Effect of La3+ on the Formation of Endohedral Zintl Clusters Featuring In/Bi Shells.

Investigating the interactions of f-block metal ions with p-block polyanions in multinary cluster compounds is becoming increasingly attractive but remains a challenge in terms of both the synthetic approach and the control of the structures that are formed during the syntheses. So far, two types of reactions were dominant for the formation of corresponding clusters: the reaction of binary anions of p-block elements in 1,2-diamino-ethane (en) solutions or the reaction of organobismuth compounds with corresponding f-block metal complexes in THF. Herein, we report the synthesis of [La@In2Bi11]4- (1) and its doubly µ-Bi-bridged analogue in the doubly [K(crypt-222)]+-coordinated {[K(crypt-222)]2[La@In2Bi11](µ-Bi)2[La@In2Bi11]}4- (2) as their [K(crypt-222)]+ salts [K(crypt-222)]41 and [K(crypt-222)]42, respectively, achieved by reactions of [InMes3] and [La(C5Me4H)3] (Mes = mesityl, C5Me4H = tetramethylcyclopentadienyl) with K10Ga3Bi6.65/crypt-222 (crypt-222 = 4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane) in en. In the absence of [La(C5Me4H)3], the otherwise unchanged reactions afford the anions [Bi6(InMes)(InMes2)]3- (3) and [Mes3In-InMes3]2- (4) instead, which can be isolated as their [K(crypt-222)]+ salts [K(crypt-222)]33 and [K(crypt-222)]24·tol (tol = toluene), respectively. The {Bi6} fragment observed in anion 3 is assumed to be one of the key intermediates not only toward the formation of 1 and 2 but also on the way to more general bismuth rich compounds.

Bismuth-Based Metal Clusters─From Molecular Aesthetics to Contemporary Materials Science.

ConspectusBismuth-based research has become a highly topical field in recent years, yielding remarkable prospects for new fundamental insights and new materials applications, ranging from innovative catalysts to novel pharmaceuticals, due to this heavy metal's virtually nonradioactive and nontoxic properties. Given that the 6s2 electron pair can be stereochemically active under certain circumstances, bismuth atoms adopt a variety of coordination modes and bonding environments with oxidation states ranging from (formally) +V to -III. As a consequence, bismuth-based compounds cover the entire spectrum from simple coordination compounds to much more unusual cluster cations and cluster anions exhibiting metal-metal bonding in a homoatomic manner, or in concert with other s-, d-, p-, or f-block metal atoms. Such bismuth clusters show high potential for the development of new bismuth-based materials, but they are also interesting objects by themselves. Given the relatively recent development of bismuth-rich cluster molecules, a deep understanding of their properties─including unprecedented structural features, complex electronic structures, substantial heavy metal aromaticity, as well as their formation pathways─is still in its infancy. The topic thus spans a broad range from highly sophisticated synthetic chemistry through interdisciplinary experimental and theoretical analyses to materials science.Based on our recent work and several notable reports from other groups, this article will highlight the successful access to a number of novel bismuth-rich cluster ions emerging from both solution-based approaches and solid-state chemistry. It will shed light on the unique structural and electronic properties that cause chemical and physical peculiarities of such compounds. Selected examples include, but are not limited to, (1) the first encapsulation of actinide ions in intermetalloid clusters which additionally served to manifest substantial all-metal π-aromaticity with a (calculated) record ring current per electron; (2) a large metalloid {Zn12} unit stabilized in a porphine-related {Zn8Bi16} moiety in [K2Zn20Bi16]6-; (3) the largest assembly of bismuth atoms within one molecule, observed in [{Ru(cod)}4Bi18]4- that consists of two Bi-Bi-linked "[{Ru(cod)}2Bi9]2-" subunits.Notably, cluster growth has remained largely a black box, which is starting to be revealed, however. We discuss possible formation pathways of such (multi)metallic nanoarchitectures on the basis of smaller subunits that were detected by mass spectrometric analyses and could also be captured upon reaction with organometallic complexes. In addition to the intrinsic structural and electronic properties of the cluster anions and cluster cations reviewed herein, we will briefly introduce the emerging usage of bismuth-based compounds in material science and give an outlook to future developments.

Between Elemental Match and Mismatch: From K12 Ge3.5 Sb6 to Salts of (Ge2 Sb2 )2- , (Ge4 Sb12 )4- , and (Ge4 Sb14 )4.

The solid mixture "K2 GeSb" was shown to comprise single-crystalline K12 Ge3.5 Sb6 (1), a double salt of K5 [GeSb3 ] with carbonate-like [GeSb3 ]5- anions, and the metallic Zintl phase K2 Ge1.5 . Extraction of 1 with ethane-1,2-diamine in the presence of crypt-222 afforded [K(crypt-222)]+ salts of several novel binary Zintl anions: (Ge2 Sb2 )2- (in 2), (Ge4 Sb12 )4- (in 3), and in the presence of [AuMePPh3 ] also (Ge4 Sb14 )4- (in 4). The anion in 2 represents a predicted, yet heretofore missing pseudo-tetrahedral anion. 4 comprises a cluster analogous to (Ge4 Bi14 )4- and (Ga2 Bi16 )4- , and thus one of the most Sb-rich binary p-block anions. The unprecedented cluster topology in 3 can be viewed as a defect-version of the one in 4 upon following a "dead end" of cluster growth. The findings indicate that Ge and Sb atoms are at the border of a well-matching and a mismatch elemental combination. We discuss the syntheses, the geometric structures, and the electronic structures of the new compounds.

Tetrahedral [Sb(AuMe)4 ]3- Occurring in Multimetallic Cluster Syntheses: About the Structure-Directing Role of Methyl Groups.

The anion of [K(crypt-222)]3 [Sb(AuMe)4 ]⋅py (1; crypt-222=4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane; py=pyridine) represents a rare example of a homoleptic heavy p-block metal atom being surrounded by four free-standing transition metal complex fragments, and the third example for a corresponding Sb compound. In contrast to all reported complexes of this type, the transition metal atoms possess twofold coordination only, hence the complex as a whole does not exhibit significant steric shielding or further linkage of the metal atoms. This is reflected in a high flexibility, as confirmed by slight deviations from a tetrahedral coordination of the Sb atom in the crystal and soft vibrational modes. An alternative pyramidal conformer, observed for a related arsenic compound with terminal phosphine ligands, is apparently disfavored owing to electron correlation effects. The compound is formed in a reaction that in another solvent or at other reactant concentrations yields salts of ternary cluster anions. By a combined experimental and theoretical study of different reaction conditions and previously unidentified side-products, we provide insight into multimetallic cluster synthesis reactions.

Insights into Formation and Relationship of Multimetallic Clusters: On the Way toward Bi-Rich Nanostructures.

Bismuth-rich polyanions show a unique potential in constructing nanostructured bismuth-based materials, but they are still poorly investigated. We use a ternary precursor of the nominal composition "K5Ga2Bi4" for the formation of [K(crypt-222)]+ salts of novel Bi-rich polyanions [Bi@Ga8(Bi2)6]q- (q = 3, 5; in 1), (Ga2Bi16)4- (in 2), and [{Ru(cod)}4Bi18]4- (in 3). Their bismuth contents exceed that of the largest homoatomic polyanion, Bi113-. The numbers of bismuth atoms in the anions in 2 and 3 furthermore surmount that of the Bi-richest binary main-group anion, (Ge4Bi14)4-, and they equal (2) or surmount (3) that reported for the anion and the cations with the largest number of Bi atoms so far, [K2Zn20Bi16]6-, [(Bi8)Ru(Bi8)]6+, and [(Bi8)Au(Bi8)]5+. Compounds 1 and 2 were obtained from reaction mixtures that contain [La(C5Me4H)3], apparently assisting in the network formation without being included in the products. In the presence of [Ru(cod)(H2CC(Me)CH2)2], yet another reaction pathway leads to the formation of the anions in 3 (conformers 3a and 3b), which are Bi-Bi linked dimers of two "[{Ru(cod)}2Bi9]2-" subunits. They comprise the largest connected assemblies of Bi atoms within one molecule and may be viewed as snapshots on the way toward even larger polybismuthide units and, ultimately, new bismuth modifications. Mass spectrometry allowed insight into the processes in solution that precede the cluster formation. In-depth quantum chemical studies were applied to explain structural peculiarities, stabilities of the observed isomers, and bonding characteristics of these bismuth-rich nanoarchitectures. The work demonstrates the high potential of the method for the access of new Bi-based materials.

Atom Exchange Versus Reconstruction: (Gex As4-x )x- (x=2, 3) as Building Blocks for the Supertetrahedral Zintl Cluster [Au6 (Ge3 As)(Ge2 As2 )3 ]3.

The Zintl anion (Ge2 As2 )2- represents an isostructural and isoelectronic binary counterpart of yellow arsenic, yet without being studied with the same intensity so far. Upon introducing [(PPh3 )AuMe] into the 1,2-diaminoethane (en) solution of (Ge2 As2 )2- , the heterometallic cluster anion [Au6 (Ge3 As)(Ge2 As2 )3 ]3- is obtained as its salt [K(crypt-222)]3 [Au6 (Ge3 As)(Ge2 As2 )3 ]⋅en⋅2 tol (1). The anion represents a rare example of a superpolyhedral Zintl cluster, and it comprises the largest number of Au atoms relative to main group (semi)metal atoms in such clusters. The overall supertetrahedral structure is based on a (non-bonding) octahedron of six Au atoms that is face-capped by four (Gex As4-x )x- (x=2, 3) units. The Au atoms bind to four main group atoms in a rectangular manner, and this way hold the four units together to form this unprecedented architecture. The presence of one (Ge3 As)3- unit besides three (Ge2 As2 )2- units as a consequence of an exchange reaction in solution was verified by detailed quantum chemical (DFT) calculations, which ruled out all other compositions besides [Au6 (Ge3 As)(Ge2 As2 )3 ]3- . Reactions of the heavier homologues (Tt2 Pn2 )2- (Tt=Sn, Pb; Pn=Sb, Bi) did not yield clusters corresponding to that in 1, but dimers of ternary nine-vertex clusters, {[AuTt5 Pn3 ]2 }4- (in 2-4; Tt/Pn=Sn/Sb, Sn/Bi, Pb/Sb), since the underlying pseudo-tetrahedral units comprising heavier atoms do not tend to undergo the said exchange reactions as readily as (Ge2 As2 )2- , according to the DFT calculations.

Peculiar All-Metal σ-Aromaticity of the [Au2 Sb16 ]4- Anion in the Solid State.

Gas-phase clusters are deemed to be σ-aromatic when they satisfy the 4n+2 rule of aromaticity for delocalized σ electrons and fulfill other requirements known for aromatic systems. While the range of n values was shown to be quite broad when applied to short-lived clusters found in molecular-beam experiments, stability of all-metal cluster-like fragments isolated in condensed phase was previously shown to be mainly ascribed to two electrons (n=0). In this work, the applicability of this concept is extended towards solid-state compounds by demonstrating a unique example of a storable compound, which was isolated as a stable [K([2.2.2]crypt)]+ salt, featuring a [Au2 Sb16 ]4- cluster core possessing two all-metal aromatic AuSb4 fragments with six delocalized σ electrons each (n=1). This discovery pushes the boundaries of the original idea of Kekulé and firmly establishes the usefulness of the σ-aromaticity concept as a general idea for both small clusters and solid-state compounds.

All-Metal Antiaromaticity in Sb4 -Type Lanthanocene Anions.

Antiaromaticity, as introduced in 1965, usually refers to monocyclic systems with 4n π electrons. This concept was extended to all-metal molecules after the observation of Li3 Al4 (-) in the gas phase. However, the solid-phase counterparts have not been documented to date. Herein, we describe a series of all-metal antiaromatic anions, [Ln(η(4) -Sb4 )3 ](3-) (Ln=La, Y, Ho, Er, Lu), which were isolated as the K([2.2.2]crypt) salts and identified by single-crystal X-ray diffraction. Based on the results obtained from the chemical bonding analysis, multicenter indices, and the electron-counting rule, we conclude that the core [Ln(η(4) -Sb4 )3 ](3-) fragment of the crystal has three locally π-antiaromatic Sb4 fragments. This complex represents the first locally π-antiaromatic all-metal system in the solid state, which is stabilized by interactions of the three π-antiaromatic units with the central metal atom.

A niobium-necked cluster [As3Nb(As3Sn3)](3-) with aromatic Sn3(2-) .

We describe here the synthesis and characterization of a ternary cluster compound [As3Nb(As3Sn3)](3-) (1), in which a niobium(v) atom is coordinated by an As3(3-) triangle and a bowl-type As3Sn3(5-) ligand. Cluster 1 was synthesized by dissolving K8NbSnAs5 (2) in the presence of [2.2.2]crypt in ethylenediamine solution, filtered and layered with toluene, then crystallized in the form of [K([2.2.2]crypt)]3[As3Nb(As3Sn3)]·en·tol. The flower-vase shaped compound 1 features a new structure type, rather different from the known Zintl phases. The stability and bonding of 1 are elucidated via extensive bonding analyses. The Sn3 ring is found to have σ-aromaticity featuring a delocalized Sn-Sn-Sn σ bond. Electronic structure calculations confirm the Nb(v) oxidation state and weak Nb-Sn and Sn-Sn bonding, in addition to the normal Nb-As and As-As bonds.

An All-Metal Aromatic Sandwich Complex [Sb3Au3Sb3](3-).

A sandwich complex, as exemplified by ferrocene in the 1950s, usually refers to one metal center bound by two arene ligands. The subject has subsequently been extended to carbon-free aromatic ligands and multiple-metal-atom "monolayered" center, but not to an all-metal species. Here, we describe the synthesis of an unprecedented all-metal aromatic sandwich complex, [Sb3Au3Sb3](3-), which was isolated as K([2.2.2]crypt)(+) salt and identified by single-crystal X-ray diffraction. Quantum chemical calculations indicate that intramolecular electron transfers for the three metallic layers (Sb → Au donation and Sb ← Au back-donation) markedly redistribute the valence electrons from the cyclo-Sb3 ligands and Au3 interlayer to the Au-Sb bonds, which hold the complex together via σ bonding. Each cyclo-Sb3 possesses aromaticity with delocalized three-center three-electron (3c-3e) π bonds, which are essentially equivalent to a 3c-4e ππ* triplet system, following the reversed 4n Hückel rule for aromaticity in a triplet state.

Ligand-controlled syntheses of copper(I) complexes with metal-metal interactions: crystal structure and relativistic density functional theory investigation.

A family of di-, tri-, and tetranuclear copper(I) complexes supported by length-controlled silaamidinate ligands have been synthesized to show short Cu(I)-Cu(I) distances (2.43-2.62 Å) and feature a linear or bent metal-metal arrangement, which is elucidated by a relativistic density functional theory calculation.