Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Molecular relaxation, cyclodextrin

Cahill S, Bulusu S. (1993). Molecular-complexes of explosives with cyclodextrins. 1. Characterization of complexes with the nitramines RDX, HMX, and TNAZ in solution by H-l-NMR spin-lattice relaxation-time measurements. Magnetic Resonance in Chemistry 31 731-735. [Pg.280]

Determination of the crystal and molecular structures of the cyclohexa-amylose (a-cyclodextrin, a-CD)-methanol complex has shown that cyclohexa-amylose assumes an unstrained relaxed structure, which is stabilized by a ring of hydrogen bonds between 0-2 and 0-3 of adjacent D-glucopyranosyl residues, on inclusion of methanol.The results support the general mechanism (Figure 2) proposed for the formation of inclusion complexes. [Pg.464]


See other pages where Molecular relaxation, cyclodextrin is mentioned: [Pg.238]    [Pg.238]    [Pg.3372]    [Pg.243]    [Pg.287]    [Pg.862]    [Pg.259]    [Pg.15]    [Pg.52]    [Pg.54]    [Pg.154]    [Pg.54]    [Pg.154]    [Pg.308]    [Pg.232]    [Pg.251]    [Pg.102]    [Pg.321]    [Pg.357]    [Pg.452]    [Pg.303]    [Pg.261]    [Pg.296]    [Pg.338]    [Pg.146]    [Pg.150]    [Pg.479]    [Pg.108]    [Pg.181]   


SEARCH



Molecular relaxation, cyclodextrin complexes

Molecular relaxations

© 2024 chempedia.info