Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 192 (1991), S. 1399-1408 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Fluorescence emission of amorphous poly(ethylene terephthalate) films at wavelengths larger than that of the excimer emission was investigated. A film thickness dependence of the excitation spectra for 360 nm emission was observed. For thick films (e.g., 280 μm), their excitation spectra for 380-460 nm emission showed excitation peaks in the region of 320-360 nm, and the intensity ratio of the 370 nm emission (excited by 290 nm radiation) to the 390 nm emission (excited by 340 nm radiation) decreased with increasing thickness of the film. Apparently, the 370 nm emission (excimer) and the 380-460 nm emission originate from different species of the excited state. From the studies of model systems, dilute solutions of dimethyl terephthalate in CHCl3-acetone and dimethyl terephthalate-PMMA in CHCl3, it was found that the excitation at 340 nm is related to a \documentclass{article}\pagestyle{empty}\begin{document}$ \mathop \pi \limits^* $\end{document} ← n transition. Fluorescence emission from the S1 (n-\documentclass{article}\pagestyle{empty}\begin{document}$ \mathop \pi \limits^* $\end{document}) state and the interaction between the C=O group and the phenylene π-electrons results in the fluorescence in the 380-460 nm region.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Fluorescence spectroscopy in highly dilute solutions has been used to study the emission from naphthyl groups attached to poly(methyl methacrylate) molecules prepared by (i) free-radical polymerization, giving an essentially random distribution of naphthyl groups along the chain, and (ii) anionic polymerization, producing polymers with naphthyl groups in terminal units only. The influence of molecular architecture on the fluorescence is discussed. In particular it is shown that it is possible to incorporate one single naphthyl group at one end of a polymer chain but that attempts to introduce a controlled greater number lead to a product with a distribution of naphthyl-group constents.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 2045-2049 
    ISSN: 0887-624X
    Keywords: pyrolysis ; GC-mass spectrometry ; maleated polyethylene ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Pyrolysis-GC/mass spectrometry experiments reveal that naphthalene groups attached to maleated polyethylene as the 1-naphthylethyl ester are stable for relatively long periods of time at 170°C. Decomposition can be detected for samples heated for 2.0 min at 200°C, but even at that temperature, the extent of decomposition is very small. At higher temperatures, two of the decomposition products from the labeled polymer are readily understood: 1-vinylnaphthalene and 1-naphthylethanol can form by reactions that are well-precedented in the organic chemistry literature. At 200°C, only naphthalene is formed, which requires scission of the bond between the naphthyl ring and the C1 carbon of the ethyl group. We suggest two possible pathways for this reaction. © 1996 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 34:2045-2049, 1996
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 979-991 
    ISSN: 0887-6266
    Keywords: confocal fluorescence microscopy ; polymer blends ; polymer interfaces ; compatibilizers ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Binary blends of linear low density polyethylene (PE) and polypropylene (PP), and ternary blends of PE, PP, and EP copolymer (EPR) were prepared in a finely mixed state. In all blends the ratio of PP to PE was 85/15. In some of the blends, the PE component was labeled with a fluorescent dye; in other blends, the EPR component was labeled. These blends were investigated by laser scanning confocal fluorescence microscopy [LCFM] as a function of annealing time as well as EPR compatibilizer content. In this way we were able to follow the evolution of sample morphology and the location of the EPR in the blends. The presence of EPR in the blends retards the growth of droplets of the dispersed PE phase. When EPR was added in amounts up to 5 wt %, it tended to cover the PE droplets in patches rather than form a true core-shell structure. In the LCFM images, the EPR/PP interface appeared sharper than the EPR/PE interface. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 979-991, 1997
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...