Tetramerization of BEB-Doped Phenalenyls to Obtain (BE)8-[16]Annulenes (E = N, O).

Two (BE)8-[16]annulenes were prepared and fully characterized by experimental and quantum-chemical means (1, E = N; 2, E = O). The 1,8-naphthalenediyl-bridged diborane(6) 3 served as their common starting material, which was treated with [Al(NH3)6]Cl3 to form 1 (91% yield) or with 1,8-naphthalenediboronic acid anhydride to form 2 (93% yield). As a result, the heteroannulenes 1 and 2 are supported by four aromatic "clamps" and may also be viewed as NH- or O-bridged cyclic tetramers of BNB- or BOB-doped phenalenyls. X-ray crystallography on mono-, di-, and tetraadducts 2·thf, 2·py2, and 2·py4 showed that 2 is an oligotopic Lewis acid (thf/py: tetrahydrofuran/pyridine donor). The applicability of 2 also as a Lewis basic ligand in coordination chemistry was demonstrated by the synthesis of the mononuclear Ag+ complex [Ag(py)2(2·py4)]+ and the dinuclear Pb2+ complex 6. During the assembly of 6, the rearrangement of 2 led to the formation of two (BO)9-macrocycles linked by two BOB-phenalenyls to form a nanometer-sized cage with four negatively charged, tetracoordinated B atoms. Both 1 and 2 show several redox waves in the cathodic regions of the cyclic voltammograms. An in-depth assessment of the consequences of electron injection on the aromaticity of 1 and 2 was achieved by electronic structure calculations. 1 and 2 are proposed to exhibit aromatic switching capabilities in the [16]annulene motif.

A lens-shaped supramolecule based on the bulky pentaphosphaferrocene [CpBIGFe(η5-P5)] and CuBr2.

Besides inherent fullerene-like hollow spheres, the metallasupramolecular chemistry of pentaphosphaferrocenes and CuBr2 afforded a conceptually new product, a compact 3.2 nm sized supramolecule [{1d}6(CuBr)32(CH3CN)6] formed by six largest pentaphosphaferrocene units [CpBIGFe(η5-P5)] (1d: CpBIG = η5-C5(4-nBuC6H4)5) so far and a framework of 32 copper and 32 bromide ions.

Interplay of Anisotropic Exchange Interactions and Single-Ion Anisotropy in Single-Chain Magnets Built from Ru/Os Cyanidometallates(III) and Mn(III) Complex.

Two novel 1D heterobimetallic compounds {[MnIII(SB2+)MIII(CN)6]·4H2O}n (SB2+ = N,N'-ethylenebis(5-trimethylammoniomethylsalicylideneiminate) based on orbitally degenerate cyanidometallates [OsIII(CN)6]3- (1) and [RuIII(CN)6]3- (2) and MnIII Schiff base complex were synthesized and characterized structurally and magnetically. Their crystal structures consist of electrically neutral, well-isolated chains composed of alternating [MIII(CN)6]3- anions and square planar [MnIII(SB2+)]3+ cations bridged by cyanide groups. These -ion magnetic anisotropy of MnIII centers. These results indicate that the presence of compounds exhibit single-chain magnet (SCM) behavior with the energy barriers of Δτ1/kB = 73 K, Δτ2/kB = 41.5 K (1) and Δτ1/kB = 51 K, Δτ2 = 27 K (2). Blocking temperatures of TB = 2.8, 2.1 K and magnetic hysteresis with coercive fields (at 1.8 K) of 8000, 1600 Oe were found for 1 and 2, respectively. Theoretical analysis of the magnetic data reveals that their single-chain magnet behavior is a product of a complicated interplay of extremely anisotropic triaxial exchange interactions in MIII(4d/5d)-CN-MnIII fragments: -JxSMxSMnx-JySMySMny-JzSMzSMnz, with opposite sign of exchange parameters Jx = -22, Jy = +28, Jz = -26 cm-1 and Jx = -18, Jy = +20, Jz = -18 cm-1 in 1 and 2, respectively) and single orbitally degenerate [OsIII(CN)6]3- and [RuIII(CN)6]3- spin units with unquenched orbital angular momentum in the chain compounds 1 and 2 leads to a peculiar regime of slow magnetic relaxation, which is beyond the scope of the conventional Glaubers's 1D Ising model and anisotropic Heisenberg model.

Across the Dimensions: A Three-Component Self-Assembly of Pentaphosphaferrocene-based Coordination Polymers.

Pentaphosphaferrocenes [CpR Fe(η5 -P5 )] (Cp*=η5 -C5 Me5 ) (A), Cp''=η5 -C5 H3 tBu2 -1,3 (B)) are excellent building blocks for polymeric assemblies in supramolecular chemistry in combination with coinage metal salts of weakly coordinating anions such as AgSbF6 . Adding rigid aromatic dinitriles ortho/meta/para-(NC)2 C6 H4 in a one-pot reaction between [CpR Fe(η5 -P5 )] and AgSbF6 leads to various coordination polymers (CPs) by a three-component self-assembly. The sterical demand of the differently substituted cyclopentadiene ligands as well as the rigid constitution of the isomeric dinitriles (NC)2 C6 H4 play a key role in the formation of the isolated CPs. All CPs were characterized by NMR spectroscopy, mass spectrometry, elemental analysis, and single-crystal X-ray diffraction.

Structural Chemistry of Giant Metal Based Supramolecules.

The review presents a bird-eye view on the state of research in the field of giant nonbiological discrete metal complexes and ions of nanometer size, which are structurally characterized by means of single-crystal X-ray diffraction, using the crystal structure as a common key feature. The discussion is focused on the main structural features of the metal clusters, the clusters containing compact metal oxide/hydroxide/chalcogenide core, ligand-based metal-organic cages, and supramolecules as well as on the aspects related to the packing of the molecules or ions in the crystal and the methodological aspects of the single-crystal neutron and X-ray diffraction of these compounds.

Unusual molecular complexes of antimony fluoride dimers with acetonitrile and pyridine: structures and bonding.

The structures of two new molecular complexes of antimony pentafluoride with pyridine (Py) and acetonitrile (AN), SbF5·Py and Sb2F10·AN, and a molecular complex of antimony trifluoride Sb2F6·Py and its ionic derivative [HPy]+[Sb2F7]- in the solid state have been determined by single crystal X-ray structural analysis. The complexes Sb2F10·AN and Sb2F6·Py are the first structurally characterized compounds of dimeric antimony fluorides. To reveal the nature of bonding in the complexes and their stability, DFT computations of the electronic structure and thermodynamic characteristics were performed, in particular the analysis of the electrostatic potentials, the orbital interactions and the topology. The results indicate that the intermolecular Sb⋯F interactions can be described as a network of pnictogen bonds.

Insertion of Phosphenium Ions into a Bicyclo[1.1.0]Tetraphosphabutane Iron Complex.

By reacting [{Cp‴Fe(CO)2}2(µ,η1:1-P4)] (1) with in situ generated phosphenium ions [Ph2P][A] ([A]- = [OTf]- = [O3SCF3]-, [PF6]-), a mixture of two main products of the composition [{Cp‴Fe(CO)2}2(µ,η1:1-P5(C6H5)2)][PF6] (2a and 3a) could be identified by extensive 31P NMR spectroscopic studies at 193 K. Compound 3a was also characterized by X-ray diffraction analysis, showing the rarely observed bicyclo[2.1.0]pentaphosphapentane unit. At room temperature, the novel compound [{Cp‴Fe}(µ,η4:1-P5Ph2){Cp‴(CO)2Fe}][PF6] (4) is formed by decarbonylation. Reacting 1 with in situ generated diphenyl arsenium ions gives short-lived intermediates at 193 K which disproportionate at room temperature into tetraphenyldiarsine and [{Cp‴Fe(CO)2}4(µ4,η1:1:1:1-P8)][OTf]2 (5) containing a tetracyclo[3.3.0.02,7.03,6]octaphosphaoctane ligand.

Versatile Coordination of AgI and CuI Ions towards cyclo-As5 Ligands.

The reactions of the cyclo-As5 complex [Cp*Fe(η5 -As5 )] (B) with the AgI and CuI salts of the weakly coordinating anion (WCA) [FAl{OC6 F10 (C6 F5 )}3 ]- ([FAl]- ) are studied. These reactions allow the synthesis of the mononuclear complexes [M(η5 : η2 -B)2 ][FAl] (M=Ag (1), Cu (2)) when a ratio of B/M(FAl) 2 : 1 is used. Compound 1 shows an unusual disorder of the central AgI cation between two π-coordinating cyclo-As5 ligands, which is absent in 2 pointing to a weak interaction of the Ag center towards the cyclo-As5 ligands in B. When the ratio of B/Ag(FAl) is changed to 3 : 1 or 1 : 1, the respective coordination compounds [Ag(η2 -B)3 ][FAl] (3) and [Ag2 (η2 : η2 -B)2 ][FAl]2 (4) are accessible. The coordination modes of the cyclo-As5 units in 1, 3 and 4 are all different, reflecting the adaptive coordination behavior of B towards AgI ions. The optimized geometries in the gas phase of 1-4 are determined by DFT calculations to support the bonding situation observed in their solid-state structures.

Au-Containing Coordination Polymers Based on Polyphosphorus Ligand Complexes.

Whereas the self-assembly of pentaphosphaferrocenes [CpRFe(η5-P5)] (CpR = Cp*, Cp×, and CpBn) with Cu and Ag salts has been well-studied in the past, the coordination chemistry toward Au complexes has been left untouched so far. Herein, the results of the self-assembly processes of [CpRFe(η5-P5)] with Au salts of different anions (GaCl4-, SbF6-, and Al(OC(CF3)3)4 (TEF-)) are reported. Next to a variety of molecular coordination products, the first coordination polymers based on polyphosphorus ligand complexes and Au salts are also obtained. Thereby, a 2D coordination polymer comprising metal vacancies is isolated. In all products, the Au centers are coordinated in a linear or a trigonal planar environment. In solution, highly dynamic processes are observed. Variable-temperature NMR spectroscopy, solid-state NMR spectroscopy, and X-ray powder diffraction were applied to gain further insight into selected coordination compounds.

Three-Component Self-Assembly Changes its Course: A Leap from Simple Polymers to 3D†Networks of Spherical Host-Guest Assemblies.

One-pot self-assembly reactions of the polyphosphorus complex [Cp*Fe(η5 -P5 )] (A), a coinage metal salt AgSbF6 , and flexible aliphatic dinitriles NC(CH2 )x CN (x=1-10) yield 1D, 2D, and 3D coordination polymers. The seven-membered backbone of the dinitrile was experimentally found as the borderline for the self-assembly system furnishing products of different kinds. At x<7, various rather simple polymers are exclusively formed possessing either 0D or 1D Ag/A structural motifs connected by dinitrile spacers, while at x≥7, the self-assembly switches to unprecedented extraordinary 3D networks of nano-sized host-guest assemblies (SbF6 )@[(A)9 Ag11 ]11+ (x=7) or (A)@[(A)12 Ag12 ]12+ (x=8-10) linked by dinitriles. The polycationic nodes represent the first superspheres based on A and silver and are host-guest able. All products are characterized by NMR spectroscopy, mass spectrometry, and single-crystal X-ray diffraction. The assemblies [(A)12 Ag12 ]12+ were visualized by transmission electron microscopy.

The Missing Parent Compound [(C5 H5 )Fe(η5 -P5 )]: Synthesis, Characterization, Coordination Behavior and Encapsulation.

The so far missing parent compound of the large family of pentaphosphaferrocenes [CpFe(η5 -P5 )] (1 b) was synthesized by the thermolysis of [CpFe(CO)2 ]2 with P4 using the very high-boiling solvent diisopropylbenzene. It was comprehensively characterized by, inter alia, NMR spectroscopy, single crystal X-ray structure analysis, cyclic voltammetry and DFT computations. Moreover, its coordination behavior towards CuI halides was explored, revealing the unprecedented 2D polymeric networks [{CpFe(η5:1:1:1:1 -P5 )}Cu2 (µ-X)2 ]n (2 a: X=Cl, 2 b: X=Br) and [{CpFe(η5:1:1 -P5 )}Cu(µ-I)]n (3) and even the first cyclo-P5 -containing 3D coordination polymer [{CpFe(η5:1:1 -P5 )}Cu(µ-I)]n (4). The sandwich complex 1 b can also be incorporated in nano-sized supramolecules based on [Cp*Fe(η5 -P5 )] (1 a) and CuX (X=Cl, Br, I): [CpFe(η5 -P5 )]@[{Cp*Fe(η5 -P5 )}12 (CuX)20-n ] (5 a: X=Cl, n=2.4; 5 b: X=Br, n=2.4; 5 c: X=I, n=0.95). Thereby, the formation of the CuI-containing fullerene-like sphere 5 c is found for the first time.

Mixed Organometallic-Organic Hybrid Assemblies Based on the Diarsene Complex [Cp2 Mo2 (CO)4 (µ,η2 -As2 )], AgI Salts and N-Donor Organic Molecules.

The reaction of the organometallic diarsene complex [Cp2 Mo2 (CO)4 (η2 -As2 )] (1) with Ag[Al{OC(CF3 )3 }4 ] (Ag[TEF]) yielded the AgI monomer [Ag(η2 -1)3 ][TEF] (2). This compound exhibits dynamic behavior in solution, which allows directed selective synthesis of unprecedented organometallic-organic hybrid assemblies upon its reaction with N-donor organic molecules by a stepwise pathway, which is supported by DFT calculations. Accordingly, the reaction of 2 with 2,2'-bipyrimidine (L1) yielded the dicationic molecular compound [{(η2 -1)2 Ag}2 (µ-L1)][TEF]2 (3) or the 1D polymer [{(η2 -1)Ag}(µ-L1)]n [TEF]n (4) depending on the ratio of the reactants. However, its reactions with the pyridine-based linkers 4,4'-bipyridine (L2), 1,2-bis(4-pyridyl)ethylene (L3) and 1,2-bis(4-pyridyl)ethyne (L4) allowed the formation of the 2D polymers [{(η2 -1)Ag}2 (µ-Lx)3 ]n [TEF]2n [Lx=L2 (5), L3 (6), L4 (7), respectively]. Additionally, this concept was extended to step-by-step one-pot reactions of 1, [Ag(CH3 CN)3 ][Al{OC(CF3 )2 (CCl3 )}4 ] ([Ag(CH3 CN)3 ][TEFCl ]) and linkers L2-L4 to produce the 2D polymers [{(η2 -1)Ag}2 (µ,Lx)3 ]n [TEFCl ]2n [Lx=L2 (8), L3 (9), L4 (10), respectively].

Structures and Chemical Bonding in Antimony(III) Bromide Complexes with Pyridine.

Weakly or "partially" bonded molecules are an important link between the chemical and van der Waals interactions. Molecular structures of six new SbBr3 -Py complexes in the solid state have been determined by single-crystal X-ray diffraction analysis. In all complexes all Sb atoms adopt a pseudo-octahedral coordination geometry which is completed by additional Sb⋅⋅⋅Br contacts shorter than the sum of the van der Waals radii, with Br-Sb⋅⋅⋅Br angles close to 180°. To reveal the nature of Sb-Br and Sb-N interactions, the DFT calculations were performed followed by the analysis of the electrostatic potentials, the orbital interactions and the topological analysis. Based on Natural Bond Orbital (NBO) analysis, the Sb-Br interactions range from the covalent bonds to the pnictogen bonds. A simple structural parameter, non-covalence criterion (NCC) is defined as a ratio of the atom-atom distance to the linear combination of sums of covalent and van der Waals radii. NCC correlates with E(2) values for Sb-N, Sb-Cl and Sb-Br bonds, and appears to be useful criterion for a preliminary evaluation of the bonding situation.

The Potential of the Diarsene Complex [(C5 H5 )2 Mo2 (CO)4 (µ,η2 -As2 )] as a Connector Between Silver Ions.

The reaction of the organometallic diarsene complex [Cp2 Mo2 (CO)4 (µ,η2 -As2 )] (B) (Cp = C5 H5 ) with Ag[FAl{OC6 F10 (C6 F5 )}3 ] (Ag[FAl]) and Ag[Al{OC(CF3 )3 }4 ] (Ag[TEF]), respectively, yields three unprecedented supramolecular assemblies [(η2 -B)4 Ag2 ][FAl]2 (4), [(µ,η1 :η2 -B)3 (η2 -B)2 Ag3 ][TEF]3 (5) and [(µ,η1 :η2 -B)4 Ag3 ][TEF]3 (6). These products are only composed of the complexes B and AgI . Moreover, compounds 5 and 6 are the only supramolecular assemblies featuring B as a linking unit, and the first examples of [AgI ]3 units stabilized by organometallic bichelating ligands. According to DFT calculations, complex B coordinates to metal centers through both the As lone pair and the As-As σ-bond thus showing this unique feature of this diarsene ligand.

Iodination of cyclo-E5 -Complexes (E=P, As).

In a high-yield one-pot synthesis, the reactions of [Cp*M(η5 -P5 )] (M=Fe (1), Ru (2)) with I2 resulted in the selective formation of [Cp*MP6 I6 ]+ salts (3, 4). The products comprise unprecedented all-cis tripodal triphosphino-cyclotriphosphine ligands. The iodination of [Cp*Fe(η5 -As5 )] (6) gave, in addition to [Fe(CH3 CN)6 ]2+ salts of the rare [As6 I8 ]2- (in 7) and [As4 I14 ]2- (in 8) anions, the first di-cationic Fe-As triple decker complex [(Cp*Fe)2 (µ,η5:5 -As5 )][As6 I8 ] (9). In contrast, the iodination of [Cp*Ru(η5 -As5 )] (10) did not result in the full cleavage of the M-As bonds. Instead, a number of dinuclear complexes were obtained: [(Cp*Ru)2 (µ,η5:5 -As5 )][As6 I8 ]0.5 (11) represents the first Ru-As5 triple decker complex, thus completing the series of monocationic complexes [(CpR M)2 (µ,η5:5 -E5 )]+ (M=Fe, Ru; E=P, As). [(Cp*Ru)2 As8 I6 ] (12) crystallizes as a racemic mixture of both enantiomers, while [(Cp*Ru)2 As4 I4 ] (13) crystallizes as a symmetric and an asymmetric isomer and features a unique tetramer of {AsI} arsinidene units as a middle deck.

Metal-Deficient Supramolecule Based on a Fivefold-Symmetric Building Block.

An unprecedented cationic supramolecule [(Cp''Fe(η5 -P5 ))12 {CuNCMe}8 ]8+ 2.66 nm in diameter was selectively isolated as a salt of the weakly coordinating anion [Al{OC(CF3 )3 }4 ]- for the first time and characterized by X-ray structure analysis, PXRD, NMR spectroscopy, and mass spectrometry. Its metal-deficient core contains the lowest possible number of Cu atoms to connect 12 pentaphosphaferrocene units, providing a supramolecule with fullerene topology which, topologically, also represents the simplest homologue in the family of metal-deficient pentaphosphaferrocene-based supramolecules [{CpR Fe(η5 -P5 )}12 (CuX)20-n ]. The 12 vacant metal sites between the cyclo-P5 rings, the largest number attained to date, make this compound a facile precursor for potential inner and outer modifications of the core as well as for functionalization via the substitution of labile acetonitrile ligands.

Use of a cyclo-P4 building block - a way to networks of host-guest assemblies.

Despite the proven ability to form supramolecular assemblies via coordination to copper halides, organometallic building blocks based on four-membered cyclo-P4 ligands find only very rare application in supramolecular chemistry. To date, only three types of supramolecular aggregates were obtained based on the polyphosphorus end-deck complexes CpRTa(CO)2(η4-P4) (1a: CpR = Cp''; 1b: CpR = Cp'''), with none of them, however, possessing a guest-accessible void. To achieve this target, the use of silver salts of the weakly coordinating anion SbF6 - was investigated as to their self-assembly in the absence and in the presence of the template molecule P3Se4. The two-component self-assembly of the building block 1a and the coinage-metal salt AgSbF6 leads to the formation of 1D or 3D coordination polymers. However, when the template-driven self-assembly was attempted in the presence of an aliphatic dinitrile, the unprecedented barrel-like supramolecular host-guest assembly P3Se4@[{(Cp''Ta(CO)2(η4-P4))Ag}8]8+ of 2.49 nm in size was formed. Moreover, cyclo-P4-based supramolecules are connected in a 2D coordination network by dinitrile linkers. The obtained compounds were characterised by mass-spectrometry, 1H and 31P NMR spectroscopy and X-ray structure analysis.

From nano-balls to nano-bowls.

Pentaphosphaferrocene [Cp*Fe(η5-P5)] in combination with Cu(i) halides is capable of a template-directed synthesis of fullerene-like spheres. Herein, we present the use of a triple decker complex as template that leads to the formation of unprecedented 'nano-bowls'. These spherical domes resemble the truncated fullerenes I h-C80 and represent a novel spherical arrangement in the chemistry of spherical molecules.

Organometallic-Organic Hybrid Polymers Assembled from Pentaphosphaferrocene, Bipyridyl Linkers, and CuI Ions.

A multicomponent approach of the P n ligand complex [Cp*Fe(η5-P5)] (1: Cp* = η5-C5Me5) with the ditopic organic linkers 4,4'-bipyridine (2) or trans-1,2-di(pyridine-4-yl)ethene (3) in the presence of CuI salts of the anions [BF4]- and [PF6]- or the coordinating anion Br-, leads to the formation of four novel organometallic-organic hybrid polymers: the cationic 1D polymeric compounds [Cu4{Cp*Fe(µ3,η5:1:1-P5)}2(µ,η1:1-C10H8N2)4(CH3CN)4] n [BF4]4n (4) and [Cu4{Cp*Fe(µ3,η5:1:1-P5)}2(µ,η1:1-C10H8N2)4(CH3CN)4] n [PF6]4n (5) as well as the unique neutral threefold 2D → 2D interpenetrated networks [Cu2Cl2{Cp*Fe(µ3,η5:1:1-P5)}(µ,η1:1-C12H10N2)] n (6) and [Cu2Br2{Cp*Fe(µ3,η5:1:1-P5)}(µ,η1:1-C10H8N2)] n (7).

Anionic Hosts for the Incorporation of Cationic Guests.

Pentaphosphaferrocene [Cp*Fe(η5 -P5 )] (1 a) represents an excellent building block for the template-directed synthesis of spherical supramolecules. Here, the self-assembly of 1 a with CuI and CuII halides in the presence of the template complexes [FeCp2 ][PF6 ], [CoCp2 ][PF6 ] and [CoCp2 ] is reported, testifying to the redox behavior of the formed supramolecules. The oxidation or reduction capacity of these reactive complexes does not inhibit their template impact and, for the first time, the cationic metallocene [CoCp2 ]+ is enclosed in unprecedented anionic organometallic hosts. Furthermore, the large variety of structural motifs, as icosahedral, trigonal antiprismatic, cuboidal and tetragonal antiprismatic arrangements of 1 a units are realized in the supramolecules [FeCp2 ]@[{1 a}12 (CuBr)17.3 ] (3), [CoCp2 ]+3 {[CoCp2 ]+ @[{1 a}8 Cu24.25 Br28.25 (CH3 CN)6 ]4- } (4), {[Cp2 Co]+ @[{1 a}8 (CuI)28 (CH3 CN)9.8 ]}{[Cp2 Co]+ @[{1 a)}8 Cu24.4 I26.4 (CH3 CN)8 ]2- } (5), and [{1 a}3 {(1 a)2 NH}3 Cu16 I10 (CH3 CN)7 ] (6), respectively.