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  • 2000-2004
  • 1965-1969  (1.012)
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  • 101
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 33 (1966), S. 5-38 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Das Verhältnis der „klassischen“ zu einer „erweiterten“ Mesomerie- oder Resonanzlehre wird dargelegt. Es wird gezeigt, welche engen Grenzen einer sinnvollen Anwendung der letzteren gezogen sind, und welchen Sinn man den von ihr benutzten vermeintlichen Grenzformeln zu unterlegen hat. Die Wertlosigkeit von Versuchen, den Begriff Resonanzhybrid für das Geschehen bei chemischen Reaktionen, die über die Vorgänge zwischen einfachsten Atomen und zwei-atomigen Molekülen hinausgehen, wird dargelegt.
    Materialart: Digitale Medien
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  • 102
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 33 (1966), S. 61-69 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: An Hand der Umsetzung einer Anzahl von Cbo-Aminosäure-4-(phenylazo)-phenylestern mit Benzylamin wird deren Aminolyseverlauf nach dünnschichtchromatographischer Trennung der Reaktionsprodukte spektralphotometrisch verfolgt und der Einfluß der (Phenylazo)-phenyl- sowie der Aminosäurekomponenten der „aktivierten“ Ester auf die Reaktionsgeschwindigkeit diskutiert.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 103
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 33 (1966), S. 124-129 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Dehydroascorbinsäure liegt auf Grund von Molekulargewichtsbestimmungen in Dimethylsulfoxid monomer gelöst vor. Die dabei auftretende Gelbfärbung deutet darauf hin, daß in der im festen Zustand farblosen Verbindung Halbketalgruppierungen gespalten werden und eine freie α-Diketo-Konfiguration anzutreffen ist.
    Materialart: Digitale Medien
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  • 104
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 31 (1966), S. 320-336 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Es werden sieben verschiedene Verfahren zur Synthese des Iminodiessigsäure-Chelatharzes (= IDE-HARZ) hinsichtlich ihrer Nebenreaktionen und der Einfluß dieser Nebenreaktionen auf die Eigenschaften der resultierenden IDE-HARZE untersucht. Der einzige Syntheseweg, der dieses Chelatharz in analysenreiner Qualität liefert, ist zur Zeit die Umsetzung von chlormethylierten, vernetzten Polystyrolperlen mit Iminodiessigsäureester und nachfolgender Verseifung der Estergruppen. Dieses p. a. IDE-HARZ wurde mit DOWEX CHELATING RESIN A-1 verglichen und festgestellt, daß DOWEX A-1 außer Iminodiessigsäure-Ankergruppen noch verankerte Amino- und Aminosäure-Ankergruppen enthält. Beide Nebenankergruppen beteiligen sich an der Komplexbildung. Im starksauren Gebiet fungieren die Amino-Ankergruppen außerdem als Anionenaustauscher. DOWEX A-1, das um 1960 in den Handel gelangte, besitzt einen beträchtlichen Anteil an Amino- und Amino- säure-Ankergruppen. Dagegen enthält DOWEX A-1, das 1963/64 produziert wurde, vorwiegend Iminodiessigsäure- und Aminosäure-Ankergruppen. Der reversible Kapazitätsschwund des DOWEX A-1 kann mit der Ausbildung von Lactambindungen erklärt werden.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 105
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 32 (1966), S. 43-46 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 3-Dialkylamino-4-benzylamino-5-nitroso-uracile gehen beim Erhitzen in 3-Dialkylamino-8-phenylxanthine Über. Aus 3-Dialkylamino-4-anilino-5-nitrosouracilen entstehen mit überschüssigem Isoamylnitrit 1-Dialkylamino-alloxazine und deren 5-N-Oxide.
    Materialart: Digitale Medien
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  • 106
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 33 (1966), S. 307-308 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: P-Aminophenylessigsäure läßt sich in einfacher Weise gewinnen, in dem man das Natriumasalz der p-Nitrophenylessigsäure mit Hydrazin in wäßriger Lösung unter katalytischer Einwirkung von RANEY-Nickel umsetzt. Die erzielten Ausbeuten sind praktisch quantitativ.
    Materialart: Digitale Medien
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  • 107
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 34 (1966), S. 15-22 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Für irreversibel reduzierbare Komplexe, deren Stabilitätskonstanten nicht aus der Verschiebung der polarographisch gemessenen Halbstufenpotentiale bestimmt werden können, lassen sich auf einfache und schnelle Weise durch polarographische Messungen der Austauschgleichgewichte mit einem zusätzlichen Komplexbildner relative Stabilitätskonstanten ermitteln. Am Beispiel der Kupferkomplexe von 8-Oxychinolin, Nitrilotriessigsäure und Äthylendiamintetraessigsäure wird gezeigt, daß durch Zusatz organischer Solvenzien Stufenüberlagerungen vermieden werden, weil die Kupfernitritriacetat- und Kupferäthylen-diamintetraacetatstufen soweit irreversibel verschoben werden, daß eine polarographische Bestimmung der Gleichgewichtskonzentrationen möglich ist. Ein Übergang von wäßrigem Milieu zu Wasser-Solvens-Gemischen erweitert wesentlich die Anwendungsmöglichkeiten für polarographische Untersuchungen von Komplexen.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 108
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 34 (1966), S. 55-63 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Die Stabilität der ω-Diazofettsäureester ist abhängig von der Kettenlänge. Der Eigenzerfall gehorcht einer Kinetik I. Ordnung, β-Diazopropionester zerfällt am schnellsten. Hauptprodukte sind die Azine von ω-Formylfettsäureestern. Dagegen entstehen beim Cu-katalysierten Zerfall ungesättigte Ester mit endständiger Doppelbindung als Hauptprodukte, beim photolytischen Zerfall Dicarbonsäureester mit mittelständiger Doppelbindung. Das Produktverhältnis wird durch die Anwesenheit von Cyclohexen nicht beeinflußt.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 109
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 34 (1966), S. 172-179 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Es wird die Darstellung von 1,3-Bis-(m-natriumsulfo-phenyl)-propandion-(1,3) und 1,3-Bis-(p-natriumsulfo-phenyl)-propandion-(1,3) sowie von einigen Vorstufen beschrieben. Die bei Darstellungsversuchen beobachtete Reaktion von Sulfonsäuremethylestern mit Natriumamid liefert Natriumsulfonat und Methylamin.
    Materialart: Digitale Medien
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  • 110
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 34 (1966), S. 180-189 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Es wird über die Synthese einer Reihe einfacher und unsymmetrisch substituierter isomerer β-Thioxoketone und ihrer Ni(II)-Chelate berichtet.Die Elektronenspektren der Liganden im Bereich von 250 bis 700 mμ und ihre IR-Spektren zwischen 400 und 3800 cm-1 sowie die optischen Spektren der Ni(II)-Chelate werden beschrieben. Bei den isomeren β-Thioxoketonen werden die regelmäßigen Eigenschaftsänderungen - wie Farbe und Schmelzpunkte der Liganden und ihrer Ni(II)-Chelate, Elektronen-und IR-Spektren - in Abhängigkeit von dem in Nachbarschaft zum Carbonylschwefel befindlichen Substituenten diskutiert.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 111
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 33 (1966), S. 50-53 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 4-Methyl-pyrimidin und 6-Methyl-purin werden durch KING-Reaktion mit Jod/Pyridin in die entsprechenden Pyridiniumjodide umgewandelt und diese durch Umsetzung mit p-Nitroso-N, N-bis-(β-chloräthyl)-anilin bzw. p-Nitroso-N, N-bis-(β-hydroxyäthyl)-anilin zu den entsprechenden Nitronen umgesetzt.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 112
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 33 (1966), S. 84-95 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 1-Phenylheptadiin-(2,4) und 1-Phenylhexadiin-(2,4) wurden durch Benzylierung von Hexadiin-(1,3) bzw. Pentadiin-(1,3) dargestellt. Weitere Aryldiacetylen-Verbindungen mit Abwandlungen am aromatischen Rest entstanden auf ähnlichem Wege.  -  Wasserlösliche 1-Arylhexadiine-(2,4) konnten durch Monobenzylierung des Diacetylens und anschließende MANNICH-Kondensation gewonnen werden.
    Materialart: Digitale Medien
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  • 113
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 33 (1966), S. 113-123 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: This paper deals with a deep evaluation of the constituents of the Wax distillate in the land Balayiem Crude. Combination of different methods of analysis was applied, (distillation, adsorption chromatography, urea addition, n. d. M.-method and elementary analysis). By dewaxing processes using ABT-mix., Paraffinic Wax was obtained. The chain length of the n-Paraffinic constituents of the Waxes was found.
    Zusätzliches Material: 14 Tab.
    Materialart: Digitale Medien
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  • 114
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 34 (1966), S. 23-29 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Unterwirft man Praseodym-Terbium-Mischoxide (Pr, Tb)O1,83 einer Säureeinwirkung, so erhält man gemischte “Dioxide”, die jedoch ein gewisses Defizit an Sauerstoff, entsprechend einer Formel (Pr, Tb)O2-Δ aufweisen. Die Gitterkonstanten dieser im Fluorittyp kristallisierenden Phasen sind dem Mischungsverhältnis Pr: Tb nicht proportional, sondern weichen nach höheren Werten ab.-An Praseodymdioxid, das auf nassem Wege dargestellt ist, wird ein hoher Reinheitsgrad festgestellt.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 115
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Aus den Stabilitäts- und Dissoziationskonstanten einiger Komplexe mit gemischten Liganden des Ni(3-Methylpyridin)4,(SCN)2, und Ni(4-Methylpyridin)4,(SCN)2 und deren Clathrate besonders mit p-Xylol lassen sich Schlüsse auf die clathratbildenden Eigenschaften dieser Verbindungen ziehen.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
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  • 116
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 34 (1966), S. 168-171 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Die Selten-Erd-Titanate der allgemeinen Formel SETiO3 (SE: La, Ce, Pr, Nd, Sm, Eu Gd) wurden magnetochemisch mittels der Gouyschen Methode bei Zimmertemperatur vermessen. Dabei wurden im Falle der Titanate mit 4 f-Ionen Suszeptibilitätswerte gefunden, die sich von denen der Sesquioxide sehr wenig unterschieden, während LaTiO3 in seinem magnetischen Verhalten abweicht. Die Suszeptiblitätswerte bestätigen die Formulierung EuIITiIVO3 für Europiumtitanat und SEIIITiIIIO3 für die übrigen Selten-Erd-Titanate. Auf mögliche ferromagnetische und antiferromagnetische Eigenschaften dieser Verbindungen wird hingewiesen.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 117
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 34 (1966), S. 251-261 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Malonsäure- und Acetessigsäureanilide werden von Arylisothiocyanaten in Gegenwart molarer Mengen Alkoholat zu Thioamiden der Methantricarbonsäure bzw. α-Acetyl-malonsäure addiert. Letztere ergeben unter Abspaltung der Acetylgruppe Monothiomalonsäuredianilide. Die Reaktionen einiger Thioamide werden untersucht.
    Zusätzliches Material: 4 Tab.
    Materialart: Digitale Medien
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  • 118
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 34 (1966), S. 272-282 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: ω-Diazofettsäureester reagieren mit aromatischen und heteroaromatischen Aldehyden in guten Ausbeuten zu ω-Acyl-fettsäureestern, mit Cycloketonen unter Ringerweiterung zu den homologen ω-[Cycloalkanon-2-yl-]-fettsäureestern.
    Materialart: Digitale Medien
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  • 119
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 34 (1966), S. 283-297 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: In der vorliegenden Arbeit wurden 1-[Bicyclo-(2,2,1)-hept-5-enyl-(2)]-alkanole sowie 1-[Bicyclo-(2,2,1)-heptyl-(2)]-alkanole dargestellt und die nach verschiedenen Methoden gewonnenen Verbindungen auf ihre endo-exo-Isomerenzusammensetzung untersucht. Zur Darstellung eignen sich Umsetzungen von bicyclischen Aldehyden nach Grignard sowie die Reduktion von Ketonen und Estern. Die Reduktion von Aldehyden führt zu 2,5-Methylen-1,2,5,6-tetrahydrobenzylalkohol bzw. 2,5-Methylen-hexahydrobenzylalkohol.Die Veresterung obiger Alkohole mit Chloriden und Anhydriden von Mono- und Dicarbonsäuren liefert Verbindungen, die pharmakologische Wirkung erwarten lassen.Versuche zur Ermittlung einer eventuellen relativen Reaktionsgeschwindigkeit endo-exo-isomerer Alkohole wurden durchgeführt.
    Zusätzliches Material: 7 Tab.
    Materialart: Digitale Medien
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  • 120
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 1-16 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Approximations in the Avrami treatment of impingement which arise when the growing crystalline bodies are rods or disks are discussed, with particular reference to the single-crystal model. This model, previously fitted to the isolated primary crystallization of polymethylene, is extended to discuss the growth of the composite lamellar structures, axialites, and spherulites, and is here fitted to the crystallization of poly(ethylene oxide) and polystyrene. Both polymers are found to yield anomalous values of the Avrami exponent when analyzed in terms of the conventional Avrami equation. The new analysis reveals similarities in the behavior of all three polymers. The residual deviations remaining after the fit of the model to polymethylene and poly(ethylene oxide) follow the same pattern, and the temperature dependence of the rate constants associated with the model is similar for all three polymers.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 121
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 17-24 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Of nine glassy polymers so far investigated, eight yield evidence that fracture propagation involves the formation and breaking of craze material. All eight produce fracture surfaces exhibiting interference colors to one extent or another and even the colorless areas cause low angle x-ray scattering. Ranked in terms of decreasing ease of colored surface formation, these polymers are poly(methyl methacrylate), poly(ethyl methacrylate), polystyrene, acrylonitrile - styrene copolymer, poly-α-methylstyrene, poly(vinyl acetate), a polyhydroxy ether, and polycarbonate. Only rigid poly(vinyl chloride) has failed to show evidence of precrack craze formation.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 122
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Copolymers of ethylene with vinyl acetate, vinyl alcohol, and butene-1 have been investigated by differential thermal analysis. The method of fast heating is used to approximate a zero entropy production heating path. The activity of crystallizable units in the melt, the crystallinity, and the a-axis spacings are determined and compared with previous results for copolymers of ethylene and propylene and carbon monoxide. Carbonyl and hydroxyl groups form point defects, forming solutions in both the crystalline and amorphous regions. Methyl, ethyl, and acetate groups form large amorphous defects. The maximum melting point of polyethylene is calculated to be 142.6°C.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 123
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 53-62 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Ethylene - propylene and ethylene - butene-1 copolymers with up to 1.7 side groups per 100 carbons have been crystallized at 227°C. and under 4100-4900 atm. pressure. The resulting crystalline polymers are at least partially of extended-chain crystal morphology. Comparison with the same polymers crystallized at atmospheric pressure, which gives folded-chain crystal morphology, revealed: (1) a density higher by 0.008-0.019 g./cm.3 depending on copolymer content; (2) a similar decrease of crystallinity with side group concentration; (3) a similar decrease of the beginning of melting from 125°C. for homopolymer to 65°C. for 1.7 side groups per 100 carbons; (4) a higher (138 ± 0.8°C.) experimental maximum melting point which, in contrast, is independent of copolymer content and seems to vary only with the fraction of low molecular weight material; (5) a decreasing amount of high-melting crystals with increasing copolymer content (72-8%) and an increasing amount of low-melting crystals (27-53%) with increasing copolymer content. In addition, superheating, which reached 5.5°C. for 50°C./min. heating rates, was detected. It was concluded that high-pressure crystallization leads, at least for part of the crystals, to solid solution formation, while atmospheric pressure crystallization does not. Which mode of crystallization is achieved seems kinetically determined. Experimental techniques were dilatometry, DTA, and calorimetry.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 124
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 41-52 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The dynamic moduli, E′ dyn, and loss tangents, tan δ, of polydimethylsiloxane and polydimethyldiphenylsiloxane polymers have been investigated by an in situ technique during γ-irradiation. These viscoelastic properties were calculated and plotted as a function of irradiation exposure time by measuring the free end displacements and resonance frequencies of polymeric cantilever reeds. The reeds were swept through a small frequency range from about 20 to 100 cycles/sec. The moles of effectively elastic chains per unit volume (v) of the two unfilled polysiloxahes were calculated from in situ modulus data and compared to values obtained utilizing the swelling technique. The approximate molecular weights between entanglements, Me, of these unfilled polymers were determined by extrapolation of moduli data to zero radiation exposure. The addition of a large silica filler, SiO2, into the polymers did not alter the crosslinking rates, and the filler did not enter into polymer - filler bonding.
    Zusätzliches Material: 6 Ill.
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  • 125
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 89-99 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The effect of birefringence on the intensity of polarized scattered light from an oriented polymer film is analyzed on the basis of a model in which the scattering element is imbedded in a homogeneous birefringent matrix. The scattering intensity is shown to depend upon the polarizer and analyzer angles, the scattering angles, the sample birefringence and thickness, and the scattering coefficients for the four polarization combinations. Computer calculations for reasonable values of these parameters indicate that these corrections can be quite appreciable.
    Zusätzliches Material: 8 Ill.
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  • 126
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 101-111 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The performance of the gel permeation chromatography (GPC) technique was studied with several commercial samples of linear high density polyethylene. A comparison of these data was made with those obtained from the elution column technique based on fractional dissolution. GPC gave reproducible fractionation data in the molecular weight range of 103-106. These data were obtained from two columns in series with nominal capacity of 1-104 and 1-106A. Polyethylene fractions of known molecular weights are required as calibration standards and for many commercial polyethylenes it is necessary to increase sensitivity at molecular weight higher than 106.
    Zusätzliches Material: 8 Ill.
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  • 127
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 63-88 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A theory of tensile strength, based on the observation of cracks in specimens strained to breaking, is formulated. The treatment involves the assumption that a crack grows to a critical size by a nucleation process. When this critical size is exceeded the crack becomes unstable and propagates spontaneously to produce rupture. By comparing the predicted and measured strength, one can estimate the magnitude of the stress concentration factor in fibers. An interpretative analysis of experimental data obtained at various strain rates indicates that the resulting changes in tensile strength are due primarily to the changes in modulus.
    Zusätzliches Material: 13 Ill.
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  • 128
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 135-154 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A new method of treating experimental data on the viscous and viscoelastic properties of various polymer melts is suggested. The dependence of the apparent viscosity on the molecular weight, temperature and shear stress can be represented as the product of three independent functions, each of them having a single argument. All three functions are universal, at least in first approximation, and the dependence of the apparent viscosity on the variables indicated is determined by two parameters (glass transition temperature and critical molecular weight), characteristic of each homologous polymer series. The viscoelastic characteristics (dynamic, relaxation, creep, as well as relaxation and retardation spectra) of polymer melts are universal in shape in the linear region and contain only one individual polymer parameter, viz., maximum Newtonian viscosity. It is shown that upon normalization of certain nonlinear characteristics with respect to the maximum Newtonian viscosity, they can also be represented in the universal form.
    Zusätzliches Material: 11 Ill.
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  • 129
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 113-119 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A device for measuring the elasticity of polymer melts has been designed by one of us (B. Maxwell). The device was used to obtain the relaxation modulus in shear of a linear polyethylene melt. From these data a discrete relaxation spectrum was derived. The range of the obtained spectrum was confirmed to correspond to the terminal zone of the “entanglement plateau” of the spectrum. The limiting dynamic viscosity (as frequency approaches zero) was obtained by integrating the relaxation modulus with respect to time. The viscosity and its activation energy were found to agree closely with the flow viscosity and the flow activation energy, respectively, involved in capillary flow.
    Zusätzliches Material: 5 Ill.
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  • 130
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 155-157 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 131
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 158-160 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 132
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 121-133 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Crystalline polymers derived from cis- and trans-2-butene oxides were studied by x-ray diffraction methods. X-ray fiber and powder photographs of poly(trans-2-butene oxide) were indexed by an orthorhombic unit cell with the dimensions a = 13.72 A., b = 4.60 A., and c (chain axis) = 6.90 A.; the space group is P212121. The crystal structure of this polymer has been determined in projection. The chain has an erythro-diisotactic structure with -dl, dl- carbon sequences. The polymer has a nonplanar zigzag backbone with carbon and oxygen atoms of alternate monomer units lying nearly in a plane. Two chain molecules pass through the unit cell. The unit cell of poly(cis-2-butene oxide) is orthorhombic with lattice constants a = 11.20 A., b = 10.44 A., c (chain axis) = 7.01 A. The polymer has a threo-diisotactic structure with -dd,dd- or -ll,ll- carbon sequences. Four chain molecules pass through the unit cell. The crystal lattice is body-centered but the space group has not yet been established. The polymer has an almost fully extended zigzag chain configuration. Polymers prepared by either metal halide catalysts (FeCl3, SnCl4) or organometallic catalysts were essentially identical; the latter catalysts did, however, yield more highly crystalline polymers.
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  • 133
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 183-198 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Good yields of some crystalline γ-alkyl esters of L-glutamic acid were obtained by carrying out the esterfication with a small (20-50 mole-%) excess of alcohol in aqueous hydrochloric acid or 60-80% sulfuric acid followed by neutralization with an alkaline solution. This new method made it possible to synthesize various γ-alkyl L-glutamates, including those higher than ethyl, and consequently, various poly(γ-alkyl L-glutamates) such as methyl, ethyl, n-propyl, n-butyl, isobutyl, and isoamyl. The conformation of these poly-L-glutamates in the solid state was determined by the infrared absorption method. The molecular motions of the polymers of γ-methyl, -ethyl, -n-propyl, -n-butyl, and-isoamyl L-glutamates and poly(γ-methyl-D-glutamate) in the solid state were studied by NMR, and dielectric and mechanical measurements. At temperatures up to 400°K., the NMR spectra of poly(γ-methyl D-glutamate) can be explained only by rotational motion of the side chain. Also, from NMR results, rotational motion of C=O groups in the side chain of poly(γ-methyl D-glutamate) is expected near room temperature, and such a motion was examined by dielectric measurements. Rotation of C=O groups in the side chains of polymers of γ-methyl, γ-ethyl, γ-n-propyl, γ-n-butyl, and γ-isoamyl L-glutamate was also observed near room temperature by dielectric measurements in the frequency range from 102 to 106 cps. Activation energies obtained by dielectric and mechanical measurements were similar to those for the side chain motions of the corresponding esters of poly(methacrylic acid). Although it has been noted that the molecular motion of poly(γ-benzyl L-glutamate) in the solid state at room temperature may be related to the motion of its back bone, the molecular motion in these poly-L-glutamates at these temperatures can be explained only in terms of side-chain rotation.
    Zusätzliches Material: 8 Ill.
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  • 134
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 199-208 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The preparation of five samples of poly(methyl methacrylate) covering a wide range of tacticity and their electron irradiation to produce series of varying molecular weight are described. The glass transition temperature Tg of each polymer was determined by DTA techniques. Plots of Tg and the reciprocal of the molecular weight are well fitted in every case by a straight line. The data are also fitted to the Gibbs-DiMarzio theory and the values of the energy and free-volume parameters obtained are discussed. A method of estimating Tg of pure syndiotactic poly(methyl methacrylate) by extrapolation is presented, the value obtained being 160°C.
    Zusätzliches Material: 4 Ill.
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  • 135
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 209-226 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The principles of a method are outlined whereby one can determine the partial specific volume of a solute, V̄, by means of measurements of dn/dc using a suitable pair of equations and a simple graphical interpolation procedure. The method yields V̄ data which compare well with densitometrically obtained V̄ data if the polarizability of both solvent and solute molecules is unaffected by the solution process. It is tested successfully on solutions of polystyrene in various solvents. The method appears to be particularly attractive for measurements of the change of V̄ with temperature and also for conveniently following the time rate of changes in - such as during the coil → helix transition.
    Zusätzliches Material: 1 Ill.
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  • 136
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 173-181 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The relationship of intrinsic viscosity to the number-average molecular weight has been obtained for poly-3,4-dichlorostyrene and poly-p-cyclohexylstyrene in a few solvents. Values of (〈L2〉0/M)1/2 have been estimated for poly-3,4-dichlorostyrene and poly-p-cyclohexylstyrene through the use of the treatment of Stockmayer and Fixman. The values of (〈L〉0/M)1/2 have been obtained as 2.18 ± 0.08 and 2.52 ± 0.07 for poly-3,4-dichlorostyrene and poly-p-cyclohexylstyrene, respectively. The σ value of a series of polystyrene derivatives has been found to increase with the bulk of side groups. This seems to indicate that the σ value is mainly determined by the steric repulsion between side groups.
    Zusätzliches Material: 4 Ill.
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  • 137
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 161-171 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: It has been shown that lamellar crystals of amylose V complexes with 71 helical configuration can be obtained by using complexing agents larger in cross section than n-butanol. The electron diffraction studies indicated a new unit cell for the unheated lamellar crystals which are composed of molecules with 71 helical configuration and hold water molecules on the exterior of the helix. Furthermore, from a throughly dried specimen at 100°C. in vacuo we obtained a pattern which showed only three Debye rings. Its spacings were explained by a two-dimensional hexagonal unit cell having a = b = 14.7 A. proposed by Zaslow. It was also found that when the crystals were dispersed in methanol at room temperature, their electron diffraction pattern was the same as that of the anhydrous amylose V complex of n-butanol.
    Zusätzliches Material: 10 Ill.
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  • 138
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 243-265 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A preliminary study of the isothermal crystallization of “even-even” polyamides reveals striking similarities in spherulitic morphology. The observed variations in textural features of spherulites of nylon 210, nylon 66, nylon 610, and nylon 1010 show parallel changes during growth conditions and conform to a definite sequence of behavior. At least four different types of spherulites exist in each polymer. Optical and x-ray techniques were used to examine some of these spherulites. Crystalline platelets possessing single-crystal properties have been grown in thin films of these polymers near their respective melting points.
    Zusätzliches Material: 21 Ill.
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  • 139
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 227-242 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Polypropylene was oxidized with nitric acid in a manner contrived to remove its amorphous component. Concurrent with the loss in weight there was an increase in crystallinity, a decrease in molecular weight, a drop in melting point, and a change in visible structure. The crystalline component, which survived from polymer which had orginally crystallized isothermally, consisted of separated spherulites. These spherulites could be broken apart into lamellae which gave electron diffraction patterns like those now associated with a variety of solution-grown single crystals. As opposed to the high molecular weight of the unoxidized parents, the lamellae which survived the acid treatment consisted of short chains whose length depended on the temperature at which the parents had crystallized. If, as diffraction studies indicate, these short molecules are lined up in rank and file, then the length of the molecules and the height of the lamellae should correspond. The heights of the lamellae could not be measured precisely enough to establish an exact correlation, but the variations in average chain length calculated from viscosity data at least approximated the heights of the lamellae which were observed visually.
    Zusätzliches Material: 10 Ill.
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  • 140
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 283-288 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 141
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 267-281 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Intercrystalline links in polyethylene have been revealed by crystallizing from the melt mixtures of fractionated polymer and the linear hydrocarbon n-C32H66, the latter constituent being removed later by washing at room temperature in an organic solvent. These fibrous links measure up to 15,000 A. in length and are 30-300 A. in thickness. Molecular chains are oriented parallel to the lengths of the links, and apparently nucleate on tie molecules formed by the simultaneous crystallization of different parts of the same molecule on the surfaces of different, and often widely separated, crystals. The maximum length of the links found in a given polymer varies as the square root of molecular weight, and there are indications that molecules in the melt are much more extended than is predicted by conventional configurational statistics. The links are under tension and presumably exert a significant influence on physical properties.
    Zusätzliches Material: 10 Ill.
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  • 142
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 289-298 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Uniaxial deformation of polyethylene single crystals has been reported in the previous papers of this series. This paper presents an extension of this study to the simultaneous biaxial deformation of polyethylene single crystals. Diamond-shaped crystals containing {110} fold domains and truncated crystals containing in addition {100} domains were used in these experiments. The results show that these crystals fail at deformations as low as 6%, giving rise to cracks predominantly in the a direction. Electron diffraction patterns suggest that {310} twinning is more favorable than {110} twinning at the lower degrees of deformation. No phase change from orthorhombic to monoclinic unit cell is observed.
    Zusätzliches Material: 6 Ill.
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  • 143
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 299-311 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A model of a rubber network formed from finite, linear polymer chains is treated, using expressions from accepted elastic theory as well as relationships that have been less generally used or only implied. The resultant empirical mathematical expressions conform very closely to the predictions of the simple kinetic theory of rubber elasticity and are mathematically consistent, in that the major properties and measurements are interrelated, and apparent inconsistencies in the literature are reconciled. As a consequence, an empirical equation is developed for the relationship between elastic properties and network structure in silicone gum vulcanizates. This equation is then applied to the estimation of peroxide crosslinking efficiencies.
    Zusätzliches Material: 4 Ill.
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  • 144
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 313-325 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The effect of γ-irradiation and post-irradiation heat treatment on the specific volume versus temperature relationships of polytetrafluoroethylene (PTFE) samples (1/2-in. diameter rods) have been studied over the 40-150°C. temperature range for radiation doses up to 8.9 X 108 rad. At low doses the specific volume at any temperature decreased with dose, but above about 108 rad it increased with dose. Similarly, the rate of volumetric expansion initially decreased with dose, while, at very high doses (8.9 X 108 rad) the rate of expansion at temperatures above 100°C. exceeded that of the unirradiated PTFE. Heating at 150°C. for 100 hr. produced a substantial decrease in the specific volume and a decrease in the rate of expansion for the irradiated samples. Irradiation effects in PTFE are considered to be a result of such factors as radiation-induced chain scission, increased crystallinity, and increased void content. Changes resulting from post-irradiation heat treatment can be attributed to increased crystallinity, decreased void content, and weight loss.
    Zusätzliches Material: 2 Ill.
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  • 145
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 327-347 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Amorphous films of Lexan polycarbonate have been exposed to acetone vapor at controlled temperatures and partial pressures in order to study sorption kinetics and thermodynamics and polymer crystallization behavior. Sorption isotherms show a discontinuity is slope at or near the depressed glass transition, which itself was identified by torsion pendulum measurements. Crystallization abruptly begins to occur at partial pressures equal to or slightly above that of the solubility transition and is manifested by delayed desorption and whitening phenomena. In this process 20% crystallinity is usually developed, as measured by calorimetry which, however, produces a 40% drop in acetone solubility. Although the depressed glass temperature is near 0°C. in saturated atmospheres - a drop of 145°C. - the melting point is only depressed 60 or 70°C. Such disparity probably accounts for the enhanced polycarbonate crystallization rate in acetone over that in the dry bulk polymer above the normal Tg.
    Zusätzliches Material: 12 Ill.
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  • 146
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 349-358 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Observation of optical interference fringes at the tip of a crack in a glassy polymer allows the construction of the configurations of the crack tip and the craze that precedes it. The craze extends 25 μ beyond the crack tip in poly(methyl methacrylate) and 550 μ beyond the tip in the polystyrene studied. The craze at the crack tip in PMMA may be seen to deform elastically as much as 100% under stress before crack propagation recommences. Such deformation is estimated to account for as much as 40% of the nominal Griffith energy of crack propagation.
    Zusätzliches Material: 5 Ill.
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  • 147
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 359-363 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The temperature rise at the moving crack tip in poly(methyl methacrylate), resulting from the dissipation of the energy of crack propagation has been calculated. At velocities below 1 cm./sec., conduction of heat away from the crack plane into the bulk polymer appears to prevent any appreciable temperature increase.
    Zusätzliches Material: 2 Ill.
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  • 148
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 365-374 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Samples of polystyrene and poly(methyl methacrylate) have been prepared by bulk polymerization under conditions previously investigated in the literature. The molecular weight distributions were determined for early-conversion samples by gel permeation chromatography, and the experimental distribution curves were compared with calculated curves based on kinetic data. The agreement between the experimental and calculated curves was such as to indicate the utility of gel permeation chromatography in the investigation of polymer reaction kinetics and mechanisms.
    Zusätzliches Material: 4 Ill.
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  • 149
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 401-414 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Poly(vinyl fluoride) polymers prepared at different polymerization temperatures have been examined in the melt, oriented, and solid state by infrared spectroscopy. Bands arising from the head-to-tail and head-to-head-tail-to-tail portions of the polymer have been isolated and assigned. The head-to-head-tail-to-tail portion of the polymer crystallizes in the head-to-tail unit cell except for a portion of the 1,2-difluorethylene units which apparently have the gauche (out-of-plane) structure. The head-to-tail portion of the polymer is nearly atactic, but is somewhat rich in syndiotactic chain structure. Bands arising from local syndiotactic order are observed.
    Zusätzliches Material: 4 Ill.
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  • 150
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 375-384 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Low-temperature internal motions of the following polyesters have been investigated by broad line nuclear magnetic resonance: poly(methylene terephthalates) (2-6 methylene groups), poly[1,4-(dimethylene)cyclohexylene terephthalate], poly(diethyleneglycol terephthalate), poly(1,2-propylene terephthalate), poly(1,4-phenylene terephthalate), poly(2,2,3,3,4,4-hexafluoropentamethylene terephthalate), poly[1,4-phenylenebis(dimethyl) siloxane], and poly(2,6-dimethylphenylene oxide). No complex line structure was found for any of the samples. Molecular motions in the polyesters appear to be restricted by polar forces arising from the ester groups. Above - 196°C. the line width decreases smoothly with increasing temperatures for all polymers except poly[1,4-(dimethylene)cyclohexylene terephthalate] and poly[1,4-phenylenebis(dimethyl)siloxane]. These two show a definite transition in line width at -20°C. and +12°C., respectively, caused by the onset of considerable internal motion. At -196°C. the lattices are rigid except for polymers containing methyl groups: poly(1,2-propylene terephthalate), poly[1,4-phenylenebis(dimethyl) siloxane], and poly(2,6-dimethylphenylene oxide). Internal motion that can be ascribed to be a reorientation of the methyl groups is present at -196°C. for these three polymers, as is demonstrated by comparison of experimental second moments and those calculated on the basis of various models.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 151
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 385-400 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Replicas of fracture surfaces of fractions of linear polyethylene, which were crystallized at elevated temperatures for extended time periods, were examined by electron microscopy. Striated. lamella-type crystallites were observed for all molecular weights over the range 3.2 × 103-5.7 × 105. In agreement with Anderson's previous report, for molecular weights of 12,000 or less, the crystallite thicknesses were comparable to the extended chain length. As the molecular weight increased above this level, however, the crystallite sizes increased only slightly and hence at high molecular weights were very much smaller than the extended chain length. From the measured melting temperatures, crystallite interfacial free energies were calculated from the theory for the melting of finite size crystals comprised of chains of finite length. The crystallite interfacial free energy was found to increase with molecular weight. Based on these results, a crystallization process is outlined which allows for the formation of either extended chain crystallites, or crystallites whose size is much smaller than the extended chain length without any change in nucleation mechanism or arbitrary adjustment in growth mechanism with molecular weight.
    Zusätzliches Material: 6 Ill.
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  • 152
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 415-422 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Values of ε0ν0 the vaporization energy and volume in the hypothetical liquid state at 0°K., are derived for some simple polar and nonpolar molecules used as models for vinyl polymers. The following empirical relationship between the free volume fraction, f = (v - v0)/v, and the liquid compressibility coefficient β is demonstrated: -f2 ∝ This is applied to several vinyl polymer liquids near their glass transition temperatures, Tg, giving. fg ≃ 0.17, if the “hard-core” volume v* is considered to be independent of pressure and temperature, (i.e., v* = v0); or, fg ≃0.12, if the P,T dependence of v* is considered to be the same as that of the glass. These agree with fg values derived by Simha and Boyer from thermal expansion coefficients for the two analogous cases. An empirical viscosity-free volume equation of the Doolittle form: η = ATneb/f is applied to the glass transition, on assuming that this is an isoviscosity state and with the use of reported values for the expansion and compressibility coefficients and dTg/dP for three polymers: polystyrene, poly(methyl methacrylate), and poly(vinyl acetate). Reasonable values of b/n are thus obtained. This viscosity equation is critically examined in the light of molecular theories of liquid viscosity.
    Zusätzliches Material: 6 Tab.
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  • 153
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 447-464 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Measurements are described of the rates of crystallization and crystal melting temperatures in stretched test pieces of trans-polyisoprene, crosslinked to various degrees. The increase in rate with extension are attributed to the corresponding increases in melting temperature and hence degree of supercooling. The rise in the melting temperature of both the α- and β-crystal forms is found to be in satisfactory agreement with Flory's treatment of oriented crystallization. The changes in tensile stress are also generally in accord with the formation of oriented crystallites. For the more lightly crosslinked materials, a pronounced rise in tensile stress occurred during the later stages of crystallization, at extensions below about 100%. Reasons are given for attributing this phenomenon primarily to the relatively large contraction in volume on crystallization, rather than to the formation of folded-chain crystallites.
    Zusätzliches Material: 16 Ill.
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  • 154
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 437-446 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Light scattering and viscosity have been measured at 25°C. for dilute solutions of six unfractionated polyoxymethylene samples in the mixed solvent hexafluoroacetone-water (mole ratio 1/1.7) slightly buffered with triethylamine. Dialysis equilibrium through porous Vycor glass thimbles indicates that the polymer is strongly solvated by the hydrate (CF3)2C(OH)2, and this must be taken into account in evaluating weight-average molecular weights from the light-scattering data. Over the molecular weight range 23,000-185,000, the intrinsic viscosities (in deciliter per gram) follow the relation \documentclass{article}\pagestyle{empty}\begin{document}$ [\eta] = 8.7{\rm} \times {\rm}10^{ - 4} M_\upsilon ^{0.69} $\end{document} The corresponding unperturbed dimensions are σ = 2.3 ± 0.2 or r02/nl2 = 10.5 ± 1.5.
    Zusätzliches Material: 3 Ill.
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  • 155
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 423-435 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Short-range interactions between chain units of random copolymers in solution may be influenced by the composition or precisely by the distribution of sequence lengths of the same monomer units. Steric factors were derived for random copolymers of styrene and acrylonitrile with different compositions from the relation between the limiting viscosity number and the molecular weight. Mark-Houwink relations were obtained in methyl ethyl ketone (MEK) or in N,N′-dimethylformamide (DMF) at 30°C. for random copolymers containing 0.383 (Co-1) and 0.626 (Co-2) mole fraction of acrylonitrile, the expressions are: [η] = 3.6 X 10-4 Mw0.62, for Co-1 in MEK; [η] = 5.3 X 10-4 Mw0.61, for Co-2 in MEK; [η] = 1.2 × 10-4Mw0.77 for Co-2 in DMF. With the Stockmayer-Fixman expression, these correlations become, respectively: [η]/M1/2 = 1.24 × 10-3 + 8.0 × 10-7 M1/2; and [η]/M1/2 = 1.70 × 10-3 + 6.3 × 10-7 M1/2; and [η]/M1/2 = 1.68 × 10-3 + 31.3 × 10-7 M1/2. From the unperturbed mean-square end-to-end distances, 〈L2〉0, determined from the first terms of the latter expressions, together with 〈L2〉0f calculated by assuming the completely free rotation, gives the steric factor σ = (〈L2〉0/〈L2〉0f)1/2 as 2.25 ± 0.05 for Co-1, and 2.31 ± 0.10 for Co-2. These values of σ are close to those for polystyrene (σ = 2.22 ± 0.05) and for polyacrylonitrile (σ = 2.20 ± 0.05). Therefore, it is concluded that the dimensions of random copolymers of styrene and acrylonitrile in solution are not significantly influenced by the composition. In other words, the unperturbed dimensions are not affected by a change in the alternation tendency between styrene units with phenyl side groups having a large molar volume and acrylonitrile units with nitrile groups responsible for the electrostatic interactions. On the other hand, the long-range interactions reflect the effect of sequence length. The Huggins constant and the second virial coefficient obtained from the light-scattering measurements have optimum values at about 0.5 mole fraction of acrylonitrile, where the greatest tendency for alternation seems to exist.
    Zusätzliches Material: 4 Ill.
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  • 156
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 465-474 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Insertion poly(methyl acrylate) and poly(methyl methacrylate) were prepared from monomers adsorbed in monolayers on the surface of montmorillonite clay, both in the presence and in the absence of bifunctional crosslinkers (ethylene glycol dimethacrylate and tetramethylene glycol dimethacrylate). The insertion poly(methyl acrylate) and the crosslinked insertion poly(methyl methacrylate) and dilute-solution properties quite different from conventional polymers of these monomers, the differences including high light-scattering molecular weights combined with low viscosities, low values of the second virial coefficient, unusually large variations of the Huggins' constant k′ with the time-temperature history of the solutions, and low sedimentation velocities. These properties suggest that the insertion polymers have compact structures and are consistent with the postulate of sheetlike macromolecules. The dilute-solution properties of insertion poly(methyl methacrylate) made without crosslinker, unlike those of similarly prepared poly(methyl acrylate), were similar to those of conventional poly(methyl methacrylate). This difference in behavior is attributed to the different tendencies of the two monomers to undergo branching or crosslinking during radical polymerization.
    Zusätzliches Material: 5 Tab.
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  • 157
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 491-500 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Equations previously developed for the light scattering of polar chain polymers subjected to orientation by an electrical field are extended to the case where the elementary dipoles have arbitrary direction with respect to the chain contour. As an illustration of the theory, measurements were made of the light scattering of nitrocellulose solutions as a function of the angle of observation, the field strength, the direction of the field, and the frequency of the field. The principal results obtained were: the molecules are deformed by the electrical field; orientation is due primarily to a permanent electric moment whose component per chain segment is of the order of 4 Debye; and the relaxation times for molecular orientation are of the order of magnitude predicted by the theory of Stockmayer and Baur.
    Zusätzliches Material: 6 Ill.
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  • 158
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 501-505 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: NMR linewidth studies of nylon 66 as a function of temperature and applied tensile stress have been conducted. The principal motional transition temperature was found to be shifted to higher temperatures with stress application by 9°C./g./den. At any given temperature, increased stress resulted in an increased linewidth. An attempt was made to correlate the shift in the motional transition temperature with the concept that a segment experiencing motion must do work against the applied tensile stress.
    Zusätzliches Material: 1 Ill.
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  • 159
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 475-489 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: X-ray diffraction, sonic velocity, and birefringence measurements were used to study the variation of the apparent melting point of strained natural rubber and polychloroprene vulcanizates with elongation ratio and crystallization temperature. The procedure of Hoffman and Weeks was employed to obtain the thermodynamic melting point, tm, for each elongation ratio α. The parameter β relating to the distribution of fold lengths is unusually large for low elongation ratios and decreases into the usual range only at higher elongations. The observed variations of tm with α for these two polymers are compared with the theoretical predictions of Flory and Roe and Krigbaum. Although the predictions of the Flory theory depend somewhat upon the value assigned for the number of repeating units per statistical link, and this parameter is not well known for polychloroprene, we nevertheless conclude that his treatment offers a better representation of the melting point elevation for high elongations. Due to the approximations introduced, the treatment of Flory is not valid for lower elongations. Any attempt to improve this treatment must begin by specifying the free energy of the semicrystalline system, which implies a knowledge of the distribution of crystallite orientations and how this distribution varies with strain and with the crystallization conditions.
    Zusätzliches Material: 9 Ill.
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  • 160
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 519-520 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 161
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 523-526 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 2 Ill.
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  • 162
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 521-522 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 1 Tab.
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  • 163
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Phase equilibria between linear polyethylene and a number of organic diluents of varying type have been investigated. The diluents include aliphatic alcohols, alkyl phenols, aryl phenols, diphenyl derivatives, alkyl aryl ethers, esters, and ketones. It is found that n-octyl alcohol, n-decyl alcohol, n-lauryl alcohol, p-tert-amyl alcohol, p-octyl phenol, p-nonyl, phenol, diphenyl, diphenylmethane, diphenyl ether, benzyl phenyl ether, and anisole are Θ-solvents for linear polyethylene at temperatures between 120 and 200°C. Thermodynamic interactions are discussed in relation to the type of diluent.
    Zusätzliches Material: 10 Ill.
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  • 164
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 527-528 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 165
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 532-534 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 1 Ill.
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  • 166
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 529-531 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 167
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 535-537 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 1 Ill.
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  • 168
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 538-542 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 169
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 666-667 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 2 Tab.
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  • 170
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: In addition to the α polymorph, two crystalline forms of nylon 4, the β and δ polymorphs, have been observed and studied.The β polymorph of nylon 4, which has not been found in a pure condition, appears to be similar to the β polymorph of nylon 6. The extended planar zigzag conformation of chains, found in the α polymorph, is present also in the β polymorph. Three models have been proposed to explain the observed data. In model 1, the staggered shear of van der Waals bonded sheets found in the α polymorph is abandoned; in model 2, the sheets are displaced by 1/2 the b axis, and in model 3 the chains are arranged in a parallel array. The β polymorph is converted to the α form in air upon heating for 11 min. at 227°C. and upon immersion in water for 2 hr. Models 1 and 2 would be converted to the α polymorph by a slippage of the van der Waals bonded sheets while the conversion from model 3 would involve a rupture of hydrogen bonds, a rotation of the chains through 90°, and the reformation of hydrogen bonds. The δ polymorph is formed by rapidly quenching extruded nylon 4 against chilled rolls. It is a metastable form which has only been observed in an unoriented condition. Upon orientation it is completely converted to the α polymorph. In addition to this, its conversion to the α form occurs under conditions similar to the β-α transition. The observed diffraction pattern can be indexed on the basis of a hexagonal packing of chains. High-temperature x-ray diffraction studies of the α polymorph suggest that the δ form, or a structure similar to it, is the high-temperature form of nylon 4.
    Zusätzliches Material: 4 Ill.
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  • 171
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 943-949 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The dynamic mechanical properties of highly crosslinked epoxyamine polymer networks with nonrandomly distributed crosslinks were investigated. The transition temperatures of these polymers can be correlated with the number of CH2 groups between crosslink junctions in the aliphatic amine portions of the network. The steepness of the modulus-temperature curve is also a function of crosslink density. This is in contrast with the case of natural rubber crosslinked by sulfur or by electron irradiation, where the modulus-temperature curves have similar shapes although the glass transition temperature increases with the degree of crosslinking. An empirical distribution function, similar to the one used by Tobolsky for stress relaxation distributions, was used to describe the temperature dispersion of the dynamic moduli. Two parameters, hg and hr, are used to characterize the steepness of the dispersion curve below and above the transition temperature, respectively. It is tentatively concluded that hg correlates with the length of the CH2 sequences in the amine portion of the polymer. The quantity hr may be related perhaps to the motion involving the trifunctional nitrogen junction.
    Zusätzliches Material: 4 Ill.
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  • 172
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 951-958 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The measurement of crystallinity and orientation in poly(ethylene terephthalate) is discussed. A simple procedure is given for the estimation of orientation from the (105) plane, and it is shown that methods which use the equatorial planes are subject to certain disadvantages. In addition a method is given for the measurement of x-ray crystallinity. The technique is applied to fibers and films of various treatments and a linear relation is found between density and x-ray crystallinity.
    Zusätzliches Material: 4 Ill.
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  • 173
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 1009-1010 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 3 Ill.
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  • 174
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 959-974 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The crystal structure of poly(m-xylylene adipamide) was reinvestigated by x-ray diffraction. It is found that the helical chain model proposed by Yoda et al. needs to be corrected to a large extent. The unit cell obtained is triclinic with dimensions a = 12.01 A., b = 4.83 A., c = 29.8 A. (fiber axis), α = 75.0° = 26.0°, and γ = 65.0°, in which one molecular chain with two chemical repeating units is involved. The space group is C1i-P1. An almost planar zigzag chain conformation with a small degree of contraction from the original planar arrangement is given. The CH2 planar zigzag chain and the aromatic rings are so oriented that their planes are inclined to the c axis at an angle of a few degrees. The hydrogen-bonded sheets nearly coincide with the (100) plane and the aromatic rings are close to the (120) plane, which is nearly perpendicular to the direction of hydrogen bonding.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
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  • 175
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 975-996 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Random copolymers of N-n-butyl-, N-n-octyl-, or N-n-octadecylacrylamide with acrylonitrile were prepared in tert-butanol at 60°C. to test the effect of amide homologs as internal plasticizers. At room temperature under high deformations all samples showed brittle failure; at 100°C. flexible and resilient copolymers were obtained. At low deformations, torsional stiffness values Tf followed the equations of Wood, Fox, and Dimarzio and Gibbs, the latter two modified by use of mole fraction instead of weight fraction. Mole fraction appeared to function better than weight fraction for these special cases where wi 〉 2mi and where modulus-temperature curves were broad. Because literature values for the glass (or brittle) temperatures of homologs of poly-n-alkyl acrylates, methacrylates, n-alkyl styrenes and alkenes, and estimated values for poly-N-n-alkylacrylamides, plotted as a function of the logarithm of the number of single bonds in repeat units, extrapolate to an average value of -111°C. at a chain length of eighteen carbon atoms, and because side-chain melting points of linear eighteen carbon side-chain homologs appear to have a common value of 48-50°C. regardless of structure, it was concluded that similar glass and melting transitions are obtained when the side chain reaches eighteen carbon atoms in any series of homologs. Transitions for longer side-chain lengths then approach the limit of a polyethylene graft, where Tg is -81°C. and Tm is 137°C.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 176
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 997-1008 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The transformations of the polymorphic forms of polybutene-1 (I,II,III) were studied by infrared spectroscopy. Attenuated total reflectance spectra demonstrate that the II → I transformation occurs initially and most rapidly on the film surfaces. Electron irradiation experiments showed the II → I conversion can be suppressed by irradiation. The degree of suppression was dependent on the irradiation dose. Comparison of spectra on irradiation in air and vacuum indicate that radiation-produced radicals are scavenged by oxygen, preventing intermolecular crosslinking and allowing normal expansion of the helix during transformation. In addition, remolding an irradiated sample of II caused immediate conversion to I rather than its return to II as was noted when unirradiated samples are remolded. These observations are related to certain conformational changes in the molecular structure.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 177
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 1011-1012 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 178
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 1013-1021 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 179
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 1022-1024 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 180
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 1025-1027 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 181
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 1029-1029 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 182
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The synthesis of the cycloheptapeptide XIII (Figure 2), corresponding to the structure proposed by T. SUZUKI et al. for the antibiotic circulin A, and its crystallization as pentaphosphate are reported. This synthetic compound proved to be identical in all respects with the crystalline natural circulin A pentaphosphate.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 183
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 49 (1966), S. 997-1000 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The synthesis of 13,15-dihydro-5H-diindeno[1,2-a;1′,2′-h] fluorene in six steps starting from flourenone 4-carboxylic acid and 2,4-dichlorotoluene is described. As an intermediate product the 5, 13, 15-trioxo-derivative is obtained.
    Materialart: Digitale Medien
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  • 184
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 49 (1966) 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 185
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 49 (1966), S. 1029-1041 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The dehydration of farnesols or nerolidols is similar to that of geraniol and nerol or linalool. It yields a mixture of hydrocarbons including trans-β-farnesene, two allofarnesenes, α-curcumene, α-, β- and γ-bisabolenes, and triterpenes. The triterpenes result from dienisation of β-farnesenes or α-farnesenes with β-farnesenes, or dimerization of allofarnesenes.
    Materialart: Digitale Medien
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  • 186
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Die Oxydation α, β-ungesättigter Aldehyde mit Peroxoessigsäure in Eisessig wurde untersucht.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
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  • 187
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 49 (1966), S. 1283-1290 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Das aus Kulturen von Endothia parasitica (MURR.) AND. isolierte, optisch aktive Welketoxin Diaporthin C13H14O5 gab mit Alkali Acetaldehyd und optisch inaktive Diaporthinsäure. deren Bruttoformel auf C11H12O5 berichtigt wurde. Die Interpretation der NMR.-Spektren führte zu den Strukturformeln von Diaporthin (I) und Diaporthinsäure (III), welche durch Synthese der letzteren bewiesen wurden.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 188
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 49 (1966), S. 1302-1318 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The essential characteristics of a simple, discontinuous model system for mass transfer between two phases are discussed. It is shown that for dyeing processes that conform to this model it is possible, with the aid of the methods of non-equilibrium thermodynamics, to give an unambiguous definition of the concepts «rate of dyeing» and «affinity of dyeing», at any stage of dyeing. It is clear from the derived phenomenological equations that dyeing systems rarely reach a true equilibrium state (i.e. a stationary state of zero order), but that in general an osmotic or a DONNAN equilibrium is attained.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 189
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 49 (1966), S. 1330-1344 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The selective cleavage of the N-sulphenyl protecting group from amino-acids and peptides containing additional acid-labile protecting residues has been investigated. Among various nucleophilic reagents tested for their ability to effect rapid and specific removal of the N-sulphenyl groups, hydrogen cyanide, sulfurous acid and thioacetamide have been found to be particularly suitable. The application of this method to the solid phase synthesis of peptides is described and discussed.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 190
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 49 (1966), S. 1348-1354 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A new procedure for the resolution of DL-proline, DL-alanine and DL-isoleucine into the optical antipodes is outlined. It is based on the separation of diastereoisomeric salts of D- or L-tyrosine hydrazide with Z-DL-proline, Z-DL-alanine and Z-DL-isoleucine, by means of fractional crystallization in suitable solvents such as lower aliphatic alcohols and water. It is shown that the new method gives excellent yields even with half the molar amount of the optically active resolving agent.
    Materialart: Digitale Medien
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  • 191
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 15N-Tracer techniques have been employed to investigate the reactions of aryldiazonium ions with aryldiazosulphonates and with aryldiazotates (SUCKFÜLL-DITTMER azo syntheses), in which unsymmetrical azo compounds and o-hydroxyazo compounds respectively are formed as the main products, with concomitant elimination of molecular nitrogen.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 192
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 49 (1966), S. 1408-1415 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Die Einführung von Silylgruppen in prim. und sec. Amine, in Silylamine, Aminosilane sowie Silazane, kann durch katalytische Silylierung der entsprechenden Verbindungen mit Silanen erfolgen. Als Katalysator dienen die Alkalimetalle oder deren Hydride.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 193
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 49 (1966), S. 1475-1483 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Strongly radioactive digitoxin (6) could be isolated (without dilution) in crystalline form from young plants of Digitalis lanata after their inoculation with D-Glucose-[6-14C] using the wick method. Hydrolytic cleavage of this digitoxin gave digitoxigenin (11) and D-digitoxose (7), both being isolated in crystalline form (without dilution). The genin was found to be 4 times more active, pro mole, than the digitoxose. This can be best explained when one assumes that the plant converts 1 mole of D-glucose into 3 moles of acetic acid. After degradation of the digitoxose using NaJO4, acetaldehyde (as the crystalline p-nitrophenylhydrazone) and formic acid (as the Pb salt) could be isolated. The acetaldehyde carried 65% and the formic acid 8,45% of the activity of the digitoxose. This is compatible with the assumption that digitoxose is formed in the plant from D-glucose without re-arrangement of the carbon chain. The appreciable activity of the formic acid could be derived from the relatively large proportion of radioactivity lost (ca. 38,9%), partly in the form of C1-subunits, in the transformation of the intermediary lanosterol into digitoxigenin. This lost activity may be incorporated in unspecifically labelled D-glucose which then re-enters the biosynthetic pathway.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
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  • 194
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 49 (1966), S. 1489-1491 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: La sensibilité au choc d'un explosif chimique solide n'est pas, comme l'a pensé A. J. A. VAN DER WYK, déterminée par sa chaleur spécifique.
    Materialart: Digitale Medien
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  • 195
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 49 (1966), S. 1529-1542 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The structure and stereochemistry of some 11α- and 11β-hydroxy-9β, 10α(retro)-steroids of the androstane, pregnane and corticoid series, obtained microbiologically, has been elucidated.
    Materialart: Digitale Medien
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  • 196
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Stapelogenin, C21H30O4, shows a double bond and two hydroxyl groups which can be acetylated. On the grounds of UV.-, IR.-, and NMR-spectra as well as mass spectra, the probable structure is that of a 3β, 12β-dihydroxy-(18, 20β), (14β, 20α)-diepoxy-Δ5-pregnene (1). The exact position of the hydroxyl group, assumed to be 12β, is particularly unsure, as it could also be situated 11α- or 12α-position.
    Zusätzliches Material: 16 Ill.
    Materialart: Digitale Medien
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  • 197
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The seeds of Stapelia gigantea are very rich in ester glycosides (ca. 5,9%). Mild acid hydrolysis gave a mixture of sugars which, after paper chromatography and electrophoresis, was found to be probably composed of cymarose, oleandrose, digitoxose, arabino-2,6-dideoxyhexose (= canarose) and pachybiose. The mixture of the raw genins gave after alkaline hydrolysis a mixture of about nine deacyl genins (C, D, E, F1, F2, F3, G, H, J); the acids split off during hydrolysis were not identified. The nine deacyl genins are probably closely related pregnane derivatives. The main component (E), C21H30O4, was obtained in crystalline state, and was named stapelogenin. Its probable structure is reported in the following publication.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
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  • 198
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 49 (1966), S. 1543-1551 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Synthesis and properties of a number of 1-(3-halogeno-4-methoxy-phenyl)-1-hydroxy-2-amino-propanes, a group of new hypertensive substances, are described. One racemate has been resolved, and the optically active components have been correlated with a catecholamine of known absolute configuration.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 199
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The aminolysis of two penicillin-like compounds which cannot form penicillenic acid has been studied: 16-Aminopenicillanic acid (which is highly immunogenic) reacts directly with ε-amino groups at pH 7,4 under CO2-free conditions; the possible role of its polymerisation in this reaction remains to be studied.26-Dinitrophenylamino-penicillanic acid reacts with εamino groups at pH 7,4 as fast as benzylpenicillin and other penicillins. Its immunogenicity in the rabbit is similar to that of benzylpenicillin.
    Materialart: Digitale Medien
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  • 200
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Für den von HARINGTON synthetisierten (±)-β-Hydroxy-glutaminsäure-äthylester wird die erythro-Konfiguration bewiesen. Der daraus gewonnene (±)-3-Hydroxy-prolin-äthylester ist dementsprechend ein trans-Derivat.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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