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  • 1965-1969  (24)
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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 79 (1967), S. 683-683 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 79 (1967), S. 1028-1028 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 368 (1969), S. 254-261 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Interaction of bromotriphenylphosphonium bromide with hexamethyldisilazane in acetonitrile yields the phosphonium salt [(C6H5)3PNHSi(CH3)3]Br. Its pyrolysis or deprotonation leads to N-trimethylsilyl-triphenylphosphazene which on reaction with (C6H5)2PCl gives [P(C6H5)2]Cl. The reversible transformation of this heptaphenyl-triphosphorous nitride chloride to (C6H5)2PCl and (C6H5)3P=N—P(C6H5)2 is described as well as its reaction with sulfur to (C6H5)3P=N—P(S)(C6H5)2.
    Notes: Die Silazanspaltung von[(CH3)3Si]2NH durch (C6H5)3PBr2 liefert [(C6H5)3PNHSi(CH3)3]Br, dessen Thermolyse oder Deprotonierung zu (C6H5)3P=N—Si(CH3)3 führt. Die Reaktion des Silylphosphazens mit Diphenylphosphorchlorid ergibt [P(C6H5)2]Cl, aus dem pyrolytisch N-Diphenylphosphino-triphenylphosphazen entsteht.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 344 (1966), S. 316-322 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Bis(dimethylamino)-sulfane reacts with BF3 in petrol ether to yield a 1:1 adduct containing a B—S-bond. The same is true for the triphenyl borane adduct. Contrary to earlier statements the BH3 group in [(CH3)2N]2S · BH3 is linked to a nitrogen rather than to the sulfur atom.
    Notes: Das aus Bis(dimethylamino)-sulfan und BF3 in Petroläther darstellbare 1:1-Addukt verfügt Über eine koordinative B—S-Bindung. Gleiches gilt auch für das Triphenylboran-Addukt. Hingegen ist die BH3-Gruppe in der Verbindung [(CH3)2N]2S · BH3 entgegen früheren Anschauungen nicht Über das Schwefel-, sondern ein N-Atom gebunden.
    Additional Material: 2 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 345 (1966), S. 69-78 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: A hypothesis is presented on the formation of stable covalent metal boron bonds in molecular compounds, and the synthesis of X2B—Mn(CO)4P(C6H5)3 and XB[Mn(CO)4P(C6H5)3]2 (X = C6H5, C4H9, Cl, NR2, OCH3) is described. These compounds are more stable than the corresponding Mn(CO)5-derivatives. This is attributed to differences in the electron density at the manganese atom. 11B - NMR studies are interpreted in terms of back-donation of metal d-electrons to the tervalent boron atom.
    Notes: Nach kurzer Erörterung einiger Leitgedanken, die dem Aufbau kovalenter Bor - Metall Bindungen in molekularen Verbindungen zugrunde liegen, wird die Synthese von X2B—Mn(CO)4P(C6H5)3 und XB[Mn(CO)4P(C6H5)3]2 (X = C6H5, C4H9, Cl, NR2, OCH3) beschrieben. Diese Verbindungen sind stabiler als die entsprechenden Mn(CO)5-Derivate, was wahrscheinlich auf Unterschieden in der Elektronendichte an den Manganatomen beruht. 11B-kernresonanzspektroskopische Untersuchungen weisen auf eine Beteiligung der Metall-d-Elektronen an der Mangan--Bor-Bindung hin.
    Additional Material: 3 Tab.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 352 (1967), S. 1-10 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Metallation of 2,5-diphenyl-3,4-dimethyl-cyclo-1,3,4-triaza-2,5-diborine (“TADBH”) with lithium methyl yields the derivative TADBLi, metallated in 1 position. Its reaction with diphenyl boron chloride leads to a “triborylamine”, TADB-B(C6H5)2; mercuration can be achieved by treatment of TADBLi with HgCl2. The metathesis of TADBLi with FeCl2 provides a route to (TADB)2Fe, for which a metallocen structure is discussed for the monomeric and diamagnetic compound, thus showing the possibility of BN systems to behave chemically similar to isoelectronic CC systems.
    Notes: Die Metallierung von 2,5-Diphenyl-3,4-dimethyleyclo-1,3,4-triaza-2,5-diborin (TADBH) mit Methyllithium liefert das 1-metallierte Derivat TADBLi. Dieses reagiert mit Diphenylborchlorid zu einem „Triborylamin“ TADB-B(C6H5)2 und mit HgCl2 zu einem (TADB)2Hg. Seine Umsetzung mit FeCl2 liefert monomeres (TADB)2Fe. Auf Grund seiner Eigenschaften wird (TADB)2Fe eine den Metallocenen ähnliche Struktur zugeordnet.
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 358 (1968), S. 44-66 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: According to the ratio of the reactants the reaction of alcohols with alane in tetrahydrofurane yields alkoxyalanes [(RO)nAlH3-n]x (R = CH3, C2H5, C3H71, C4H9n, C4H9t; n = 1, 2, 3; x ≥ 2). The stability of monoalkoxyalanes towards disproportionation into AlH3 and (RO)2AlH descreases as the carbon chain of the alkyl group becomes more and more branched at the α-C-Atom, while x decreases in the same direction. On the other hand, the stability of the dialkoxyalanes increases in the reverse order.All alkoxyalanes add diborane forming alkoxyaluminium borohydrides; some other routes to their preparation are also described. The Kollonitsch product AlH3 · 3 BH3 · 3 Al(OC3 H71)3 has been confirmed, but there is convincing evidence that it is to be described as a mixture of isopropoxyaluminium borohydrides.
    Notes: Die Einwirkung von Alkoholen ROH (R = CH3, C2H5, C3H71, C4H9n und C4H9t) auf in THF gelösten Aluminiumwasserstoff liefert je nach dem Molverhältnis Mono-, Di- oder Trialkoxyalane [(RO)nAlH3-n]x (n - 1, 2, 3). Von diesen werden die Monoalkoxyalane bezüglich einer Disproportionierung in Dialkoxyalane und AlH3 um so stabiler, je stärker verzweigt die Alkylgruppe am α-C-Atom und je kleiner der Assoziationsgrad x ist, der für R - C4H9t den Wert 2 erreicht. Umgekehrt nimmt die Bildungstendenz der Dialkoxyalane zu, je kleiner der Raumbedarf der Alkylgruppe wird.Alle Alkoxyalane addieren Diboran zu Alkoxyaluminium-boranaten [(RO)nAl(BH4)3-n]x, für die einige weitere Synthesewege angegeben werden. Das von Kollonitsch aus AlH3 und B(OC3H71)3 dargestellte AlH3 · 3 BH3 · 3 Al(OC3H71)3 erweist sich als ein Gemisch von Isopropoxyaluminium-boranaten.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 77 (1965), S. 506-506 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 9
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 77 (1965), S. 734-734 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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