Six new derivatized deltahedral Zintl ions have been synthesized by reactions between the known Zintl ions Ge(9) (n-) with the halides R(3)EX and/or the corresponding anions R(3)E(-) for E=Ge or Sn. This rational approach is based on our previous discovery that these derivatization reactions are based on nucleophilic addition to the clusters. All species were structurally characterized as their salts with potassium countercations sequestered in 2,2,2-crypt or [18]crown-6 ether. The tin-containing anions were characterized also in solutions by (119)Sn NMR spectroscopy. The reaction types for such substitutions and the structures of the new anions are discussed.

One pathway toward nanomaterials with controllable band gaps is to assemble solids where atomic clusters serve as building blocks, since the electronic structures of clusters vary with size and composition. To study the role of organization in cluster assemblies, we synthesized multiple architectures incorporating As(7)(3-) clusters through control of the countercations. Optical measurements revealed that the band gaps vary from 1.1-2.1 eV, even though the assemblies are constructed from the identical cluster building block. Theoretical studies explain this variation as being a result of altering the lowest unoccupied molecular orbital levels by changing the countercations. Additional variations in the gap are made by covalently linking the clusters with species of varying electronegativity to alter the degree of charge transfer. These findings offer a general protocol for syntheses of nanoassemblies with tunable electronic properties.

The title anion was synthesized by oxidation of nido-Ge94- with Ph3P or Ph3As in ethylenediamine solution. It was structurally characterized in the compound (Rb-2,2,2-crypt)6[Ge9=Ge9=Ge9].3en (2,2,2-crypt = 4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane) crystallized from the solution. The anion is a linear trimer of nine-atom clusters with the shape of tricapped trigonal prisms elongated along two of the three prismatic edges. Each pair of clusters is connected by two exo-bonds.

Clusters have the potential to serve as building blocks of materials, enabling the tailoring of materials with novel electronic or magnetic properties. Historically, there has been a disconnect between magic clusters found in the gas phase and the synthetic assembly of cluster materials. We approach this challenge through a proposed protocol that combines gas-phase investigations to examine feasible units, theoretical investigations of energetic compositional diagrams and geometrical shapes to identify potential motifs, and synthetic chemical approaches to identify and characterize cluster assemblies in the solid state. Through this approach, we established As7(3-) as a potential stable species via gas-phase molecular beam experiments consistent with its known existence in molecular crystals with As to K ratios of 7:3. Our protocol also suggests another variant of this material. We report the synthesis of a cluster compound, As7K1.5(crypt222-K)1.5, composed of a lattice of As7 clusters stabilized by charge donation from cryptated K atoms and bound by sharing K atoms. The bond dimensions of this supercluster assembled material deduced by X-ray analysis are found to be in excellent agreement with the theoretical calculations. The new compound has a significantly larger band gap than the hitherto known solid. Thus, our approach allows the tuning of the electronic properties of solid cluster assemblies.

A tetramer of nine-atom deltahedral germanium clusters and charge 8-, [Ge9=Ge9=Ge9=Ge9]8- , has been characterized as a (Rb-18C6)(+) salt (18C6 = 18-crown-6 polyether). The clusters are connected by pairs of parallel bonds, and the electrons are delocalized over the whole anion. The size of the tetramer is of nanorod dimensions, ca. 2 nm.

Renewable polymeric materials derived from biomass with built-in phototriggers were synthesized and evaluated for degradation under irradiation of UV light. Complete decomposition of the polymeric materials was observed with recovery of the monomer that was used to resynthesize the polymers.

The type of the reactions of addition of exo-bonded groups to deltahedral Zintl ions such as Ge9(n-) has been established as addition of anionic nucleophiles. Various nucleophiles such as Ph2Bi-, Ph2Sb-, Ph- interact with the relatively low-lying LUMO of Ge9(2-) and/or the half filled HOMO of Ge9(3-) and bond to the clusters. The title anions, characterized in their (K-crypt) salts where crypt = 4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo-[8.8.8]-hexacosane, and the previously characterized [Ph2Sb-Ge9-SbPh2](2-) are made by a reaction of K4Ge9 with SbPh3 in ethylenediamine. [Ph-Ge9-SbPh2](2-) is the first ogranically functionalized deltahedral Zintl ion, i.e., a deltahedral ion with a direct carbon-cluster covalent bond, that can exists without the substituents as well. The Ge(9) clusters resemble tricapped trigonal prisms with one elongated edge (one of the three edges parallel to the pseudo 3-fold axis). The two substituents are always bonded to the vertexes of such an elongated edge. The same is true for the intercluster bond in [Ph2Sb-Ge9-Ge9-SbPh2)](4-).

Atropisomeric maleimides were synthesized and employed for stereospecific [2 + 2] photocycloaddition. Efficient reaction was observed under direct irradiation, triplet-sensitized UV irradiation, and non-metal catalyzed visible-light irradiation, leading to two regioisomeric (exo/endo) photoproducts with complete chemoselectivity (exclusive [2 + 2] photoproduct). High enantioselectivity (ee > 98%) and diastereoselectivity (dr > 99:1%) were observed under the employed reaction conditions and were largely dependent on the substituent on the maleimide double bond but minimally affected by the substituents on the alkenyl tether. On the basis of detailed photophysical studies, the triplet energies of the maleimides were estimated. The triplet lifetimes appeared to be relatively short at room temperature as a result of fast [2 + 2] photocycloaddition. For the visible-light mediated reaction, triplet energy transfer occurred with a rate constant close to the diffusion-limited value. The mechanism was established by generation of singlet oxygen from the excited maleimides. The high selectivity in the photoproduct upon reaction from the triplet excited state was rationalized on the basis of conformational factors as well as the type of diradical intermediate that was preferred during the photoreaction.