Tesis doctorals> Departament de Química

Transfer of chirality in new supramolecular complexes as design principle for future asymmetric catalysts

  • Dades identificatives

    Identificador: TDX:955
    Autors:
    Degenbeck, Helmut
    Resum:
    During the course of the thesis libraries of chiral (1,2)-diamines and prochiral 2,2’-biphenol derivatives were synthesised. The transfer of chirality from the diamine to the biphenol moiety mediated either by hydrogen bonding or coordination to a metal centre (ZnII, CuII) was demonstrated by CD (circular dicroism). The behaviour in solution of the hydrogen bonded complexes was investigated by NMR spectroscopy, UV-vis and ITC titrations (determination of association constants. The determination of absolute configurations of the ZnII complexes was achieved by X-ray structure determination and CD analyses both on the experimental and theoretical level. Last but not least, a new potentially catalytic phosphane ligand was derived from a dynamically racemic 2,2’-biphenol derivative.
  • Altres:

    Data: 2011-07-25
    Departament/Institut: Departament de Química Analítica i Química Orgànica Universitat Rovira i Virgili.
    Idioma: eng
    Identificador: http://hdl.handle.net/10803/37353
    Font: TDX (Tesis Doctorals en Xarxa)
    Autor: Degenbeck, Helmut
    Director: Vidal Ferran, Anton
    Format: application/pdf 320 p.
    Editor: Universitat Rovira i Virgili
    Paraula Clau: Circular Dichroism Chiral Induction Supramlecular Chemistry
    Títol: Transfer of chirality in new supramolecular complexes as design principle for future asymmetric catalysts
    Matèria: 547 - Química orgànica 542 - Química pràctica de laboratori. Química preparativa i experimental 34 - Dret
  • Paraules clau:

    547 - Química orgànica
    542 - Química pràctica de laboratori. Química preparativa i experimental
    34 - Dret
  • Documents:

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