Bibliothek

feed icon rss

Ihre E-Mail wurde erfolgreich gesendet. Bitte prüfen Sie Ihren Maileingang.

Leider ist ein Fehler beim E-Mail-Versand aufgetreten. Bitte versuchen Sie es erneut.

Vorgang fortführen?

Exportieren
Filter
  • Polymer and Materials Science  (152)
  • Inorganic Chemistry  (11)
  • 1
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 2811-2817 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: When hexaphenylcyclotrisilazane was heated above 450°C. at atmospheric pressure, it formed an infusible polymer of exceptional thermal and chemical stability. The polymerization, which was accompanied by elimination of benzene, is represented approximately by the equation: \documentclass{article}\pagestyle{empty}\begin{document}$\eta [({\rm C}_6 {\rm H}_5)_2 {\rm SiNH}]_3\,\, \to \,\,({\rm C}_6 {\rm H}_5 {\rm SiN})_{3n} + 3n{\rm C}_6 {\rm H}_6$\end{document} The infusible polymer was a foamed, vitreous, pale yellow solid with a high degree of stability to heat, acids, alkali, and organic solvents. A similar reaction occured with a resein that was obtained as a by-product in the preparation of hexaphenylcyclotrisilazane and with a mixture of silylamines that was obtained from the reaction of methylphenyldichlorosilane with ammonia. Coatings on aluminum and steel prepared by heating the silylamine polymers had good thermal stability and adhesion. Inclusion of a polymeric dimethylsilyl derivative of ethylenediamine improved the flexibility of the coatings.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 2
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 2773-2787 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Optically active β-(1,1-dichloroethyl)-β-propiolactone (CH3CCl2-PL), β-(1,1-dichloropropyl)-β-propiolactone (C2H5CCl2-PL), and β-(1,1-dichlorobutyl)-β-propiolactone (C3H7CCl2-PL) were synthesized with enantiomeric excesses of 100, 100, and 84%, respectively. Polymerization was conducted in bulk and toluene solution, under vacuum, using mainly ZnEt2/H2O as initiator. Osmometry analyses indicate molecular weights in the range 10,000-25,000. The polymers thus prepared are semi-crystalline and show large optical rotation values.13 C-NMR was used to show that they have a high degree of isotacticity, indicating that little or no racemization occurs in the course of polymerization. Glass transition, melting and decomposition temperatures are given as a function of the size of the substituent, and their variations are discussed.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 3
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 117-129 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The polymerization of three optically active β-1,1-dichloroalkyl β-propiolactones has been investigated in toluene, at 55°C, using aluminum triisopropoxide (Al(OiPr)3) as initiator in a range of monomer/initiator molar ratios smaller than 150. β-1,1-dichloroethyl β-propiolactone polymerizes according to a living mechanism. However, the ability to polymerize decreases with an increase in the length of the alkyl substituent. For instance, β-1,1-dichloro-n-propyl β-propiolactone is obtained only in low yields, whereas β-1,1-dichloro-n-butyl β-propiolactone does not polymerize at all. Actually, each of the lactones investigated reacts with Al(OiPr)3 in an initiation step that obeys a coordination-insertion mechanism. However, the size of the chloroalkyl substituent has a critical effect on the propagation: when the alkyl group contains more than two methylene units, the insertion of a second monomer becomes exceedingly slow.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 4
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: β-(trichloromethyl)-β-propiolactone (CCl3-PL), β-(trifluoromethyl,methyl)-β-propiolactone (CF3, Me-PL) and β-(trifluoromethyl,ethyl)-β-propiolactone (CF3,Et-PL) have been obtained by the reaction of ketene with chloral, 1,1,1-trifluoroacetone and 1,1,1-trifluorobutanone, respectively. Chiral catalysis lead to optically active monomers. The enantiomeric excess of the lactones has been measured by 1H-NMR spectroscopy, in the presence of 2,2,2-trifluoro-1-(9-anthryl)ethanol or an europium chiral shift reagent. Polymerizations have been carried out in bulk or in toluene, at 60°C or 80°C, using mainly organometallic initiators. The Polymers become insoluble and crystalline at enantiomeric excesses over 80% for CCl3-PL and 70% for CF3,Me-PL. Melting temperatures were recorded from 238 to 268°C for poly(CCl3-PL) and from 78 to 100°C for poly(CF3,Me-PL), depending upon the molecular weight and the enantiomeric excess. The 13C-NMR specroscopy of poly(CCL3-PL) indicates that the polymerization of the corresponding lactone leads to polymers of increasing degrees of isotacticity with the enantiomeric excess of the monomer.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 5
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 6
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1593-1607 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: R(+) and S(-) enantiomers of α-methyl β-propiolactone (MPL) have been synthesized from the corresponding α-methyl β-hydroxymethylpropionates and racemic MPL from methyl methacrylate. The optical purity and absolute configuration of these lactones were determined using 1H-NMR spectroscopy after complexation with a chiral compound: 2,2,2-trifluoro-1-(9-anthryl)-ethanol. Optical purities of 100% were obtained for both the S(-) ([α0]D25 = -10.4°, c = 1.3 g/dL in CHCl3) and the R(+) ([α0]D25 = +10.5°, c = 1.0 g/dL in CHCl3) enantiomers. The corresponding racemic and optically active polylactones [poly(MPL)] were prepared by anionic polymerization, in bulk and in solution, as well as poly(MPL)s of intermediate optical purities. The polymers thus obtained are optically active ([α0]D25 = 16.2° in CHCl3 for the optically pure polymer, S configuration) and exhibit significant differences. For example, the racemic poly(MPL) is soluble in several organic solvents such as tetrahydrofuran, benzene, CCl4, CH2Cl2, hexafluoroisopropanol, and CHCl3, whereas the optically active poly(MPL)s are soluble in CHCl3 and hexafluoroisopropanol only. Moreover, racemic poly(MPL) is amorphous whereas optically active poly(MPL)s are semicrystalline for optical purities larger than 51%. Melting temperatures and enthalpies of fusion of the semicrystalline polylactones vary with optical purity whereas glass transition temperatures remain invariant for all polymers, at about -28°C. The poly(MPL) of highest optical purity exhibits a melting temperature of 95°C and an enthalpy of fusion of 61 J/g.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 7
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 29 (1991), S. 555-570 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Modification of fluorine-containing polymers has recently received much attention due to new chemistries allowing for refunctionalization of these materials, especially their surfaces. In this article results are discussed which demonstrate various interesting modifications (including incorporations of —OH and oxygen comprised functionality) to expanded poly(tetrafluoroethylene) (ePTFE) surfaces. This is effected through the use of low damage, radio frequency glow discharge (RFGD) processes. The low damage conditions, which preserve the original pore structure/morphology of these RFGD treated materials, are supported by Scanning Electron Microscopy (SEM) while the resulting atomic and molecular effects are investigated through other surface analytical methodology. All materials reported in this investigation have been subjected to intensive structural analyses utilizing Electron Spectroscopy for Chemical Analysis (ESCA), Attenuated Total Reflectance Fourier Transform Infrared spectroscopy (ATR-FTIR), and wettability profiles obtained through contact angle measurements using a large series of liquids having varying surface tensions and surface reactive functionality. Through this multitechnique analysis of both expanded PTFE and poly(vinylidene fluoride) (PVDF) treated surfaces, a model is supported which illustrates surfaces possessing both high and low energy regions comprising both oxygen and fluorine functionality in close molecular proximity.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 8
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 29 (1991), S. 719-727 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The scope of polyformal formation from nitro- and fluorodiols has been explored further with a series of α, ω-diols. Polymers with M̄ns of 2000-4000 were generally obtained but M̄ns approaching 10,000 are possible in some cases. Effects of monomer structure and reaction parameters on polymer molecular weight are described. The polymers were characterized by GPC, 1H-NMR, and DSC analysis.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 9
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Recent work in our laboratories has fully characterized the surface region of a segmented poly(ether-urethane) (PEU) extending from the air/polymer interfacial region through bulk depths in the micron range. This characterization utilized energy and angle dependent Electron Spectroscopy for Chemical Analysis (ESCA), Attenuated Total Reflectance-Fourier Transform Infrared Spectroscopy (ATR-FTIR), and Comprehensive Wettability Profiling (contact angle using a homologous series of liquids) as defined by Zisman. In this study this same multi-analytical-technique approach is used to elucidate changes in these PEU surfaces induced through an H2O Radio Frequency Glow Discharge (RFGD) plasma. This investigation reports both qualitative and quantitative changes due to the modification treatments as well as the permanency of the changes effected on these surfaces through the plasma treatment. From our analyses, the amount of surface residing polyurethane (hard segment) is observed to increase due to a proposed plasma etching mechanism. Further, the addition of oxygen containing functionality is detected at the modified surfaces unique with respect to the unmodified PEU. These surface modifications which show large increases in wettability, are finally observed to be semi-permanent over a time period of 6 months.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 10
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The synthesis and optical resolution of α-phenyl β-amino-ethylpropionate led to the preparation of optically active α-phenyl β-propiolactones (PhPL) of different optical purities. The enantiomeric excess of PhPL was determined using 200 MHz 1H-NMR spectroscopy, after complexation with tris[3-(trifluoromethyl hydroxymethylene)-d-camphorato]europium III. It was then polymerized, in bulk and in solution, using a potassium acetate/crown ether complex as initiator. The optically active poly(PhPL)s thus obtained are insoluble in most organic solvents, whereas atactic poly(PhPL)s are soluble in CCl4, CHCl3, and dichloroethane. Several differences are observed between the physical properties of optically active and atactic poly(PhPL)s. However, atactic poly(PhPL)s are semi-crystalline polymers, similar to poly(α-disubstituted β-propiolactone)s, but in contrast with poly(α-methyl β-propiolactone). Melting (Tf) and glass transition temperatures, as well as enthalpy of fusion (ΔH), vary with the optical purity of the polymers. For example, atactic poly(PhPL) exhibits a Tf = 94°C and ΔH = 9 J/g as compared to Tf = 119°C and ΔH = 37 J/g for a poly(PhPL) having an enatiomeric excess of 50%.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
Schließen ⊗
Diese Webseite nutzt Cookies und das Analyse-Tool Matomo. Weitere Informationen finden Sie hier...