Solutions intermolecular hydrogen bonds

Unexpectedly strong intermolecular hydrogen bonding has been reported by IR spectroscopic studies for tetrahydro-4,7-phenanthroline-l,10-dione-3,8-dicarboxylic acids, which exist in the oxo-hydroxy form 165 in both solid state and in solution [78JCS(CC)369].Tlie conclusion was based on comparison of B-, C-, and D-type bands for 165 and their dimethyl esters (detection of hydrogen bonding) and on analysis of IR spectra in the 6 /xm region (pyridine- and pyridone-like bands). 

Exopolysaccharides in solution have an ordered helical conformation, which may be single, double or triple for example, xanthan forms a double or triple helix (Figure 7.3c). These are stabilised by intermolecular hydrogen bonds. The helical conformation makes the exopolysaccharide semirigid and the molecules can move large volumes of solution. These volumes overlap even at low concentrations of exopolysaccharide, giving rise to relatively high viscosities. 

Poly(acrylic acid) is very soluble in water as are its copolymers with maleic and itaconic acids. Solutions of 50 % by mass are easily obtained. The isomer of PAA, poly(ethylene maleic acid), is not so soluble. However, solutions of PAA tend over a period of time to gel when their concentration in water approaches 50 % by mass (Crisp, Lewis Wilson, 1975) this is attributed to a slow increase in the number of intermolecular hydrogen bonds. Copolymers of acrylic acid and itaconic acid are more stable in solution and their use has been advocated by Crisp et al. (1975, 1980). 

The carboxyl functions in the new structures are buried within the clefts in a manner that discourages the formation of the intermolecular hydrogen bonded dimers which are usually observed in the solution and solid phases. Unusual acid-base behavior is one consequence. In the smallest system 11 (represented by the benzene spacer) a tremendous difference in pKa s (6 units) can be observed for the two ionizations 14). 

Bushuk BA, Rubinov AN, Stupak AP (1987) Inhomogeneous broadening of spectra of dye solutions due to intermolecular hydrogen bonding. J Appl Spectros 47 1251-1254... 

Infra-red, microwave, and X-ray photoelectron spectroscopy Infra-red and ultra-violet spectroscopy has been widely used for investigating the structure of intermolecularly hydrogen-bonded complexes in the solid state (Novak, 1974) and in solution (Zundel, 1976, 1978 Clements et al., 1971a,b,c Pawlak et al., 1984). By analysing the infra-red spectra of equimolar liquid mixtures of amines with formic or acetic acid, the relative importance of structures [10] and [11] was estimated (Lindemann and Zundel, 1977). It was proposed that [10] and [11] make equal contributions to the observed structure of the complex when the p -value of the carboxylic acid is approximately two units lower than that of the protonated amine. 

Intramolecular hydrogen bonding can be observed in dilute solutions of di and poly hydroxy compounds in CC14, where no intermolecular hydrogen bonds are formed. Under these conditions a number of cyclic and acyclic diols have two bonds and others have single band in the O-H stretching mode region. 

A solution-state and solid-state nuclear magnetic resonance study of the complex and its separate components in both their neutral and ionized (TMP hydrochloride and SMZ sodium salt) forms was undertaken in order to elucidate the TMP-SMZ interactions. Inspection of the data for the complex in the solid state shows that the 13C chemical shifts are consistent with the ionic structure proposed by Nakai and coworkers105 (14). Stabilization of the complex is achieved by the resulting ionic interaction and by the formation of two intermolecular hydrogen bonds. 

Thus, in these two examples the most stable species in solution is not that found in die crystal. The long lifetimes of the metastable species in solution at low temperatures may indicate that the dissolution process leads initially to polymolecular aggregates in which the intermolecular hydrogen bonds are maintained. 

The values of the fractionation factors in structures [15]-[21] are not strictly comparable since they are defined relative to the fractionation in different solvent standards. However, in aqueous solution, fractionation factors for alcohols and carboxylic acids relative to water are similar and close to unity (Schowen, 1972 Albery, 1975 More O Ferrall, 1975), and it seems clear that the species [15]-[21] involving intermolecular hydrogen bonds with solvent have values of cp consistently below unity. These observations mean that fractionation of deuterium into the solvent rather than the hydrogen-bonded site is preferred, and this is compatible with a broader potential well for the hydrogen-bonded proton than for the protons of the solvents water, alcohol and acetic acid. 

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