Up till now anionic mercury clusters have only existed as clearly separable structural units in alloys obtained by highly exothermic reactions between electropositive metals (preferably alkali and alkaline earth metals) and mercury. There is, however, weak evidence that some of the clusters might exist as intermediate species in liquid ammonia [13]. Cationic mercury clusters on the other hand are exclusively synthesized and crystallized by solvent reactions. Figure 2.4-2 gives an overview of the shapes of small monomeric and oligomeric anionic mercury clusters found in alkali and alkaline earth amalgams in comparison with a selection of cationic clusters. For isolated single mercury anions and extended network structures of mercury see Section 2.4.2.4. [Pg.173]

Alkaline-earth Metal- and Tin(+2)-Phosphorus and -Arsenic Clusters... [Pg.412]

Alkaline-earth Metal—and Tin(+2)—Phosphorus and—Arsenic Clusters 1419... [Pg.419]

Obviously, it is possible to produce bigger clusters at Aig = 4.76 by stabilizing them with suitably sized cations, available by electroequivalent substitution of alkali metal by alkaline earth metal cations. [Pg.30]

An elegant access to larger cluster units is to make use of preformed smaller clusters as they occur, e.g., in Zintl phases [8, 9]. The phase KSi (or K4Si4) contains homoatomic Si4 tetrahedra, and thus a salt-like formulation (Na )4[Si4]" with a formal electron transfer is appropriate (Fig. 1) [10]. Such homoatomic anionic building blocks occur in binary or ternary intermetallic phases A E and A Pn j with A being an alkali and alkaline-earth metal, and E = Si-Pb and Pn = P-Bi. These phases are generally available in good quantities, and - since a few members... [Pg.92]

The coordination compounds of the alkaline-earth metals are becoming increasingly important to many branches of chemistry and biology. A considerable degree of structural diversity exists in these compounds, and monomers up to nonametallic clusters and polymeric species are known. [Pg.450]

A. Simon, Alkali and alkaline earth metal suboxides and subnitrides. In M. Driess and H. Noth (eds.), Molecular Clusters of the Main Group Elements, Wiley-VCH, Weinheim, 2004, pp. 246-66. [Pg.459]


See other pages where Alkaline earth metal clusters is mentioned: [Pg.172]    [Pg.17]    [Pg.172]    [Pg.17]    [Pg.169]    [Pg.169]    [Pg.174]    [Pg.180]    [Pg.162]    [Pg.30]    [Pg.63]    [Pg.370]    [Pg.237]    [Pg.41]    [Pg.18]    [Pg.170]    [Pg.246]    [Pg.256]    [Pg.391]    [Pg.415]    [Pg.419]    [Pg.346]    [Pg.283]    [Pg.26]    [Pg.31]    [Pg.39]    [Pg.166]    [Pg.69]    [Pg.91]    [Pg.372]    [Pg.397]    [Pg.138]   
See also in sourсe #XX -- [ Pg.15 ]




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