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Crown-ether-isocyanide gold

As indicated above in chiral mesophases, the introduction of a functional group in mesogenic stmctures offers the opportunity to achieve functional LCs. With this aim, mesomorphic crown-ether-isocyanide-gold(I) complexes (26) have been prepared recently [38]. The derivatives with one alkoxy chain show monotropic SmC mesophases at or close to room temperature. In contrast, the complexes with three alkoxy chains behave as monotropic (n = 4) or enantiotropic (n > 4) LCs. The structure of the mesophases could not be fully eluddated because X-ray diffraction studies in the mesophase were unsuccessful and mesophase characterization was made only on the basis of polarized optical microscopy. These complexes are luminescent not only in the solid state and in solution, but also in the mesophase and in the isotropic liquid state at moderate temperatures. The emission spectra of 26a with n=12 were... [Pg.378]

Figure 2.40 Euminescent fluorinated crown-ether-isocyanide gold(I) metallo-mesogens... Figure 2.40 Euminescent fluorinated crown-ether-isocyanide gold(I) metallo-mesogens...
Arias, J., Bardaji, M. and Espinet, P. (2008) Luminescence and Mesogenic Properties in Crown-Ether-Isocyanide or Carbene Gold(I) Complexes Luminescence in Solution, in the Solid, in the Mesophase, and in the Isotropic Liquid State. Inorganic Chemistry, 47, 3559-3567. [Pg.394]

Espinet also investigated liquid crystalline gold complexes (Scheme 76) of crown ether isocyanides 139 [142],... [Pg.187]


See other pages where Crown-ether-isocyanide gold is mentioned: [Pg.90]    [Pg.90]   


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