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  • Inorganic Chemistry  (765)
  • 1980-1984
  • 1975-1979  (765)
  • 1970-1974
  • 1978  (765)
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Publisher
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  • 1980-1984
  • 1975-1979  (765)
  • 1970-1974
Year
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978) 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic 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
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 1-12 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Determination of Activation Parameters of Spironorcaradiene-Spirocycloheptatriene Equilibria by Line Shape Analysis of 1H and 13C NMR SpectraLine shape analysis of 1H and 13C NMR spectra is used for the determination of activation parameters of the valence isomerization of substituted spironorcaradienes/spirocycloheptatrienes 5 ⇌ 6. Whereas the values obtained for the dibenzo-spironorcaradienes 5a, b are comparable with the data of simple norcaradiene derivatives, those of tetrachloro derivatives 5c, d show considerable differences.
    Notes: Die Linienformanalyse der 1H- und 13C-NMR-Spektren wird zur Bestimmung der Aktivierungsparameter der Valenzisomerisierung von verschieden substituierten Spironorcaradienen zu Spirocycloheptatrienen 5 ⇌ 6 herangezogen. Während die Aktivierungsparameter bei Dibenzospironorcaradienen 5a, b vergleichbar sind mit denen der einfachen Norcaradienderivate, treten bei den Daten der Tetrachlorderivate 5c, d erhebliche Abweichungen auf.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 42-55 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Allyl Radicals with Bicyclo[3.2.1]octane Skeleton, a Contribution to the Problem of Homoconjugative InteractionsThe ESR spectra of allyl radicals with bicyclo[3.2.1]octane skeleton were analyzed in order to investigate the possibility of nonbonding interactions in free radicals. The similarity of the spin density distribution in radicals 7 and 8 demonstrates that 7 has the character of a bicyclic allyl radical. There is no significant interaction between HOMO allyl and LUMO double bond in 7. The same is true for the radical having a fused benzene ring instead of the double bond.
    Notes: Radikale mit Bicyclo[3.2.1]octan-Gerüst wurden ESR-spektroskopisch untersucht, um Aussagen über nichtbindende Wechselwirkungen in Radikalen zu gewinnen. Die Ähnlichkeit der Spindichteverteilung in 7 und 8 zeigt, daß 7 den Charakter eines bicyclischen Allylradikals besitzt. Eine merkliche Wechselwirkung wischen HOMO-Allyl und LUMO-Doppelbindung in 7 existiert nicht. Gleiches gilt, wenn anstelle der Doppelbindung ein Benzolrest anelliert ist. Die experimentellen Befunde werden mit INDO-Rechnungen verglichen.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 56-64 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Mechanism of the Thermal Isomerisation of O-2-Butenyl O,O-Dimethyl Thiophosphate. Kinetic StudyThe thermal isomerisation of O-2-butenyl O,O-dimethyl thiophosphate (1b) (scheme 3) obeys first order rate law. Solvent polarity does not affect the parameters of activation, but influences a little the rate constants. The kinetic data and the observed “special” salt effect lead to the conclusion that the isomerisation proceeds by a dissociative mechanism. Ion pairs as intermediates are proposed.
    Notes: Die thermische Isomerisierung von Thiophosphorsäure-O-2-butenylester-O,O-dimethylester (1b) (Schema 3) verläuft nach einem Geschwindigkeitsgesetz 1. Ordnung. Die Polarität des Mediums beeinflußt nicht die Aktivierungsparameter und übt lediglich einen minimalen Einfluß auf die Geschwindigkeitskonstanten aus. Die kinetischen Daten und der festgestellte „spezielle“ Salzeffekt lassen den Schluß zu, daß diese Isomerisierung einem intramolekularen ionischen Mechanismus folgt. Als ionische Zwischenstufe werden Ionenpaare postuliert.
    Additional Material: 1 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 1210-1216 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Phosphorus, 73: 1,2-Diphenyldiphosphane1,2-Diphenyldiphosphane (1) is formed, contrary to results given in the literature, by the reaction of KHPPh with 1,2-dibromoethane. Pure 1 is obtained by hydrolysis or alcoholysis of Me3Si(Ph)P-P(Ph)SiMe3 in the dark. It is stable at - 30°C. 1 disproportionates at room temperature to give PhPH2, higher homologues of the series H2[PPh]n, especially H2[PPh]3, and cyclic phenylphosphanes [PPh]n, mainly [PPh]5. These rearrangements are accelerated by light, phosphides, and strong acids and bases. With K(Ph)P—P(Ph)K, Me3Si(Ph)P—P(Ph)SiMe3, and P2Ph4 1 reacts to give the asymmetric diphosphanes K(Ph)P—P(Ph)H, Me3Si(Ph)P—P(Ph)H, and Ph2P—P(Ph)H, respectively. The NMR, IR, and Raman spectra are discussed.
    Notes: 1,2-Diphenyldiphosphan (1) wird - entgegen Literaturangaben - bei der Reaktion von KHPPh mit 1,2-Dibromethan gebildet. Reines 1 ist durch Hydrolyse oder Alkoholyse von Me3Si(Ph)P - P(Ph)SiMe3 unter Lichtausschluß erhältlich und bei - 30°C beständig. Es disproportioniert bei Raumtemperatur in PhPH2, höhere Homologe der Reihe H2[PPh]n  -  insbesondere H2[PPh]3 - und cyclische Phenylphosphane [PPh]n  -  vor allem [PPh]5. Diese Umlagerungen werden durch Licht, Phosphide sowie starke Säuren und Basen beschleunigt. Mit K(Ph)P—P(Ph)K, Me3Si(Ph)P—P(Ph)SiMe3 oder P2Ph4 reagiert 1 zu den unsymmetrischen Diphosphanen K(Ph)P—P(Ph)H, Me3Si(Ph)P—P(Ph)H bzw. Ph2P—P(Ph)H. Die NMR-, IR- und Raman-Spektren von 1 werden diskutiert.
    Additional Material: 1 Tab.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 1223-1227 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organic Syntheses by Means of Transition Metal Complexes, 6: Synthesis of Ketenimines via Ketenimine Complexes, Isocyanide Carbene Addition and Ketenimine Carbene Rearrangement in Metal ComplexesTransition metal carbene complexes of the Fischer type, e. g. pentacarbonyl(methoxymethyl-carbene)chromium(0), add isocyanides to give ketenimine complexes (1). Ligand displacement by excess isocyanide affords ketenimines (3), which can be isolated in good yields. In contrast to free ketenimine, the nucleophilic attack on ketenimine coordinated to a metal occurs at the terminal carbon atom leading to carbene complexes. The structures of the ketenimine complexes of chromium (1) and tungsten (2), the product of isomerization (5)(2) of the chromium complex, and the products formed by addition of methanol or water (6 and 7, resp.)(2) are discussed, using 13C NMR data.
    Additional Material: 1 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978) 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 1233-1238 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Polycyclic Compounds, X: A Facile Synthesis of (Partially Hydrogenated) Benz[a]anthracenes with Functional GroupsThe hexa- and decahydrobenz[a]anthracenes 3 and 5 are available in a one step synthesis by Diels-Alder reaction of the tetrahydrobenzo[b]furans 2 with 2,3-didehydronaphthalene (1) or with the naphthalene-endoxide 4. The interconversions 3 → 6, 7 and 8 and 5 → 9 show that many hydroxy- and oxosubstituted (partially hydrogenated) benz[a]anthracenes can be obtained from the primary adducts 3 and 5.
    Notes: Die Hexa- und Decahydrobenz[a]anthracene 3 und 5 sind in einem einstufigen Verfahren durch Diels-Alder-Reaktionen der Tetrahydrobenzo[b]furane 2 mit 2,3-Didehydronaphthalin (1) bzw. mit dem Naphthalin-endoxid 4 zugänglich. Die Reaktionsfolgen 3 → 6, 7 und 8 sowie 5 → 9 zeigen die vielfältigen Abwandlungsmöglichkeiten der Primäraddukte 3 und 5 zu hydroxy- und oxo-substituierten (partiell hydrierten) Benz[a]anthracenen auf.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 1253-1263 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Vinyl Cations, 26: Syntheses and Solvolyses of Vinyl FluoridesThe vinyl fluorides 5-8 were prepared by treatment of the corresponding olefins with BrF and subsequent dehydrobromination. The solvolysis reactions in various solvents were studied. The products and their rates of solvolysis measured under different conditions point to a vinyl cation mechanism of the solvolysis reactions.
    Notes: Die Vinylfluoride 5-8 wurden durch Umsetzung der entsprechenden Olefine mit BrF und sich anschließende Dehydrobromierung dargestellt und die Solvolysereaktionen in mehreren Lösungsmitteln untersucht. Die Reaktionsprodukte sowie die unter verschiedenen Bedingungen gemessenen Solvolysegeschwindigkeiten deuten auf einen Verlauf der Solvolyse über Vinylkationen.
    Additional Material: 5 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 1264-1274 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Bicyclofulvenes, IV: Syntheses of Methylenetricyclo[4.2.1.02,5]nonane- and -tricyclo[3.2.1.02,4]octane DerivativesThe synthesis of 9-methylenetricyclo[4.2.1.02,5]nonane (3), 8-methylenetricyclo[3.2.1.02,4]octane (2) and their derivatives as well as that of methylenehomocubane (37) and 9-methylenepentacyclo-[4.3.0.02,4.03,8.05,7]nonane (38) is described.
    Notes: Die Darstellung von 9-Methylentricyclo[4.2.1.02,5]nonan (3), 8-Methylentricyclo[3.2.1.02,4]octan (2) und ihrer Derivate, sowie von Methylenhomocuban (37) und 9-Methylenpentacyclo-[4.3.0.02,4.03,8.05,7]nonan (38) wird beschrieben.
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