ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

X
feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Inorganic Chemistry  (6,538)
  • Organic Chemistry  (4,565)
  • Chemical Engineering  (2,596)
  • 1980-1984  (9,508)
  • 1920-1924  (4,191)
Collection
Keywords
Publisher
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Untersuchungen über den Thermischen Zerfall von n-Dodecylcyclopentan in der Gasphase (1982)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 324 (1982), S. 964-972 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Investigations on the Thermal Decomposition of n-Dodecylcyclopentane in the Gas PhaseIn the thermal decomposition of n-dodecylcyclopentane at 670 and 750°C in a laboratory tubular reactor mixtures of hydrogen and 57 and 113 hydrocarbons respectively are formed. The mixtures have been analyzed and identified by capillary gas chromatography and by mass spectrometry. The distribution of the reaction products is used for mechanistic discussions.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19823240615
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Kinetische Untersuchungen zur Pyrolyse von Mono-n-alkyl-cyclohexanen (1983)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 325 (1983), S. 66-74 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetic Investigations of the Pyrolysis of Mono-n-alkyl-cyclohexanesThe thermal decomposition of cyclohexane and six mono-n-alkylcyclohexanes was studied kinetically in a metallic laboratory tubular reactor at 650 to 850°C and atmospheric pressure.Kinetic parameters were found to be a function of length of the alkylic side chain. A comparison with analogous parameters of n-paraffins and the unsubstituted cyclohexane allowed the conclusion that C—C-scission in the alkylic chain is the initial reaction in pyrolysis of n-alkylcyclohexanes followed by radical attacks to all C—H-bonds of the feed molecules.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19833250109
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Flexural fatigue of marine laminates reinforced with woven roving of E-glass and of Kevlar® 49 aramidPresented at the 34th Annual Meeting of the SPI Reinforced Plastics/Composites Institute, New Orleans, Louisiana (January 30, 1979). (1981)
    Brookfield, Conn. : Wiley-Blackwell
    Polymer Composites 2 (1981), S. 61-67 
    Details
    ISSN: 0272-8397
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: A comparison of the flexural fatigue characteristics of E-glass and Kevlar® 49 aramid in polyester and vinyl ester resin hand lay-ups typical of boat hull laminates is presented. Data on unidirectional E-glass and aramid composites from epoxy preimpregnated tapes are reported for comparison. The data indicate that while the initial flexural strength of E-glass woven roving laminates is greater than that of aramid laminates, the runout stress of aramid laminates at 106 fatigue cycles is similar or superior to glass. S-N curves for aramid laminates are flatter indicating better flexural fatigue resistance.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pc.750020204
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 4
    Electronic Resource
    Electronic Resource
    Characterization of electron beam crosslinked poly(styrene-block-ethylene-co-butylene-block-styrene) (1983)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 23 (1983), S. 510-515 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A saturated triblock copolymer, poly(styrene-block-ethylene-co-butylene-block-styrene) was chemically crosslinked using trimethylol propane trimethacrylate, TMPTM, and subjected to electron beam radiation. The gel percent, Gehman ten second modulus, and stress relaxation were measured to characterize the materials as a function of crosslinker concentration and radiation level. A time-temperature super-position master curve was generated at 63°C for 3 percent TMPTM and 5 Mrads of radiation, which indicated rubbery plateau behavior at long times of measurement, as opposed to the uncrosslinked material, which continued to creep and flow. The main locus of crosslinking was within the polystyrene phase, which explains reduced creep and stress relaxation only for long times of measurement and/or high temperatures. Based on shifts of the glass transition temperatures, it was estimated that 11 to 16 percent poly(ethylene-co-butylene) was dissolved in the polystyrene phase.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760230906
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 5
    Electronic Resource
    Electronic Resource
    2, 3-Disubstituted γ-Butyrolactams from the Michael-Additions of Doubly Deprotonated, Optically Active β-Hydroxycarboxylates to Nitroolefins. Preliminary Communication (1980)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 63 (1980), S. 2005-2009 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conjugate addition of the chiral, non-racemic alkoxy-enolates 5 and 6 to nitroolefins furnishes the hydroxynitroesters 7-13, which are catalytically hydrogenated to give the lactams 14-18. The configuration of adduct 7 from nitroethylene was elucidated by NMR. analysis of the acetal 20 derived from 7. The assignment establishes that the reaction follows the stereochemical rule of attack depicted in 21 and previously deduced for other electrophiles, i.e. formation of erythro-products of type 3b and 4b. No stereocontrol was found at the newly formed chiral centers in α- and β-position to the NO2 group of 8-12.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19800630727
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 6
    Electronic Resource
    Electronic Resource
    Über die Einwirkung von Schwefelchlorür auf tertiäre aromatische Arsine. (Beitrag zur Kenntnis der Konstitution des Schwefelchlorürs) (1921)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 54 (1921), S. 2479-2489 
    Details
    ISSN: 0365-9631
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19210540936
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 7
    Electronic Resource
    Electronic Resource
    Formation and dissociation mechanism of amide complexes. VPart IV, see [1]. Interconversion of dimeric and monomeric Cu2+-complexes with 1,8-diamino-3,6-diaza-2,7-octanedione: Comparison between the reactivity of terminal and internal amide groups (1982)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 65 (1982), S. 753-761 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The protonation and deprotonation rates of the coordinated amide groups in the Cu2+-complexes of 1,8-diamino-3,6-diaza-2,7-octanedione (DED = L) have been studied by stopped-flow techniques. Starting at low pH from Cu2+ and DED the dimeric Cu2L24+-complex, fully formed within the mixing time of the stopped-flow instrument, reacts in two consecutive steps to yield the final product CuLH-2. The rate constants of the forward and backward reactions have been determined and are given in Table 1. The intermediate was identified as Cu2L2H-22+ by measuring its VIS.-absorption spectrum.The rate constants for the interconversion of the amide groups from the O- to the N-coordinated form in the Cu2+-complexes of DED, 2,10-dioxo-1, 4, 8, 11 tetraazaundecane (DANA) and triglycine (TRIGLY) are compared with each other. It is shown that these rate constants are similar, no matter whether the amide group is terminal or internal as long as the rotation is easily possible as is the case in the dimeric species Cu2L24+ and Cu2L2H-22+. However, for CuLH-2 the inter-conversion only takes place after opening of one of the chelate rings in a rapid protonation preequilibrium.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19820650313
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 8
    Electronic Resource
    Electronic Resource
    Di- und Polyaminozucker, XXIII. Eliminierungsvorgänge bei der Synthese der 2,3-Diamino-2,3-didesoxy-D-glucose (1980)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 3089-3093 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Di- and Polyamino Sugars, XXIII. Elimination Reactions Accompanying the Synthesis of 2,3-Diamino-2,3-dideoxy-D-glucoseBy-products of the synthesis of 2,3-diamino-2,3-dideoxy-D-glucose were found to be hex-2- and -3-enopyranosides (4, 5). Structure proofs by spectroscopy were corroborated by hydroboration and direct elimination reactions.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19801130924
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 9
    Electronic Resource
    Electronic Resource
    1H- und 13C-NMR-Untersuchungen an N-Acyl-imino-dithio-kohlensäure-S,S-dimethylestern (1983)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 325 (1983), S. 1011-1015 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H- and 13C-N.M.R. Investigations of N-Acyl-imino-dithiocarbonic-S,S-dimethylester
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19833250618
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 10
    Electronic Resource
    Electronic Resource
    31P- und 195Pt-NMR-Untersuchungen an Diplatin(I)-Komplexen des Typs [Pt2(μ-SPR2)2L2] (L = PR3, PhP(OPh)2, P(OPh)3, CNR)VIII. Mitteilung aus der Reihe Sekundäre Phosphinochalkogenide; VII. Mitteilung s. (1983)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 504 (1983), S. 117-127 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 31P and 195Pt N.M.R. Investigations on Diplatinum (I) Complexes of the Type [Pt2(μ-SPR2)2L2] (L = PR3, PhP(OPh)2, P(OPh)3, CNR)31P-, 195Pt-chemical shifts and 195Pt-31P- resp. 31P-31P-coupling constants of a series of doubly bridged diplatinum(I) complexes are reported. 31P-coordination chemical shifts of the terminal ligands of complexes of type [Pt2(μ-SPR2)2(P′R3′)2] and some of the various coupling constants are strongly influenced by the π-acceptor strength of these ligands. J(195Pt-195Pt) is found to change the sign among the series of complexes investigated. Thermal singlett triplet exitation giving rise to the paramagnetism of these complexes observed by preliminary EPR-measurements and confirmed by EHT-calculations is deduced from the large values of 2J(P-P′) and 3J(P′P′) as well as the unusually high temperature dependence of some coupling constants and other NMR features. The chemical stability of the doubly bridged core, the coordination shifts of the bridging phosphorus atoms and EHT-calculations suggest a view of aromaticity of the [Pt2(μ-SPR2)2](M-M) unit of these complexes.
    Notes: Es werden 31P-, 195Pt-chemische Verschiebungen und 195Pt31P-Kopplungskonstanten einer Reihe von doppelt verbrückten Diplatin(I)-Komplexen mitgeteilt. 31P-koordinationschemische Verschiebungen der ternären Liganden von Komplexen des Typs [Pt2(μ-SPR2)2(P′R3′)2] und verschiedene Kopplungskonstanten werden stark von der π-Akzeptor-Stärke dieser Liganden beeinflußt. J(195P-195Pt) wird innerhalb der Reihe der untersuchten Komplexe mit wechselndem Vorzeichen gefunden. Aus den großen Werten von 2J(Pt-P′) und 3J(P′P′) sowie der ungewöhnlich starken Temperaturabhängigkeit einiger Kopplungskonstanten und anderen NMR-Eigenschaften wird auf Paramagnetismus dieser Komplexe aufgrund thermischer Singlett-Triplett-Anregung geschlossen, der in vorläufigen EPR-Messungen gefunden und durch EHT-Rechnungen gestützt wird. Die chemische Stabilität des doppelt verbrückten Kerns, die koordinationschemischen Verschiebungen der Brückenphosphoratome und EHT-Rechnungen weisen auf Aromatizität der [Pt2(μ-SPR2)2](M-M)-Einheit dieser Komplexe hin.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19835040915
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...