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.

Dimers and 2D Networks of Adamantane-Related Ternary Organosilicon Coinage Metal Sulfide Clusters.

Adamantane-type organotin sulfide clusters were recently shown to react with coinage metal phosphine complexes under replacement of an organic substituent by a metal-phosphine unit. An extension of such studies involving the silicon-based congener [(PhSi)4S6] (A) revealed that the cluster core will be partly disassembled and a {PhSi} moiety is replaced by a coinage metal phosphine complex to form [(Et3PAg)3(PhSi)3S6] (B) and [Na2(thf)2.33][(Me3PCu)(PhSi)3S6] (C). Herein, we present an extension of this work upon variation of the reactants and reaction conditions. Besides the isolation of crystalline precursor complexes [CuCl(PMe2Ph)3] (1) and [AgCl(PMe2Ph)2]2 (2), the study addresses reactions of A with AgCl and a phosphine ligand in CH2Cl2, upon which A is completely disassembled to form [(Ph3P)3Ag(µ-S)SiCl2Ph] (3). In another case a CH2 group, most likely stemming from CH2Cl2, was attached to the ligand, thus generating [{PhCl(S)SiSCH2P(Ph2)CH2CH2}2] (4). Upon using CuCl and 1,4-bis(diphenylphosphino)butane (dppb) we isolated the phosphine-bridged analog of B, [{(dppbCu2)CuP(Ph2)(CH2CH2)(PhSi)3S6}2] (5). In order to receive the yet elusive silver homolog of C, we used PMe2Ph as a bulkier ligand. This way we generated a 2D coordination polymer of the desired composition, [Na2(thf)1.5][(Me2PhPAg)(PhSi)3S6] (6). UV-visible spectra of 6 indicated a bandgap of 3.89 eV, thus blue-shifted in regards to B and C.

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.

Origin of the Nonlinear Optical Response in Organotetrel Molecules, (Hetero)adamantane-Type Clusters with Organic Substituents, and Related Species.

The nonlinear optical response of (hetero)adamantane-type clusters and organotetrel molecules with the general formula [(RT)4E6] and [TR4] (T = group 14, R = organic substituents, E = S, CH2) is investigated from first principles. These clusters have been reported to efficiently convert infrared radiation into white light and are therefore extremely attractive functional materials for a multitude of applications. We demonstrate that the optical nonlinearities of the clusters in the range from 0 to 3 eV have their origin in electronic transitions within the substituents. The cluster core does not directly take part to the generation process; however, it strongly affects the intensity of the linear and nonlinear response. The relationships between optical properties and cluster symmetry, stoichiometry, substituent field, core composition, and further structural characteristics are investigated by systematical variation of R and T. This also demonstrates the possibility to finely tune the intensity as well as the frequency dependence of the optical response. Upon formation of cluster dimers, the intensity of the nonlinearities depends on the overall dimer geometry. In the case of heterogeneous dimers, the optical response strongly resembles that of a dominant cluster. Similarly, upon formation of cluster crystals, the compound inherits the optical characteristics of the parent molecules.

Strain-Induced Structural Rearrangement Towards a White-Light-Emitting Adamantane-Type Cluster Dimer.

Group 14/16 adamantane-type hybrid clusters of the type [(RT)4E6] (T = group 14 element, E = group 16 element, R = organic group) have been reported to emit white-light when irradiated in an amorphous state with a continuous-wave (CW) infrared laser diode. This effect is enhanced if the cluster core is varied from a binary to a more complex composition. To further explore this phenomenon, we synthesized clusters with a multinary R/R'-T/T'-E/E' composition, including isolobal replacement of E with CH2, in [(2-NpSi){CH2Sn(S)Ph}3] (1, Np = naphthyl). When expanding one of the CH2 moieties to a C2H4 group, thus generating a R/R'-T/T'-E/E'/E'' cluster composition, we unexpectedly observed a dimerization of the initially formed, yet non-isolable adamantane-like cluster [(2-NpSi){CH2Sn(S)Ph}2{C2H4Sn(S)Ph}] (2) to [(2-NpSi){CH2Sn(S)Ph}2{C2H4Sn(S)Ph}]2 (3), exhibiting a heretofore unprecedented cluster architecture. Both monomeric 1 and dimeric 3, show white-light emission as thin films. The nonlinear optical response of the compounds was also modelled with DFT methods.

Ion-Selective Assembly of Supertetrahedral Selenido Germanate Clusters for Alkali Metal Ion Capture and Separation.

Supertetrahedral chalcogenido (semi)metalate cluster-based frameworks possess high selectivity for alkali metal cations, matching the specific charge density of their inner surfaces, which enables their use as ion-exchange materials. Aggregates of the supertetrahedral chalcogenido metalate cluster offer even new perspectives for metal ion capture and separation. Herein, we report on ionothermal preparation of two corresponding model compounds, (C2C1Im)7[Cs@GeII4(GeIV4Se10)4] (1) and (C2C1Im)10[Na5(CN)6@Cu6(Ge4Se10)4(Cu)] (2). Their formation is reliant on one specific cation type each, Cs+ for 1 and Na+ for 2, thus providing promising separation potential during crystallization. Compound 1 is based on the largest discrete binary selenido germanate cluster reported to date and the first mixed-valent chalcogenido germanate(II/IV) supertetrahedron. Moreover, it adds to the few examples of chalcogenides capable of capturing Cs+ ions. Its high selectivity for Cs+ compared to that of Li+, Na+, K+, and Rb+ was confirmed by single-crystal X-ray diffraction, energy-dispersive X-ray spectroscopy, and electrospray ionization mass spectrometry. Quantum chemical studies indicate that smaller ions, K+ and Rb+, could also be embedded in an isolated cluster assembly, but as the cluster aggregate slightly distorts for crystallization, the selectivity for Cs+ becomes exclusive in the salt. The anionic substructure of compound 2 is based on a two-dimensional network of supramolecular assemblies and exhibits an exclusive preference for Na+. This work thus provides the first comprehensive insight into the selective incorporation of specific alkali metal ions into supramolecular aggregates of supertetrahedral chalcogenide clusters, as a promising basis for new ion trapping techniques─especially for heavy alkali metal ions that pose environmental challenges.

Insights into molecular cluster materials with adamantane-like core structures by considering dimer interactions.

A class of adamantane-like molecular materials attracts attention because they exhibit an extreme non-linear optical response and emit a broad white-light spectrum after illumination with a continuous-wave infrared laser source. According to recent studies, not only the nature of the cluster molecules, but also the macroscopic structure of the materials determines their non-linear optical properties. Here we present a systematic study of cluster dimers of the compounds AdR4 and [(RT)4 S6 ] (T = Si, Ge, Sn) with R = methyl, phenyl or 1-naphthyl to gain fundamental knowledge about the interactions in the materials. For all compounds, a similar type of dimer structures with a staggered arrangement of substituents was determined as the energetically most favorable configuration. The binding energy between the dimers, determined by including London dispersion interactions, increases with the size of the core and the substituents. The cluster interactions can be classified as substituent-substituent-dominated (small cores, large substituents) or core-core-dominated (large cores, small substituents). Among various possible dimer conformers, those with small core-core distances are energetically preferred. Trimer and tetramer clusters display similar trends regarding the minimal core-core distances and binding energies. The much lower energy barrier determined for the rotation of substituents as compared to the rotation of the cluster dimers past each other indicates that the rotation of substituents more easily leads to different conformers in the material. Thus, understanding the interaction of the cluster dimers allows an initial assessment of the interactions in the materials.

Ionothermal Approach to Homo- and Heteroleptic Alkylation of Tellurido Mercurate Clusters for Assembly in Lamellar Crystal Structures.

The selective methylation and butylation of chalcogenido metalate clusters by utilizing imidazolium-based ionic liquids turned out to be not only a comparably mild but at the same time also the only known method for postsynthetic alkylation of such species in order to increase their solubility. For additional impact on the crystal structures, selective alkylation with longer alkyl chains was addressed by utilizing the ionic liquid (C10C1Im)[BF4] (C10 = decyl group at position 1 and C1 = methyl group at position 3 of the cation's Im = imidazolium ring) for ionothermal syntheses of functionalized tellurido mercurate clusters. Herein, we report three novel compounds, two of which comprise cluster anions that exhibit a selective organic functionalization of their terminal telluride ligands upon in situ alkylation with the ionic liquid: [Hg6Te6(Te2)2(TeDec)2]6- (in 1; Dec = decyl) represents the first decylated chalcogenido metalate cluster. A unique heteroleptic functionalization, combining methylation and decylation, was achieved for the second cluster, [Hg6Te6(Te2)2(TeDec)(TeMe)]6- (in 2; Me = methyl). The third cluster is purely inorganic, but based on the same cluster core architecture: [Hg4Te2(Te2)2(Te3)2]4- (in 3) comprises a tritelluride unit instead of two HgTeR groups (R = Me, Dec). As a consequence of the long alkyl chains, both at the cluster and at the charge-compensating cations, all three crystal structures are characterized by lamellar assemblies of cations and anions. For further comparison of the properties of the organometallic versus purely inorganic compounds, vibrational and optical properties of crystalline samples of the compounds comprising clusters 1 and 3 were studied by means of infrared, Raman, and UV-visible spectroscopy. The results clearly show the effect of the presence of an organic decoration (in 1) relative to its absence (in 3), reflected by a red shift of the band gap energy (1 → 3) and a replacement of the Te-C bands (in 1) with bands for tritelluride units (in 3).

[M@Sn14-xSbx]q- (M = La, Ce, or U; x = 6-8; q = 3, 4): Interaction of 4f or 5f Metal Ions with 5p Metal Atoms in Intermetalloid Clusters.

The impact of 4f metal ions Ln3+ (Ln = La or Ce) versus 5f metal ions Un+ (n = 3 or 4) on the compositions and distribution of 5p metal atoms in the cluster shells of endohedral species [M@Sn14-xSbx]q- (M = La, Ce, or U; x = 6-8; q = 3, 4) was studied by means of combined experimental and quantum chemical investigations. While all known f-block metal ion-centered endohedral clusters possessed combinations of larger main group metal atoms so far (Sn/Bi or Pb/Bi), resulting in mixtures of 13- and 14-atom cages, the 14-atom cages reported herein comprise exclusively Sn and Sb atoms and therefore are challenged in accommodating the large 4f and 5f ions. We show that the clusters form in reactions of (Sn2Sb2)2- anions with [Ln(C5Me4H)3] or [U(C5Me4H)3Cl], and that salts of [La@Sn6Sb8]3-, [La@Sn7Sb7]4-, [U@Sn8Sb6]4-, and [U@Sn7Sb7]3- can be isolated from them. The assignment of Sn versus Sb in the encapsulating cage follows a simple rule. Different central atoms cause only slight differences in this regard and with respect to distortions of the cluster shells. The reactions also yielded the salt of the new binary anion (Sn4Sb4)2- that was recently predicted by quantum chemical studies.

Low-Cost, Multifunctional, and Sustainable Sodium Sulfido Ferrate(II).

We introduce Na2[Fe3S4], comprising anionic layers, synthesized by a simple and straightforward solid-state method based on the fusion of binary sulfides of abundant sodium and iron. The structure crystallizes in a trigonal lattice with honeycomb cavities, as well as 25% of statistical iron vacancies in the crystal structure. The compound depicts high dielectric constants from 998 to 1850 at a frequency of 1 kHz depending on the sintering temperature, comparable with benchmark dielectric materials. According to the complex electrochemical impedance results, the compound depicts an electrical conductivity at ambient temperature. Optical investigations reveal a band gap of 1.64 eV, which is in agreement with an electronic band gap of 1.63 eV computed by density functional theory calculations. Magnetometry results reveal an antiferromagnetic behavior with a transition at 120 K. These findings introduce Na2[Fe3S4] as a sustainable multifunctional material with potential for a variety of electronic and magnetic applications.

Electronic structure and bonding in endohedral Zintl clusters.

Endohedral Zintl clusters-multi-metallic anionic molecules in which a d-block or f-block metal atom is enclosed by p-block (semi)metal atoms-are very topical in contemporary inorganic chemistry. Not only do they provide insight into the embryonic states of intermetallic compounds and show promise in catalytic applications, they also shed light on the nature of chemical bonding between metal atoms. Over the past two decades, a plethora of endohedral Zintl clusters have been synthesized, revealing a fascinating diversity of molecular architectures. Many different perspectives on the bonding in them have emerged in the literature, sometimes complementary and sometimes conflicting, and there has been no concerted effort to classify the entire family based on a small number of unifying principles. A closer look, however, reveals distinct patterns in structure and bonding that reflect the extent to which valence electrons are shared between the endohedral atom and the cluster shell. We show that there is a much more uniform relationship between the total valence electron count and the structure and bonding patterns of these clusters than previously anticipated. All of the p-block (semi)metal shells can be placed on a ladder of total valence electron count that ranges between 4n+2 (closo deltahedra), 5n (closed, three-bonded polyhedra) and 6n (crown-like structures). Although some structural isomerism can occur for a given electron count, the presence of a central metal cation imposes a preference for rather regular and approximately spherical structures which maximise electrostatic interactions between the metal and the shell. In cases where the endohedral metal has relatively accessible valence electrons (from the d or f shells), it can also contribute its valence electrons to the total electron count of the cluster shell, raising the effective electron count and often altering the structural preferences. The electronic situation in any given cluster is considered from different perspectives, some more physical and some more chemical, in a way that highlights the important point that, in the end, they explain the same situation. This article provides a unifying perspective of bonding that captures the structural diversity across this diverse family of multimetallic clusters.

Charge Makes a Difference: Molecular Ionic Bismuth Compounds.

Key challenges in modern synthetic chemistry include the design of reliable, selective, and more sustainable synthetic methods, as well as the development of promising candidates for new materials. Molecular bismuth compounds offer valuable opportunities as they show an intriguing spectrum of properties that is yet to be fully exploited: a soft character, a rich coordination chemistry, the availability of a broad variety of oxidation states (at least +V to -I) and formal charges (at least +3 to -3) at the Bi atoms, and reversible switching between multiple oxidation states. All this is paired with the status of a non-precious (semi-)metal of good availability and a tendency towards low toxicity. Recent findings show that some of these properties only come into reach, or can be substantially optimized, when charged compounds are specifically addressed. In this review, essential contributions to the synthesis, analyses, and utilization of ionic bismuth compounds are highlighted.

Assembly of One to Four As4 Analogues, (Ge2 As2 )2- or (Ge3 As)3- , in the Coordination Sphere of [PhM]+ , [MesM]+ , or M2+ (M=Zn, Cd, Hg).

Pseudo-tetrahedral units of p-block atoms proved to be excellent building blocks for novel molecular architectures and for introducing new elemental combinations which are not otherwise accessible. In this work, we present a series of clusters obtained by reactions of binary Ge/As anions with [MPh2 ] (M=Zn, Cd, Hg; Ph=phenyl). The study is grounded on the fact that the binary reactant gained by extracting the solid 'K2 GeAs' with ethane-1,2-diamine (en) co-exists as (Ge2 As2 )2- and (Ge3 As)3- in solution. This allows for a larger variety of products by 'selecting' the most suitable species for the final ternary complex to crystallize. The reactions afforded the unprecedented first step of the corresponding interaction, thus attachment of (MPh)+ to a pseudo-tetrahedral unit in [PhZn(Ge3 As)]2- (1) and [PhHg(Ge3 As)]2- (2), and complex anions with two, three, or four units, [(Ge3 As)Zn(Ge2 As2 )]3- (3), [Cd3 (Ge3 As)3 ]3- (4), and [Zn3 (Ge3 As)4 ]6- (5). Quantum chemistry confirmed the compositions and the positions of the Ge or As atoms, beside explaining structural peculiarities. The subtle impact of different [MR2 ] reactants was additionally studied by corresponding reactions using [ZnMes2 ] (Mes=mesityl), which showed success in selectively crystallizing [MesZn(Ge3 As)]2- (6). Based on our findings, we derive a suggestion of the underlying reaction cascade.

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.

Reactive Solubilization of Heterometallic Clusters by Treatment of (TrBi3 )2- Anions (Tr=Ga, In, Tl) with [Mn{N(SiMe3 )2 }2 ].

Lowering the charge of Zintl anions by (element-)organic substituents allows their use as sources of (semi)metal nanostructures in common organic solvents, as realized for group 15 anions or Ge9 4- and Sn9 4- . We developed a new strategy for other anions, using low-coordinate 3d metal complexes as electrophiles. [K(crypt-222)]+ salts of (TrBi3 )2- anions dissolved in situ in Et2 O and/or THF when reacted with [Mn(hmds)2 ]. Work-up afforded soluble [K(crypt-222)]+ salts of [{(hmds)2 Mn}2 (TlBi3 )]2- (in 1), [{(hmds)2 Mn}2 (Bi2 )]2- (in 2), and [{(hmds)Mn}4 (Bi2 )2 ]2- (in 3) (crypt-222=4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane; Tr=Ga, In, Tl; hmds=N(SiMe3 )2 ), representing rare cases of Zintl clusters with open-shell metal atoms. 1 comprises the first coordination compound of the (TlBi3 )2- anion, 2 features a diamond-shaped {Pn2 M2 } unit, and 3 is a mixed-valent MnI /MnII compound. The uncommon electronic structures in 1-3 and magnetic coupling were studied by comprehensive DFT calculations.

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.

Systematic Access of Ternary Organotetrel-Copper Chalcogenide Clusters by [PhTE3 ]3- Anions (T=Si, Sn; E=S, Se).

Fragmentation reactions of organotetrel chalcogenide heteroadamantane-type clusters [(PhT)4 E6 ] (T/E=Si/S (1); Si/Se; Sn/S, and Sn/Se) by addition of the corresponding sodium chalcogenide gave salts of the general formula Na3 [PhTE3 ], with T/E=Si/S (2); Si/Se (3); Sn/S (A); Sn/Se (4). Reaction of these salts with [Cu(PPh3 )3 Cl] gave a series of organotetrel-copper chalcogenide clusters [(CuPPh3 )6 (PhTE3 )2 ] with T/E=Si/S; (5), Si/Se (6), Sn/S (7) and Sn/Se (8). Compounds 5-8 share a common structural motif with two intact {PhTE3 } units coordinating a Cu6 moiety, which was previously reported with other ligands, and for the Sn and Ge congeners only. If the Sn/Se reaction system was allowed to crystallize more slowly, single crystals of compound [(CuPPh3 )6 (PhSnSe3 )3 Cu3 SnSe] (9) were obtained, which are based on a larger cluster structure. Hence, 9 might form from 8 through incorporation of additional cluster fragments. The experimentally and quantum chemically determined optical properties were compared to related clusters.

Pyrene-Terminated Tin Sulfide Clusters: Optical Properties and Deposition on a Metal Surface.

Herein, we present the synthesis of two pyrene-functionalized clusters, [(Rpyr Sn)4 S6 ]⋅2 CH2 Cl2 (4) and [(Rpyr Sn)4 Sn2 S10 ]⋅n CH2 Cl2 (n=4, 5 a; n=2, 5 b; Rpyr =CMe2 CH2 C(Me)N-NC(H)C16 H9 ), both of which form in reactions of the organotin sulfide cluster [(RN Sn)4 S6 ] (C; RN =CMe2 CH2 C(Me)N-NH2 ) with the well-known fluorescent dye 1-pyrenecarboxaldehyde (B). In contrast, reactions using an organotin sulfide cluster with another core structure, [(RN Sn)3 S4 Cl] (A), leads to formation of small molecular fragments, [(Rpyr Cl2 Sn)2 S] (1), (pyren-1-ylmethylene)hydrazine (2), and 1,2-bis(pyren-1-ylmethylene)hydrazine (3). Besides synthesis and structures of the new compounds, we report the influence of the inorganic core on the optical properties of the dye, which was analyzed exemplarily for compound 5 a via absorption and fluorescence spectroscopy. This cluster was also used for exploring the potential of such non-volatile clusters for deposition on a metal surface under vacuum conditions.

Introducing Distinct Structural and Optical Properties into Organotin Sulfide Clusters by the Attachment of Perylenyl and Corannulenyl Groups.

We report the introduction of distinct optical properties into organotin sulfide clusters by the attachment of extended polycyclic aromatic organic molecules. This was realized by the reactions of [(RNSn)4S6] (RN = CMe2CH2CMeNNH2) with 3-perylenecarbaldehyde and corannulenecarbaldehyde, respectively. The reaction with the first reactant leads to the formation of two products [(RperylSn)3S4][SnCl3] [1a; Rperyl = CMe2CH2CMeNNCH(C20H11)] and [(RperylSn)3S4Cl] (1b). Structural differences between these two compounds are reflected in their different optical absorption and luminescence behavior, yet in both cases, the main emission is red-shifted relative to 3-perylenecarbaldehyde. The second organic molecule affords the compound [(RcorSn)4Sn2S10] [2; Rcor = CMe2CH2CMeNNCH(C20H9)] with intriguing optical properties, including a broad emission with essentially no shift in λmax compared to corannulenecarbaldehyde. All compounds were obtained as single crystals, and their structures were determined by means of single-crystal X-ray diffraction. The optical properties of the highly luminescent compounds were investigated by means of emission and time-resolved photoluminescence spectroscopy measurements.

Different Chemical Environments of [Ge4Se10]4- in the Li+ Compounds [Li4(H2O)16][Ge4Se10]·4.33H2O, [{Li4(thf)12}Ge4Se10], and [Li2(H2O)8][MnGe4Se10], and Ionic Conductivity of Underlying "Li4Ge4Se10".

The crystalline selenido germanates [Li4(H2O)16][Ge4Se10]·4.3H2O (1), [{Li4(thf)12}Ge4Se10] (2), and [Li2(H2O)8][MnGe4Se10] (3) (thf = THF = tetrahydrofuran) were obtained by an extraction of a glassy ternary phase of the nominal composition Li4Ge4Se10 (=Li2S·2GeSe2) with water (1) or THF (2) and slow evaporation of the solvent or by being layered with MnBr2 in H2O/MeOH (3), respectively. The compounds contain known selenido germanate anions, however, for the first time with Li+ counterions. This is especially remarkable for the prominent ∞3{[MnGe4Se10]2-} open-framework structure, which was reported to crystallize with (NMe4)+, Cs+, Rb+, and K+ counterions, but it has not yet been realized with the smallest alkali metal cation. Impedance spectroscopic studies on Li4Ge4Se10 classify the glassy solid as a moderate Li+ ion conductor.