Cluster chemistry blocks

Mathematical cluster chemistry/Metal-metal interactions in transition metal clusters with donor ligands/Electron count versus structural arrangement in clusters based on a cubic transition metal core with bridging Main Group elements/Metalloboranes/ Clusters with interstitial atoms from the p-block How do Wade s rules handle them /Diverse naked clusters of the heavy Main Group elements Electronic regularities and analogies... 

G1.2 Applications of high-performance liquid chromatography to metal carbonyl and cluster chemistry G1.3 Surface-mediated syntheses of metal clusters G1.4 Trimetallic units as building blocks in cluster chemistry... 

With the exception of polynuclear boron hydrides, cluster chemistry has developed mainly over the past 40 years. Prior to this a number of compormds that would now be classified as clusters had been but their nature was not recognized. It is perhaps interesting to ask the question of why cluster compounds, that is molecules containing metal-metal bonds, were considered prior to 1940 to be a relatively uncommon feature in inorganic chemistry The problem was in part associated with the dominance of organic chemistry coupled with the difficulties in the rapid determination of the structure of compounds of this type. The determination of the X-ray structure of relatively simple compounds could take months or years to accomplish. As stated above, for the s and p block elements the compounds were also generally found to be unstable to air and moisture, whilst for the d and f block the compounds were often very complex in structure and the stoichiometry difficult to assess. This led to a general lack of appreciation of the occurence and stability of metal-metal or element-element bonds. 

The importance of surface characterization in molecular architecture chemistry and engineering is obvious. Solid surfaces are becoming essential building blocks for constructing molecular architectures, as demonstrated in self-assembled monolayer formation [6] and alternate layer-by-layer adsorption [7]. Surface-induced structuring of liqnids is also well-known [8,9], which has implications for micro- and nano-technologies (i.e., liqnid crystal displays and micromachines). The virtue of the force measurement has been demonstrated, for example, in our report on novel molecular architectures (alcohol clusters) at solid-liquid interfaces [10]. 

Abstract Amino acids are the basic building blocks in the chemistry of life. This chapter describes the controllable assembly, structures and properties of lathanide(III)-transition metal-amino acid clusters developed recently by our group. The effects on the assembly of several factors of influence, such as presence of a secondary ligand, lanthanides, crystallization conditions, the ratio of metal ions to amino acids, and transition metal ions have been expounded. The dynamic balance of metalloligands and the substitution of weak coordination bonds account for the occurrence of diverse structures in this series of compounds. 

Metalloboranes, 4 172 exopolyhedral, 4 208-210 main group element, 4 207-208 transition element, 4 205-207 Metallo-carbohedrene clusters, 4 648 Metallocarboranes, 4 170 as catalysts, 4 217-218 economic aspects, 4 229 exopolyhedral, 4 215-216 f-block element, 4 225-226 host-guest chemistry-carborane anticrowns, 4 216-217 structural systematics, 4 176-179 transition metal, 4 210-215 Metallocene catalysis, MAO in, 16 92-93. 

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