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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 1983-1985 
    ISSN: 0044-2313
    Keywords: Metal hydrides ; rhodium ; lithium ; crystal structure ; neutron diffraction ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Structure of Li3RhH6  -  a Ternary Hydride with Isolated [RhH6]3- OctahedraThe ternary rhodium hydride Li3RhH6 was synthesized by the reaction of lithium hydride with rhodium under a hydrogen pressure of 80 bar. X-ray investigations on powdered samples and an elastic neutron diffraction experiment on the deuterated compound led to the complete structure determination (space group: Pnma, Z = 4). The atomic arrangement is isotypic to the Na3RhH6 structure type. The crystal structure contains isolated [RhH6]3- octahedra, which are separated by the lithium ions.
    Notes: Die Synthese von Li3RhH6 gelingt durch Umsetzung von Lithiumhydrid mit feinverteiltem Rhodium unter einem Wasserstoffdruck von 80 bar. Röntgenographische Untersuchungen an pulverförmigen Proben und ein elastisches Neutronenbeugungsexperiment an der deuterierten Verbindung führten zur Strukturaufklärung (Raumgruppe: Pnma, Z = 4). Die Verbindung ist isotyp zu der von Na3RhH6 und enthält isolierte [RhH6]3--Oktaeder, die durch die Lithiumionen separiert werden.
    Additional Material: 2 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 566 (1988), S. 31-38 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Structure of Ternary Platinum Hydrides A3PtH5 with A ≙ K, Rb or CsThe ternary platinum hydrides A3PtH5 (A ≙ K, Rb or Cs) have been synthesized by the reaction of the binary alkali metal hydrides with platinum sponge in a pure hydrogen atmosphere. The crystal structure was determined by X-ray investigations on powdered samples and neutron diffraction experiments on the deuterated compounds. The room temperature modifications (space group P4/mbm) contain planar [PtH4]2--groups and additional hydride ions which are coordinated by A ions exclusively. These crystal structures are isotypic with those of the fluorides A3PdF5 (A ≙ Rb, Cs). In the cubic high temperature modifications of Rb3PtH5 and Cs3PtH5 (space group Pm3m) the movements of the [PtH4]2- groups result in an atomic arrangement corresponding to that of a perovskite according to the formula (PtH4)HA3.
    Notes: Die Synthese der ternären Platinhydride A3PtH5 (A ≙ K, Rb oder Cs) gelingt durch Umsetzung der binären Alkalimetallhydride mit Platinschwamm in einer hochreinen Wasserstoffatmosphäre. Röntgenograhische Untersuchungen an pulverförmigen Proben und Neutronenbeugungsexperimente an den deuterierten Verbindungen führten zur Strukturaufklärung. Die Atomanordnungen in den Raumtemperatur-Modifikationen (Raumgruppe: P4/mbm) enthalten neben planaren [PtH4]2--Baugruppen Hydridionen, die ausschließlich von A-Ionen koordiniert sind. Der Strukturaufbau entspricht dem der ternären Fluoride A3PdF5 (A ≙ Rb, Cs). In den kubischen Hochtemperatur-Modifikationen von Rb3PtH5 und Cs3PtH5 (Raumgruppe: Pm3m) existieren, bedingt durch Bewegungsvorgänge in den [PtH4]2--Gruppen, perowskitartige Strukturen, entsprechend der Schreibweise (PtH4)HA3.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 1318-1321 
    ISSN: 0044-2313
    Keywords: Metal hydrides ; platinum ; high pressure synthesis ; crystal structure ; neutron diffraction ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: High-pressure Synthesis and Structure of Rb2PtH6 and Cs2PtH6, Ternary Hydrides with K2PtCl6-StructureThe ternary platinum hydrides Rb2PtH6 and Cs2PtH6 were synthesized by the reaction of rubidium hydride and cesium hydride, respectively, with platinum sponge under a hydrogen pressure above 1 500 bar at 500°C. X-ray investigations on powdered samples and elastic neutron diffraction experiments on the deuterated compounds at the time-of-flight spectrometer POLARIS led to their complete structure determination. Their atomic arrangements are isotypic with that of K2PtCl6 containing isolated [PtH6]2--octahedra (space group: Fm3m, Z = 4).
    Notes: Die Synthese von Rb2PtH6 und Cs2PtH6 gelingt durch Umsetzungen von Rubidiumhydrid beziehungsweise Caesiumhydrid mit Platinschwamm bei einem Wasserstoffreaktionsdruck 〉 1 500 bar und einer Temperatur von 500°C. Röntgenographische Untersuchungen an pulverförmigen Proben und elastische Neutronenbeugungsexperimente an den deuterierten Verbindungen mit Hilfe des Flugzeitspektrometers POLARIS führten zur vollständigen Strukturaufklärung. Die beiden Hydride kristallisieren im K2PtCl6-Typ mit isolierten [PtH6]2--Oktaedern (Raumgruppe: Fm3m, Z = 4).
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 623 (1997), S. 184-190 
    ISSN: 0044-2313
    Keywords: Mixed Hexahydridodeuteridoplatinates(IV) ; 195Pt{1H}MAS NMR ; Raman ; IR Spectra ; Normal Coordinate Analysis ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation, 195Pt NMR, IR, Raman Spectra, and Normal Coordinate Analysis of the Complex Ions [PtHnD6-n]2-, n = 0-6The extremely air and moisture sensitive hexahydridodeuteridoplatinates(IV) K2[PtHnD6-n], n = 0-6, have been prepared by high pressure reactions at 500°C and 1500 bar. The solid homoleptic compounds K2[PtH6] and K2[PtD6] and mixtures of K2[PtHnD6-n] prepared with varying H/D ratios have been investigated by 195Pt{1H} MAS NMR and by IR and Raman spectroscopy. Because of the high mobility of the atoms in the solid clearly resolved NMR spectra without sidebands are obtained exhibiting relatively sharp, isotropic 195Pt resonances (Δv1/2 = 400 Hz) at -990 ± 1 ppm for K2[PtH6] and -1034 ± 1 ppm for K2[PtD6]. Starting with K2[PtH6] the signals of the complexes with mixed ligand spheres are arranged systematically with an average high field shift of -9.5 ppm per substituted hydrideligand. By quantitative evaluation of the integrated intensities the statistical formation of the individual complexions within the mixtures is derived. The molecular vibrations in the IR and Raman spectra of the pure homoleptic compounds and the heteroleptic species in the mixtures are assigned with the aid of normal coordinate analyses. The Pt-H valence force constant is 2.13 mdyne/Å.
    Notes: Die äußerst luft- und feuchtigkeitsempfindlichen Hexahydridodeuterido-platinate(IV) K2[PtHnD6-n], n = 0-6, sind durch Hochdruckreaktionen bei 500°C und 1500 bar dargestellt worden. An den festen homoleptischen Verbindungen K2[PtH6] und K2[PtD6] und den mit unterschiedlichen H/D-Verhältnissen präparierten Gemischen K2[PtHnD6-n] sind die 195Pt-{1H}-MAS-NMR- sowie die IR- und Raman-Spektren aufgenommen worden. Wegen der hohen Mobilität der Atome in den Festkörpern erhält man gut aufgelöste, seitenbandenfreie NMR-Spektren mit relativ scharfen, isotropen 195Pt-Signalen (Δv1/2 = 400 H/z) bei -990 ± 1 ppm für K2[PtH6] und -1034 ± 1 ppm für K2[PtD6]. Ausgehend von K2[PtH6] ordnen sich die Signale der Komplexe mit gemischter Ligandensphäre mit einem systematischen Hochfeldshift von durchschnittlich -9,5 ppm pro substituiertem Hydridliganden an. Aus der quantitativen Auswertung der integralen Intensitäten folgt die statistische Bildung der einzelnen Komplexionen in den Gemischen. Die Molekülschwingungen in den IR- und Raman-Spektren der reinen homoleptischen Verbindungen und der heteroleptischen Spezies in den Gemischen werden durch Normalkoordinatenanalysen zugeordnet. Für die Pt—H-Valenzkraftkonstante ergibt sich ein Wert von 2,l3 mdyn/Å.
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 622 (1996), S. 1145-1149 
    ISSN: 0044-2313
    Keywords: Metal hydrides ; manganese ; high pressure synthesis ; crystal structure ; neutron diffraction ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: K3MnH5, the First Salt-like Manganese HydrideK3MnH5 and K3MnD5 were synthesized by the reaction of potassium hydride (deuteride) with manganese powder under a hydrogen pressure above 3000 bar at 875 K. X-ray investigations on powdered samples and elastic neutron diffraction experiments on the deuterated compound at the time-of-flight spectrometer LAD in the temperature range 5-600 K led to the complete structure determination. The atomic arrangement is isotypic with that of Cs3[CoCl4]Cl (space group: 14/mcm, Z = 4). The structure of K3MnH5 contains isolated [MnH4]2--tetrahedra and additional hydrogen ions which are exclusively coordinated by potassium cations. The magnetic susceptibilities show Curie-Weiss behaviour. At temperatures below 50 K there are obviously antiferromagnetic interactions.
    Notes: Die Synthese von K3MnH5 bzw. K3MnD5 gelingt durch Umsetzung von Kaliumhydrid (-deuterid) mit Manganpulver bei einem Wasserstoffreaktionsdruck 〉 3000 bar und einer Temperatur von 875 K. Röntgenographische Untersuchungen an pulverförmigen Proben und elastische Neutronenbeugungsexperimente an der deuterierten Verbindung mit Hilfe des Flugzeitspektrometers LAD in Abhängigkeit von der Temperatur (5-600 K) führten zur vollständigen Strukturaufklärung.Die Atomanordnung enthält neben isolierten [MnH4]2--Tetraedern Hydridionen, die ausschließlich von Kaliumionen koordiniert sind. Der Strukturaufbau entspricht dem im Cs3[CoCl4]Cl (Raumgruppe: 14/mcm, Z = 4). Die Temperaturabhängigkeit der magnetischen Suszeptibilitäten zeigt oberhalb von 50 K Curie-Weiss-Verhalten. Unterhalb 50 K treten offensichtlich antiferromagnetische Kopplungen auf.
    Additional Material: 4 Ill.
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  • 6
    Publication Date: 2009-03-19
    Print ISSN: 1098-0121
    Electronic ISSN: 1550-235X
    Topics: Physics
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  • 7
    Publication Date: 2016-09-01
    Print ISSN: 0031-9007
    Electronic ISSN: 1079-7114
    Topics: Physics
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  • 8
    Publication Date: 2019
    Description: 〈p〉The band inversion in topological phase matters bring exotic physical properties such as the topologically protected surface states (TSS). They strongly influence the surface electronic structures of the materials and could serve as a good platform to gain insight into the surface reactions. Here we synthesized high-quality bulk single crystals of Co〈sub〉3〈/sub〉Sn〈sub〉2〈/sub〉S〈sub〉2〈/sub〉 that naturally hosts the band structure of a topological semimetal. This guarantees the existence of robust TSS from the Co atoms. Co〈sub〉3〈/sub〉Sn〈sub〉2〈/sub〉S〈sub〉2〈/sub〉 crystals expose their Kagome lattice that constructed by Co atoms and have high electrical conductivity. They serves as catalytic centers for oxygen evolution process (OER), making bonding and electron transfer more efficient due to the partially filled orbital. The bulk single crystal exhibits outstanding OER catalytic performance, although the surface area is much smaller than that of Co-based nanostructured catalysts. Our findings emphasize the importance of tailoring TSS for the rational design of high-activity electrocatalysts.〈/p〉
    Electronic ISSN: 2375-2548
    Topics: Natural Sciences in General
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  • 9
    Publication Date: 2002-08-01
    Print ISSN: 1618-2642
    Electronic ISSN: 1618-2650
    Topics: Chemistry and Pharmacology
    Published by Springer
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  • 10
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