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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 7 (1973), S. 357-364 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We describe a method to optimize simultaneously Slater orbital exponents. The procedure is based on Newton's method and requires the derivatives of the energy as a function of the exponents. The calculation of these derivatives is described explicitly. The method has been applied to the hydrogen molecule.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of plant pathology 92 (1986), S. 43-47 
    ISSN: 1573-8469
    Keywords: biochemical resistance ; Phoenix dactilifera L. ; Fusarium oxysporum f. sp.albedinis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Description / Table of Contents: Samenvatting In een hexaanextract van wortels van de dadelpalm, cv. Black Boo Stammi die resistent is tegen de Bayoudziekte, bevonden zich stoffen die de sporekieming en de groei van kiembuizen onderdrukken. Dit gold voor alle drie isolaten vanFusarium oxysporum f. sp.albedinis, die werden getoetst. In extracten van de vatbare cultivar Jihel werden de kieming en de groei niet geremd.
    Notes: Abstract An hexane extract from roots of Black Boo Stammi, a cultivar of date palm, resistant toFusarium oxysporum f. sp.albedinis, contained substances which inhibited the spore germination and the growth of the germ tubes of the three isolates of the pathogen that were tested. Extract from roots of Jihel, a susceptible cultivar, lacked these substances.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 7 (1975), S. 637-638 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Substituent effects on chemical shifts of cyclopropane derivatives are investigated by 13C NMR. When we introduce pairwise corrections in empirical correlations, the theoretical chemical shifts of trisubstituted cyclopropanes are in good agreement with experimental values.
    Notes: Les effets de substituants sur les déplacements chimiques de dérivés cyclopropaniques ont été étudiés par RMN du carbone-13. Les déplacements chimiques théoriques de cyclopropanes trisubstitués sont en bon accord avec les valeurs expérimentales lorsqu'on introduit dans les corrélations des paramètres d'interaction du second ordre.
    Additional Material: 2 Tab.
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  • 4
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The 13C NMR spectra of 43 benzothiazoles have been recorded in DMSO-d6. All carbon atoms have been attributed in an unambigous way owing to substituent effects in position 4, 5, 6 or 7. We discuss variations of chemical shifts as a function of the nature of the substituent in position 2 (equation of type: Δδ = aF+bR+cQ+d′), annelation in the benzoheterocyclic series, and prototropic tautomerism in the benzothiazolic series (in the case of the substituent in the 2-position being an OH, SH or NHR group).
    Notes: Les spectres de résonance magnétique nucléaire due carbone-13 de 43 benzothiazoles ont été enregistrés dans le diméthylsulfoxyde hexadeutérié. Tous les carbones ont été attribués de facon non ambiguë, grǎce aux effets de substituant sur les positions 4, 5, 6 ou 7. Nous discutons des variations des déplacements chimiques en fonction de la nature du substituant en 2 (équation triparamétrique du type: Δδ = aF+bR+cQ+d′), de l'annélation en série benzohétérocyclique et de la tautomérie prototropique en série benzothiazolique (dans le cas où le substituant en position 2 représente un groupement OH, SH ou NHR).
    Additional Material: 1 Ill.
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  • 5
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: We have recorded the 13C n.m.r. spectra of thiones and thioethers in the 1,3-diazole and 1,3-diazine series with various alkyl substituents at the nitrogen atoms. Some analogous oxygen containing heterocycles were also examined. We have shown that in the thiocarbonylated compounds the thiol ⇄ thione equilibrium is displaced towards the thione form, but that 13C n.m.r. gives only qualitative results. In the sulphur containing derivatives the isopropyl group is in a fixed conformational position because of the steric hindrance of the sulphur atom. Substitution by a tert-butyl group leads to unexpected γ values. We ascribe this phenomenon to ring deformation or to variations in the valence angles of the substituted nitrogen atoms.
    Notes: Nous avons enregistré les spectres de RMN du carbone-13 de thiones et de thioethers, en série diazolique et diazinique-1,3, diversement substitués sur les atomes d'azote par des groupements alkyles, ainsi que certaines des structures oxygénées homologues. Toutes les raies de résonance ont été attribuées. Dans le cas des dérivés thiocarbonylés, nous montrons que l'équilibre thiol ⇄ thione est déplacé vers la forme thione, mais que la RMN du carbone-13 ne peut conduire qu'à une évaluation qualitative de la position de cet équilibre. L'analyse des effets de substituant montre que, contrairement aux composés oxygénés, le groupement isopropyle adopte dans les dérivés soufrés une conformation privilégiée par suite de l'encombrement stérique dǔ à l'atome de soufre. La substitution par un groupement tertiobutyle conduit à des valeurs des effets γ inattendus. Nous attribuons ce phénomène à des déformations de cycle ou à des variations des angles valentiels de l'azote porteur du substituant, provoquées par des interactions stériques entre le substituant et le cycle correspondant. Nous relions ces modifications à certaines modalités de la réactivité, et à des résultats de spectroscopie photoélectronique.
    Additional Material: 5 Tab.
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  • 6
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 33S NMR spectra have been obtained in the FT mode for some sulphones and sulphonic acids. The investigated compounds show narrow resonance lines. In the case of sulphones, the range of 33S chemical shifts is sufficiently wide, i.e. the effects due to changes in substituents are significant enough to allow further use of the 33S NMR of sulphones for quantitative analysis in petroleum chemistry.
    Additional Material: 1 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 5 (1973), S. 573-578 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Calculations are presented as evidence for the existence of a tautomeric equilibrium in thiamine and its polyphosphoric esters. The relative position of the equilibrium in these compounds is considered. Most of the experimental observations can be explained by the results of the calculations.
    Notes: Nous mettons en évidence l'existence d'un équilibre de tautomérie dans la thiamine et ses esters phosphoriques. Et nous évaluons la position relative de l'équilibre dans ces différents composés. Le calcul permet de relier un grand nombre d'observations expérimentales.
    Additional Material: 7 Tab.
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  • 8
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Azido-tetrazole equilibrium is observed in the case of a solution of tetrazolo [5,1-b] benzothiazole in CDCl3, using proton magnetic resonance at 250 MHz. Analysis of the spectra obtained yields the chemical shifts and the coupling constants of the two tautomeric forms.
    Notes: Nous avons observé l'équilibre azide-tétrazole dans le cas du tétrazolo [5,1-b] benzothiazole par résonance magnétique nucléaire du proton à 250 MHz, en solution dans le deutériochloroforme. L'analyse des spectres a permis la détermination des déplacements chimiques et des constantes de couplage des deux formes tautomères.
    Additional Material: 1 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 7 (1975), S. 89-93 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The NMR spectra of five benzodiazepinones are determined over a range of temperature. They indicate that the seven ring has a twist-boat shape, which inverts more or less rapidly according to the nature of substituents. The activation parameters and the rates of inversion are determined and the substituent effects are discussed.
    Notes: Les modifications, en fonction de la température, des spectres RMN de cinq benzodiazépinones permettent de mettre en évidence un équilibre entre deux formes pseudo-bateaux du cycle à sept liaisons. Les auteurs calculent les paramétres d'activation et la constante de vitesse d'inversion et discutent le rǒle des substituants.
    Additional Material: 5 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 8 (1976), S. 518-521 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The predominant spatial arrangement of the methyl ring substituents of some dioxaphospholanes was determined by means of 1H, 13C and 31P n.m.r. This study also provides some information about the conformations of these molecules.
    Notes: L'étude en RMN du 1H, 13C et 31P d'hétérocycles dioxaphospholaniques a permis d'identifier sans ambiguité la position des substituants sur le cycle et aussi d'accéder à un certain nombre d'informations relatives à la stéréochimie de la molécule.
    Additional Material: 6 Tab.
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