Molecular ions or neutral compounds known as "metal cluster compounds" are made up of three or more different metals and exhibit strong metal-metal interactions. Fe2(CO)9 and Fe3(CO)12 were swiftly isolated as a result of the rapid formation of metal carbonyl clusters like Ni(CO)4 and Fe(CO)5. The "unsupported" Mn-Mn link in Mn2(CO)10 was found by Rundle and Dahl, proving that metals may form bonds with one another in molecules. Using [Rh13(CO)24H3]2 as an example, Paolo Chini demonstrated in the 1970s how to build very big clusters from platinum metals. The single-crystal X-ray diffraction technique has been useful in this field of cluster chemistry. Low-valent early metal halides frequently consist of clusters with strong M-M bonding. In contrast, there is abundant metal-halide bonding in the higher halides of these metals and almost all of the late transition metals. It was proven that ferredoxin contains Fe4S4 clusters in the 1970s, and nitrogenase later had a distinct MoFe7S9 active site revealed. Although some of the Fe-S clusters have catalytic properties, they primarily act as redox cofactors. In the field of bioinorganic chemistry, numerous Fe-S clusters with CO as ligands have also been discovered. Metal atom clusters called elementoid clusters have more direct contacts between the elements than between the elements and ligands because they are stabilised by ligands. Ligand stabilised cores of Al77, Ga84, and Pd145 are examples of structurally characterised clusters.
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