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Supramolecular sheet

Maji, S. K., Haidar, D., Drew, M. G. B., Banerjee, A., Das, A. K., and Banerjee, A. (2004). Self-assembly of /1-turn forming synthetic tripeptides into supramolecular //-sheets and amyloid-like fibrils in the solid state. Tetrahedron 60, 3251-3259. [Pg.211]

Keywords Hydrogen bonding Supramolecular chains Supramolecular sheets Coordination Guanidine... [Pg.40]

Figure 4.9. Schematic representations of the crystal structures of the salts of enantiopure 5 with / -substiluted 1-arylethylamines in success, (a) Less soluble salts, in which the formation of a stable supramolecular hydrogen-bond sheet, the realization of efficient CII—ti interaction, and the close packing of the sheets are achieved, (b) More soluble salts, in which efficient CH n interaction is not realized and the close packing of the supramolecular sheets a stable supramolecular hydrogen-bond sheet is not formed, (c) More soluble salts, in which a stable supramolecular hydrogen-bond sheet is formed and the close packing of the supramolecular sheets is achieved, while efficient interaction is not realized. Figure 4.9. Schematic representations of the crystal structures of the salts of enantiopure 5 with / -substiluted 1-arylethylamines in success, (a) Less soluble salts, in which the formation of a stable supramolecular hydrogen-bond sheet, the realization of efficient CII—ti interaction, and the close packing of the sheets are achieved, (b) More soluble salts, in which efficient CH n interaction is not realized and the close packing of the supramolecular sheets a stable supramolecular hydrogen-bond sheet is not formed, (c) More soluble salts, in which a stable supramolecular hydrogen-bond sheet is formed and the close packing of the supramolecular sheets is achieved, while efficient interaction is not realized.
Foggasy and co-workers. In many cases, the hydrogen-bond chains form a supramolecular sheet. Thus it is strongly suggested that the chiral discrimination of racemic amines by enantiopure 9 mainly occurs through the formation of a supramolecular hydrogen-bond sheet (chain) of (9-H), which interact with the amine to discriminate its chirality. [Pg.242]

As shown in Table 5.4, the resolution efficiencies for the p-substituted 1-phenyl-efhylamine derivatives were greatly improved, as was expected, when p-methyl-and p-methoxymandelic acids were used in the place of mandelic acid. These results strongly support our explanation that two factors, hydrogen-bonding interaction to form a supramolecular sheet consisting of 2i-columns and van der Waals interaction between the sheets, govern the stability of diastereomeric salts [11]. The same factors were also found in the diastereomeric salts of racemic arylalka-noic acids with enantiopure amino alcohols [12]. [Pg.137]


See other pages where Supramolecular sheet is mentioned: [Pg.129]    [Pg.211]    [Pg.212]    [Pg.214]    [Pg.215]    [Pg.216]    [Pg.217]    [Pg.217]    [Pg.219]    [Pg.220]    [Pg.88]    [Pg.135]    [Pg.136]    [Pg.136]    [Pg.137]    [Pg.138]    [Pg.138]    [Pg.139]    [Pg.504]    [Pg.504]    [Pg.457]   
See also in sourсe #XX -- [ Pg.137 ]




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