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Mesogen ligand

In the above complexes, mesogens were formed by the complexation of mesogenic ligands to a metal centre. Using entirely different chemistry, Ghedini and co-workers had previously used the same approach in obtaining palladium complexes of... [Pg.292]

In the above section, we have established some simple ideas concerning the way in which a metal may influence liquid crystal properties when bound to mesogenic ligands. The behaviour may also be influenced by lateral substituents which may... [Pg.299]

In many cases the uncomplexed ligand also demonstrates mesogenic behaviour, but incorporation of a metal increases the phase transition temperatures over those of the mesogenic ligands. [Pg.218]

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. [Pg.366]

Compounds presented in Scheme 9 have provided evidence for the influence of the otherwise rarely investigated />-anilino-ethynyl group and a variety of auxiliary ligands on the luminescence, NLO, and mesogenic properties of this type of complexes.98... [Pg.260]

In a search for liquid crystalline phases, a series of (/>-alkoxy-phenyl)isocyanide complexes was prepared from (Me2S)AuCl and the corresponding ligands RNG, where R = C H2n + iO-C6H4 with n = 2-12 (in even numbers).206 The chlorides were converted into the bromides and iodides in metathesis reactions using KBr/KI. Mesogenic behavior was found for most of the new materials with transition temperatures in the range from ca. 95 to 160 °C. [Pg.281]

Similar work was carried out with ligands featuring different flexible or rigid spacers (X = -C(0)0-, -C=C-, -CH2-CH2-) and terminal alkoxy groups where n = 9-12. These compounds and the carbene complexes derived therefrom by addition of alcohols also show mesogenic properties (Scheme 49).211 212... [Pg.282]

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. [Pg.422]


See other pages where Mesogen ligand is mentioned: [Pg.422]    [Pg.350]    [Pg.371]    [Pg.399]    [Pg.99]    [Pg.80]    [Pg.131]    [Pg.145]    [Pg.228]    [Pg.427]    [Pg.399]    [Pg.55]    [Pg.83]    [Pg.282]    [Pg.2486]    [Pg.422]    [Pg.350]    [Pg.371]    [Pg.399]    [Pg.99]    [Pg.80]    [Pg.131]    [Pg.145]    [Pg.228]    [Pg.427]    [Pg.399]    [Pg.55]    [Pg.83]    [Pg.282]    [Pg.2486]    [Pg.361]    [Pg.363]    [Pg.372]    [Pg.411]    [Pg.582]    [Pg.259]    [Pg.281]    [Pg.52]    [Pg.428]    [Pg.161]    [Pg.406]    [Pg.408]    [Pg.409]    [Pg.413]    [Pg.413]    [Pg.414]    [Pg.414]    [Pg.414]    [Pg.418]    [Pg.419]    [Pg.421]    [Pg.422]    [Pg.423]    [Pg.425]    [Pg.426]    [Pg.426]   
See also in sourсe #XX -- [ Pg.408 , Pg.423 ]




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