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  • Artikel: DFG Deutsche Nationallizenzen  (4)
  • Chemistry  (3)
  • ^1H NMR  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Amsterdam : Elsevier
    Phytochemistry 28 (1989), S. 3437-3442 
    ISSN: 0031-9422
    Schlagwort(e): Fagaceae ; MS. ; Quercus spicata ; ^1H NMR ; ^1^3C NMR ; hexacosanic acid ; lupeol ; pentacyclic triterpenes ; querspicatin A ; querspicatin B
    Quelle: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Thema: Biologie , Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 391-400 
    ISSN: 0887-624X
    Schlagwort(e): cardanol ; polyurethane ; thermoplastic polyurethane ; differential scanning calorimetry ; dynamic mechanical thermal analyzer ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A novel thermoplastic polyurethane was prepared from cardanol, a renewable resource and a waste of the cashew industry. Cardanol was recovered from cashew nut shell liquid (CNSL) by double vacuum distillation. It was characterized by CHN analysis and IR, 1H-NMR, and 13C-NMR spectroscopy techniques. Cardanol is a meta-substituted long chain phenol. The long aliphatic chain unit substituent was found to be a monoene. The monomer, 4-[(4-hydroxy-2-pentadecenylphenyl)diazenyl]phenol was prepared from cardanol. It was a dihydroxy compound as characterized by CHN analyzer, UV, and 1H-NMR spectroscopy. The polyurethane was synthesized from this dihydroxy compound by the treatment with 4,4′-diphenylmethane diisocyanate (MDI) in dimethylformamide (DMF) solvent at 80-90°C under nitrogen atmosphere. The polymer was characterized by 1H-NMR, FTIR, and UV spectroscopy. The elemental analysis was done for determining the percentage content of C, H, and N, and the intrinsic viscosity [η] of polymer showed 1.85 dL/gm. Thermogravimetric investigations (TGA) of the cardanol, the dihydroxy compound, and the polyurethane were performed to study their decomposition. The semicrystalline nature of the PU was confirmed by differential scanning calorimetry (DSC) and dynamic mechanical thermal analyzer (DMTA). The wide-angle X-ray diffraction (WAXS) study of PU shew a broad amorphous halo indicative of absence of crystallinity in the polymer, which has been explained as due to strong hydrogen bonding in the hard phase. PU may possibly be useful as a telecommunication and as a nonlinear optical material. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 391-400, 1998
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 3139-3144 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 425 (1976), S. 277-280 
    ISSN: 0044-2313
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Kinetik und Mechanismus der Reduktion von Kobalt(III)-Trisacetylacetonat durch Hydrazin in saurem MediumDie Kinetik der Reduktion von Kobalt(III)-Trisacetylacetonat durch Hydrazin in wäßrig-perchlorsaurer Lösung wurde unter unterschiedlichen Bedingungen untersucht.
    Notizen: The kinetics of reduction of tris(acetylacetonato)cobalt(III) by hydrazine in aqueous perchloric acid medium have been studied under different conditions. The complex Co(acac)3 and its protonated form Co(acac)2(acacH+) are both reduced by N2H4 with specific rate constants kR and kH,R respectively. These reactions occur concurrently with the self reduction of the complex in acid media having a specific rate constant kH. From detailed analysis of the effects of acid and hydrazine concentration on the rate, values of kH, kR and kH,R have been determined at 30°, 40° and 50°C at an ionic strength of 2 and from these the corresponding activation parameters ΔH≠ and ΔS≠ have been evaluated. The mechanism appears to involve the formation of intermediates in which N2H62+ is hydrogen bonded to Co(acac)3 and Co(acac)2(acacH+) respectively each of which possibly decomposes (rate determining) by H atom transfer from N2H62+ to the bound acetylacetonate ligand, leading to an electron transfer to cobalt(III) forming cobalt(II).
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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