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Secondary dialkylammonium

Self-assembly of secondary dialkylammonium ions with macrocyclic polyethers and formation of pseudorotaxanes 96CC1483. [Pg.269]

M. C. T. Fyfe, J. F. Stoddart, (Supra)molecular Systems Based on Crown Ethers and Secondary Dialkylammonium Ions , Adv. Supramol Chem 1998, 5,1-53. [Pg.220]

Pseudorotaxanes and Rotaxanes Incorporating Macrocyclic Polyethers and Secondary Dialkylammonium Salts as their Components... [Pg.146]

Complexes formed between secondary dialkylammonium ions and crown ethers having fewer than 24 atoms in their macrocycles have been observed to occur in a face-to-face manner. See a. Metcalfe, J.C., Stoddart, J.F. and Jones, G. (1977) Journal of the American Chemical Society,... [Pg.156]

Secondary dialkylamines are selectively acylated in the presence of primary amines by complexation of the latter with 18-crown-6 and a proton source. As the cavity in 18-crown-6 is ca. 2.7 A , secondary dialkylammonium salts are less efficiently complexed. ... [Pg.402]

Complexes of primary alkylanunonium salts and secondary dialkylammonium salts have been observed with diazaparacyclophanes. ... [Pg.404]

Another wide family of purely organic interlocked systems has been developed by Stoddart s group, based on hydrogen bonding and on donor-acceptor interactions. Suitably sized crown ethers can form pseudorotaxane complexes with appropriate secondary dialkylammonium ions which rely on N —H - 0 and C—H - 0 hydrogen bonds for stabiUzation. Similarly, a r-electron rich component, in interaction with a r-electron deficient moiety (traditionally cyclobis(paraquat-p-phenylene), CBPQ T, 21, ... [Pg.417]


See other pages where Secondary dialkylammonium is mentioned: [Pg.335]    [Pg.220]    [Pg.220]    [Pg.352]    [Pg.130]    [Pg.369]    [Pg.433]    [Pg.346]    [Pg.702]    [Pg.704]    [Pg.706]    [Pg.715]    [Pg.729]    [Pg.740]    [Pg.550]    [Pg.555]    [Pg.550]    [Pg.555]    [Pg.1063]    [Pg.1774]    [Pg.1775]   
See also in sourсe #XX -- [ Pg.372 ]




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Dialkylammonium

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