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Cholesteryl substituted mesogens

Table 5.1-7 Cholesteryl (cholest-5-ene) substituted mesogens, cont. ... Table 5.1-7 Cholesteryl (cholest-5-ene) substituted mesogens, cont. ...
The hydrosilylation-allylation protocol is applicable to the syntheses of dendritic polyols . The hydroboration-oxidation of G0-G3 dendrimers prepared in accordance with the synthetic routes shown in Scheme 24 give the corresponding dendritic polyols, GO-OH-G3-OH, which are characterized by H NMR and MALDI-TOF analyses. Further modifications of the dendritic polyols with cholesteryl chloroformate yield unique dendrimers possessing 12, 36 and 108 cholesteryl units, providing the first examples of flexible dendrimers substituted with rigid mesogenic units that are expected to have unusual liquid crystalline properties . The second generation polyol dendrimer 264... [Pg.1758]

See other pages where Cholesteryl substituted mesogens is mentioned: [Pg.765]    [Pg.40]    [Pg.59]    [Pg.968]    [Pg.968]    [Pg.1758]    [Pg.44]    [Pg.870]    [Pg.839]    [Pg.526]    [Pg.528]    [Pg.26]   


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Cholesteryl

Mesogen

Mesogenicity

Mesogens

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