On pyridine chloronium cations.

We present the first solid-state structural evidence of mono- and bis(pyridine)chloronium cations. The latter was synthesized from a mixture of pyridine, elemental chlorine and sodium tetrafluoroborate in propionitrile at low temperatures. The mono(pyridine) chloronium cation was realized with the less reactive pentafluoropyridine, using ClF, AsF5, and C5F5N in anhydrous HF. During the course of this study, we also investigated pyridine dichlorine adducts and found a surprising disproportionation reaction of chlorine that depended on the substitutional pattern of the pyridine. Electron richer dimethylpyridine (lutidine) derivatives favor full disproportionation into a positively and a negatively charged chlorine atom which forms a trichloride monoanion, while unsubstituted pyridine forms a 1 : 1 py·Cl2 adduct.

A decacationic ferrocene-based metallostar.

Decacationic metallostars have been prepared by the reaction of permercurated ferrocene FeC10(HgO2CCF3)10 with superacidic (C5F5NH)(SbF6) (pK a = -11 estimated in H2O) in multigram scale. In the resulting compound, [FeC10Hg10(NC5F5) n ][SbF6]10, the labile pentafluoropyridine ligands are readily displaced by acetonitrile (MeCN) or tetrahydrothiophene (THT). In the X-ray structure of [FeC10Hg10(THT)10][SbF6]10·24 MeCN no cation-anion contacts between mercury and fluorine were observed. Moreover, cyclic voltammetry measurements of [FeC10(Hg(MeCN))10]10+ and [FeC10(Hg(THT))10]10+ revealed a (quasi)reversible one-electron oxidation of Fe(ii) to Fe(iii). From the reaction of [FeC10(Hg(MeCN))10]10+ with MoF6 as oxidant the ferrocenium cation [FeC10(Hg(MeCN))10]11+ was obtained and characterized via single crystal XRD. These electrophilic metallostars are promising potential building blocks for the synthesis of dendritic architectures containing a robust, tenfold functionalized ferrocene core.

Increasing the oxidation power of TCNQ by coordination of B(C6F5)3.

The oxidation power of the cyanocarbon TCNQ (tetracyano-quinodimethane) can be significantly increased to approximately E = +0.9 V vs. Cp2Fe by coordination of up to four equivalents of the strong fluorinated Lewis acid B(C6F5)3, resulting in a highly reactive but easy-to-use oxidation system. Thianthrene and tris(4-bromophenyl)amine were oxidized to the corresponding radical cations. Dianionic [TCNQ·4 B(C6F5)3]2- was formed upon reduction with two equivalents of ferrocene or decamethylcobaltocene. [TCNQ·4 B(C6F5)3]- and [TCNQ·4 B(C6F5)3]2- are rare cases of redox-active weakly-coordinating anions.

Eightfold Electrophilic Methylation of Octacyanotungstate [W(CN)8]4-/3-: Preparation of Homoleptic, Eight-Coordinate Methyl Isocyanide Complexes [W(CNMe)8]4+/5.

Homoleptic eightfold coordinated methyl isocyanide complexes of W(IV) and W(V) have been prepared for the first time. The reaction of [NBu4]4[W(CN)8] with methyl triflate (MeOTf) gives [W(CNMe)8][OTf]4. The even stronger methylating mixture of methyl fluoride (MeF) and arsenic pentafluoride (AsF5) in liquid sulfur dioxide (SO2) is able to fully alkylate both [NBu4]4[W(CN)8] and [NBu4]3[W(CN)8]. The paramagnetic octakis(methyl isocyanide)tungsten(V) complex [W(CNMe)8][AsF6]5 is thermally highly unstable above -30 °C. All compounds have been characterized via single-crystal X-ray diffraction and IR, Raman, and NMR or EPR spectroscopy.

Tenfold Metalation of Ferrocene: Synthesis, Structures, and Metallophilic Interactions in FeC10 (HgX)10.

The permercuration of ferrocene was achieved by reacting ferrocene with 10 equivalents of mercury(II) butyrate Hg(O2 CC3 H7 )2 in a facile one-pot reaction in multi-gram scale and high yields. The butyrate groups in FeC10 (HgX)10 (X=O2 CC3 H7 ) can be exchanged by treatment with trifluoro- or trichloroacetic acid (X=O2 CCF3 , O2 CCCl3 ). Substitution of the trifluoroacetate groups by halides (X=Cl, F) proceeds easily in aqueous THF. The completeness of metalation was confirmed by NMR and vibrational spectroscopy, mass spectrometry, as well as elemental analysis. Additionally, the first crystal structures of permetallated metallocenes are presented: FeC10 (HgX)10 (X=Cl, O2 CCF3 , O2 CCCl3 ).

The [2+2] cycloaddition product of perhalogenated cyclopentadienyl cations: structural characterization of salts of the [C10Cl10]2+ and [C10Br10]2+ dications.

Instead of monomeric cyclopentadienyl cations, the low-temperature reaction of hexachloro- and hexabromocyclo-pentadiene (C5Cl6 and C5Br6) with powerful Lewis acids SbF5 and AsF5 in SO2ClF yields salts of perhalogenated dications [C10Cl10][Sb3F16]2 and [C10Br10][As2F11]2 which are characterized via single crystal X-ray diffraction and NMR spectroscopy. Additionally, this reactivity is rationalized by quantum-chemical calculations.