Extension and Fusion of Cyclic Polyantimony Units.

The synthesis and characterization of a series of polyantimony anionic clusters are reported. The products [(NbCp)2Sb10]2-, [MSb13]3- (M = Ru/Fe), and [MSb15]3- (M = Ru/Fe) were isolated as either K(18-crown-6) or K([2.2.2]-crypt) salts. The Sb10 ring contained in the [(NbCp)2Sb10]2- cluster can be viewed as an extension of two envelope-like cyclo-Sb5 units and represents by far the largest monocyclic all-antimony species. The clusters [MSb13]3- and [MSb15]3- (M = Ru/Fe) illustrate the variability of crown-like Sb8 ring motifs and reveal the fusion of different antimony fragments featuring unique Sb-Sb chain-like units. The reported synthetic approaches involve the fabrication of a variety of distinctive polyantimony anionic clusters, enhancing our understanding of the coordination chemistry of heavier group 15 elements.

[K2(Bi@Pd12@Bi20)]4-: An Endohedral Inorganic Fullerene with Spherical Aromaticity.

Inorganic fullerene clusters have attracted widespread attention due to their highly symmetrical geometric structures and intrinsic electronic properties. However, cage-like clusters composed of heavy metal elements with high symmetry are rarely reported, and their synthesis is also highly challenging. In this study, we present the synthesis of a [K2(Bi@Pd12@Bi20)]4- cluster that incorporates a {Bi20} cage with pseudo-Ih symmetry, making it the largest main group metal cluster compound composed of the bismuth element to date. Magnetic characterization and theoretical calculations suggest that the spin state of the overall cluster is a quartet. Quantum chemical calculations reveal that the [Bi20]3- cluster has a similar electronic configuration to C606- and the [Bi@Pd12@Bi20]6- cluster exhibits a unique open-shell aromatic character.

Synthesis and Characterization of [Fe3 (As3 )3 (As4 )]3- , a Binary Fe/As Zintl Cluster With an Fe3 Core.

We report here the synthesis and structural characterization of the first binary iron arsenide cluster anion, [Fe3 (As3 )3 (As4 )]3- , present in both [K([2.2.2]crypt)]3 [Fe3 (As3 )3 (As4 )] (1) and [K(18-crown-6)]3 [Fe3 (As3 )3 (As4 )]⋅en (2). The cluster contains an Fe3 triangle with three short Fe-Fe bond lengths (2.494(1) Å, 2.459(1) Šand 2.668(2) Šfor 1, 2.471(1) Å, 2.473(1) Šand 2.660(1) Šfor 2), bridged by a 2-butene-like As4 unit. An analysis of the electronic structure using DFT reveals a triplet ground state with direct Fe-Fe bonds stabilizing the Fe3 core.

Missing Link in the Growth of Lead-Based Zintl Clusters: Isolation of the Dimeric Plumbaspherene [Cu4Pb22]4.

We report here the structure of an endohedral plumbaspherene, [Cu4Pb22]4-, the gold analogue of which was previously postulated to be a "missing link" in the growth of larger clusters containing three and four icosahedral subunits. The cluster contains two [Cu2Pb11]2- subunits linked through a Cu2Pb4 trigonal antiprism. Density functional theory reveals that the striking ability of mixed Pb/coinage metal Zintl clusters to oligomerize and, in the case of Au, to act as a site of nucleation for additional metal atoms, is a direct consequence of their nd10(n + 1)s0 configuration, which generates both a low-lying (n + 1)s-based LUMO and also a high-lying Pb-centered HOMO. Cluster growth and nucleation is then driven by this amphoteric character, allowing the clusters to form donor-acceptor interactions between adjacent icosahedral units or to additional metal atoms.

Inorganic Ferrocene Analogue [Fe(P4)2]2.

Inorganic metallocene derivatives containing only cyclo-Pn ligands have been targeted for more than 20 years, but their syntheses have never been achieved by pursuing the conventional route of using P4 phosphorus except for the generation of [Ti(η5-P5)2]2-. Herein, we report a facile one-step method for the synthesis of the homoleptic iron complex [Fe(P4)2]2- by the Zintl-phase-type precursor KP. 31P NMR analyses indicate that upon dissolving the KP phase in ethylenediamine P42- was generated only in the presence of 2,2,2-crypt. The amounts of cation-sequestering agents, the type of iron precursor, and their consuming ratio have a decisive impact on the yield of [Fe(P4)2]2-. Both the FeII and the FeIII precursors can oxidize P42- to give a concomitant product [(P7)Fe(P4)]3-, which can be partially inhibited by the addition of potassium to produce relatively pure crystalline [K(2,2,2-crypt)]2[Fe(P4)2].

Solution-Based Group 14 Zintl Anions: New Frontiers and Discoveries.

ConspectusGroup 14 Zintl anions [Ex]q- (E = Si-Pb, x = 4, 5, 9, 10) are synthetically accessible, and their diverse chemical reactivity makes them valuable synthons in the construction of larger nanoclusters with remarkable structures, intriguing patterns of chemical bonding, and tunable physical and chemical properties. A plethora of novel cluster anions have now been isolated from the reactions of polyanionic [Ex]q- precursors with low-valent d-/f-block metal complexes, main-group organometallics, or organics in polar aprotic solvents. The range of products includes intermetalloid clusters with transition metal atom(s) embedded in main-group element cages, organometallic Zintl anions in which [Ex]q- acts as a ligand, intermetallic Zintl anions where [Ex]q- is bridged by ligand-free transition metal atom(s), organo-Zintl anions where [Ex]q- is functionalized with organic-group(s), and oligomers formed through oxidative coupling reactions. The synthesis and characterization of these unconventional complexes, where important contributions to stability come from ionic, covalent, and metal-metal bonds as well as weaker aurophilic and van der Waals interactions, extend the boundaries of coordination chemistry and solid-state chemistry. Substantial progress has been made in this field over the past two decades, but there are still many mysteries to unravel related to the cluster growth mechanism and the controllable synthesis of targeted clusters, along with the remarkable and diverse patterns of chemical bonding that present a substantial challenge to theory. In this Account, we hope to shed some light on the relationship between structure, electronic properties, and cluster growth by highlighting selected examples from our recent work on homoatomic deltahedral [Ex]q- anions, including (1) germanium-based Zintl clusters, such as the supertetrahedral intermetallic clusters [M6Ge16]4- (M = Zn, Cd) and the sandwich cluster {(Ge9)2[η6-Ge(PdPPh3)3]}4- with a heterometallic Ge@Pd3 interlayer; (2) tin-based intermetalloid clusters [Mx@Sny]q- and the application of [Co@Sn9]4- in bottom-up synthesis; and (3) lead clusters with precious metal cores, including the largest Zintl anion [Au12Pb44]8-. In addition to their intrinsic appeal from a structural and electronic perspective, these new cluster anions also show promise as precursors for the development of new materials with applications in heterogeneous catalysis, where we have recently reported the selective reduction of CO2.

[Nb@Ge13/14 ]3- : New Family Members of Ge-Based Intermetalloid Clusters.

During the past two decades, single-atom-centered medium-sized germanium clusters [M@Gen ] (M=transition metals, n>12) have been extensively explored, both from theoretical perspectives and experimental gas-phase syntheses. However, the actual structural arrangements of the Ge13 and Ge14 endohedral cages are still ambiguous and have long remained an unresolved problem for experimental implementation. In this work, we successfully synthesize 13-/14-vertex Ge clusters [Nb@Ge13 ]3- (1) and [Nb@Ge14 ]3- (2), which are structurally characterized and exhibit unprecedented topologies, neither classical deltahedra nor 3-connected polyhedral structures. Theoretical analysis indicates that the major stabilization of the Ge backbones arises due to the substantial interaction of Ge 4p-AOs with the endohedral Nb 4d-AOs through three/four-center two-electron bonds with an enhanced electron density accumulated over the shortest Nb-Ge13 contact in 1. Low occupancies of the direct two-center two-electron (2c-2e) Nb-Ge and Ge-Ge σ bonds point to a considerable degree of electron delocalization over the Ge cages revealing their electron deficiency.

Single-Metal-Encapsulated Double-Cage [Pt@Sn17 ]4- : An Exception from Group 14 Endohedral Clusters.

Group 14 endohedral clusters containing a metal center inside usually possess a single cage topological structure, but here an unexpected single-metal-filled double-cage cluster, [Pt@Sn17 ]4- (1 a) is reported. It can be seen as a combination of the more extended Pt-filled [Pt@Sn9 ] cage and hollow [Sn9 ] cage sharing a central Sn atom, which is offset from the central position. This double-cage species represents the largest group 14 intermetalloid cluster encapsulating a single transition metal atom. DFT calculations show that the capsule-like architecture of [Sn17 ]4- , similar to that found in [Pt2 @Sn17 ]4- , is unstable if filled with a single Pt atom and collapses to the title cluster 1 a upon geometry optimization. Deviation of the central Sn atom occurs due to the vibronic coupling as a consequence of pseudo-Jahn-Teller distortion leading to the bent Cs -symmetrical structure, in contrast to the more symmetrical D2d cage previously reported in [Ni2 @Sn17 ]4- .

Synthesis and Characterization of Ternary Clusters Containing the [As16]10- Anion, [MM'As16]4- (M = Nb or Ta; M' = Cu or Ag).

The [Nb@As8]3- anion was first isolated from solution in 1986, and a number of isostructural [M@Pn8]n- clusters (M = Nb, Cr, or Mo; Pn = As or Sb; n = 2 or 3) have since been reported. We show here how anions of this class can be used as synthetic precursors that, in combination with sources of low-valent late transition metals (Cu and Ag), generate ternary polyarsenide cluster anions with unprecedented structural motifs. Chain type [MM'As16]4- (M = Nb or Ta; M' = Cu or Ag) units are found in compounds 2-5. These clusters contain a nortricyclane-like As7 cage and a [M@As8] crown, linked by a single As atom, and represent a fusion of two quite distinct branches of polyarsenide chemistry. Our analysis of the electronic structure confirms that the cluster retains many of the features of the component units. Electrospray ionization mass spectrometry reveals a series of smaller component ions containing 8-12 As atoms, the density functional theory-computed structures of which can be understood in terms of the pseudoelement concept. This work not only presents a new type of coordination mode for As clusters but also offers a point of entry for the rational design of multinary arsenic-based materials.

Electronic structures and properties of dianionic pentacarbonyls [TM(CO)5]2- (TM = Cr, Mo, W).

Density functional theory (DFT) calculations were employed to study the stabilities, electronic structures, and vibrational and bonding properties of dianionic pentacarbonyls [TM(CO)5]2- (TM = Cr, Mo, W). A D3h symmetry structure with singlet state was found to be the ground state and C-O stretching vibrational frequencies range from 1719 to 1766 cm-1, which are in excellent agreement with the experimental observations. The calculation results on bond dissociation energy for the CO loss revealed their stabilities. By employing energy decomposition analysis (EDA), the bonding nature between TM2- and (CO)5 was disclosed, in which the [TM(d)]2-→(CO)5π backdonations contribute largely to the orbital interactions while σ donation from the lone pair of CO to metal contributes moderately. Compared with those in the isoelectronic neutral hexacarbonyls TM(CO)6, the π backdonations are obviously larger in [TM(CO)5]2- because there are two extra electrons in (n- 1)d AOs of the center transition metal.

Open Shells in Endohedral Clusters: Structure and Bonding in the [Fe2@Ge16]4- Anion and Comparison to Isostructural [Co2@Ge16]4.

The anionic cluster [Fe2@Ge16]4- has been characterized and shown to be isostructural to the known D2h-symmetric α isomer of the cobalt analogue [Co2@Ge16]4-. Together with the known pair of compounds [Co@Ge10]3- and [Fe@Ge10]3-, the title compound completes a set of four closely related germanium clusters that allow us to explore how the metal-metal and metal-cage interactions evolve as a function of size and of the identity of the metal. The results of spin-unrestricted density functional theory (DFT) and multiconfigurational self-consistent field (MC-SCF) calculations present a consistent picture of the electronic structure where transfer of electron density from the metal to the cage is significant, particularly in the Fe clusters where the exchange stabilization of unpaired spin density is an important driving force.

[Sn8 ]6- -Bridged Mixed-Valence ZnI /ZnII in {[K2 ZnSn8 (ZnMes)]2 }4- Inverse Sandwich-Type Cluster Supported by a ZnI -ZnI Bond.

Since [Sn8 ]6- was discovered from the solid-state phase in 2000, its solution chemistry has been elusive due to the high charges and chemical activity. Herein, we report the synthesis and characterization of an inverse sandwich-type cluster dimer {[K2 ZnSn8 (ZnMes)]2 }4- (1 a), in which the highly charged [Sn8 ]6- is captured by mixed-valence ZnI /ZnII to form the dimer {closo-[Zn2 Sn8 ]}2 moieties bridged by a Zn-Zn bond. Such Zn-Sn cluster not only exhibits a novel example of mixed-valence ZnI /ZnII for stabilizing highly active anion species, but also indicates the [Sn8 ]6- cluster can act as a novel bridging ligand, like arene, with a η4 :η4 -fashion. Theoretical calculations indicate that a significant delocalization of electrons over Zn atoms plays a vital role in the stabilization of the [Sn8 ]6- species. The AdNDP and magnetic response analyses clearly showed the presence of local σ-aromaticity in three cluster fragments: two ZnSn4 caps and Sn8 square antiprism.

[Cu4@E18]4- (E = Sn, Pb): Fused Derivatives of Endohedral Stannaspherene and Plumbaspherene.

We report the synthesis of two new cluster anions, [Cu4@E18]4- (E = Sn, Pb), in which a Cu4 subunit is incorporated into a continuous E18 tetrel cage. Both anions are characterized by X-ray crystallography and mass spectrometry, complemented by quantum-chemical calculations that highlight the relationships to known Zintl clusters, including the stannaspherenes and plumbaspherenes [M@Sn12]q- and [M@Pb12]q-, the Matryoshka bronze [Sn@Cu12@Sn20]12-, and also [Pd2@E'18]4- (E' = Ge, Sn).

Spherical Aromaticity of All-Metal [Bi@In8 Bi12 ]3-/5- Clusters.

The chemical bonding of Zintl clusters is still an evolving and hot topic in modern chemistry. In this paper we synthesized a novel [K([2.2.2]crypt)]4 [In8 Bi13 ] complex in a condensed phase. The quantum chemical calculations and X-ray data revealed that the compound consists of the 1:1 mixture of [Bi@In8 Bi12 ]3- and [Bi@In8 Bi12 ]5- clusters. To the date, those clusters are the largest binary clusters composed of In and Bi elements. Herein, we introduce a spherical aromatic description of chemical bonding for such clusters. We show through AdNDP, ELF, and induced magnetic field and quantitative NICS analyzes that both clusters are spherically aromatic which explains their high symmetry, stability, and peculiar magnetic properties. We believe that this work will help researchers in the further development and understanding of chemical bonding in Zintl clusters.

σ-Aromaticity-Induced Stabilization of Heterometallic Supertetrahedral Clusters [Zn6 Ge16 ]4- and [Cd6 Ge16 ]4.

In this work, the largest heterometallic supertetrahedral clusters, [Zn6 Ge16 ]4- and [Cd6 Ge16 ]4- , were directly self-assembled through highly-charged [Ge4 ]4- units and transition metal cations, in which 3-center-2-electron σ bonding in Ge2 Zn or Ge2 Cd triangles plays a vital role in the stabilization of the whole structure. The cluster structures have an open framework with a large central cavity of diameter 4.6 Šfor Zn and 5.0 Šfor Cd, respectively. Time-dependent HRESI-MS spectra show that the larger clusters grow from smaller components with a single [Ge4 ]4- and ZnMes2 units. Calculations performed at the DFT level indicate a very large HOMO-LUMO energy gap in [M6 Ge16 ]4- (2.22 eV), suggesting high kinetic stability that may offer opportunities in materials science. These observations offer a new strategy for the assembly of heterometallic clusters with high symmetry.

Record Low Ionization Potentials of Alkali Metal Complexes with Crown Ethers and Cryptands.

Electronic properties of series of alkali metals complexes with crown ethers and cryptands were studied via DFT hybrid functionals. For [M([2.2.2]crypt)] (M=Li, Na, K) extremely low (1.70-1.52 eV) adiabatic ionization potentials were found. Such low values of ionization energies are significantly lower than those of alkali metal atoms. Thus, the investigated complexes can be defined as superalkalis. As a result, our investigation opens up new directions in the designing of chemical species with record low ionization potentials and extends the explanation of the ability of the cryptates and alkali crown ether complexes to stabilize multiple charged Zintl ions.

Synthesis, Crystal Structures, and Photochemical Properties of a Family of Heterometallic Titanium Oxo Clusters.

The incorporation of heterometallic atoms into the structure of titanium-oxygen nanomaterials is one of the known and effective strategies to develop new high-performance photovoltaic active materials. In this study, we have synthesized three benzoic acid-stabilized heterometallic titanium oxo clusters with the different transition metals Co, Cu, and Cd, formulated as [Ti4Co2(µ2-O)2(µ3-O)2(C6H5COO)12(CH3CN)2]·2CH3CN (1), [Ti5Cu4(µ3-O)6(C6H5COO)16] (2), and [Ti12Cd5(µ2-O)(µ3-O)15(µ4-O)2(C6H5COO)22(C6H5COOH)(CH3CN)]·CH3CN·C6H5COOH (3), and then we characterized their structures. UV-vis spectroscopy analysis revealed an enhanced UV-vis-light absorption of those heterometallic clusters. The density functional theory calculations indicated that charge transfer occurs from the p orbital of O atoms to the d orbital of Ti atoms in the TiO core (O → Ti) as well as from the metal to the core in 1 and 2. We also measured the photocurrent response and photocatalytic H2 evolution, which shows enhancement in the photocurrent intensity and good H2 evolution ability because of the cooperative effect of heterometal doping in titanium oxo clusters.

Structure and Bonding in [Sb@In8 Sb12 ]3- and [Sb@In8 Sb12 ]5.

We report the characterization of the compound [K([2.2.2]crypt)]4 [In8 Sb13 ], which proves to contain a 1:1 mixture of [Sb@In8 Sb12 ]3- and [Sb@In8 Sb12 ]5- . The tri-anion displays perfect Th symmetry, the first completely inorganic molecule to do so, and contains eight equivalent In3+ centers in a cube. The gas-phase potential energy surface of the penta-anion has eight equivalent minima where the extra pair of electrons is localized on one In+ center, and these minima are linked by low-lying transition states where the electron pair is delocalized over two adjacent centers. The best fit to the electron density is obtained from a model where the structure of the 5- cluster lies close to the gas-phase transition state.

Designed Cluster Assembly of Multidimensional Titanium Coordination Polymers: Syntheses, Crystal Structure and Properties.

The exploitation of new titanium-based coordination polymers (Ti CPs) with high crystallinity is difficult but highly desirable for their potential applications in photocatalysis. Herein, a cluster-cooperative assemble strategy is developed to synthesize Ti CPs. By utilizing various bifunctional ligands containing carboxylate acids and N-donor groups, we successfully assembled the zero-dimensional (0D) [(Ti3 O)(iPrO)8 ]2+ or [(Ti4 O2 )(iPrO)6 ]6+ clusters into one-dimensional (1D) tube-, ribbon-, or helical chain-shape architectures, two-dimensional (2D) layered structures, and a rare parallel 2D→three-dimensional (3D) polycatenation framework with various copper iodide dopants, including rhombus- or wing-shaped Cu2 I2 and tetrahedron- or ladder-shaped Cu4 I4 . The as-synthesized compounds display strong absorption in the visible region with narrow band gaps ranging from 1.70 to 2.72 eV and exhibit good photocatalytic activities in the degradation of organic pollutants.

Aromaticity and Antiaromaticity in Zintl Clusters.

Originally, the concepts of aromaticity and antiaromaticity were introduced to explain the stability and reactivity of unsaturated organic compounds. Since then, they have been extended to other species with delocalized electrons including various saturated systems, organometallic compounds, and even inorganic clusters and molecules. In this Minireview, we focus on the most recent progress of using these concepts to guide experimental synthesis and rationalize geometrical and electronic structures of a particular family of polyanions composed of Group 14 and 15 elements, namely Zintl clusters.