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1,1 -Binaphthalene-2,2 -dicarboxylic acids

Kano has studied extensively the recognition of anions and zwitterions by both native and derivatized cyclodextrins [ 16]. The native (3-cyclodextrin com-plexation properties were examined with respect to binaphthyl derivatives. For both l,T-binaphthalene-2,2,-dicarboxylic acid and l,T-binaphthalene-2,2 -diol phosphate almost no chiral recognition was observed. The enantiomers of binaphthyl-2,2 -dicarboxylic acid were better distinguished using a per-O-methylated (3-cyclodextrin derivative in place of the native (3-cyclodextrin. [Pg.33]

Compounds with a zigzag structure along one axis can be obtained by the reaction of 2,2 -dihydroxy-l,l -binaphthalene-6,6 -dicarboxylic acid (6.51) with salts of manganese, copper, cobalt or cadmium. In these networks (6.52), hydrogen bonds between the ID zigzags play a fundamental role in the cohesion of the crystal. [Pg.207]


See other pages where 1,1 -Binaphthalene-2,2 -dicarboxylic acids is mentioned: [Pg.18]    [Pg.18]    [Pg.85]    [Pg.479]    [Pg.576]    [Pg.106]    [Pg.73]    [Pg.247]    [Pg.393]    [Pg.18]    [Pg.18]    [Pg.139]    [Pg.191]    [Pg.79]    [Pg.52]   
See also in sourсe #XX -- [ Pg.18 ]




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1,1 - binaphthalen

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