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Hydrogen bonds inter-associating

Many biological processes involve an associa tion between two species in a step prior to some subsequent transformation This asso ciation can take many forms It can be a weak associ ation of the attractive van der Waals type or a stronger interaction such as a hydrogen bond It can be an electrostatic attraction between a positively charged atom of one molecule and a negatively charged atom of another Covalent bond formation between two species of complementary chemical re activity represents an extreme kind of association It often occurs in biological processes in which aide hydes or ketones react with amines via imine inter mediates... [Pg.728]

Solubility in Water. Alkyl halides and alcohols differ markedly from one another in their solubility in water. All alkyl halides are insoluble in water, but low-molecular-weight alcohols (methyl, ethyl, n-propyl, and isopropyl) are soluble in water in all proportions. Their ability to participate in inter-molecular- hydrogen bonding not only affects the boiling points of alcohols, but also enhances their water solubility. Flydrogen-bonded networks of the type shown in Figure 4.5, in which alcohol and water molecules associate with one another, replace the alcohol-alcohol and water-water hydrogen-bonded networks present in the pure substances. [Pg.150]

Fig. 30. — Packing arrangement of 4-fold antiparallel double helices of potassium hyaluronate (32). (a) Stereo view of a unit cell approximately normal to the line of separation of the two helices. The two chains in each duplex, drawn in open and filled bonds for distinction, are linked by not only direct hydrogen bonds, but also water bridges. Inter double-helix hydrogen bonds are mediated between hydroxymethyl and iV-acetyl groups. Potassium ions (crossed circles) at special positions have only a passive role in the association of hyaluronate chains. Fig. 30. — Packing arrangement of 4-fold antiparallel double helices of potassium hyaluronate (32). (a) Stereo view of a unit cell approximately normal to the line of separation of the two helices. The two chains in each duplex, drawn in open and filled bonds for distinction, are linked by not only direct hydrogen bonds, but also water bridges. Inter double-helix hydrogen bonds are mediated between hydroxymethyl and iV-acetyl groups. Potassium ions (crossed circles) at special positions have only a passive role in the association of hyaluronate chains.
DSC studies have shown that modification alters thermal transition temperatures and the overall enthalpy (AHgei) associated with gelatinization (Tables 10.13 and 10.14). Upon hydroxypropylation, the reactive groups introduced into the starch chains are capable of disrupting the inter-and intra-molecular hydrogen bonds, leading to an increase in accessibility by water that lowers... [Pg.307]

The results of a study of the laser-Raman spectra of sucrose are summarized in Table IX. The most important features observed187 when the concentration was varied consisted in shifts of the frequencies of the CH2OH group, which are sensitive to intra- and inter-molecular hydrogen-bonding. In addition, the association of D-glucose with D-fructose that leads to the... [Pg.79]

We have already mentioned that water molecules self-associate through hydrogen bonding, and various forms of polymers exist in bulk water. Same is the situation with ethanol. In hydrated ethanol inter-molecular association between water and ethanol molecules occurs through H-bonding. A hydrogen bond exists when (1) there is evidence of a bond and (2) this bond involves a hydrogen atom already bonded to another atom. Thus the bond formation process can be written... [Pg.69]

Noncovalent interactions are weak inter- or intramolecular interactions that result from a combination of electrostatic interactions (ionic), hydrogen bonding, hydrophobic interactions (stacking or intercalation), and van der Waals interactions (dipole-dipole or induced dipole-induced dipole). Complexes formed by these types of interactions are usually fragile. This property is often essential to their biological function, which depends on the equilibria between the associated and free forms of these molecules. [Pg.319]


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See also in sourсe #XX -- [ Pg.97 ]

See also in sourсe #XX -- [ Pg.97 ]




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