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101.
Oxidizing Elemental Platinum with Oleum under Harsh Conditions: The Unique Tris(disulfato)platinate(IV) [Pt(S2O7)3]2− Anion 下载免费PDF全文
Jörn Bruns Prof. Dr. Thorsten Klüner Prof. Dr. Mathias S. Wickleder 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(24):7222-7227
For the first time, direct oxidation of elemental platinum by a mineral acid to its tetravalent state was observed in course of the reaction of platinum with oleum (65 % SO3) in the presence of barium carbonate. The reaction has been carried out in torch‐sealed glass ampoules at 160 °C and gave yellow single crystals of Ba[Pt(S2O7)3](H2SO4)0.5(H2S2O7)0.5 (triclinic, P$\bar 1$ , Z=2, a=992.05(2), b=1069.07(3), c=1114.22(3) pm, α=69.49(7), β=72.96(2), γ=72.93(1)°, V=1033.95(5) Å3). The structure of Ba[Pt(S2O7)3](H2SO4)0.5(H2S2O7)0.5 exhibits the unique tris‐(disulfato)‐platinate anion [Pt(S2O7)3]2? with three chelating disulfate groups coordinated to the platinum atom. Charge balance is achieved by the Ba2+ ions, which are coordinated by (S2O7)2? groups from the platinate complex and by disordered sulfuric acids and disulfuric acid molecules. Thermal decomposition of the bulk material revealed elemental platinum and barium sulfate as decomposition residual. 相似文献
102.
The Origin of the Selectivity and Activity of Ruthenium‐Cluster Catalysts for Fuel‐Cell Feed‐Gas Purification: A Gas‐Phase Approach 下载免费PDF全文
Dr. Sandra M. Lang Prof. Dr. Thorsten M. Bernhardt Marjan Krstić Prof. Dr. Vlasta Bonačić‐Koutecký 《Angewandte Chemie (International ed. in English)》2014,53(21):5467-5471
Gas‐phase ruthenium clusters Run+ (n=2–6) are employed as model systems to discover the origin of the outstanding performance of supported sub‐nanometer ruthenium particles in the catalytic CO methanation reaction with relevance to the hydrogen feed‐gas purification for advanced fuel‐cell applications. Using ion‐trap mass spectrometry in conjunction with first‐principles density functional theory calculations three fundamental properties of these clusters are identified which determine the selectivity and catalytic activity: high reactivity toward CO in contrast to inertness in the reaction with CO2; promotion of cooperatively enhanced H2 coadsorption and dissociation on pre‐formed ruthenium carbonyl clusters, that is, no CO poisoning occurs; and the presence of Ru‐atom sites with a low number of metal–metal bonds, which are particularly active for H2 coadsorption and activation. Furthermore, comprehensive theoretical investigations provide mechanistic insight into the CO methanation reaction and discover a reaction route involving the formation of a formyl‐type intermediate. 相似文献
103.
A membrane-assisted solvent extraction (MASE) method is presented for the extraction of several non-ionic organophosphorus chemicals from wastewaters samples followed by LC-MS/MS determination. The method was developed for a variety of chlorinated phosphates (trichloroethyl, tichloropropyl) and non-chlorinated phosphates (triphenyl, tributyl) used as flame retardants and for plasticizers such as triethylhexyl and tris-butoxyethyl phosphate. Parameters such as extracting solvent, sample volume and ionic strength, extraction temperature and time were optimized. The final method provides good quantification limits (1-25 ng L(-1)) and linearity (R2>0.9978). Method precision was also good at high concentrations (5% mean RSD at the 500 ng L(-1) level) but decreased at lower concentrations (20% mean RSD at the 20 ng L(-1) level). MASE yields lower matrix effects than SPE in a successive LC-MS/MS analysis of these compounds, avoiding the need for standard addition for quantification. When applied to wastewater samples comparable results were obtained using either MASE with internal standard calibration or SPE with standard addition. 相似文献
104.
Kreickmann T Diedrich C Pape T Huynh HV Grimme S Hahn FE 《Journal of the American Chemical Society》2006,128(36):11808-11819
The bis(benzene-o-dithiol) ligands H(4)-1, H(4)-2, and H(4)-3 react with [Ti(OC(2)H(5))(4)] to give dinuclear triple-stranded helicates [Ti(2)L(3)](4)(-) (L = 1(4)(-), 2(4)(-), 3(4)(-)). NMR spectroscopic investigations revealed that the complex anions possess C(3) symmetry in solution. A crystal structure analysis for (PNP)(4)[Ti(2)(2)(3)] ((PNP)(4)[14]) confirmed the C(3) symmetry for the complex anion in the solid state. The complex anion in Li(PNP)(3)[Ti(2)(1)(3)] (Li(PNP)(3)[13]) does not exhibit C(3) symmetry in the solid state due to the formation of polymeric chains of lithium bridged complex anions. Complexes [13](4)(-) and [14](4)(-) were obtained as racemic mixtures of the Delta,Delta and Lambda,Lambda isomers. In contrast to that, complex (PNP)(4)[Ti(2)(3)(3)] ((PNP)(4)[15]) with the enantiomerically pure chiral ligand 3(4)(-) shows a strong Cotton effect in the CD spectrum, indicating that the chirality of the ligands leads to the formation of chiral metal centers. The o-phenylene diamine bridged bis(benzene-o-dithiol) ligand H(4)-4 reacts with Ti(4+) to give the dinuclear double-stranded complex Li(2)[Ti(2)(4)(2)(mu-OCH(3))(2)] containing two bridging methoxy ligands between the metal centers. The crystal structure analysis and the (1)H NMR spectrum of (Ph(4)As)(2)[Ti(2)(4)(2)(mu-OCH(3))(2)] ((Ph(4)As)(2)[(16]) reveal C(2) symmetry for the anion [Ti(2)(4)(2)(mu-OCH(3))(2)](2)(-). For a comparative study the dicatechol ligand H(4)-5, containing the same o-phenylene diamine bridging group as the bis(benzene-o-dithiol) ligands H(4)-4, was prepared and reacted with [TiO(acac)(2)] to give the dinuclear complex anion [Ti(2)(5)(2)(mu-OCH(3))(2)](2)(-). The molecular structure of (PNP)(2)[Ti(2)(5)(2)(mu-OCH(3))(2)] ((PNP)(2)[17]) contains a complex anion which is similar to [16](2)(-), with the exception that strong N-H...O hydrogen bonds are formed in complex anion [17](2)(-), while N-H...S hydrogen bonds are absent in complex anion [16](2)(-). 相似文献
105.
The heterodinuclear complex [LCuIIVIVO] 1 was synthesized by using a new unsymmetric dinucleating ligand based on 1,8-naphthalenediol, whereas the homodinuclear CuIICuII complex 2 has a bridging beta-diketimineamid unit. Here we report on the synthesis, molecular structures, and magnetic properties of 1 and 2. In the solid state, both complexes dimerize to tetranuclear entities 1(2) and 2(2). The intradimer interaction in both complexes is ferromagnetic because of the orthogonality of the magnetic orbitals (J12 = +45.6 cm(-1) in 1 and +4.8 cm(-1) in 2). The interdimer interaction in 1 is also ferromagnetic, giving a St = 2 ground state. 相似文献
106.
107.
Dipl.‐Chem. Alexander Rupp Dr. Nataliya Roznyatovskaya Dr. Harald Scherer Dr. Witali Beichel Petra Klose Carola Sturm Dr. Anke Hoffmann Dr. Jens Tübke Prof. Dr. Thorsten Koslowski Prof. Dr. Ingo Krossing 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(31):9794-9804
Several, partly new, ionic liquids (ILs) containing imidazolium and ammonium cations as well as the medium‐sized [NTf2]? (0.230 nm3; Tf=CF3SO3?) and the large [Al(hfip)4]? (0.581 nm3; hfip=OC(H)(CF3)2) anions were synthesized and characterized. Their temperature‐dependent viscosities and conductivities between 25 and 80 °C showed typical Vogel–Fulcher–Tammann (VFT) behavior. Ion‐specific self‐diffusion constants were measured at room temperature by pulsed‐gradient stimulated‐echo (PGSTE) NMR experiments. In general, self‐diffusion constants of both cations and anions in [Al(hfip)4]?‐based ILs were higher than in [NTf2]?‐based ILs. Ionicities were calculated from self‐diffusion constants and measured bulk conductivities, and showed that [Al(hfip)4]?‐based ILs yield higher ionicities than their [NTf2]? analogues, the former of which reach values of virtually 100 % in some cases.From these observations it was concluded that [Al(hfip)4]?‐based ILs come close to systems without any interactions, and this hypothesis is underlined with a Hirshfeld analysis. Additionally, a robust, modified Marcus theory quantitatively accounted for the differences between the two anions and yielded a minimum of the activation energy for ion movement at an anion diameter of slightly greater than 1 nm, which fits almost perfectly the size of [Al(hfip)4]?. Shallow Coulomb potential wells are responsible for the high mobility of ILs with such anions. 相似文献
108.
A Chiral Thioxanthone as an Organocatalyst for Enantioselective [2+2] Photocycloaddition Reactions Induced by Visible Light 下载免费PDF全文
Dr. Rafael Alonso Prof. Dr. Thorsten Bach 《Angewandte Chemie (International ed. in English)》2014,53(17):4368-4371
Thioxanthone 1 , which was synthesized in a concise fashion from methyl thiosalicylate, exhibits a significant absorption in the visible light region. It allows for an efficient enantioselective catalysis of intramolecular [2+2] photocycloaddition reactions presumably by triplet energy transfer. 相似文献
109.
Improving Site‐Directed RNA Editing In Vitro and in Cell Culture by Chemical Modification of the GuideRNA 下载免费PDF全文
Paul Vogel Marius F. Schneider Jacqueline Wettengel Dr. Thorsten Stafforst 《Angewandte Chemie (International ed. in English)》2014,53(24):6267-6271
Adenosine‐to‐inosine deamination can be re‐addressed to user‐defined mRNAs by applying phosphothioate/2′‐methoxy‐modified guideRNAs. Dense chemical modification of the guideRNA clearly improves performance of the covalent conjugates inside the living cell. Furthermore, careful positioning of a few modifications controls editing selectivity in vitro and was exploited for the challenging repair of the Factor 5 Leiden missense mutation. 相似文献
110.
Thorsten Gehrmann Julio Lloret Fillol Dr. Hubert Wadepohl Prof. Dr. Lutz H. Gade Prof. Dr. 《Angewandte Chemie (International ed. in English)》2009,48(12):2152-2156
Breaking the chain : Reaction of a zirconium hydrazinediide with organoazides gives 2‐pentazene‐1,4‐diyl complexes, such as [Zr(N2TBSNpy){N(Ad)N3NPh2}] (C gray, N blue, Si green, Zr turquoise), by formal [2+3] cycloaddition. Bonding within the N5 chain is investigated using density functional calculations. These complexes thermally eject N2 to give side‐on bonded diazenides.