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Hydrogen-bonded hydration

For hydrates, the question is, to what extent does the nitrogen atom lone pair contribute to hydrogen bonding in amine hydrates Hydrogen bonding is expected to explain the difference between gaseous and solid ammonia couplings. [Pg.98]

Fig. 12. A drawing of the crystal structure of adenine hydrochloride hemi-hydrate. Hydrogen bonds are indicated by dashed lines. The dimensions were calculated from the coordinates given by Cochran (11). Fig. 12. A drawing of the crystal structure of adenine hydrochloride hemi-hydrate. Hydrogen bonds are indicated by dashed lines. The dimensions were calculated from the coordinates given by Cochran (11).
Meot-Ner M 1984 Ionic hydrogen bond and ion solvation 2. Solvation of onium ions by 1-7 water molecules. Relations between monomolecular, specific and bulk hydration J. Am. Chem. Soc. 106 1265-72... [Pg.1359]

The ideas of Frank, Evans and Kauzmann had a profound influence on the way chemists thought about hydrophobic effects in the decades that followed However, after the study of the hydrophobic hydration shell through computer simulations became feasible, the ideas about the hydrophobic hydration gradually changed. It became apparent that the hydrogen bonds in the hydrophobic hydration shell are nof or only to a minor extent, stronger than in normal water which is not compatible with an iceberg character of the hydration shell. [Pg.15]

As is suggested frequently , this term might well result from the restriction of the hydrogen bonding possibilities experienced by the water molecules in the first hydration shell. For each individual water molecule this is probably a relatively small effect, but due to the small size of the water molecules, a large number of them are entangled in the first hydration shell, so that the overall effect is appreciable. This theory is in perfect agreement with the observation that the entropy of hydration of a nonpolar molecule depends linearly on the number of water molecules in the first hydration shell ". ... [Pg.16]

In summary, a wealtli of experimental data as well as a number of sophisticated computer simulations univocally indicate that two important effects underlie the acceleration of Diels-Alder reactions in aqueous media hydrogen bonding and enforced hydrophobic interactionsIn terms of transition state theory hydrophobic hydration raises the initial state more tlian tlie transition state and hydrogen bonding interactions stabilise ftie transition state more than the initial state. The highly polarisable activated complex plays a key role in both of these effects. [Pg.24]

If one would ask a chemist not burdened with any knowledge about the peculiar thermodynamics that characterise hydrophobic hydration, what would happen upon transfer of a nonpolar molecule from the gas phase to water, he or she would probably predict that this process is entropy driven and enthalpically highly unfavourable. This opinion, he or she wo ild support with the suggestion that in order to create room for the nonpolar solute in the aqueous solution, hydrogen bonds between water molecules would have to be sacrificed. [Pg.166]


See other pages where Hydrogen-bonded hydration is mentioned: [Pg.350]    [Pg.107]    [Pg.148]    [Pg.164]    [Pg.93]    [Pg.231]    [Pg.221]    [Pg.54]    [Pg.304]    [Pg.426]    [Pg.148]    [Pg.245]    [Pg.243]    [Pg.350]    [Pg.107]    [Pg.148]    [Pg.164]    [Pg.93]    [Pg.231]    [Pg.221]    [Pg.54]    [Pg.304]    [Pg.426]    [Pg.148]    [Pg.245]    [Pg.243]    [Pg.207]    [Pg.207]    [Pg.209]    [Pg.351]    [Pg.425]    [Pg.245]    [Pg.567]    [Pg.1739]    [Pg.2591]    [Pg.43]    [Pg.57]    [Pg.270]    [Pg.303]    [Pg.136]    [Pg.16]    [Pg.16]    [Pg.16]    [Pg.17]    [Pg.17]    [Pg.18]    [Pg.24]    [Pg.54]    [Pg.99]    [Pg.99]    [Pg.165]    [Pg.166]    [Pg.166]    [Pg.167]    [Pg.167]   
See also in sourсe #XX -- [ Pg.426 ]




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