Gold mesogens

Gold(III) usually displays a square planar geometry, typically observed in d8 metallic complexes such as palladium(II), platinum(II), rhodium(I) and iridium (I), for which an enormous number of liquid crystals have been described [3-5], mainly as orthometallated compounds. However, only a gold(III) metallomesogen has been published. Since the first gold mesogen was reported in 1986, many other compounds have been described. 

---

As we will see below, N, SmA and SmC are the most typical mesophases found for gold mesogens. 

There has been a series of previous reviews on metallomesogens [3, 4] and even a book [5]. There is a also specific review of gold mesogens, published in 1999 [6]. 

Figure 7.14 N, N-heterocyclic bis(carbene) gold mesogen and schematic representation of the bilayer. R = C H2 +i n = 12, 14, 16.

Most gold mesogens with perhaloaryl ligands as promesogen also contain isocyanide (mesogen or promesogen) ligands. Therefore, they were introduced in Section 7.2.5.3. 

Lateral monofluorination of the p-alkoxyphenyl isocyanide system [XAu (CNC6H40C H2 +i)] (X = C1, Br, I), in ortho-(3-F) (6a) and meta-(2-F) (6b) positions relative to the alkoxy chain was also studied [18]. None of the free fluorinated ligands is a LC, but their gold complexes display mesomorphic properties. This is a typical case of a promesogenic ligand which yields a mesogen upon coordination to a metal. 

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... 

The nematic nanoparticies have been prepared by a two step synthetic process. First, gold nanopartides are covered with an alkylthiol monolayer (hexyl- and dodecylthiol) in a second step, the alkylthiol-nanoparticles are reacted with the functionalized thiol mesogen in dichloromethane at room temperature to obtain the monolayer-protected liquid crystal gold nanopartides. These materials are chemically stable and display a nematic mesophase at room temperature [67, 68]. Other examples include liquid crystal gold nanopartides functionalized by hexaalkoxy-substituted triphenylene [69]. 

Several mixtures of hexanethiol capped gold nanopartides and triphenylene based discotic LCs have been studied. These mixtures display liquid crystal behavior (columnar mesophases) and an enhancement in the DC conductivity, due to the inclusion of gold nanoparticies into the matrix of the organic LC [70]. Other studies of mixtures of gold nanoparticies with mesogens indude a series of cholesteryl phenoxy alkanoates. The inclusion of the nanopartides does not change the inherent liquid crystal properties of the cholesteryl derivative but the mesophases are thermally stabilized [71]. 

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. 

Hie first helical SmC mesophase for a gold(I) mesogen has been prepared by means of complexation to an enantiomerically pure chiral isocyanide (Figure 7.32) [30]. This... 

---