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  • 1
    Publication Date: 1938-09-01
    Print ISSN: 0002-7863
    Electronic ISSN: 1520-5126
    Topics: Chemistry and Pharmacology
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  • 2
    Publication Date: 1978-01-01
    Print ISSN: 0014-3057
    Electronic ISSN: 1873-1945
    Topics: Chemistry and Pharmacology , Physics
    Published by Elsevier
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  • 3
    Publication Date: 1939-08-01
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Published by Springer Nature
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 60 (1938), S. 2255-2262 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 144 (1939), S. 287-288 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] THE original solubility measurements on crystalline swine pepsin led to the conclusion that the crystals consisted of a single puro protein or several closely related proteins1. Since that time, it has become apparent in this and other laboratories2,5 that pepsins ...
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  • 6
    ISSN: 0025-116X
    Keywords: Chemistry ; 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
    Die Makromolekulare Chemie 177 (1976), S. 2069-2078 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die nomogene Lösungspolymerisation von Tritylmethacrylat in Hexamethylphosphortriamid (HMPT) mit 2,2′-Azodiisobutyronitril bei 60°C wurde untersucht. Die durch die NMR-Spektroskopie gefundene isotaktische Kettenstruktur war für dieses Polymer weniger bedeutend als bei dem im Fällungsmittel Benzol dargestellten Poly(tritylmethacrylat).Die Lösungseigenschaften von Poly(tritylmethacrylat) wurden in HMPT bei 25°C untersucht. Die Beziehungen zwischen der Grenzviskositätszahl, den Knäueldimensionen und dem Gewichtsmittel des Molekulargewichts wurden aufgestellt. Die ungestörte Dimension 〈r02〉1/2 wurde durch Viskositäts- und Lichtstreuungsmessungen mit Hilfe der Extrapolationen von Kurata-Stockmayer, Stockmayer-Fixman, Cowie, Inagaki-Kurata und Baumann bestimmt.Die Knäuelausdehnung in HMPT bei 25°C ist mittelgroß. Die Beziehung zwischen der Kettenbeweglichkeit und dem Molvolumen der Seitenkette zeigt, daß Poly(tritylmethacrylat)-wegen der Größe der Estergruppe und auch der starken Wechselwirkung zwischen den aromatischen Ringen-eine kleinere Kettenbeweglichkeit als die anderen Polymethacrylate hat.
    Notes: Trityl methacrylate was polymerized with 2,2′-azodiisobutyronitrile at 60°C in a homogeneous hexamethylphosphoric triamide (HMPT) solution. The isotactic microstrucutre found by NMR spectroscopy was less important for this polymer than for poly(trityl methacrylate) prepared in benzene, a precipitating medium.Some aspects of the hydrodynamic behaviour of poly(trityl methacrylate) were examined in HMPT at 25°C. Relations between the intrinsic viscosity, the root-mean-square end-to-end dimension, and the weight average molecular weight were established. The unperturbed dimension 〈r02〉1/2 was determined from viscosity and light scattering measurements using the well known extrapolation methods of Kurata-Stockmayer, Stockmayer-Fixman, Cowie, Inagaki-Kurata, and Baumann.Poly(trityl methacrylate) adopts a moderately expanded conformation in HMPT at 25°C. The correlation of the chain rigidity with the molar volume of the side group of polymethacrylic esters shows that poly(trityl methacrylate) has a higher chain rigidity than other polymethacrylates on account of the steric hindrance of the trityl group and of the strong interactions between the aromatic rings.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Lösungseigenschaften von Poly(5-p-menthylmethacrylate) und Poly(2-tert-butylphenylmethacrylat) werden nach verschiedenen Methoden in guten und idealen Lösungsmitteln bestimmt. Die Kettenbeweglichkeit wird mit Hilfe der umgestörten Dimension berechnet; σ ist 3, 1 für das Poly(5-p-menthylmethacrylat) und 2,6 für das Poly(2-tert-butylphenylmethacrylat). Diese Werte werden mit denen einiger anderer Polymethacrylate verglichen, die voluminöse Substituenten in der Kette besitzen. Der Einfluß einer großen Gruppe in der ortho-Stellung von Cyclohexyl- und Phenylringen wird auf Grund der sterischen Behinderung und der spezifischen Wechselwirkungen diskutiert.
    Notes: The solution properties of poly(5-p-menthyl methacrylate) and poly(2-tert-butylphenyl methacrylate) are determined by several methods in good and ideal solvents. The flexibilities σ calculated on the basis of the unperturbed dimensions are 3,1 and 2,6, resp. These values are compared with those found for other polymethacrylates with bulky substituents. The influence of a large group in ortho position at the cyclohexyl and the phenyl rings is discussed in terms of steric hindrance and specific interactions.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 149 (1971), S. 177-183 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Mikrotaktizität von radikalisch polymerisierten Polymethacrylaten, die in der Seitenkette des Monomeren immer größere Gruppen haben, wird durch die dochaufgelösten Kernresonanzspektren der entsprechenden Polymethylmethacrylate bestimmt.Die Syndiotaktizität vermindert sich schrittweise von Polymethylmethacrylat bis zu Polytriäthylmethylmethacrylat in der Reihe der gesättigten Polymeren. Die aromatischen Polymethacrylate haben eine geringere Syndiotaktizität als die entsprechenden gesättigten Polymeren. Polytritylmethacrylat stellt den Extremfall dar.Die Mikrotaktizität der Polymeren folgt sowohl aus der Größe und der Polarisierbarkeit der Estergruppe als auch aus der Wirkung, die die aromatischen Ringe aufeinander ausüben.
    Notes: The microtacticity of polymethacrylates prepared by radical initiated polymerization of monomers with side groups of increasing bulkiness is determined by high resolution nuclear magnetic resonance of the corresponding poly(methyl methacrylates).The syndiotacticity decreases systematically from poly(methyl methacrylate) to poly(triethylmethyl methacrylate) in the series of the saturated polymers.The aromatic polymethacrylates have a lower syndiotacticity than the corresponding saturated polymers and poly(trityl methacrylate) is the extreme case.The microtacticity of the polymers is undoubtedly determined by the bulkiness and the polarisability of the ester group as well as by specific interaction between the aromatic rings.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 9 (1971), S. 3595-3606 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetic behavior of the 60Co-initiated copolymerization at 25°C of styrene with vinyl acetate at 1100 and 2000 rad/hr was studied. As in the case of thermal and photochemical copolymerizations of these monomers, the growing chains are particularly rich in styrene units, and the overall rate is affected by a diluent effect due to the vinyl acetate monomer. However, in the case of the radiation copolymerization, this effect is partially counterbalanced by an increase of the initiation rate with the vinyl acetate concentration; the polymerization rate curve shows a maximum at a vinyl acetate molar fraction of 0.25. This effect is due to the very different free radical yields of these two monomers. The experimental results may be understood on the basis of a kinetic scheme which involves an energy transfer process from the excited vinyl acetate molecules to the styrene monomer and a termination reaction of the growing chains by very short styrene radicals when the mixture is rich in vinyl acetate.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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