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Triamide gelators

Novel triamide gelator 44 based on 4,4, 4"-triaminotriphenylamine and stearic acid was prepared by the group of Shirota [34]. Triaminotripheny-lamine was reacted with high-purity stearic acid in mesitylene at 164 °C for 8 h with constant removal of water (Scheme 10). [Pg.90]

Fig. 8 Triamide gelators based on l,3,5-benzenetricarbox)4ic acid and cis-1,3,5-cyclo-hexanetricarboxylic acid and proposed unidirectional hydrogen-bonded organization in the gels of 42 and 43... Fig. 8 Triamide gelators based on l,3,5-benzenetricarbox)4ic acid and cis-1,3,5-cyclo-hexanetricarboxylic acid and proposed unidirectional hydrogen-bonded organization in the gels of 42 and 43...
Scheme 10 Preparation of triamide gelator 44 (a) mesitylene, 165 C, 8 h, under nitrogen... Scheme 10 Preparation of triamide gelator 44 (a) mesitylene, 165 C, 8 h, under nitrogen...
Much more efficient triamide geiators were prepared from cis-1,3,5-cyclohexanetricarboxyhc acid and long-chain alkylamines (Fig. 8) [33]. Geiators 42 and 43 exhibited excellent gelation of various hpophihc solvents (hexane, cyclohexane, benzene, toluene, chlorobenzene, and pyridine) and also of kerosene. [Pg.90]


See other pages where Triamide gelators is mentioned: [Pg.77]    [Pg.93]    [Pg.77]    [Pg.93]    [Pg.91]    [Pg.241]   
See also in sourсe #XX -- [ Pg.83 , Pg.90 ]




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