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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 75 (1953), S. 3272-3273 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry 45 (1953), S. 2311-2317 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The first paper of the series contained the theoretical prediction that syndiotactic propagation could be favored over isotactic propagation in free radical polymerization by the nature of the monomer substituent group. To check this hypothesis the steric structure of polymers of vinyl acetate and certain haloacetates was investigated. X-ray examination of the polyvinyl esters and the solubility of derived alcohol polymers indicate that the degree of regularity increases in the order: acetate 〈 monochloroacetate 〈 polychloroacetates 〈 trifluoroacetate. The influence of the substituent group is limited in the polyvinyl esters because only the trifluoroacetate shows true crystallinity, and, even in this polymer, the average length of the regular sequences appears to be small. The above order of regularity suggests that the electrostatic factor is more important than the steric factor in the stereoregulated polymerization of vinyl esters. The regular sequences of the trifluoroacetate are indicated to have a syndiotactic configuration from the chain repeat distance. The polymerization of the ester is believed to involve predominantly syndiotactic propagation, with relatively frequent interruptions of isotactic propagation. The generalizations agree with results reported for other stereoregular radical polymerizations. Conceivably, syndiotactic propagation may be preferred for free radical polymerization in general, and polymers produced under radical conditions may be more regular than has been realized.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 3077-3086 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Stability of low molecular weight (D.P. 〈 300) polychloral has been found to be a function of the amine used as the polymerization initiator. The polymer produced with diethylamine unzips much more rapidly than that made with triethylamine. This investigation also showed that ester endcaps provide little protection from amine-induced depolymerization. The amine-initiated copolymer of chloral and dichloroacetaldehyde behaves anomalously in that it is unstable in the presence of normally inert organic solvents. Mechanisms are proposed to account for these observations.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 951-964 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A study was made of the effect of polymerization temperature on the syndiotacticity of polyvinyl formate. Vinyl formate was polymerized with ultraviolet light initiation in the temperature range from -20 to +30°C. The value of (Ep  -  Et)/2 obtained, 4.5 kcal./mole, is characteristic of those values obtained by other workers for the free radical-initiated polymerization of vinyl acetate. A linear relationship was found to exist between the viscosities of the polyvinyl formates and those of the derived polyvinyl alcohols. The degree of polymerization of polyvinyl formate may be calculated from the equation: [η] = 4.42 × 10-3 DP0.63. The low temperature polymerization of vinyl for- mate results in more syndiotactic polymer, as shown by x-ray diffraction. Polyvinyl for-mate obtained at more elevated polymerization temperatures did not demonstrate the same degree of order. No difference was found between the infrared spectra of the polyvinyl formates. The polyvinyl alcohol derived from polyvinyl formate polymerized at low temperatures (0 to -35°C.) exhibits water resistance and forms a colored iodine complex similar to that obtained with the syndioactic polyvinyl alcohol derived from polyvinyl trifluoroacetate. Conventional polyvinyl alcohol and that derived from polyvinyl acetate polymerized at -30°C. do not exhibit the same properties. Minor differences in the 1,2-glycol content in the various polyvinyl alcohols do not account for the differences in the observations. The amount of head-to-head addition in various vinyl aliphatic esters seems to be related to the inductive strength of the acid portion of the ester. No difference was found between the crystallinities of the various polyvinyl alcohols, as measured by film density. Heat treatment increases the crystallinities about the same amount, but the water resistance of the stereoregular materials remains higher. From the good correlation between the observations made on polyvinyl formate and the derived polyvinyl alcohol, it is concluded that syndiotactic polyvinyl formate, and hence syndiotactic polyvinyl alcohol, is obtained by the low temperature free radical-initiated polymerization of vinyl formate. Increased syndiotacticity is more readily obtained in polyvinyl formate than in polyvinyl acetate, indicating the greater influence of inductive effect compared with the steric effect in controlling stereoregularity during free-radical propagation.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Chloral was polymerized by means of cationic and anionic initiators and the products compared. Anionic catalysts readily produce high molecular weight polymer (DP ∼ 300-600), but a DP of only 200 could be produced with cationic catalysts. The anionic system apparently initiates and propagates polymerization much more readily than the cationic system. This effect is attributed to the inductive effects of the chlorine atoms on the chloral. Little difference was found when products of similar DP were compared as to x-ray diffraction pattern, infrared spectrum and tractability. This is believed due to the single type of structure which is sterically favored. Various cyclic compounds of chloral could not be made to undergo polymerization under cationic initiation. The conditions required to effect ring opening were too rigorous to enable polymerization to take place.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polychloral diol, unlike polyoxymethylene diol, is not readily capped in the presence of alkali catalysts. Polychloral is capped under acid conditions by acid anhydrides and chlorides and does not appear to undergo degradation during the process. Evidence for end-capping is provided by infrared analysis in the case of the low DP polychloral, metachloral. End-capped polychlorals possess good stability towards hot dimethylformamide and good stability at elevated temperatures (255°C.). From the melting points of copolymers, polychloral itself is estimated to have a melting point of about 460°C. The high melting point is consistent with the rigidity of the polymer chain. A means of estimating the DP of the polymer is proposed, based on a form of endgroup analysis. By this technique, metachloral is estimated to have a DP of about 50.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The copolymerization of chloral and dichloroacetaldehyde (DCA) has been studied with the use of organometallic compounds as initiators. The alkylzincs were the most effective catalysts, giving good conversions to copolymers of apparently high molecular weight. The polymerizations were best carried out at temperatures below -40°C. at an initiator concentration of at least 0.4 mmole/mole of monomers. The copolymerization proceeds to high conversions in toluene as the solvent, but the presence of small amounts of either n-heptane or tetrahydrofuran greatly decreases the yield. This, coupled with the fact that little polymerization occurs at DCA concentrations above 70 mole-%, leads to the proposal of a propagation reaction mechanism involving the coordination of the monomeric aldehydes with a cyclic zinc alkoxide dimer. Monomer reactivity ratios with chloral as M1 and DCA as M2 were r1 = 1.50 and r2 = 0.65. The copolymer is stiff and inelastic with a tensile strength of ca. 6000 psi.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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