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  • Chirality  (2)
  • chiral solvating agents  (1)
  • 1
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 4 (1992), S. 43-49 
    ISSN: 0899-0042
    Schlagwort(e): chiral discrimination ; enantiomeric separation ; chiral solvating agents ; asymmetric synthesis ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1434-193X
    Schlagwort(e): Binaphthyls ; Chirality ; Circular dichroism ; Dendrimers ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: ---The absorption and CD spectra of a series of Fréchet (compounds 7-10) and backfolding (compounds 11-12) dendrimers derived from enantiopure (S)-2,2′-dihydroxy-1,1′-binaphthalene have been recorded (THF) in the range 200-350 nm. All the compounds examined show a positive couplet between 200 and 240 nm (1B transition of the 2-naphthol chromophore), the intensity of which (Δεmax of the low-energy branch) ranges between 100 and 40. By means of the DeVoe polarizability model the intensity of the 1B couplet has been calculated vs. the dihedral angle θ. This analysis provides θ angles of 95-110° for the Fréchet dendrimers and 100-110° for the backfolding compounds. These values clearly indicate that the torsional angle θ, defined by the two naphthalene planes, never exceeds the critical value of 110°. This investigation confirms the wide utility of CD spectroscopy to provide geometrical information that cannot be obtained by other types of structural analysis.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 2591-2597 
    ISSN: 1434-193X
    Schlagwort(e): Cascade molecules ; Dendrimers ; Chirality ; Amides ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The synthesis of the first and second generation of enantiopure dendrimers based on a chiral trans-3,4-dihydroxypyrrolidine is reported. Benzenepolycarboxylic acids were used as central nucleus to afford linear and radial growth, and terephthalic acid was used as spacer between the pyrrolidine nuclei. The analysis of the chiroptical properties ([α]D, circular dichroism) of these new dendrimers suggests that those with radial growth present a self organisation of chiral units.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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