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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Applied physics 24 (1981), S. 39-43 
    ISSN: 1432-0630
    Keywords: 34,61 ; 80 ; 85.30
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract The range parameters of boron in silicon have been measured using the10B(n,α)7 Li-nuclear reaction. The results indicate that the distributions can be perfectly modeled using Pearson IV distributions with 4 moments. The range is very well described by theoretical calculations, whereas the higher moments show a strong deviation from theory.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Structure Reactivity Relations of Coordinatively Unsaturated Chelate Complexes. III. Acceptor Tendency of Nickel and Cobalt Chelates with Tridentate Di-anionic Schiff Base LigandsThe reactivity of nickel and cobalt chelate complexes of the type 3 with several donors is compared by isolation of stable adducts. In the case of nickel the reactivity is vigorously influenced by the substituents R1 and R2. The equatorial and the axial unoccupied coordination centers of the nickel chelates exhibit a markedly different behaviour. The cobalt(II) chelates - all of them are high spin complexes - favour O-donors. The complicate composition of the adducts point to a polynuclear structure. With pyridine, high spin diadducts have been isolated probably with coordination number 5 for the metal.
    Notes: Die Reaktionsfähigkeit von Nickel- und Cobalt-Chelaten des Typs 3 gegenüber verschiedenen Donatoren wird durch Isolierung stabiler Addukte verglichen. Im Fall der Nickel-Chelate wird die Reaktivität stark durch die Substituenten R1 und R2 beeinflußt. Gegenüber N-Donatoren besteht eine ausgeprägte Differenzierung zwischen äquatorialer und axialen Koordinationslücken. Die Cobalt(II)-Chelate, die alle zum high-spin-Typ gehören, bevorzugen allgemein O-Donatoren. Die komplizierte Zusammensetzung der Addukte deutet auf Mehrkernstrukturen hin. Mit Pyridin wurden high-spin-Diaddukte, vermutlich mit Koordinationszahl 5 des Zentralatoms, isoliert.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 497 (1983), S. 206-212 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Structure Reactivity Correlations in Coordinatively Unsaturated Chelate Complexes. IV. Reaction of Dioxygen with Cobalt(II) Chelates of Tridentate Di-anionic Schiff Base LigandsThe high-spin cobalt(II) chelates 3 form with pyridine isolable adducts which are also high-spin complexes. In the case 3 b a low-spin mono-adduct is indicated by ESR spectroscopy, which is changed time-dependently into a stable quadratic-pyramidal form. With 1, 10-phenanthroline 3 b forms a low-spin mono-adduct. The spectrophotometric titration of 3 d with pyridine indicates an equilibrium A + 2 Py ⇌ APy2 (β2 = 0,36 M-2) where A represents probably the tetrameric form of 3 d. In pyridine, 3 a, 3 b, and 3 d react with O2 in an 1:1 ratio; 3 c binds O2 in the ratio 2:1. The formation of superoxo complexes is indicated by ESR spectroscopy for the complexes 3 a, 3 b, and 3 d. 3 b reacts with O2 in piperidine to give the free superoxide ion. In n-butylamine a species is formed which seems to be an ion pair with direct interactions between the free O2- ion and the coordinated amine nitrogen.
    Notes: Die high-spin-Cobalt(II)-Chelate 3 bilden mit Pyridin isolierbare Addukte, die ebenfalls zum high-spin-Typ gehören. Bei 3 b ist ESR-spektroskopisch ein low-spin-Addukt nachweisbar, das sich zeitabhängig in eine stabile quadratisch-pyramidale Form umwandelt. Mit 1,10-Phenanthrolin bildet 3 b ein low-spin-Monoaddukt. Die spektrophotometrische Titration von 3 d mit Pyridin zeigt ein Gleichgewicht A + 2 Py ⇌ APy2 an (β2 = 0,36 M-2), worin A vermutlich das Tetramere von 3 d ist. In Pyridin reagieren 3 a, 3 b und 3 d im Verhältnis 1:1, 3 c im Verhältnis 2:1 mit O2. ESR-spektroskopisch sind bei 3 a, 3 b und 3 d Superoxokomplexe nachweisbar. 3 b bildet mit O2 in Piperidin freies Superoxid und in n-Butylamin eine Spezies, deren ESR-Spektrum auf ein Ionenpaar mit direkter Wechselwirkung zwischen freiem O2- und koordiniertem Aminstickstoff hindeutet.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 469 (1980), S. 109-114 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: N-Alkyl-aminomethane Phosphonic Acid Dialkyl Ester via Hexahydro-s-triazinesN-substituted hexahydro-s-triazines (—CH2—NR—)3 react with HP(O)(OR1)2 forming the corresponding aminomethane phosphonic acid esters R—NH—CH2—P(O)(OR)1)2, in which depending on the substituents R and R1 exact reaction conditions are necessary to prepare 1-31. These compounds are not formed by interaction of (—CH2—NR—)3 with phosphorous acid.
    Notes: N-substituierte Hexahydro-s-triazine (—CH2—NR—)3 reagieren mit Phosphorigsäure-dialkylestern HP(O)(OR(1)2 unter Bildung der entsprechenden Aminomethanphosphonsäureester R—NH—CH2—P(O)(OR1)2 (1-31), wobei in Abhängigkeit der Substituent R und R1 exakte Reaktionsbedingungen zur Bildung von 1-31 einzuhalten sind. Die Reaktion zwischen (—CH2—NR—)3 und phosphoriger Säure ist für die Darstellung von 1-31 ungeeignet.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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