ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

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

Proceed reservation?

Export
Filter
  • Chemistry  (2)
  • O-protonation  (1)
  • 1995-1999  (3)
  • 1990-1994
  • 1975-1979
  • 1965-1969
  • 1995  (3)
Collection
Publisher
Years
  • 1995-1999  (3)
  • 1990-1994
  • 1975-1979
  • 1965-1969
Year
  • 1
    ISSN: 1573-9171
    Keywords: nonamethylmetallocenecarbaldehydes ; iron ; ruthenium ; osmium ; molecular structure ; intramolecular hydrogen bond ; interionic hydrogen bond ; O-protonation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The products ofO-protonation of metallocenecarbaldehydes C5Me5MC5Me4CHO (M = Fe, Ru, Os) with HBF4 and CF3COOH were obtained for the first time, the adducts [C5Me5MC5Me4CH(OH)]+BF− being isolated in a pure state. The structures of the adducts depend on the nature of the metal and the anion and are governed by the correlation between their basicities. For example, the Fe-containing adducts have an open fulvenoid structure with an interionic hydrogen bond irrespective of the nature of the anion X (X = BF4 −, CF3COO−). In the case of the Ru- and Os-containing adducts in which the metal atoms are more basic than iron, the competition between the metal atom and the anion for the formation of a hydrogen bond with the OH group is clearly manifested in the IR and1H NMR spectra. In the presence of the weakly basic BF4 − anion, a cyclic structure with an intramolecular M...HO hydrogen bond is formed, while in the presence of a more basic F− or CF3COO− anion. it transforms to the open fulvenoid structure with an interionic hydrogen bond. The structures of the compounds obtained were determined by IR and1H NMR spectra, and the structure of the (C5Me5RuC5Me4CHOH)+...F− salt was proved by X-ray diffraction analysis.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1227-1234 
    ISSN: 0887-624X
    Keywords: polyanilines ; derivatives ; chemical synthesis ; oxidation state ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Syntheses of parent polyaniline and methyl, methoxy, and ethoxy ortho-substituted polyanilines were performed using the conventional chemical methodology and monitored using the new open-circuit-potential (Voc) profile technique. The intermediate pernigraniline oxidation state was identified and isolated at the Voc maximum (A) during the conventional chemical synthesis of poly(o-methoxyaniline) in the emeraldine oxidation state. The introduction of the substituent on the aniline ring leads to longer polymerization times and lower Voc values. Syntheses in the presence of two different monomers in solution were also investigated and showed preferential polymerization of the monomer with the lowest Voc potential. All polymers produced were characterized by elemental analysis, gel permeation chromatography, UV-VIS spectroscopy, and cyclic voltammetry. The influence of the substituent on the Voc profile and on the polymer characteristics are rationalized in terms of steric and electronic effects. © 1995 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 57 (1995), S. 751-765 
    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: The influence of fiber type and fiber-surface properties on matrix flow behavior was investigated using structural reaction injection-molding (SRIM). The influence of fiber type, fiber-surface properties, and matrix type on strength properties in elastomeric composites reinforced with nonwoven fibrous structures was investigated using tensile tests on elastomer composite samples from SRIM and latex coagulation (LC) fabrication methods and the microbond strength method on individual fibers. The fibers used were PET, LLDPE, and p-aramid. Fibers were treated with epoxy, styrene, and isocyanate derivatives, which make the surface chemically reactive. Treatments were also made with NaOH and a copolymer of polyester and polyol ether, causing a change in the fiber surface energy. The matrix types were polyurethane elastomer and natural rubber. The results show that the surface treatments which produced a change in the surface energy influenced the flow rate of the matrix polymer during the composite fabrication process. The treatments resulted in chemically reactive fiber surfaces which improved the fiber-matrix bond strength without affecting the Young's modulus of the composite material. Good correlation was found between bond strength and surface energy including the dispersive component of surface energy in the case of polyurethane elastomer and surface-modified PET fibers. The age of the polyurethane matrix has a marked influence on the bond strength. The fiber volume fraction in composites has a strong influence on the Young's modulus of the elastomer composite. © 1995 John Wiley & Sons, Inc.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...