Clusters have been the subject of intense investigations since their famous definition launched by Cotton in 1963, and the area has expanded ever since. One obvious development addresses the widening of the definition of what to call a cluster: from purely (transition) metal−metal linked assemblies, as per Cotton's early denomination, to nonmetal/metal clusters or purely nonmetal cages, like fullerenes, and even noncovalent aggregates such as water clusters. The other extension concerns the broadened spectrum of compositions within the aforementioned cluster types and their corresponding structures that range from trinuclear motifs to clusters with sizes in the range of the hemoglobin unit. This review article reports on one cluster family that has its origins in traditional Zintl anion chemistry but has undergone rapid development in recent years, namely, ligand-free clusters that combine main group and transition metal atoms. Depending on the position of the transition metal atom(s), one refers to such clusters as intermetalloid (endohedral) clusters or as a special type of heterometallic clusters. The predominant synthetic access makes use of soluble Zintl anions. Other pathways for their preparation include traditional solid state reactions of according element combinations or bottom-up syntheses employing low valent organo-main group element sources. This survey will shed light on all of these approaches, with an emphasis on the syntheses that employ soluble Zintl anion compounds. The article will give a comprehensive overview of the currently known compounds, their different synthesis protocols, and analytic techniques for determination of their compositions, structures, and further properties. Additionally, this survey will report peculiarities of bonding situations found within some of the cluster molecules, which were studied by means of sophisticated quantum chemical investigations.

The encapsulation of actinide ions in intermetalloid clusters has long been proposed but was never realized synthetically. We report the isolation and experimental, as well as quantum chemical, characterization of the uranium-centered clusters [U@Bi12](3-), [U@Tl2Bi11](3-), [U@Pb7Bi7](3-), and [U@Pb4Bi9](3-), upon reaction of (EE'Bi2)(2-) (E = Ga, Tl, E' = Bi; E = E' = Pb) and [U(C5Me4H)3] or [U(C5Me4H)3Cl] in 1,2-diaminoethane. For [U@Bi12](3-), magnetic susceptibility measurements rationalize an unprecedented antiferromagnetic coupling between a magnetic U(4+) site and a unique radical Bi12(7-) shell.

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Reactions of [K(crypt-222)] (TlBi )⋅0.5 en (1 b) with [Ru(cod)(H CC(Me)CH ) ] (A) in 1,2-diaminoethane (en) led to the formation of two compounds with new bismuth-rich cluster anions, [K(crypt-222)] [Bi {Ru(cod)} ]⋅1.5 en (2) and [K(crypt-222)] [Tl Bi {Ru(cod)}]⋅2 tol (3), alongside the salt of a binary nido cluster, [K(crypt-222)] (Tl Bi )⋅2 en (4). The anions in 2 and 3 are two further examples of rare heterometallic clusters containing Ru atoms. As one cod ligand is retained on each Ru atom in both clusters, the anions may be viewed as intermediates on the way towards larger, ligand-free intermetalloid clusters. Quantum-chemical studies provided insight into the bonding situation in these clusters. According to these studies, the anion of 2 features both electron-precise and electron-deficient parts. Electrospray ionization mass spectrometry analysis indicated that the clusters undergo stepwise fragmentation.

Clusters containing tin atoms show a huge variety of molecular structures, chemical as well as physical properties.