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  • 1970-1974  (1,189)
  • 1930-1934
  • 1971  (1,189)
  • Organic Chemistry  (689)
  • Physics  (500)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 85-114 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements of the small-angle scattering power and the degree of crystallinity in melt-crystallized high-density polyethylene have been used to evaluate the “amorphous” density in situ by the relation, \documentclass{article}\pagestyle{empty}\begin{document}$ (2\pi/V)\int_0^\infty {S\tilde g} (S)dS = (\rho_{\rm c} - \rho_{\rm a})^2 \upsilon_{{\rm er}} (1 - \upsilon_{{\rm er}}) $\end{document} where V is the irradiated volume and ḡ(S) is the “slit-smeared” absolute intensity. The amorphous density is a function of sample history and is always higher than the extrapolated melt density. After slit-height correction, and within the experimental error, the ratio of the two observed long periods is 2:1 at all temperatures (25--126°C). The lamellar thickness and the average interlamellar spacing are obtained from the degree of crystallinity and the first corrected long period. At increasing temperatures between 25°C and 110°C, the lamellae become thinner while the interlamellar zone expands by almost half. Over this range the changes are reversible with temperature. Above 110°C, both the lamellae and the interlamellar region expand with temperature. The thickening is partially reversible upon recooling. Other results obtained include measurements of stacking disorder and of microstructural changes with crystallization temperature and with time at ambient temperature.
    Additional Material: 16 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 143-160 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Work on two sheet organosilicon polymers, one derived from the mineral chrysotile and the other from the mineral apophyllite, is described. This work provides direct evidence that both these polymers are composed of sheets. In addition, it shows that in the chrysotile-derived polymer the sheets curl into scrolls, and that in the apophyllite-derived polymer the sheets are essentially flat.
    Additional Material: 14 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 209-243 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The shear creep and creep recovery behavior of narrow molecular weight distribution polystyrene samples of low molecular weight, 1.1 × 103, 3.4 × 103, and 1.57 × 104 are reported as a function of temperature, near and above the glass temperature. Time-temperature equivalence for the total creep compliance is found to be nonapplicable, and in fact the steady-state recoverable compliance, Je, is a strong function of temperature. The time-scale shift factors for the recoverable compliance are analyzed in the light of free volume theory. Viscosity data are presented for samples with molecular weights between 1.1 × 103 and 6.0 × 105. The temperature dependence of the characteristic time constant ηJe can be explained in terms of free volume concepts whereas that of viscosity η cannot. Effects of residual molecular weight heterogeneity are demonstrated.
    Additional Material: 18 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 295-311 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A theoretical calculation of the Hv light-scattering patterns for deformed three-dimensional spherulites is presented. Affine deformation is assumed. The optic axis of the scattering element is allowed to lie at an arbitrary angle ß to the radius which is permitted to change in the course of the deformation in a manner that may depend upon the angular location in the spherulite. The consequences of twisting of the optic axis about the spherulite radius are also explored.
    Additional Material: 10 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 331-343 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The adsorption of polydimethylsiloxane polymers from solution on glass has been studied. The amount of polymer adsorbed depends markedly on the solvent because of specific solvent - surface interactions. The presence of silanol groups in the polymer, particularly as endgroups, markedly increases the amount of polymer adsorbed. Large differences are shown between the adsorption of the commercially available, and fully trimethylsilylated polydimethylsiloxanes of narrow molecular weight distribut on. Possible adsorption mechanisms are discussed.
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 383-384 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 421-430 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A method is given for the analysis of long-chain branching in polymers by using combined GPC and intrinsic viscosity measurements. A computer program was written to evaluate branching indices by a tabular, iterative method. The method was applied to the evaluation of long-chain branching in low-density polyethylene.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 431-435 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effects of stereoregularity on the low-temperature relaxation processes were studied by dynamic mechanical measurements on isotactic and syndiotactic polyisobutyl methacrylates (iso-PiBMA and syn-PiBMA). The α, β, and γ relaxation processes were observed in both stereoregular forms. Both the α, and β loss peaks were at lower temperatures for iso-PiBMA than for syn-PiBMA. The γ loss peak was observed at about -155°C at 30 Hz for both forms, and the apparent activation energy of this process was same for both samples within experimental error (6.7 ± 0.5 kcal/mole). It was reduced from these results that the α and β processes are both considerably influenced by the isotactic configuration but the γ process is not.
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 15-26 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The gelation reaction of acetoguanamine with formaldehyde was investigated in the light of the gelation theory for tetrafunctional amino resins described in the previous paper. The gel time and extents of reaction of formaldehyde, amino groups, and imino groups varied with the molar ratio in the feed, but values of K (the ratio of the rate constant for condensation to that for addition) and k (the ratio of the rate constant for addition of the imino group to that of the amino group) were nearly constant. When the catalyst concentration was increased, the gel time, extents of reaction of each functional group, and the values of K and k varied; in particular K increased markedly. From the results of varying the molar ratio and concentration of acidic catalyst, it was found that the number of methylol groups per molecule of acetoguanamine at the gel point was influenced by the reaction conditions but the number of methylene linkages per molecular of acetoguanamine was nearly constant at about 0.6, regardless of reaction conditions. The number-average molecular weights up to the gel point varied with the reaction conditions, but at the gel point they were all nearly constant at about 385.
    Additional Material: 10 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 543-555 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Photocurrents developed in polyethylene in the wavelength range 360-180 nm have been measured. The action spectra show features which can be related to the corresponding features in the absorption spectrum, and in addition there is electron injection from the metal electrode at a wavelength determined by the electrode material. The time dependence of the response indicates that a long-lived space charge is formed in the material.
    Additional Material: 6 Ill.
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  • 11
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 569-576 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Large photocurrents have been observed in films of some simple polymers (containing no π-orbitals), of which poly(vinyl fluoride) is a typical example. Not only are the currents large (up to 10-5 A/cm2) but also they are capable of being excited by light in the visible wavelength region where absorption by the polymer is too low to be detectable. The results indicate that the effects are electronic, rather than ionic, in nature.
    Additional Material: 4 Tab.
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  • 12
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 577-584 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It was previously shown that for a stationary random copolymer of A, B, and C, we have in general p(AB) + p(AC) = p(BA) + p(CA), etc., in place of p(AB) = p(BA) which is valid for a stationary binary copolymer. Here, p(AB) for example, is the probability that a randomly picked pair of consecutive comonomers in the polymer consists of an A followed by a B. For a stationary ternary copolymer produced by a first-order Markovian addition mechanism, we show that PABPBCPCA/PACPCBPBA = k, where k is a constant characteristic of a particular set of three monomers but independent of its composition. Here, PAB is the conditional probability of finding a monomer of B given that its immediate predecessor is an A. We further show that if the individual rate constants of the monomer additions involved take a special form such as used in the Alfrey-Price Q-e scheme, then we have k = 1 irrespective of the kinds of monomers, and in addition we have p(AB) = p(BA), p(AC) = p(CA), etc. Thus, although these latter results were previously proposed by Ham as an alternative basis to supplant the Q-e scheme, they may rather be regarded as mathematical consequences of special assumptions adopted for the form of the individual rate constants. For a stationary random copolymer of four components A, B, C, and D, we have p(AB) + p(AC) + p(AD) = p(BA) + p(CA) + p(DA), etc., in general. For a first-order Markovian four-component copolymer, we show that there are seven different combinations of the conditional probabilities that are constants (k1, k2,…, k1) independent of the monomer composition. Again, if we assume the same special form for the rate constants involved, we find that all the seven constants k1, k2, …, k7 reduce to unity and p(XY) = p(YX) for X,Y, = A, B, C, D.
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  • 13
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 717-729 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Several copolymers as well as homopolymers of vinylidene chloride and vinyl chloride have been examined by Raman spectroscopy. Probabilities of concentrations of monomer sequences have been calculated from known reactivity ratios. Surface scattering intensities at some frequencies were found to be linearly proportional to specific microstructure concentrations. Normalization of scattering intensities was accomplished using the intensity of the CH2 asymmetric stretching mode at 2926 cm-1, which is common to all samples examined. Good correlation was found for the concentrations of comonomer sequences {B}, {BB}, {BBB}, {AA} and {AAAA} in which A denotes vinylidene chloride and B vinyl chloride.
    Additional Material: 16 Ill.
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  • 14
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 99-107 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polarography of Nickel (II) in the presence of DL-tryptophan has been studied in KNO3 supporting electrolyte. Nickel yields two irreversible steps which are due to the formation of two varieties of complex in sluggish equilibrium with each other. The reduction is an irreversible, kinetically controlled process as evidenced from cyclic voltammetry and i-t curves. Rate constants of the processes are evaluated. The effect of temperature is described.
    Additional Material: 4 Ill.
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  • 15
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 108-114 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch potentiometrische bzw. photometrische pH-Titration wurden Protonierungskonstanten von 1-substituierten Butandion-(2,3)monoximen (1 und 2) und -dioximen (3) bestimmt. Die zu den Monoximen 1 und 2 gehörigen Anionen sind mesomeriestabilisiert. Bei den quaternären Ammoniumkationen 1a, 1b, 1d und 2g wird daher in erster Stufe die Oxim-, in zweiter Stufe die Ammoniumgruppierung deprotoniert. Für die lg cK11 bzw. lg cK12 der Verbindungen 1 und 2 besteht eine lineare Freie-Energie-Polare-Energie-Beziehung. Von den verschiedenen Protonierungsstufen der Dioxime 3 existieren Tautomere. Die von den Amindioximen 3 d, 3e und 3 f abgeleiteten quaternären Ammoniumkationen können daher in erster Stufe sowohl ein Ammonium- als auch ein Oximproton abspalten, und sie unterscheiden sich damit charakteristisch von 1 a, 1 b, 1 d und 2 g.
    Additional Material: 1 Ill.
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  • 16
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aus 2-Desoxyribose bildet sich in saurem Medium 3-Acetylacrolein. Dieses reagiert mit 3,5-Dihydroxytoluol (Orcin) im Sinne einer aldolartigen Aldehyd-Phenol-Kondensation über eine zwischengeschaltete Oxydation zu einer Reihe violetter und blauer Farbstoffe. Die Hauptkomponenten wurden präparativ dünnschichtchromatographisch dargestellt und als 9-(2-Acetylvinyl)-dimethyl-hydroxy-3-isoxanthone 2 und 1-(Dimethyl-3-isoxanthonyl)-2-[(dimethyl-dihydroxy-9-methyl-xanthenyl)-9]-äthylene 4 charakterisiert. Die Bildung von 4 erfolgt aus 2 und Orcin. Die Farbstoffe haben den Charakter von Säure-Base-Indikatoren mit stark pH-abhängigen Elektronenspektren. Sie sind in protonisierter Form die Träger der Farbreaktion (2: λmax = 575 nm; 4: λmax = 595 nm).
    Additional Material: 8 Ill.
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 371-376 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The condensation of acetylacetone with anthranilic acid in presence of piperidine as the condensing agent gives acetylacetoneanthranilic acid SCHIFF'S base (H2AA) which forms complexes with Zinc (II) and Palladium (II). The dissociation constants of H2AA have been determined by interpolation at half n̄ values and also by algebraic method which give the values 4.85 and 8.25 at 30° ± 1 °C for the dissociation constants. The stability constants of Zinc (II) and Palladium (II) complexes have been determined adopting CALVIN and MELCHIOR'S extension of BJERRUM'S method and the values of log k1 are found to be 2.92 and 3.97 respectively at 30° ± 1 °C. In these complexes 1:1 metal-ligand stoichiometry is observed.
    Additional Material: 4 Ill.
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  • 18
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 411-421 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Russian Abstract.
    Abstract: It seems advisable to investigate polycondensation processes extended systematically from low to high conversion by carefully chosen model systems, considering the statistical data available on the processes themselves and the relationship between structure and properties of the resulting polymers. In a previous paper (Rev. Gén. Caoutchouc Plastiques, Éd. Plastiques, 4, (1967) 111) dealing with conventional crosslinking agents, the possibility was suggested to perform polycondensation processes approaching more closely the classical random distribution. This can be achieved with symmetrical monomers having functional groups well spaced out to avoid substitution effects and cyclisation. Cyclisation is also rendered more difficult by greater stiffness of the structure of the monomers. This paper shows by some examples that, in favourable cases, the deviation from the classical random distribution can be reduced to the limits of experimental error, thus enabling the physical properties to be compared with the results of comparatively simple model calculations.
    Notes: Es ist ratsam, Polykondensationsprozesse an äußerst sorgfältig gewählten Modellsystemen zu studieren, und zwar systematisch von niedrigeren nach höheren Umsätzen, und indem man die Kenntnis der Prozesse selbst, der resultierenden Struktur der Produkte, und deren strukturgebundenen physikalischen Eigenschaften gleichzeitig auf statistischer Basis vertieft. In einem früheren Bericht (Rev. Gén. Caoutchouc Plastiques, Éd. Plastiques, 4, 1967, 111) über bekannte organische und anorganische Netzformer wurde auf die Möglichkeit hingewiesen, Polykondensationssysteme zu entwickeln, die den reinen klassischen Zufallsverteilungen in viel besserer Näherung folgen. Hierzu wählt man symmetrische Monomere mit räumlich weit auseinanderliegenden Funktionen, um Substitutionseffekte und Ringschlüsse weitgehend zu vermeiden; weiterhin werden Ringschlüsse auch durch Steifheit der Monomerstruktur sehr erschwert. In diesem Vortrag wird an einigen Beispielen belegt, daß man so tatsächlich die Abweichungen vom klassischen (cyclenfreien) Zufallsmodell in günstigen Fällen erwartungsgemäß bis zur Grenze der Unmeßbarkeit zurückdrängen kann, und daß sich das deshalb lohnt, weil man dann physikalische Eigenschaften der Produkte mit relativ einfachen Modellrechnungen vergleichen kann.
    Additional Material: 7 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 422-446 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Russian Abstract.
    Abstract: The non-equilibrium polycondensation is one of the processes developed in the efforts taken to discover new routes of syntheses in polymer chemistry. It applies to various routes of synthesis, such as polyrecombination, oxidative dehydropolycondensation, polycyclisation, polycondensation of dicarboxylic acids with diamines or bis-phenols and others.The characteristic features of the non-equilibrium polycondensation consist in the absence of reversible equilibrium reactions, high values of the equilibrium constants leading practically to the irreversibility of the process and, in contrast to equilibrium polycondensation, the possibility to prepare copolymers exclusively from monomers. In addition, it offers the essential advantages residing in the wider molecular weight distribution than that of polymers obtained by equilibrium polycondensation.The paper describes experimental results demonstrating the advantages of the non-equilibrium polycondensation. Various examples are presented that prove the non-equilibrium polycondensation a promising process for the synthesis of commercially valuable polymers.
    Notes: Die Entwicklung synthetischer Richtungen in der Polymerchemie führte zu einer Reihe neuer Syntheseverfahren, darunter auch der Nichtgleichgewichts-Polykondensation. Diese umfaßt die Polyrekombination, die oxydative Dehydropolykondensation, die Polycyclisierung, die Polykondensation von Dicarbonsäurechloriden mit Diaminen oder Bisphenolen u. a.Die Merkmale der Nichtgleichgewichts-Polykondensation sind: Fehlen reversibler Reaktionen während der Synthese; hohe Werte der Gleichgewichtskonstante und damit eine Nichtumkehrbarkeit des Prozesses sowie die Möglichkeit, im Gegensatz zur Gleichgewichts-Polykondensation Copolymere nur aus Monomeren zu erhalten.Ein wesentlicher Unterschied besteht auch in einer breiteren Verteilung der relativen Molekülmassen als bei Produkten, die durch Gleichgewichts-Polykondensation erhalten werden.Im Vortrag werden experimentelle Befunde mitgeteilt, die die genannten Besonderheiten der Nichtgleichgewichts-Polykondensation anschaulich illustrieren. An einer Reihe von Beispielen wird gezeigt, daß die Nichtgleichgewichts-Polykondensation ein aussichtsreiches Verfahren von praktisch wertvollen Polymeren ist.
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  • 20
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    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 294-300 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,5-Diacyl-2-alkyl-diaminoguanidine 1 cyclisieren unter Wasserabspaltung zu 3-(Nα-Alkyl-Nβ-acylhydrazino)-5-aryl-1,2,4-triazolen 3. Die Cyclisierung der 1-Acyl-2-alkyl-5-carbamoyldiaminoguanidine 2 führt zu 2-Alkyl-3-[semicarbazido-(1)]-5-aryl-1,2,4-triazolen 5. Aus 3 und 5 lassen sich durch Säurehydrolyse die entsprechenden Hydrazinotriazole 4 und 6 darstellen.
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  • 21
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    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 301-308 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Es wurden hochtemperaturbeständige Azopigmente auf der Basis von 3-Amino-phthalsäureimid hergestellt. Durch Einführung von Chlorsubstituenten konnte die Lichtechtheit günstig beeinflußt werden. Die Migrationsechtheit wurde durch Molekülverdopplung entscheidend verbessert.
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  • 22
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    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 385-386 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 23
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 447-460 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Russian Abstract.
    Abstract: The concept of tacticity, originally established for vinyl polymers, is shown to be valid also for condensation polymers if extended to include some particularities. From this point of view the preparation and properties of exclusively isotactic polyesters from lactic acid and substituted β-hydroxy propionic acid are described. Ditactic polyurethanes were prepared from tartaric acid esters. In contrast to tactic vinyl polymers, the condensation polymers obtained show optical activity.A special kind of steric regularity was found to be possible in polyesters and polyamides having built-in single bonds with hindered rotation. Thermal isomerisation of these polyesters may result in removal of their tacticity. The kinetics of this reaction were investigated.Cis-tacticity and trans-tacticity was observed to occur in condensation polymers having C=C or N=N double bonds in the backbone chain. The preparation of some of these polymers is reported, including experiments based on a photolytic polyreaction. The application of catalysts or light led to isomerisation at the double bonds.
    Notes: Der Begriff der Taktizität wurde ursprünglich nur für Vinylpolymere konzipiert; es wird gezeigt, daß er unter Berücksichtigung einiger Besonderheiten auch auf Polykondensate anwendbar ist. Unter diesem Gesichtspunkt werden Herstellung und Eigenschaften von rein isotaktischen Polyestern auf der Basis von Milchsäure und substituierten β-Hydroxypropionsäuren geschildert. Beispiele für ditaktische Polyurethane lassen sich von Weinsäure-Estern ableiten. Zum Unterschied von taktischen Vinylpolymeren sind diese genannten Polykondensate optisch aktiv.Eine besondere Art von sterischer Regelmäßigkeit ist bei Polyestern und Polyamiden durch den Einbau von drehungsbehinderten Einfachbindungen möglich. Bei diesen Polyestern kann die thermische Isomerisierung zum Verlust der Taktizität führen. Die Kinetik dieser Reaktion wird studiert.Cis-Taktizität oder trans-Taktizität kann bei Polykondensaten mit C=C- oder N=N- Doppelbindungen in der Hauptkette auftreten. Die Herstellung von einigen derartigen Polymeren wird beschrieben; unter anderem wird eine photolytische Polyreaktion erprobt. Durch Einwirkung von Katalysatoren oder Licht tritt Isomerisierung an den Doppelbindungen ein.
    Additional Material: 2 Ill.
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  • 24
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971) 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 25
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 561-568 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Herstellung von Estern aus Alkalisalzen verschiedener Carbonsäuren mit Alkylhalogeniden in Gegenwart von tertiären Aminen oder quartären Ammoniumsalzen wird am Modellbeispiel Natriumbenzoat/Benzylchlorid/Triäthylamin untersucht und die Abhängigkeit der Reaktion von verschiedenen Parametern bestimmt. Die Ergebnisse sind durch die Annahme einer zusätzlichen Reaktionsphase an der Festkörperoberfläche erklärbar. Als Katalysator wirkt das quartäre Ammoniumion, tertiäre Amine sind nur als Vorstufe anzusehen.
    Additional Material: 9 Ill.
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  • 26
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 594-601 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 4-Arylidene-2-phenyl-2-imidazolin-5-ones 1 react with Grignard reagents in a boiling ether-benzene mixture to yield 4-diarylmethyl derivatives 2 together with their oxidation products 3 and 4. The exocyclic double bond in 5 also undergoes addition reaction with the same reagents to yield 4-triarylmethyl derivatives 6. Alkylation of 2 affords the 4-alkylimidazolones 7 and 8.
    Additional Material: 3 Tab.
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  • 27
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 579-584 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Acidity constants of 3-, 4- and 5-chloro-o-toluidinium ions have been measured at 25° in aqueous dioxane media containing 20, 45, 70 and 72 wt.% of 1.4-dioxane by pH metry. The necessary correction factors to convert pH meter readings into stoichiometric pH have been evaluated. The relation between the strength of anilinium ions and various solvent properties has been discussed. A HAMMETT type relation has been developed for correlating the acid strength of these disubstituted anilinium ions with HAMMETT's structural parameters.
    Additional Material: 3 Ill.
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  • 28
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 642-645 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Phenylazocarbonamide liefern nach N-Chlorierung mit tert.-Butylhypochlorit in Chloroform in einer Fragmentierungsreaktion kristallines Phenyldiazoniumchlorid 4 in hoher Ausbeute. Auch N-Chlor-cyclohexyl-azocarbonamid ist fragmentierbar.
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  • 29
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 686-698 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Umsetzung von o-Xylylendihalogeniden mit Ammoniak und einigen seiner Derivate (Benzylamin, N,N-Diphenylhydrazin, Carbonsäurehydrazide, Harnstoff, Cyanamid) liefert Isoindolin 2, 2-substituierte Isoindolin- und o-Xylylendiaminderivate.Eine neue Methode zur Darstellung von 2 aus o-Xylylendihalogeniden und Cyanamid wird beschrieben.
    Additional Material: 6 Tab.
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  • 30
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 706-714 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Treatment of 4-arylazo-2-alkoxy-2-thiazolin-5-ones 4a-f with glycine or phenylhydrazine effects their conversion into 1-aryl-5-alkoxy-1 H-1,2,4-triazole-3-carboxylic acid derivatives 5a-j, with the loss of hydrogen sulfide. On the other hand, the reaction of the 2-ethoxy (4a-c) and the 2-isopropyloxy (4g-i) derivatives with strong basic amines involves the loss of an alkyl mercaptan to yield the N-substituted amines 7d-j of 1-aryl-Δ2-1,2,4-triazolin-5-one-3-carboxylic acids. The 2-benzyloxy derivatives 4d-f react with the same reagents to give the N-substituted amides 2a-g of 1-aryl-Δ2-1,2,4-triazolin-5-thione-3-carboxylic acids, with the loss of benzyl alcohol.Hetero-ring opening of 4, followed by recyclisation, occurs upon treatment with ethyl or phenyl magnesium halides to yield the triazolinethione derivatives 13 a-c.
    Additional Material: 2 Tab.
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  • 31
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 722-729 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Es wird über Versuche zur Synthese von 1,3-Oxathiolium-Salzen aus S-Ketomethylen sowie o-Hydroxyphenyl-thiolester-Derivaten berichtet. Die Salze bilden sich nur bei der Einwirkung von starken Mineralsäuren (HClO4) auf o-Hydroxyphenyl-thiolester bzw. auf ihre zugehörigen Ausgangsverbindungen, während unter gleichen Bedingungen die entsprechenden S-Ketomethylenderivate nicht reagieren. Diese cyclisieren dafür aber in Gegenwart überschüssiger Thiosäuren zu 1,3-Dithiolium-Salzen, deren Struktur, ebenso wie die der 1,3-Oxathiolium-Salze, an Hand analytischer und spektroskopischer Daten gesichert wurde.
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  • 32
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 754-762 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: IR-Spektren von höheren und verzweigten Trialkylcyanosilanen bestätigen, daß diese wie das Trimethyl- und Triäthylcyanosilan aus Gemischen der Normal- und Isoform bestehen. Die Alkylgruppen haben auf die Lage der CN- und NC-Schwingungsbanden und auf das Verhältnis von Normal-: Isoform keinen Einfluß. In Bis-[dialkyl(iso)cyano]-disiloxanen, die durch Jodieren der betreffenden Dihydrogendisiloxane und anschließende Umsetzung mit Silbercyanid hergestellt wurden, tritt die Isoform stärker hervor.
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  • 33
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 768-772 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Tab.
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  • 34
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Tab.
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  • 35
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 778-780 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 36
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 889-898 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Infrarotspektren von Butan-, Hexan,- Heptan-, Octan- und Decanarsonsäure sowie von Phenyl-, o-Methylphenyl-, p-Methylphenyl-, p-Äthylphenyl- und p-Diphenyl-arsonsäure werden im Bereich von 400-3500 cm-1 mitgeteilt und die Frequenzen zugeordnet. In den Spektren der Alkanarsonsäuren können im üblichen Erwartungsbereich keine As—C-Valenzschwingungen nachgewiesen werden. Die Bindung eines Phenylringes an den Arsonsäurerest macht die Spektren im Gebiet der AsO-Valenzfrequenzen unübersichtlich. Die Unterscheidung dieser Banden von den CH-out-of-plane-Schwingungen ist unsicher.
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  • 37
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 905-916 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Der elektronenstoßinduzierte Abbau von Trimethylphenoxysilanen (H3C)3Si—O—C6H4R (R = —H und —Cl, —Br, —CH3, —NH2, —NO2 jeweils in ortho-, meta-und para-Stellung) wird beschrieben. Die Hauptfragmentierunsreaktion besteht in der Abspaltung eines Methylradikals vom Molekülion. Für die Ausbeute dieser Reaktion ergibt sich eine HAMMETT-Korrelation. Der Ausdruck lg [(I(M-15)/IM)R(I(M-15)/IM)H] nimmt mit steigendem Wert für die σ-Konstante zu. Diese Abhängigkeit wird auf der Grundlage der Quasi-Gleichgewichts-Theorie der Massenspektren als Folge des Substituenteneinflusses auf die Geschwindigkeit der Spaltungsreaktion und den Anteil der Molekülionen, der die zum Ablauf der Reaktion erforderliche Aktivierungsenergie besitzt, interpretiert. Zur Diskussion dieses Substituenteneffektes werden die mit der Elektronenstoßmethode bestimmten Ionisationspotentiale und die Aktivierungsenergien für die Spaltungsreaktion M+ → (M-15)+ + ·CH3 herangezogen.
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  • 38
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 935-939 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bei Reaktion des L-α-Narcotins mit Bromcyan und nachfolgender Hydrolyse entsteht D-β-Narcotin, d.h. es tritt spezifische Inversion nur an C-1 ein. ROBINSON und Mitarbeiter hatten eine spezifische Inversion an C-9 mittels methanolischer Kalilauge verwirklicht. Durch Kombination beider Methoden lassen sich die vier Narcotin-Isomeren sowie die zwei Racemate herstellen.
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  • 39
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 969-976 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 3 (5)-Amino-pyrazol liefert mit 1,3-Dicarbonylverbindungen R1COCH2COR2 5, 7-disubstituierte Pyrazolo[1,5-a]pyrimidine. Wenn R1 ≠ R2, erhält man definierte Bicyclen über substituierte 5-Vinylamino-1-p-toluolsulfonyl-pyrazole, z.B. 15, die aus 5-Amino-1-p-toluolsulfonyl-pyrazol, R1COCH2COR2 und katalytischen Mengen Aminsalzen gewonnen werden. Bei der Methylierung von 7-Hydroxy-5-methyl-pyrazolo [1, 5-a]pyrimidin 11 werden 4, 5-Dimethyl-(20a) und 1, 5-Dimethyl-pyrazolo [1, 5-a]pyrimidin- (7) (21a) isoliert. Ein O-Alkyl-Derivat von 11 wird aus 7-Chlor-5-methyl-pyrazolo [1,5-a]pyrimidin und C3H7ONa gewonnen. Die Strukturen 15, 20a und 21a werden durch Diskussion von τ- und J-Werten (1H-NMR-Spektren) für die Pyrazol-Protonen festgelegt.
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  • 40
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971) 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 41
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 956-968 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Addition verschiedener elektrophiler Agenzien an ω-Methoxyolefine wurde untersucht, um Aufschluß über eine Methoxygruppenbeteiligung zu erhalten. Eine derartige Beteiligung konnte bei der Addition von Chlor und Brom an 5-Methoxypenten-(1) nachgewiesen werden; hier entstehen zu 10-15% die entsprechenden 2-Halogenmethyltetrahydrofurane, und zu 50-60% tritt Umlagerung unter Verschiebung der Methoxygruppe ein. Die Addition von Chlor oder Brom an 6-Methoxyhexen-(1) liefert zu 15-20% die entsprechenden 2-Halogenmethyltetrahydropyrane, eine Methoxylgruppenwanderung ist nicht nachweisbar. Die Reaktion von Chlor oder Brom mit 4-Methoxybuten-(1) und mit 7-Methoxyhepten-(1) liefert ausschließlich 1, 2-Additionsprodukte.Bei der Anlagerung von Chlor an Allyl-methyl-äther erhält man außer 73% 2,3-Dichlor-1-methoxypropan infolge nebenher ablaufender Dreikomponentenreaktionen 12% 1,2,3-Trichlorpropan, 7% 1,3-Dimethoxy-2-chlorpropan und 8% 1, 2-Dimethoxy-3-chlorpropan. Bei der Addition von 2,4-Dinitrophenylsulfenylchlorid und von Quecksilberacetat an ω-Methoxyolefine tritt weder Umlagerung noch Ringschluß ein. Mit 2, 4-Dinitrophenylsulfenylchlorid entstehen nebeneinander Markownikow- und anti-Markownikow-Produkte, der Anteil des Markownikow-Produktes steigt mit wachsender Kettenlänge vom Allyl-methyl-äther bis zum 7-Methoxyhepten-(1).
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  • 42
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 993-998 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The formation of ternary complexes of the type MAB (where M = Cu(II), Ni(II), Zn(II) or Cd(II); A = nitrilotriacetic acid and B = glycine, α-alanine or dl-aspartic acid) has been shown by potentiometric studies. The nature of titration curves indicates that the secondary ligand B is added stepwise to the initially formed metal nitrilotriacetates. The formation constants (log KMAB) and the free energies of formation (ΔF°) of the mixed complexes have been calculated at 25 ± 1 °C and m̈ = 0.10 (KNO3) at different pH values. The formation constants of the resulting 1:1:1 ternary complexes follow the order Cu(II) 〉 Ni(II) 〉 Zn(II) 〉 Cd(II).
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  • 43
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In conformity with the assumption that light fastness depends upon the electron density of the azo centre, it is now shown that condensation of the aldehyde function in p-aryl azo salicylaldehydes with hydroxylamine, semicarbazide, aniline, phenylhydrazine, 2,4-dinitrophenylhydrazine and ethylene diamine causes in most cases an increase in light fastness on nylon 6 as a result of the decreased electron attracting properties of the functions as compared with the aldehyde function. Aftertreatment of dyeings from arylazo salicylaldehydes or arylazo acetophenone with ethylene diamine causes a similar increase. Further confirmation of this observation is obtained in case of monoazo dyestuffs derived from salicylaldehyde and derivatives which contain the sulphonic acid group when applied as acid dyestuffs on Nylon 6. Application of the latter dyes on wool revealed an analogous tendency only in case of dyes derived from 2-naphthylamine-4, 8-disulphonic acid.
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  • 44
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 1051-1059 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Es werden die Elektronenanlagerungs-Massenspektren einer Reihe von 22,26-Epiminocholestanen verschiedenen Sättigungs- und Substitutionsgrades sowie unterschiedlicher Stereochemie an C-22 und C-25 vergleichend untersucht. Neben dem M-1-Peak wird als typischer Spaltprozeß bei dieser Verbindungsklasse Fragmentierung zwischen C-20 und C-22 beobachtet, die zu einem um 98 bzw. bei Acetylepiminocholestanen 140 Masseneinheiten unterhalb der Molmasse liegenden Peak führt. Eine Ausnahme bilden Δ22-ungesättigte Vertreter, bei denen eine solche Spaltung ausbleibt und die stattdessen einen charakteristischen, durch Ion-Molekül-Reaktion mit Sauerstoff resultierenden M + 14-Peak zeigen. Daneben tritt in allen Fällen Abspaltung von Wasser bzw. Acetyl auf.
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  • 45
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 1070-1080 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Am Beispiel einfacher Methylverbindungen CH3X wurden aus Eigenvektoren und Eigenwerten von Allvalenzelektronenrechnungen in CNDO/2-Näherung Größen berechnet, die der 13C—H-, der geminalen H—H-Kopplungskonstante bzw. der 13C-chemischen Verschiebung der Methylgruppen proportional sein sollen. Die theoretischen Größen werden mit den entsprechenden experimentellen Werten verglichen. Güte und Grenzen der Näherungsverfahren werden diskutiert.
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  • 46
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 1101-1109 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mit einem Allvalenzelektronen-SCF-Verfahren - der INDO-Methode - wird die Elektronenstruktur des Tri- und Pentamethincyanins untersucht. An ausgewählten Modellen wird für die möglichen geometrischen Anordnungen der Trimethincyanin-Einzelmoleküle in Doppelmolekülen die relative energetische Stabilität abgeschätzt. Die Berechnungen bestätigen die schon früher festgestellte starke Ladungsalternation und einen weitestgehenden Bindungsausgleich entlang der Polymethinkette. Die Elektronendichteverteilung wird duch die Zusammenlagerung von Trimethincyaninmolekülen zu Doppelmolekülen wenig verändert. Das Modell mit einer „mauerwerkartigen“ Anordnung erweist sich als das stabilste.
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  • 47
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 1118-1124 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Eine auf Acrylnitril und Hydrazin basierende Synthese von 3(5)-Hydroxy-pyrazol 5a durch Sulfinateliminierung aus 1-(p-Toluolsulfonyl)-pyrazolidon-(3) in nicht-wäßrigem Milieu wird beschrieben. Die Methylierung von 5a liefert Gemische von 5-Hydroxy-1-methyl-pyrazol 5b und 1,2-Dimethyl-pyrazolon-(3) 7. 5b wird chemisch eindeutig durch Sulfinateliminierung aus 2-Methyl-1-(p-toluolsulfonyl)-pyrazolidon-(3), 5-Hydroxy-1-cyclohexyl-pyrazol durch Dehydrieren von 2-Cyclohexyl-pyrazolidon-(3) gewonnen. Die Methylierung von 5a mit 2 Mol p-Toluolsulfonsäure-methylester in DMF liefert in guter Ausbeute 7, analog ergibt 3(5)-Hydroxy-5(3)-methyl-pyrazol 1,2,5-Trimethyl-pyrazolon-(3).
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  • 48
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 1125-1130 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Phenol und Anilin werden durch Rhodanamin 1 in para-Stellung rhodaniert, p-Toluidin in ortho-Stellung. Acetophenon ergibt unter Verbrauch von zwei Mol 1 2-Amino-4-phenyl-5-rhodano-thiazol 6. Von β-Dicarbonylverbindungen abgeleitete Enamine 7 a, b, c werden zu Rhodan-enaminen 8 a, b, c rhodaniert, aus denen leicht Amino-thiazole, das Dithiin 10 und das Thiazolon 11 erhalten werden können.
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  • 49
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 31-44 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Für die Synthese von heterologen Indanon-(2)-Derivaten werden eine Reihe von ortho-Bis-acetonitrilen und die entsprechenden Diessigsäuren und -ester, wie z. B. Pyrrol- und Thiophen-3, 4-bis-acetonitrile sowie-3,4-diessigsäureester dargestellt. Die DIECKMANN-Cyclisierung führt nur bei dem Thiophenderivat 8 in guter Ausbeute zum gewünschten Ketoester 18, dessen tautomere Formen NMR-spektroskopisch charakterisiert wurden. Aus 18 wird ein Thiophen-Analoges zum Indanon-(2) 19 in hoher Ausbeute erhalten. Dagegen ergibt die Pyrrolverbindung 12 bei gleicher Synthesenfolge nur Spuren des Heterologen 22. Das Ausbleiben des Ringschlusses beim Pyrrolabkömmling aus geometrischen Gründen wird als unwahrscheinlich angesehen.
    Additional Material: 1 Ill.
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  • 50
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bei der gemeinsamen Einwirkung von Phenolen und N-Methylanilin auf Arylcyanate katalysieren die Phenole die N-Methylanilin-Addition zu Isoharnstoffen und N-Methylanilin die Phenol-Addition zu Kohlensäure-diesterimiden. Die Reaktionen verlaufen über sechsgliedrige übergangszustände und sind durch stark negative Aktivierungsentropien (≈ -43 cal/Mol · grd) gekennzeichnet. Substituenteneffekte wirken sich unterschiedlich aus. Bei substituierten Arylcyanaten ist die Elektrophilie der OCN-Gruppe, bei substituierten Phenolen die Stärke der Assoziate maßgebend für die Reaktionsgeschwindigkeit. In den letzteren Fällen lassen sich daher die Additionsgeschwindigkeiten durch lineare Beziehungen der Form lg k = a · Δ\documentclass{article}\pagestyle{empty}\begin{document}$ \widetilde{v} $\end{document}OH - b beschreiben.
    Additional Material: 3 Ill.
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  • 51
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 115-128 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Pyrazolidon-(3) und dessen C-Alkyl-Derivate werden am N-1 acetyliert und benzoyliert, Aus 1-Acyl-pyrazolidonen-(3) erhält man mit Dimethylsulfat in Wasser oder DMF 2-Methyl-1-acyl-pyrazolidone-(3), mit Benzylhalogeniden in Alkoholen oder Methyläthylketon 2-Benzyl-1-acyl-pyrazolidone-(3), dagegen mit Diäthylsulfat in Alkoholen, Methyläthylketon oder DMF das O-Äthyl-Derivat, z. B. 3-Äthoxy-1-benzyol-Δ-pyrazolin. Die N-2-substituierten 1-Acyl-pyrazolidone-(3) werden sauer zu 2-substituierten Pyrazolidonen-(3) hydrolysiert. Alle Strukturen sind durch kritische Diskussion des chemischen Verhaltens, der IR- und 1H-NMR. Spektren gesichert.Durch Cu-katalysierte saure Dehydrogenierung von 2-Methyl-pyrazolidon-(3) und von 2-Methyl-1-acetyl-pyrazolidon-(3) erhält man nahezu quantitativ 5-Hydroxy-1-methylpyrazol, entsprechend aus 2-Benzyl-pyrazolidon-(3) (8e) 5-Hydroxy-1-benzyl-pyrazol. Die Alkalispaltung von 8e liefert 1-(β-Carboxy-äthyl)-2-benzyl-hydrazin.
    Additional Material: 3 Tab.
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  • 52
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-Methyl-penten-(2)-al 1 erhält man durch Aldolkondensation von Propionaldehyd bei 150° an Calciumhydroxid in einer Ausbeute von 42%; bei 300° an 33 Gew.-% Kaliumhydroxid auf Bimsstein in einer Ausbeute von 57% d. Th.Die Kondensation von Propionaldehyd mit Formaldehyd bei 300% an Kaliumhydroxid bzw. Calciumhydrogenphosphat-Kontakten (optimale Katalysatorkonzentration: 10 Gew.-%) liefert 2-Methylacrolein 2 in Ausbeuten von 56-61% (berechnet auf eingesetzten Propionaldehyd).Das Temperaturoptimum beider Reaktionen wurde ermittelt.Der Vorteil dieser Verfahren liegt neben den guten Ausbeuten besonders bei den leicht und billig herzustellenden Katalysatoren. Die Zahl der Nebenprodukte ist gering.
    Additional Material: 2 Ill.
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  • 53
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 153-160 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Als Modellreaktionen zur Aufklärung der Kinetik und des Mechanismus der Oxydation tertiärer C—H-Bindungen durch Permanganat in alkalischen Lösungen wurde die Oxydation von Diphenylessigsäure untersucht. Es wurde gezeigt, daß bis zu Laugenkonzentrationen von etwa 1 m ein Mechanismus unter direktem oxydativen Angriff des Permanganats auf die tertiäre C—H-Bindung überwiegt und im geschwindigkeitsbestimmenden Schritt eine H—übertragung erfolgt. Die Geschwindigkeitskonstante beträgt 3,3 · 10-3 1 mol-1 s-1 bei 20°C und der kinetische Deuteriumisotopieeffekt 7,8.Mit steigender Laugenkonzentration wird in zunehmendem Maße ein radikalischer Mechanismus unter Beteiligung von OH-Radikalen wirksam. Dies drückt sich in einer charakteristischen Zunahme der Geschwindigkeitskonstanten mit steigender Laugenkonzentration sowie in einer Abnahme des kinetischen Isotopieeffektes aus.Es wird eine Variante zur kinetischen Analyse der beiden Mechanismen angegeben und die Geschwindigkeitskonstante für die Reaktion der OH-Radikale mit der tertiären C—H-Bindung zu 1,4 · 107 1 mol-1 s-1 bei 20°C bestimmt.
    Additional Material: 2 Ill.
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  • 54
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 229-235 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1-Alkyl-, 1-Cycloalkyl-, 1-Aralkyl-, 1-Aryl- und 1-Acyl-pyrazolidone-(3) liefern mit Formaldehyd und sekundären Aminen N-2-MANNICH-Derivate, deren Struktur durch kritische Diskussion ihrer 1H-NMR- und IR-Spektren festgelegt wird. Die hydrogenolytische Spaltung von 2-Morpholinomethyl-1-benzyloxycarbonyl-pyrazolidon-(3) 8c ergibt quantitativ 1-Benzyloxycarbonyl-pyrazolidon-(3) 6c.
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  • 55
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 205-210 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch Aminomethylierung von α,ω-Dinitroalkanen entstehen symmetrische Bis-MANNICH-Basen, die nach Überführung in ihre Dihydrochloride zu Dinitroalkadienen thermolysiert werden. Zur Struktursicherung dienen NMR-Spektren und die Addition von p-Toluidin.
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  • 56
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 218-228 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Über entsprechende Phosphorsäure-monoamid-dichloride 5 werden Triamide 8 mit zwei Äthyleniminresten und dem Rest eines hydrophoben Amins synthetisiert, wobei als letzteres neben Heptyl-, Dodecyl-, Cyclohexyl- und β-Phenyl-äthylamin ein antimitotisches α-Phenyl-β-(4-alkoxy-phenyl)-äthylamin (1f, 1g) dient. Eine Methode zur Darstellung von (+)- und (-)-[α-Phenyl-β-(4-äthoxyphenyl)-äthyl]-amid-phosphorsäure-dichlorid 5h und 5i wird angegeben.Aus Phosphoryl-N-Lost-dichlorid 6 wird das Dimorpholid 9k und Bis-(β-phenyl-äthyl)-amid 9e, aus Thiophosphoryl-N-Lost-dichlorid 7 eine Reihe von Thiophosphoryl-N-Lost-diamiden 10 b, 10 d-g, 10i gewonnen. Die Stereoisomerie bei der Kombination von Thiophosphoryl-N-Lost mit zwei Resten der antimitotischen Amine 1f, 1g wird diskutiert. Aus der Diskussion der Cl⊖-Abspaltung u.a. folgt, daß Phosphoryl-N-Lost-diamide des Typs 9k desaktivierte N-Lost-Derivate sind, Thiophosphoryl-N-Lost-diamide dagegen nicht.
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  • 57
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 259-264 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cyclohexyl- und Butyl-dichlorarsine RAsCl2 reagieren mit Natrium im Molverhältnis 1:2 zu den Cyclopolyarsinen (RAs)n. Während die n-Butyl- und Isobutyl-cyclopolyarsine als pentamere Verbindungen vorliegen, konnten im Falle der Cyclohexyl-, tert.-Butyl- und sek.-Butyl-cyclopolyarsine tetramere Strukturen nachgewiesen werden. Die Molekülgröße wurde durch kryoskopische Molmassebestimmungen und in einigen Fällen auch durch Massenspektren und Röntgenstrukturuntersuchungen ermittelt. Am Beispiel des Tetra-tert.-butyl-cyclotetraarsins wird das chemische Verhalten gegenüber Alkalimetallen, Halogenen und Methyljodid näher studiert.
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  • 58
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 277-286 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Acide Verbindungen werden durch Dimethylformamid-dimethylacetal entweder methyliert (Phthalimid, p-Toluolsulfonsäure-methylamid, Phenol, Benzoesäure, Dihexylphosphinsäure, Salzsäure) oder in Tetramethylammoniumsalze (Ditosylimid, 2,4,6-Trichlorphenol, Pikrinsäure, Trifluoressigsäure, Diphenylphosphinsäure) bzw. in Tetramethylformamidiniumsalze (p-Toluolsulfonsäure, Perchlorsäure) überführt. Entscheidend für den verschiedenartigen Ablauf der Reaktionen ist die Acidität der Ausgangsverbindung.
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  • 59
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 339-348 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Am Beispiel der p-Phenylendiamine wird gezeigt, daß mit dem einfachsten quantenchemischen Rechenverfahren, der HMO-Methode, eine Reihe photographischer Eigenschaften, wie Entwicklungsgeschwindigkeiten, Kupplungsgeschwindigkeiten u.a., in Abhängigkeit vom Substituenteneinfluß zufriedenstellend vorausgesagt werden können.
    Additional Material: 7 Tab.
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  • 60
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 331-338 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Es wurden die integralen Intensitäten charakteristischer Absorptionsbanden im Infrarotgebiet sowie die Dipolmomente einiger substituierter Arylchlorkohlensäureester bestimmt. Die Wurzel aus den integralen Intensitäten wurde mit den HAMMET-Konstanten σ in Beziehung gebracht. So konnte gezeigt werden, daß elektronenaffine Gruppen einen besonderen Einfluß auf die Elektronenstruktur der Chlorkohlensäuregruppe ausüben, der sich vor allem an der Aryl-Sauerstoffbindung bemerkbar macht. Der Einfluß auf die Carbonylgruppe und die Acyl-Sauerstoffbindung ist klein, während der auf die C—Cl-Bindung noch geringer ist.
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  • 61
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971) 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 62
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 357-370 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Zerfallsreaktionen der Tetraalkoxysilane Si[—O—(CH2)nCH3]4 (n = 0-4) und Si[—O—(CH2)nCH(CH3)2]4 (n = 0, 1, 2) bei Elektronenstoß in der Ionenquelle des Massenspektrometers werden wiedergegeben. Sie bestehen im Abbau der primär durch Fragmentierung aus dem Molekülionen gebildeten Ionen (Alkyl-O-)3Si+ und (Alkyl-O-)3Si—OCH2+. Diese Abbaureaktionen sind Folgen von Wasserstoffumlagerungen, in deren Verlauf Aldehyd- und Olefinabspaltungen miteinander konkurrieren. Im allgemeinen überwiegt die Olefinabspaltung. Die Besonderheiten dieser Reaktionen bei der Fragmentierung der verschiedenen Tetraalkoxysilane werden diskutiert.
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  • 63
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 377-384 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mit einer thermokinetischen Methode wurde an einer kontinuierlichen Strömungsapparatur die Kinetik der Cumolhydroperoxidzersetzung mit Schwefelsäure in einem äquimolaren Phenol-Aceton-Gemisch zwischen 40 und 60 °C untersucht. Außerdem wurde der Einfluß von Wasser und Acetophenon im gleichen Temperaturbereich kinetisch verfolgt. Weiterhin konnten die Aktivierungsparameter und die Reaktionsenthalpie ermittelt werden.
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  • 64
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 397-410 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Russian Abstract.
    Abstract: The paper presents the essential rules underlaying the polycondensation of the title components in organic solvents in the presence of tertiary amines on heating or at comparatively low temperatures. With hydrogen chloride resulting as a low molecular reaction product the condensation proceeds under non-equilibrium conditions. Conducting the condensation at higher temperatures, however, may be accompanied by destructive exchange reactions of the polymer with the starting material or between the polymer molecules themselves, affecting the molecular weight of the polymers obtained. Investigations of the kinetics of polycondensation of terephthalic acid with 9,9-bis-(4-hydrophenyl)-fluorene and 4,4′-(hexahydro-4,7-methyleneindan-5-ylidine)-diphenol at 150 to 200°C in a solvent with high boiling point showed the polyesterification to proceed by an anionic mechanism with formation of acylium ions at the start of and during the reaction.The polycondensation of dicarboxylic acid chlorides with bisphenols was found to depend largely on the components and composition of the initial mixture, temperature and other factors involved. Particularly, the kind of medium chosen for the polycondensation process reflects in the supramolekular structure and, thereby, in the physical properties of the polymer obtained.The results of experiments carried out to clarify the importance of tertiary amines in the polyesterification reaction in solvents at low temperature suggest two catalytic mechanisms, a nucleophilic and a general basic one.
    Notes: Im Vortrag werden die wichtigsten Gesetzmäßigkeiten der Polykondensation von Dicarbonsäurechloriden mit Bisphenolen in einem organischen Lösungsmittel unter Erwärmen oder bei relativ niedrigen Temperaturen in Gegenwart eines tertiären Amins betrachtet. Im Hinblick auf das niedermolekulare Reaktionsprodukt-Chlorwasserstoff-ist die Polykondensation dann ein Nichtgleichgewichtsprozeß. Wird sie jedoch bei höherer Temperatur durchgeführt, so können destruktive Austauschreaktionen des entstehenden Polykondensats mit den Ausgangsstoffen und zwischen den Makromolekülen auflaufen, wodurch die Molmassenverteilung der Polyarylate beeinflußt wird.Aus Untersuchungen zur Kinetik der Polykondensation von Terephthalsäurechlorid mit 9,9-Bis-(4-hydroxyphenyl)-fluoren und 5,5-Di-(4-hydroxyphenyl)-perhydro-4, 7-methylenindan in einem hochsiedenden Lösungsmittel bei 150 bis 300 °C geht hervor, daß die Polyveresterung nach einem ionischen Mechanismus unter Bildung von Acylium-Ionen verläuft.Von Bedeutung für die Polykondensation von Dicarbonsäurechloriden mit Bisphenolen sind: Verhältnis und Natur der Ausgangsstoffe; Reaktionstemperatur und Art des Mediums. Die Natur des Mediums beeinflußt die Ausbildung der übermolekularen Struktur des Polykondensats.Für die Polyveresterung durch tertiäre Amine bei niedrigen Temperaturen wird eine nucleophile Katalyse und eine allgemeine Basenkatalyse diskutiert.
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  • 65
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 387-396 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Russian Abstract.
    Abstract: The theory of Flory is extended to include the polycondensation in solution. The rate of the process is shown to be affected by the reactivity of the functional groups and their accessibility, considered to be the probability of interactions resulting in reactions. The accessibility depends strongly on the degree of coiling of the reactants.Calculations were performed to test the concept of the dependence of the polycondensation in solution on the chain length of the polymer and the nature of the solvent. The activation energy was found to increase with the degree of coiling of the reactants.The model reaction of 2, 2-bis-(p-hydroxyphenyl)propane with phenyl chloroformate and the polycondensation of 2,2-bis-(p-hydroxyphenyl)propane with its bis-chloroformate were investigated in the mixed solvents nitrobenzene/decaline and nitrobenzene/p-dichlorobenzene. With the first solvent the polarity and the dissolving quality decrease with increasing content of decaline. In the second mixture only the polarity changes with the content of dichlorobenzene.The rate of the model reaction is hardly affected by the composition of the solvent mixture.In the polymer system the rate is likewise hardly affected if only the polarity of the solvent mixture is changed. Lower dissolving quality caused differences of the kinetic constants ranging over one order. The results seem to support the theoretical considerations.
    Notes: Es wird eine Erweiterung der FLORYschen Theorie für Polykondensationsreaktionen in Lösung vorgeschlagen. Danach wird die Prozeßgeschwindigkeit vor allem von zwei Faktoren beeinflußt, von der Reaktivität der funktionellen Gruppen und von ihrer Akzessibilität - der Wahrscheinlichkeit einer zur Reaktion führenden Wechselwirkung. Die Akzessibilität ändert sich ihrerseits stark mit dem Knäuelungsgrad der Reaktanten.Zur Prüfung der Konzeption, daß die Kinetik von Lösungspolykondensationsreaktionen von der Kettenlänge der Makromoleküle und von der Natur des Lösungsmittels abhängt, wurden Berechnungen vorgenommen. Sie ergaben, daß die Aktivierungsenergie von Polykondensationsreaktionen in Lösung mit dem Knäuelungsgrad der Reaktanten zunimmt.Experimentell untersucht wurde die Modellreaktion von 2, 2-Bis-(p-hydroxyphenyl)propan und Chlorkohlensäurephenylester sowie die Polykondensation von 2, 2-Bis-(p-hydroxyphenyl)propan mit dessen Bis-chlorkohlensäureester in den Lösungsmittelgemischen Nitrobenzol/Dekalin und Nitrobenzol/p-Dichlorbenzol. Im erstgenannten System sinken Polarität und Lösungsmittelgüte für das Polymere mit steigendem Dekalingehalt. In der zweiten Mischung ändert sich mit dem Dichlorbenzolanteil nur die Polarität.Die Geschwindigkeit der Modellreaktion wird durch die Zusammensetzung des Lösungsmittels kaum beeinflußt.Beim makromolekularen System wird die Reaktionsgeschwindigkeit ebenfalls nur gegeringfügig beeinflußt, wenn man allein die Polarität des Lösungsmittelgemisches verändert. Bei Verringerung der Lösungsmittelgüte dagegen treten Unterschiede in den kinetischen Konstanten von einer Größenordnung auf. Diese Ergebnisse scheinen die Richtigkeit der theoretischen Erörterungen zu bestätigen.
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  • 66
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 461-483 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Russian Abstract.
    Abstract: Siloxane oligomers containing two hydroxyl, amino or anhydride groups were obtained by applying the reactions known to lead to Si—C bonds.Polycondensation of these monomers with suitable bifunctional reactants resulted in siloxane-modified polyesters, phenolformaldehyde resins, polyamides, polyestermides and polyimides the properties of which, such as softening point, solubility and thermostability were investigated. The siloxane containing polyimides proved to be soluble and melting polymers that resisted heating up to 400 degrees C in the presence of air oxygen.Polyimides of similar properties but being composed of different siliciumorganic units were obtained by polycondensation of an imide-containing bis-silanol with dichloro-Si compounds. This process eliminates the laborious preparations of siliciumorganic diamines.Condensation polymerisation of organic polymers with siliciumorganic polymers having one or two reactive functional groups in their molecules allow to prepare siloxane-modified block and graft polymers as well cross-linked products.
    Notes: Mit Hilfe der bekannten Reaktionen zur Knüpfung von Si—C-Bindungen haben wir oligomere Polysiloxane mit zwei Hydroxyl-, Amino- und Anhydridgruppen hergestellt:Durch Polykondensation dieser Monomeren mit geeigneten bifunktionellen Partnern wurde eine Reihe siloxanmodifizierter Polyester, Phenol-Formaldehydharze, Polyamide, Polyesterimide und Polyimide synthetisiert und einige ihrer Eigenschaften (z. B. Erweichungspunkt, Löslichkeit, Thermostabilität) untersucht. Die siloxanhaltigen Polyimide waren beispielsweise löslich, schmelzbar und in Gegenwart von Luftsauerstoff bis gegen 400 °C beständig.Polyimide mit ähnlichen Eigenschaften, aber verschiedenen siliciumorganischen Bauelementen waren durch Polykondensation eines imidhaltigen Bis-Silanols mit Dichlor-Si-Verbindungen zugänglich. Bei diesem Verfahren erübrigt sich die präparativ oft aufwendige Synthese der entsprechenden siliciumorganischen Diamine.Polykondensationsreaktionen von organischen mit siliciumorganischen Polymermolekülen, die eine oder zwei zur Reaktion miteinander befähigte funktionelle Endgruppen besitzen, ermöglichten den Aufbau von siloxanmodifizierten Block- und Pfropfcopolymeren sowie vernetzten Produkten.
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    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 529-545 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Russian Abstract.
    Abstract: Phosphorus-containing polymers are known to have valuable properties, primarily the ability of self-extinction. Most favorable results were obtained with substances including phosphorus and chlocrine in their molecules. However, up to now attention was given predominantly to polymers having C—O—P bonds.The present paper describes the synthesis of phosphorus and phosphorus and chlorine containing polymers with C—P bonds using methylol derivatives of phosphorus. Bis-(p-carbomethoxyphenoxymethyl) methylphosphinoxide was used as a phosphine oxide derivative. This phosphorus-containing dicarboxylic acid was reacted with glycols to give phosphorus-containing polyesters and copolyesters. With glycols in excess the reaction led to phosphorus-containing and mixed oligomers which after reaction with diisocyanates yielded polyurethanes, copolyurethanes and urethane block copolymers.Esterification of bis(hydroxymethyl)phosphonic acid with acrylic and methacrylic acid yielded monomers which, when subjected to polymerisation, gave phosphorus-containing polyesteracrylates and methacrylates and, in addition, could be copolymerised with acrylic and methacrylic acid.Mono- and dicondensation products of hypophosphorous acid with chloral, being considered as chlorine-containing methylol derivatives of phosphinic and phosphonic acids, led to polyurethanes.
    Notes: Bekanntlich neigen phosphorhaltige Polymere zum Selbstverlöschen. Die besten Ergebnisse wurden erzielt, wenn im Molekül gleichzeitig Phosphor und Chlor vorhanden sind. Meist wurde jedoch bis jetzt den phosphorhaltigen Polymeren mit C—O—P-Bindungen Aufmerksamkeit gewidmet.Von uns wurden Polymere mit C—P-Bindungen synthetisiert, die nur Phosphor oder gleichzeitig Phosphor und Chlor enthalten. Zu diesem Zweck wurden einige Methylolderivate des Phosphors herangezogen. Von Derivaten des Phosphintyps wurde Bis-(p-carbomethoxyphenoxymethyl)-methylphosphinoxid als phosphorhaltige Dicarbonsäure herangezogen. Durch Umsetzung dieser Säure mit Glykolen wurden phosphorhaltige Polyester und Copolyester dargestellt. Im Falle eines Überschusses der Glykole wurden auch phosphorhaltige und gemischte Oligomere erhalten, aus denen durch Reaktion mit Diisocyanaten Polyurethane, Copolyurethane und Blockpolyurethane synthetisiert werden konnten.Durch Veresterung von Bis-(hydroxymethyl)-phosphonsäure mit Acryl- und Methacrylsäure wurden polymerisierbare Monomere erhalten und dann in phosphorhaltige Polyesteracrylate und -methacrylate überführt sowie mit Acryl- und Methacrylsäure copolymerisiert.Mono- und Dikondensationsprodukte der hypophosphorigen Säure mit Chloral können als chlorhaltige Methylolderivate von Phosphin- und Phosphonsäuren aufgefaßt werden; sie wurden bei der Synthese von Polyurethanen verwendet.
    Additional Material: 11 Ill.
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  • 68
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 569-578 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polarographic behaviour of thio-acetic acid (RSH) at dropping mercury electrode (d.m.e.) has been investigated in presence of KNO3 in the pH range 2-10.5 at 30.0 ± 0.2°C in 50% alcoholic medium at 0.2 M ionic strength. Well defined anodic waves were obtained at all pH values in the concentration range studied. At pH 〈 2.2 and 〉 10.5 ill defined anodic waves were obtained. The effect of pH, concentration of RSH, temperature, drop time and alcohol on the wave characteristic and the mechanism of the reaction occurring at the surface of the mercury drop have been studied in detail. A small prewave was also observed at pH 9.1 and 10.5, which has been assigned adsorption characteristics. The reversibility of the reaction mechanism was confirmed by a number of methods. The wave is diffusion controlled and reversible involving one electron transfer process: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm RSH} + {\rm Hg}\rightleftharpoons{\rm RSH}g + {\rm H}^ + + {\rm e} $$\end{document}Mathematical and experimental evidence shows that the anodic wave of RSH at. d.m.e. does not correspond to formation of (RSSR) but to a mercury compound RSHg according to the above equation. The diffusion coefficient and temperature coefficient for (30-45°C) of id at pH 4.0 and 9.1 have been found to be 1.698; 1.965 × 10-6 cm2/sec and 1.08%; 1.20% per degree respectively. The dissociation constant pKa was found to be 4.25 by the plot of E1/2 vs. pH. The linearity of id with RSH concentrations provides a rapid and precise method for the determination of RSH down to 0.2 mM.
    Additional Material: 4 Ill.
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  • 69
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 614-625 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Titelverbindungen wurden NMR-, UV- und CD-spektroskopisch untersucht. An Hand der chemischen Verschiebung der Protonen des Zuckerrestes wurde für alle untersuchten N-β-D-Glucopyranoside eine anti-Konformation nachgewiesen. Das Vorzeichen der Cotton-Effekte der Glucopyranoside und Desoxyribofuranoside hängt außer von der Konfiguration wesentlich von der Struktur des Aglykons ab. Veränderungen in unmittelbarer Nähe des glykosidischen Stickstoffatoms (6-Azathymin- und Pyridazon-(3)-Derivate) führen zu einer Umkehr des Vorzeichens der Cotton-Effekte.
    Additional Material: 5 Ill.
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  • 70
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 602-606 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ausgehend von 2,4,6-Trichlor-5-methyl-pyrimidin läßt sich über 2,4,6-Trifluor-5-methyl-pyrimidin und 5-Methyl-2,4-dibenzyloxy-6-fluor-pyrimidin durch nachfolgende Abhydrierung der Benzylgruppen 6-Fluor-thymin in guter Ausbeute gewinnen. Die Verbindung ist im Gegensatz zu 6-Fluor-uracil in wäßriger Lösung stabil und daher als biologisch aktive Substanz einsetzbar. Mit NH3 oder Benzylamin reagiert 6-Fluor-thymin leicht zu 6-Amino- bzw. 6-Benzylamino-thymin.
    Additional Material: 1 Tab.
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  • 71
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 626-635 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch Umsetzung von Brenzcatechincarbonat 1 mit Alkoholen, Aminen und Hydrazinen werden Kohlensäureester, Urethane, Harnstoffe, Semicarbazide und Carbohydrazide hergestellt. Durch thermische Zersetzung von N-Alkyl-carbamidsäure-(2-hydroxyphenyl)-estern 6 werden Alkylisocyanate gewonnen.
    Additional Material: 8 Tab.
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  • 72
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 667-677 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In der Umsetzung von N-Acyl- und N-Äthoxycarbonyl-α-aminoketonen 1 mit Nitrosierungsmitteln wurde eine neue Methode zur Darstellung von 3-Acyl-1,2,4-oxadiazolen 3 gefunden. Als instabile Zwischenverbindungen sind die α-Hydroximinoderivate von 1, die C,N-Diacyl-formamidoxime bzw. C-Acyl-N-äthoxycarbonyl-formamidoxime 2, anzunehmen, welche vermutlich aus den primär gebildeten N-Nitrosoderivaten von 1 entstehen.
    Additional Material: 2 Tab.
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  • 73
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 3(1)H-Imidazo[4,5-h]chinoline sind interessante ampholytische Chelatbildner, da sie in koordinativ günstiger Position zu einer N-Donatorfunktion - auf Grund der Tautomerie dieser Verbindungen - eine acide NH-Gruppe enthalten. Durch Kondensation von 5, 7-Dinitro-8-amino-chinolin mit Carbonsäuren unter reduzierenden Bedingungen wurden verschiedene C-2-substituierte 3(1)H-Imidazo[4,5-h]chinoline erhalten, die in Abhängigkeit vom Carbonsäurerest C-5-amino- bzw. -hydroxysubstituiert sind. Die Kondensation von 5-Nitro-7,8-diamino-chinolin mit Carbonsäuren ergibt in Gegenwart von Polyphosphorsäure C-2-substituierte 5-Nitro-3(1)H-imidazo[4,5-h]chinoline. Die Konstitution der erhaltenen Verbindungen wird durch massenspektroskopische Untersuchungen bestätigt. An unterschiedlich 15N-markierten Verbindungen konnte der Fragmentierungsmechanismus verschiedener 3(1) H-Imidazo[4,5-h]chinoline aufgeklärt werden. Durch quantenchemische Berechnungen des 3(1)H-Imidazo[4, 5-h]chinolins und verschiedener Substitutionsprodukte konnten Hinweise über die Lage der Tautomeriegleichgewichte, die Säure-Base-Eigenschaften, das UV-Spektrum sowie über das reaktive Verhalten dieser Verbindungen erhalten werden.
    Additional Material: 13 Ill.
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  • 74
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 715-721 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Acetylation of 4-hydroxy-1-thiocoumarin 1 b in the presence of phosphorus oxychloride yields the 3-acetyl derivative 2, which condenses with aromatic aldehydes to give the corresponding 3-cinnamoyl derivatives 3 a-e, and yields 3-arylazo-4-hydroxy-1-thiocoumarins 4 a-d upon treatment with aromatic diazonium salts.Whereas treatment of 1 b with primary amines results in the formation of 4-substituted amino derivatives 5 a-c, 3-acetyl-4-hydroxy-1-thiocoumarin 2 reacts with the same reagents to yield the 3-α-alkyliminoethyl derivatives 7 a-c.Treatment of 1 b with phenylhydrazine affords the 4-phenylhydrazine derivative 5 d. On the other hand, 2 reacts with the same reagent to yield a mixture of the phenylhydrazone 9 and the pyrazolo-1-thiocoumarin 10.
    Additional Material: 1 Tab.
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  • 75
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 737-744 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch Umsetzung von Chinonen mit N,N-disubstituierten Aryl-thioamiden in Gegenwart saurer Kondensationsmittel wird ein neuer Typ farbiger heterocyclischer Verbindungen mit kondensiertem 1,3-Oxathiolium-System erhalten. Es wird über die optimalen Herstellungsbedingungen sowie über einige charakteristische Spektraldaten dieser Verbindungsklasse berichtet.
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  • 76
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 785-794 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The condensation of phenyl-, p-tolyl-, p-anisyl-, and p-chlorophenyl isopropyl ketones with dimethyl methylsuccinate in the presence of potassium t-butoxide, gave the crystalline (E)-4-aryl-3-methoxycarbonyl-2-methyl-4-isopropyl-but-3-enoic acidsi.e., Ar and COOCH3 in trans-position. The nomenclature of cis/trans isomers used herein follows the IUPAC 1968 Tentative Rules, Section E, Fundamental Stereochemistry, J. org. Chemistry 35, 2849 (1970). See also: J. E. BLACKWOOD, C. L. GLADYS, K. L. LOENING, A. E. PETRARCA and J. E. RUSH, J. Amer. chem. Soc. 90, 510 (1968); Introduction to Subject Index of Chem. Abstr. 66 (1963). 1 as major products. These esters resisted oxidation, and the position of the double bond was indicated by their infrared absorption, as well as that of some derived products. Their configuration followed from their conversion to the 4-acetoxy-2-naphthoates 2. The condensation also gave oily half-ester fractions which proved to contain small amounts of the (Z)-isomers 5 by their conversion (in low yields) to the oxoindenyl acids 6.
    Additional Material: 9 Tab.
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  • 77
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 811-816 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch radikalische Addition von N-Chlorurethan und N,N-Dichlorurethan an Cholesten-(2), Cholesterylacetat und Androstenolonacetat erhält man die entsprechenden vicinalen Chlorurethane, die mit Alkali zu Carbäthoxyaziridinen und Aziridinen umgesetzt werden.
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  • 78
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 849-854 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new method for preparing 2-mercaptoacetamide and N-alkyl-2-mercaptoacetamides has been described. Electronic spectra of sixteen N-alkyl and N-aryl-2-mercaptoacetamides have been compared with corresponding substituted acetamides and discussed. The results reveal the possibility of an intra-molecular hydrogen-bonding between —NH hydrogen and sulphur of —SH group.
    Additional Material: 3 Ill.
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  • 79
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 882-888 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Sowohl durch Umsetzung von α-Brommethyl- als auch von α,α-Dibrommethyl-aryl-ketonen mit Hydrazin lassen sich 1-Amino-4-aryl-1,2,3-triazole darstellen, deren reduktive Desaminierung 1-H-4-Aryl-1,2,3-triazole liefert.
    Additional Material: 2 Tab.
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  • 80
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 1065-1069 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Darstellung von 3-Alkyl-50-guanidino-1,2,4-oxadiazolen 1a-x aus Cyanguanidinen und aliphatischen Nitriloxiden wird beschrieben. Hydrolyse und Oxydation der erhaltenen Reaktionsprodukte werden untersucht.
    Additional Material: 1 Tab.
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  • 81
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Konfigurationszuordnung für die Sulfinylgruppe von Sulfoxiden S-alkylierter L-Cystein-Derivate kann, da in dieser Reihe ein Standard existiert, durch Vergleich der ORD- und CD-Spektren, aber auch durch Vergleich enzymkinetischer Daten erfolgen. Das Verhalten bei Ionenaustausch und Chromatographie läßt ebenfalls Schlüsse auf die Absolutkonfiguration am asymmetrischen Schwefelatom zu.
    Additional Material: 6 Ill.
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  • 82
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 1113-1117 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch Umsetzung von β-Chlorvinyl-methin-immoniumsalzen mit N, N-disubstituierten Thioacetamiden in Essigsäureanhydrid entstehen die neuartigen 2-Dialkylamino-thiapyryliumsalze 10. Diese reagieren mit CH-aciden Verbindungen zu substituierten 2-Methylen-2H-thiapyranen 11. Die UV-S-Absorptionen der Verbindungen 10 und 11 werden mitgeteilt.
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  • 83
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 1139-1142 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch Hydrierung von 3-Hydroxy-14β-Δ1.3.5(10).8-östratetraenon-(17) 1 werden ent-8α, 13α-Östron 2 und 8α, 14β-Östron 3 erhalten. Die Reaktion wurde sowohl mit optisch aktivem als auch mit racemischem Material durchgeführt.
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  • 84
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    Journal für Praktische Chemie/Chemiker-Zeitung 313 (1971), S. 1155-1172 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Das Reaktivitätsverhalten von 18 monosubstituierten Styrolen bei der radikalischen Copolymerisation mit Styrol wird im Rahmen der Näherungen von HÜCKEL und PARISER-PARR-POPLE MO-theoretisch untersucht. Die unter Zugrundelegung verschiedener Modelle errechneten Reaktivitätsindizes werden mit experimentellen r-Werten bzw. den daraus mittels des ALFREY-PRICE-Schemas errechneten Q- und e-Werten korreliert; die erhaltenen Korrelationen werden diskutiert.
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  • 85
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 755-758 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mass flux entering the Fick's diffusion equation is considered as an arbitrary analytical function of concentration, concentration gradient, and of the gradient of concentration gradient. The restrictions imposed on the flux by the principle of material objectivity are stated and briefly discussed.
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  • 86
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 759-762 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 87
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1287-1303 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The viscoelasticity and volume expansion of the raw polymerizate of ethylene-propylene copolymer with vinyl chloride grafts, and of the individual components has been studied. The raw polymerizate (composite) and the pure ethylene-propylene-vinyl chloride graft copolymer were found to consist of two phases. The pure graft copolymer has an ethylene-propylene matrix containing some fraction of poly(vinyl chloride) (PVC) grafts and a microphase with the remainder of the PVC grafts. The raw polymerizate consists of a PVC matrix plasticized with ethylene-propylene chains and a microphase of the ethylene-propylene copolymer. An attempt has been made to calculate the participation of components in microphases and the minimum dimension of the PVC microphase aggregates.
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  • 88
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1333-1339 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The lattice-theory equations for the surface tension of polymer solutions based on the parallel-layer model have been extended to include more than two components. The surface tensions of tetrachloroethylene solutions of some blended polydimethylsiloxane fluids have been measured at room temperature. The results are in nearly quantitative agreement with the theoretical calculations.
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  • 89
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1371-1378 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new relaxation process, explaining the change of elasticity in rubberlike polymers at critical stress (0.1-0.5 kgf/cm2) has been discovered. This process is characterized by the low value of activation energy (weak temperature dependence of relaxation times) and large sizes of kinetic units (strong dependence of relaxation time on stress). Critical stress depend on temperature and for rubberlike polymers turns to zero at 40°-60°C. Mechanism of the phenomena can be explained by the existence of the ordered molecular microregions, creating additional crosslinking points of nonchemical nature with free chains of the network, breaking up at critical stress. Observed phenomena is analogous to the process of forced rubber elasticity of those polymers in glassy state. Critical stress is analogous to the limit of forced rubber elasticity below glass transition temperature.
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  • 90
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1449-1469 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Wide-line NMR spectra have been obtained on an oriented sample of drawn nylon 66 fibers at temperatures between -196°C and 200°C and at alignment angles between the fiber axis and the magnetic field of 0°, 45°, and 90°. At -196°C, 20°C, and 180°C, the complete angle dependence of the NMR spectrum has been measured. The second moments of these spectra have been compared to theoretical second moments calculated for various models of chain segmental motion in an attempt to elucidate the mechanisms involved in the low-temperature segmental motion (γ process) and the high-temperature segmental motion (αc process). In agreement with earlier suggestions, the present results indicate that the γ process consists of segmental motion in noncrystalline regions. The overall decrease in second moment caused by the γ process is consistent with a model in which all noncrystalline segments rotate around axes nearly fixed in space. Furthermore, this decrease shows a pronounced dependence on the alignment angle. It is believed that this is due to tie molecules which become highly oriented along the fiber axis during drawing; their axes of rotation will therefore be nearly parallel to the fiber axis. The segments in noncrystalline entities such as chain folds and chain ends are less well oriented along the fiber axis and make an essentially isotropic contribution to the second moment decrease. The second moment at 180°C indicates the presence of considerable motion in the crystalline regions, and this motion is denoted the αc process. The second moment Sc of the crystalline regions is strongly dependent on the alignment angle, the predominant feature being a relatively high value of the second moment when the fiber axis is directed parallel to the magnetic field. This is in qualitative, but not quantitative, agreement with the motional model recently advanced by McMahon, which assumes full rotation of the chains around their axes. Excellent quantitative agreement with experiment has been obtained by superimposition of rotational oscillation around the chain axis of amplitude roughtly 50°, and torsion of the chains with neighboring CH2 groups oscillating around the C—C bond with a relative amplitude of about 40°. A model in which the chains perform rotational jumps of 60° between two equilibrium sites has also been considered (60° flip-flop motion). A distinction between this model and rotational oscillation has not been possible.
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  • 91
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1525-1529 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 6 Ill.
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  • 92
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1553-1577 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: As is well known, the chemical potentials of polymer and solvent in solution and, hence, the Flory-Huggins interaction parameter χ can be determined from scattered light intensities from dilute and concentrated solutions of the polymer in the solvent concerned. Preferably, measurements should be performed at temperatures as low as possible, provided the temperature exceeds the cloudpoint for the concentration used. It is shown that the lower the temperature and, consequently the higher the scattered light intensity, the better is the accuracy of the parameters obtained. At each temperature the scattered light intensity shows a maximum at some concentration. Below the theta temperature the ratio of scattered light intensity and concentrations also shows a maximum at some concentration. The values and the concentrations of these maxima for various temperatures enable the maximum of the spinodal to be determined. The spinodal itself can be determined by an extrapolation procedure of the reciprocal scattered light intensities. Measurements have been performed with three narrow-distribution polystyrene samples in cyclohexane. On the basis of the results, χ, and its dependence on concentration, temperature, and molecular weight can be determined to high accuracy.
    Additional Material: 13 Ill.
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  • 93
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1641-1655 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The morphology of high-density polyethylene crystallized under simultaneous pressure and shear in an Instron capillary viscometer has been examined by scanning electron microscopy, electron microscopy, and selected-area electron diffraction. Two distinct fibrous morphologies were observed in these unusually transparent strands. The outer sheath was composed of fibers, 3000 Å in diameter, aligned parallel to the extrusion direction and apparently interconnected by a lamellar cross texture. A highly crystalline ribbon texture composed of fine fibers, 200-250 Å in diameter, dominated the inner core. Sharp-spot electron diffraction patterns obtained from these central ribbons indicated a high degree of c-axis orientation parallel to the fibers and an extended-chain crystal structure. The melting behavior of both irradiated and unirradiated strands examined by differential scanning calorimetry was consistent with the formation of two distinct crystalline morphological units.
    Additional Material: 11 Ill.
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  • 94
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1681-1691 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of the nature of exchangeable cations on the tacticity of poly(methyl methacrylate) (PMMA) prepared from montmorillonite-MMA adsorption complexes was investigated. The strength of ion-dipole interactions was estimated either by the value of the electrostatic interaction potential or by the value of the carbonyl-stretching frequency shift. It was shown that Pi, the percentage of isotactic triads in the polymer, increases with increasing strength of the ion-dipole interactions, while the persistence ratio and the mean length of closed isotactic (or syndiotactic) sequences remain essentially unchanged regardless of the nature of the cation. It was shown that values of Pi may vary from 0.15 for weakly interacting ions to 0.5 for strongly interacting ones, reaching at the upper limit the value calculated from the model proposed in a previous paper, thus confirming its validity.
    Additional Material: 6 Ill.
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  • 95
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1693-1702 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Differential thermal analysis (DTA) of some commercial nylons has disclosed some anomalous phenomena with respect to the glass transition, generally considered to occur at 40-50°C. On the first heat cycle the transition occurs normally. On cooling, however, no corresponding transition occurs, and on an immediate rerun the transition has disappeared. If another DTA thermogram is made after a few hours, the transition begins to reappear, but at a temperature lower by a few degrees. After about five days rest, the transition is again normal in size and temperature. On annealing at 75°C, the 43°C transition is pushed up to about 92°C. On resting after annealing, transitions appear at both 40 and 92°C. These phenomena are explained in terms of the slow formation of a hydrogen-bonded network in the amorphous regions of the polymer. It is the disruption of this network that is normally considered to be the glass transition in nylons. The network is slow in re-forming because of problems involved in matching up potential hydrogen-bonding sites, which are, of course, distributed at intervals along the polymer chain. The temperature at which the network is disrupted is apparently dependent not so much on the ratio of bonding to nonbonding sites, as on the temperature at which it was formed.
    Additional Material: 6 Ill.
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  • 96
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1793-1805 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Detailed critical examinations of three aspects of nitric acid treatment of polyethylene are reported. (1) The endgroups introduced by the nitric acid are examined. It is concluded that in samples degraded to a single-crystal traverse stage, carboxyl features only as endgroup, and conversely each chain-end is terminated by such a group. Consequently, the carboxyl content can be used for quantitative characterization of the cut chain length. The function and position of the nitro group remains unexplained. (2) The morphological selectivity of the nitric acid-induced degradation is scrutinized. It is concluded that the crystal core is attacked and thinned by the acid; the slowing down of the reaction is principally due to accumulation of reaction products. Accordingly, the usual distinction between a vulnerable amorphous layer and a resistant crystal core is not justified on the basis of such degradation experiments. It follows that meaningful structural information is obtained only when the relevant crystal properties are studied as a function of chain cutting, assessed from the molecular weight distribution (GPC), as opposed to that of degradation time alone. (3) The role of sample consistency and reagent strength has been examined. It is demonstrated that for the reaction to be sufficiently uniform throughout the sample for the results to be meaningful, the reaction rate has to be slow compared to the rate at which the reagent diffuses into the specimen. To realize these conditions, finely dispersed samples and weak reagents were found to be favorable
    Additional Material: 7 Ill.
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  • 97
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1871-1885 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Several samples of a copolymer were examined by means of equilibrium centrifugation in a density gradient. The results for the samples without compositional distribution (homogeneous polymers) were used to determine the relation between the chemical composition and the distance from the center of rotation. For one of the homogeneous polymers a quantitative analysis of the schlieren curve was made in order to show the kind of accuracy that can be achieved. For the inhomogeneous polymer it was found that the schlieren curve could, in principle, be described quantitatively by the assumption that fluctuations in composition are independent of fluctuations in molecular weight, but on this basis the average square of the fluctuations in composition is more than four times smaller than the value derived from chromatographic data. A more satisfactory explanation of the experimental results is provided by assuming a linear correlation between average molecular weight and composition, but it is not claimed that this is necessarily the only model that explains the data.
    Additional Material: 3 Ill.
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  • 98
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1887-1905 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Time-dependent, apparent heat capacities of glucose, poly(vinyl chloride), polystyrene, selenium, poly(methyl methacrylate), and poly(2,6-dimethyl-1,4-phenylene ether) in the glass transition region were determined by differential thermal analysis. The thermal history was set by linear cooling at rates between 0.007 and 160°C/min. Linear heating for analysis was carried out at rates between 0.3 and 600°C/min. Average activation energies of 52, 81, 90, 54, 77, and 108 kcal/mole, respectively, were evaluated by using the hole theory of glasses previously developed. Within experimental limitations all data could be described quantitatively by the theoretical expressions using only one parameter, the number of frozen-in holes, to described the thermal history. Experimental and theoretical limitations are discussed.
    Additional Material: 10 Ill.
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  • 99
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1915-1918 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 100
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A mathematical development interrelating the orientation distribution functions of three kinds of orientation units for a polymer spherulite (i.e., a crystal lamella, a crystallite, and a given reciprocal lattice vector of the crystallite) is formulated on the basis of series expansions of the distribution functions in generalized spherical harmonies. Two types of uniaxial deformation models of a polyethylene spherulite, taking account of micronecking and untwisting of crystal lamellae, and of chain tilting and untwisting of crystal lamellae, respectively, both in addition to affine deformation of the lamellae are discussed. The models are tested by comparison of the theoretical orientation distribution functions of some reciprocal lattice vectors of the crystallite with the results of x-ray diffraction experiments.
    Additional Material: 13 Ill.
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