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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 114 (1981), S. 3499-3504 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phosphonium Hydrogendichlorides, II: Three Crystal Structures in ComparisonBy means of crystal structure analysis the compounds [(4-CH3OC6H4)(CH3)PCl2][ClHCl] (1), [(4-CH3OC6H4)PCl3][ClHCl] (2), and [(4-C2H5OC6H4)PCl3][ClHCl] (3) are confirmed as phosphonium hydrogendichlorides and the number of existing geometric parameters of hydrogen bonding between Cl atoms in crystals is substantially increased. The symmetric hydrogendichloride anions who the shortest distances Cl…Cl (312.1 pm in 2) and the largest distance of this kind (328.8 pm also in 2) is observed in the anion with the shortest Cl-H bond.
    Notes: Durch Kristallstrukturanalyse werden die Verbindungen [(4-CH3OC6H4)(CH3)PCl2][ClHCl] (1), [(4-CH3OC6H4)PCl3][ClHCl] (2) und [(4-C2H5OC6H4)PCl3][ClHCl] (3) als Phosphonium-hydrogendichloride bestätigt und die vorhandenen geometrischen Daten zur Wasserstoffbrückenbindung zwischen Cl-Atomen in Kristallen deutlich vermehrt. Die symmetrischen Hydrogendichlorid-Anionen zeigen die kürzesten Abstände Cl…Cl (312.1 pm in 2), und der längste Abstand dieser Art (328.8 pm ebenfalls in 2) wird beim Anion mit der kürzesten Bindung Cl—H beobachtet.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 479 (1981), S. 75-83 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Crystal Structures of Acid Hydrates and Oxonium Salts. XVIII. Melting Diagram H2O—HF and Structures of the 1:1 and a 1:2 PhaseThe quasi binary system H2O-HF contains three intermediate phases of compositions 1:1, 1:2, and 1:4, which melt at -36, -78 (decomposition), and -100°C. With a composition of 1:2 there is also a low-temperature phase (transition at -103°C) and a metastable phase. The 1:1 phase is orthorhombic, space group Pnma, z = 4, a = 621.6, b = 418.4, c = 623.3 pm at -62°C. One of the 1:2 phases (assignment still to be done) is monoclinic, space group P21/c, z = 4, a = 347.8, b = 603.9, c = 1141.5 pm, β = 96.57° at -95°C. Both crystal structures are those of oxonium salts, H3OF and H3OFHF, respectively, and built up by strong hydrogen bonds.
    Notes: Das quasibinäre System H2O-HF enthält drei intermediäre Phasen der Zusammensetzungen 1:1, 1:2 und 1:4, die bei -36, -78 (Zersetzung) und -100°C schmelzen. Mit 1:2-Zusammensetzung gibt es auch noch eine Tieftemperaturphase (Umwandlung bei -103°C) und eine metastabile Phase. Die 1:1-Phase kristallisiert orthorhombisch, Raumgruppe Pnma, z = 4, a = 621,6, b = 418,4, c = 623,3 pm bei -62°C. Eine der 1:2-Phasen (die Zuordnung steht noch aus) kristallisiert monoklin, Raumgruppe P21/c, z = 4, a = 347,8, b = 603,9, c = 1141,5 pm, β = 96,57° bei -95°C. Beide Kristallstrukturen sind die von Oxoniumsalzen, H3OF bzw. H3OFHF, und durch starke Wasserstoffbrücken geprägt.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 121 (1988), S. 1841-1845 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Characteristics of Fluorinated BenzofuransDihydrobenzofurans 4a-c and g-j were synthesized from 2-acetyl-1,4-benzoquinone (1) and β-diketones 2a-c and g-j and dehydrated to benzofurans 5a-i. The structure of 5d was examined by X-ray analysis. Reaction of quinone 9 and diketone 2g yielded directly fluorinated benzofurans 11a and 12b. The abnormal 1H-NMR spectra of benzofurans 5d,f and 11a are discussed. Formation of ketone hydrates 12a,b and 13 was detected.
    Notes: Die Dihydrobenzofurane 4a-c und g-j wurden aus 2-Acetyl-1,4-benzochinon (1) und den β-Diketonen 2a-c und g-j dargestellt und zu den Benzofuranen 5a-i dehydratisiert. Die Struktur von 5d wurde röntgenographisch untersucht. Durch Umsetzung von 1,4-Benzochinon (9) mit dem Diketon 2g wurden direkt die fluorierten Benzofurane 11a und 12b erhalten. Besonderheiten in den 1H-NMR-Spektren der Benzofurane 5d,f und 11a werden diskutiert, und eine Keton-Hydrat-Bildung (12a,b und 13) wird nachgewiesen.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1871-1875 
    ISSN: 0009-2940
    Keywords: Oxidation by HOF ; Hypofluorous acid ; Addition compounds of HOF and HF with acetonitrile ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxidation Reactions with HOF and Adducts of HOF and HF with AcetonitrileIn acetonitrile solution HOF oxides CF3SSCF3 via CF3S(O)nSCF3 (n = 1, 2) to yield [CF3S(O)2]2O. Analogously, CF3Se(O)OH and CF3SeX (X = Cl, Br) are oxidized via CF3Se(VI) intermediates to provide finally [CF3Se(O)2]2O. With CH3CN at low temperatures HOF and HF form 1:1 adducts, whose structures have been elucidated by low-temperature X-ray structure analysis. Additional proof for the formation of CH3CN · HF in the liquid phase is provided.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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