Transition metal clusters alkali metals

Transition Metal-Doped Alkali Metal Clusters.153... 

If the octahedral and icosahedral 13-atom nickel clusters are representative, an inhomogeneous magnetic field is not a good tool for separating isomers of transition metal clusters. This result is reminiscent of the fact that geometry plays no strong role in the ionization potential variation of alkali clusters (80). However, many calculations must be made before we can be definitive here. 

Within this context, the present article concentrates on transition metal cluster complexes of cobalt, iron and manganese with mixed chalcogen/carbonyl ligand spheres obtained by reaction of simple binary metal carbonyls with alkali-metal sulfides, alkali-metal thiolates or transition-metal thiolate complexes and their selenium or tellurium counterparts. 

H2S, SO2, S and CS2 have all been used as sources of sulfido atoms to introduce atomic sulfur into transition metal clusters. For example, the reaction of a solution of [Rh(CO)2(acac)] and alkali carboxylates with H2S or SO2 at high tern-... 

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]

The polyhedral boranes and carboranes discussed above may be regarded as boron clusters in which the single external orbital of each vertex atom helps to bind an external hydrogen or other monovalent atom or group. Post-transition main group elements are known to form clusters without external ligands bound to the vertex atoms. Such species are called bare metal clusters for convenience. Anionic bare metal clusters were first observed by Zintl and co-workers in the 1930s [2-5], The first evidence for anionic clusters of post-transition metals such as tin, lead, antimony, and bismuth was obtained by potentiometric titrations with alkali metals in liquid ammonia. Consequently, such anionic post-transition metal clusters are often called Zintl phases. 

Hetero-atomic clusters, moreover, may be derived from the binary structures mainly through the introduction of late transition or earlier post-transition elements. Examples of ternary alloys containing such structures are the alkali metal salts of centred clusters In10Me10 (Me = Ni, Pd, Pt), Tl12 Me12- (Me = Mg, Zn, Cd, Hg), etc. The crystal structure of the phase Na T Cdi x)27 (0.24 < x < 0.33)... 

Modem work on these and related bare post-transition element clusters began in the 1960s after Corbett and coworkers found ways to obtain crystalline derivatives of these post-transition element clusters by the use of suitable counterions. Thus, crystalline derivatives of the cluster anions had cryptate or polyamine complexed alkali metals as countercations [8]. Similarly, crystalline derivatives of the cluster cations had counteractions, such as AlCLj, derived from metal halide strong Lewis acids [9]. With crystalhne derivatives of these clusters available, their structures could be determined definitively using X-ray diffraction methods. 

Polymetallic anions, prepared by dissolution of alloys of the alkali and post-transition metals in amine solvents (often with a complexand for the alkali metal cation), have been characterized in crystalline and solution phases. Clusters TlSng3, Ge92 (with 20 skeletal bonding electrons), Sn93- (21 skeletal e) and Bi95+ (22 skeletal e) possess a tricapped trigonal prismatic structure, symmetry D3A, with variations of dimensional detail which correlate with the electron population.291 292 This structure is a ctoso-deltahedron, and with 20 (2h + 2) skeletal electrons can be construed to be three-dimensionally aromatic.292 The 22e clusters M94 (M = Ge, Sn, Pb) occur as the C4v monocapped square antiprism, a nido polyhedron. 

Of particular significance in this respect has been the ability to prepare, characterize and study most intriguing species, the alkalides [2.79, 2.80] and the electrides [2.80, 2.81] containing an alkali metal anion and an electron, respectively, as counterion of the complexed cation. Thus, cryptates are able to stabilize species such as the sodide [Na+ c 9]Na- and the electride [K+ c 9]e-. They have also allowed the isolation of anionic clusters of the heavy post-transition metals, as in ([K+ c cryp-tand]2 Pb52-) [2.82]. 

A further consequence of intermediate-range interactions adding up are very high almost isotropic repulsive barriers around compact clusters. This has consequences for the density scaling [32] and favors small islands with more narrow distributions of sizes and spacings than the ones obtained without interactions [29]. We finally note that atomic superlattices with smaller lattice constant may be stabilized by dipolar interactions of relatively short range. The most prominent examples for such interactions are alkali metals on metal surfaces. A phase transition from a dilute liquid into a well-ordered solid has been reported for Cs/Ag/Si(lll)-( /3 x %/3) [33]. 

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