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.

Confined Lewis Pairs: Investigation of the X- →Si20 Interaction in Halogen-Encapsulating Silafulleranes.

A joint theoretical and experimental study on 32 endohedral silafullerane derivatives [X@Si20 Y20 ]- (X=F-I; Y=F-I, H, Me, Et) and T h ${T_h }$ -[Cl@Si20 H12 Y8 ]- (Y=F-I) is presented. First, we evaluated the structure-determining template effect of Cl- in a systematic series of concave silapolyquinane model systems. Second, we investigated the X- →Si20 interaction energy ( E int ${E_{{\rm{int}}} }$ ) as a function of X- and Y and found the largest E int ${E_{{\rm{int}}} }$ values for electron-withdrawing exohedral substituents Y. Given that X- ions can be considered as Lewis bases and empty Si20 Y20 clusters as Lewis acids, we classify our inseparable host-guest complexes [X@Si20 Y20 ]- as "confined Lewis pairs". Third, 35 Cl NMR spectroscopy proved to be highly diagnostic for an experimental assessment of the Cl- →Si20 interaction as the paramagnetic shielding and, in turn, δ ${\delta }$ (35 Cl) of the endohedral Cl- ion correlate inversely with E int ${E_{{\rm{int}}} }$ . Finally, we disclose the synthesis of [PPN][Cl@Si20 Y20 ] (Y=Me, Et, Br) and provide a thorough characterization of these new silafulleranes.

B2,N4-Doped Heptacenes: Ambipolar Charge-Transfer Compounds with Deep LUMO Levels.

The B2,N4-doped heptacene H4 in which two N,N'-dihydrophenazine units are linked by two BMes bridges (Mes = mesityl) was synthesized via fourfold Buchwald-Hartwig coupling between 2,3,6,7-tetrachloro-9,10-dimesityl-9,10-dihydro-9,10-diboraanthracene and o-phenylenediamine (tBuXPhos-Pd-G3, DBU/NaOTf, 2-MeTHF, 50 °C, 16 h). Upon exposure to ambient air, H4 is oxidized to its N,N'-dihydro form H2; further oxidation with MnO2 furnishes the di(phenazine) derivative H0. Stirring under a blanket of H2 in the presence of Pd/C hydrogenates H0 back to H2 and ultimately H4. Yellow-colored H0 is a remarkably good electron acceptor with a LUMO-energy level of -3.9 eV; upon irradiation with a 405 nm LED in the presence of THF or 1,4-cyclohexadiene, H0 accepts two H atoms to furnish H2. One-electron reduction of H0 yields the isolable radical-anion salt Li[H0] (lithium naphthalenide, THF, -30 °C to rt). The ambipolar compounds H2 and H4 possess a navy blue and deep purple color, respectively, due to charge-transfer interactions from the electron-rich N,N'-dihydrophenazine donor(s) to the electron-accepting B2C4 core.

Regioselective Derivatization of Silylated [20]Silafulleranes.

Silafulleranes with endohedral Cl- ions are a unique, scarcely explored class of structurally well-defined silicon clusters and host-guest complexes. Herein, we report regioselective derivatization reactions on the siladodecahedrane [nBu4N][Cl@Si20(SiCl3)12Cl8] ([nBu4N][1]), which has its cluster surface decorated with 12 SiCl3 and 8 Cl substituents in perfect Th symmetry. The room-temperature reaction of [nBu4N][1] with excess iBu2AlH in ortho-difluorobenzene (oDFB) furnishes perhydrogenated [nBu4N][Cl@Si20(SiH3)12H8] ([nBu4N][2]) in 50% yield; the non-pyrophoric [2]- is the largest structurally authenticated (by X-ray diffraction) hydridosilane known to date. A simple switch from pure oDFB to an oDFB/Et2O solvent mixture suppresses core hydrogenation and results in the formation of [nBu4N][Cl@Si20(SiH3)12Cl8] ([nBu4N][3]). In addition to the exhaustive Cl/H exchange at all 44 Si-Cl bonds of [1]- and the regioselective 36-fold silyl group hydrogenation, we achieved the simultaneous introduction of Me substituents at all 8 SiCl vertices along with the conversion of all 12 SiCl3 to SiH3 groups by treating [nBu4N][1] with Me2AlH/Me3Al in oDFB ([nBu4N][Cl@Si20(SiH3)12Me8], [nBu4N][4]; 73%). Quantum-chemical free-energy calculations find an SN2-Si-type hydrogenation of the exohedral SiCl3 moieties in [1]- (trigonal-bipyramidal intermediate) slightly preferred over metathesis-like SNi-Si substitutions (four-membered transition state). Cage hydrogenation likely occurs via SNi-Si processes. The experimentally demonstrated influence of an Et2O co-solvent, which drastically increases the respective reaction barriers, is attributed to the increased stability of the resulting iBu2AlH-OEt2 adduct and its higher steric bulk compared to free iBu2AlH.

A Hydride-Substituted Homoleptic Silylborate: How Similar is it to its Diborane(6)-Dianion Isostere?

The B-nucleophilic 9H-9-borafluorene dianion reacts with 9-chloro-9-silafluorene to afford air- and moisture-stable silylborate salts M[Ar2 (H)B-Si(H)Ar2 ] (M[HBSiH], M=Li, Na). Li[HBSiH] and Me3 SiCl give the B-pyridine adduct Ar2 (py)B-Si(H)Ar2 ((py)BSiH) or the chlorosilane Li[Ar2 (H)B-Si(Cl)Ar2 ] (Li[HBSiCl]) in C6 H6 -pyridine or THF. In both cases, the first step is H- abstraction at the B center. The resulting free borane subsequently binds a py or thf ligand. While the py adduct is stable at room temperature, the thf adduct undergoes a 1,2-H shift via the cyclic B(µ-H)Si intermediate BHSi, which is afterwards attacked at the Si atom by a Cl- ion to give Li[HBSiCl]. DFT calculations were employed to support the proposed reaction mechanism and to characterize the electronic structure of BHSi. Treatment of Li[HBSiCl] with the N-heterocyclic carbene IMe introduces the neutral donor at the Si atom and leads to Ar2 (H)B-Si(IMe)Ar2 (HBSi(IMe)), a donor-acceptor-stabilized silylene.

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.

Three- and Five-Membered Anionic Chains of Pnictogenylboranes.

An unprecedented family of three- and five-membered substituted anionic derivatives of parent pnictogenylboranes is herein reported. Reacting various combinations of the pnictogenylboranes H2 E'-BH2 -NMe3 (E'=P, As) with pnictogen-based nucleophiles MER1R2 (E=P, As; R1=H, R2=t Bu; R1=R2=Ph; M=Na, K) allows for the isolation of the unsymmetrical products [Na(18-crown-6)][H2 E'-BH2 -EHt Bu] (3: E=E'=P; 4: E=E'=As; 5: E=As, E'=P) and [M(C)][H2 E'-BH2 -EPh2 ] (7: E=E'=P, M=Na, C=18-crown-6; 8: E=E'=As; M=K, C=[2.2.2]cryptand; 9: E=P, E'=As, M=Na, C=[2.2.2]cryptand; 10: E=As, E'=P, M=K, C=[2.2.2]cryptand). [Na(18-crown-6)][H2 As-BH2 -t BuPH-BH3 ] (6) is only accessible by a different pathway, using t BuPH2 , BH3 ⋅ SMe2 and NaNH2 as starting materials. Additionally, the synthesis of symmetrical diphenyl-substituted compounds [M(18-crown-6)][Ph2 E-BH2 -EPh2 ] (11: E=P, M=Na; 12: E=As, M=K) is reported which can be regarded as isostructural inorganic, negatively charged analogs of dppm (1,1-bis(diphenylphosphino)methane) and dpam (1,1-bis(diphenylarsino)methane). Furthermore, an elongation of the pnictogen boron backbone in compounds 3, 7 and 9' (similar compound to 9, stabilized however by 18-crown-6), is attainable by reacting them with the pnictogenylboranes H2 E'-BH2 -NMe3 leading to corresponding five-membered chain-like compounds [Na(18-crown-6)][H2 E-BH2 -R1R2P-BH2 -E'H2 ] (E=E'=P, R1=H, R2=t Bu (13); E=E'=P, R1=R2=Ph (14); E=E'=As, R1=R2=Ph (15); E=P, E'=As, R1=R2=Ph (16)). Finally, the thermodynamics of the reaction pathways were evaluated by quantum chemical computations.

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.

Synthesis and Reactivity of a Cyclooctatetraene-Like Polyphosphorus Ligand Complex [Cyclo-P8 ].

The thermolysis of Cp'''Ta(CO)4 with white phosphorus (P4 ) gives access to [{Cp'''Ta}2 (µ,η2 : 2 : 2 : 2 : 1 : 1 -P8 )] (A), representing the first complex containing a cyclooctatetraene-like (COT) cyclo-P8 ligand. While ring sizes of n >6 have remained elusive for cyclo-Pn structural motifs, the choice of the transition metal, co-ligand and reaction conditions allowed the isolation of A. Reactivity investigations reveal its versatile coordination behaviour as well as its redox properties. Oxidation leads to dimerization to afford [{Cp'''Ta}4 (µ4 ,η2 : 2 : 2 : 2 : 2 : 2 : 2 : 2 : 1 : 1 : 1 : 1 -P16 )][TEF]2 (4, TEF=[Al(OC{CF3 }3 )4 ]- ). Reduction, however, leads to the fission of one P-P bond in A followed by rapid dimerization to form [K@[2.2.2]cryptand]2 [{Cp'''Ta}4 (µ4 ,η2 : 2 : 2 : 2 : 2 : 2 : 2 : 2 : 1 : 1 : 1 : 1 -P16 )] (5), which features an unprecedented chain-type P16 ligand. Lastly, A serves as a P2 synthon, via ring contraction to the triple-decker complex [{Cp'''Ta}2 (µ,η6 : 6 -P6 )] (B).

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.

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.

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.

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.

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.

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.

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.

The Lewis-Base-Stabilized Diphenyl-Substituted Arsanylborane: A Versatile Building Block for Arsanylborane Oligomers.

The synthesis and properties of the diphenyl-substituted arsanylborane Ph2 AsBH2 SMe2 (1) and Ph2 AsBH2 NMe3 (2) stabilized by a Lewis base (LB) were reported. These compounds were obtained by reaction of KAsPh2 with IBH2 -LB (LB=SMe2 , NMe3 ). Compounds 1 and 2 were used as starting materials for oligomeric/ polymeric arsinoboranes. The neutral species, H3 B-Ph2 AsBH2 NMe3 (3) and Br3 B-Ph2 AsBH2 NMe3 (4), were synthesized by reaction with H3 B and Br3 B, respectively. Upon reaction with IBH2 -LB (LB=SMe2 , NMe3 ), the cationic oligomeric group-13/15-based compounds [(Me3 NBH2 AsPh2 BH2 NMe3 )]I (5) and [H2 B(Ph2 AsBH2 NMe3 )2 ]I (6) were obtained. All compounds were completely characterized. In addition, the oxidation of Ph2 AsBH2 NMe3 with chalcogens was studied. The sulfur Ph2 As(S)BH2 NMe3 (7 b) and selenium Ph2 As(Se)BH2 NMe3 (7 c) oxidation products were both isolated and fully characterized, whereas the bis(trimethylsilyl)peroxide oxidated arsinoborane Ph2 As(O)BH2 NMe3 (7 a) was not stable enough and could only be characterized in solution. DFT computations supported the decomposition pathway of this compound.

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.

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).