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  • 1
    ISSN: 0170-2041
    Keywords: Calculations, AM1 and INDO, S-CI ; Cyanomethylene compounds ; Pyrazolones ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: (Dicyanomethylene)pyrazolones 1a, b are treated with some indoles and pyrroles. The resulting disubstituted malono-nitriles 2a-f, 4a-e, 6 yield cyanomethylene compounds 3a-f, 5a-e, 7 by irreversible thermal or photochemical decomposition. The compounds exist in different isomeric forms. Structures are proven by NMR spectroscopy and X-ray analysis. UV-Vis data are discussed by means of AM1 and INDO/S-CI calculations.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die grenzflächenaktivitä wäßriger Lösungen von Melamin-Formaldehyd-Harzen wurde in verschiedenen Stufen der Harzynthese untersucht. Zur Bildung von Mikrokapseln geeignete, partiell methanolveretherte Melamin-Form-aldehyd-Harze sind reaktionsfähige grenzflächenaktive Verbindungen. Die Bildung der Kapselwände aus diesen Verbindungen ist eine Einkomponenten-Grenzflächenpolykondensation.
    Notes: The surface activity of aqueous solutions of melamine formaldehyde resins was investigated at different stages of the resin synthesis. Partially methanol etherigied melamine formaldehyde resins, which are able to form microcapsules, are reactive surface active compounds. The formation of capsuole walls with these resins proved to be a one-component interfacial polycondensation reaction.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Biomaterials 2 (1991), S. 37-40 
    ISSN: 1045-4861
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Previous studies have shown that synthetic calcium phosphate ceramics are biocompatible materials capable of providing scaffolding for new bone growth as well as osteogenesis. In particular, hydroxylapatite (HA) is less soluble than β-tricalcium phosphate (β-TCP) which has a higher degree of bioactivity. An implant made of dense hydroxylapatite shows substantially less bone growth than an implant made of a suitable HA/TCP ratio.1 Therefore, since biological response to the two materials is different, it is essential to have some means of determining the ratio of hydroxylapatite to β-tricalcium phosphate to ensure quality control of the synthetic ceramic as well as optimum biological response. In this study, a calibration curve was developed for x-ray diffractometer examination of mixtures of HA and β-TCP. The accuracy of using the diffractometer was compared to the accuracy of a powder camera, and it was determined that the diffractometer correctly identified the ratio within a range of 3% while the powder camera was accurate within a 20% range. This study showed that with an appropriate calibration curve, the HA/TCP ratio can be determined to a greater degree of accuracy using an x-ray diffractometer than by powder camera methods.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 123 (1990), S. 375-379 
    ISSN: 0009-2940
    Keywords: Cyclophanes / Hostguest chemistry / Macrocyclic compounds / Phanes / Supramolecular chemistry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New Watersoluble Macrobicyclic CavitiesThe watersoluble macrobicyclic compounds 1, 3, 5a, and 5b have been synthesized for the first time bearing large endolipophilic cavities of different sizes and shapes. They were studied with respect to their interactions towards lipophilic guest compounds. The “in/out” isomerism of the hitherto largest endolipophilic cavities 4a, 4b, 5a, and 5b has been investigated by 1H-, 13C-NMR spectroscopy and FAB mass spectrometry. The absence of significant 1H-NMR high-field shifts in hostguest studies is attributed to the rigidity of cavities 1 and 3, whilst the isomeric cavities 5a and 5b contain very large openings. Orientational fluorescence spectroscopy investigations, however, suggest hostguest interactions of the isomers 5a and 5b with ammonium 8-anilino-1-naphthalenesulfonate (8,1-ANS).
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 123 (1990), S. 859-867 
    ISSN: 0009-2940
    Keywords: Crown compounds / Host-guest chemistry / Macropentacyclic compounds / Phanes / Supramolecular chemistry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Pentamacrocyclic Tris-Crown Hosts. - Selective Binding of Cationic, Anionic, and Neutral Guest CompoundsThe tris-crown host compounds 1-4 were synthesized for the first time. The X-ray crystal structures of 2 and of the 1:3 complex of 1 and KSCN were determined. Whereas in the free crown 2 a less well preorganized molecular cavity is encountered, in the complex of 1 with KSCN one potassium ion is bound to each crown ether unit. One of the three SCN- anions is situated in the interior of the cavity and in addition is disordered in such a way as to be bound to the K+ using partially the S atom of the SCN- ion. Organic guest molecules like 1,2-, 1,3-, 1,5-, 2,6-, and 2,7-naphthalenediol as well as β-naphthol in acidic water solution are bound selectively in the interior of the cavities of the host molecules 2 and 3, but not by 1 and 4, the cavities of which seem to be too small and too large, respectively. In contrast, the binding of α-naphthol and of smaller phenolic guest molecules like phenol, resorcinol, pyrocatechol, phloroglucinol, pyrogallol, and 1,2,4-trihydroxy-benzene with the host 1-4 is much less pronounced (1H- NMR highfield shifts).
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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