Soft confinement of water in aliphatic alcohols: MIR/NIR spectroscopic and DFT studies.

Here, we present the first examination of the state of water under a soft confinement in eight aliphatic alcohols including cyclopentanol, 1-pentanol, 1-hexanol, 1-heptanol, 1-octanol, 1-decanol, 2-octanol and 3-octanol. Due to relatively large size of the aliphatic part, water has limited solubility in all studied alcohols. Water content in saturated solutions was determined by Karl Fischer titration and correlated with the spectroscopic data. This way, we determined the molar absorptivity of the ν2+ν3 combination mode. The effect of addition of water and temperature variation was monitored by ATR-IR and NIR spectroscopy. Analysis of the experimental results was guided by DFT calculations, which provided the structures, harmonic MIR spectra and binding energies of selected alcohol-water complexes. Our studies demonstrated that the state of water in alcohols is related to its solubility, which depends on structure of solvent molecules. The solubility of water in 1-alcohols decreases on increasing of the chain length, but for long chain alcohols this effect is less evident. More apparent solubility reduction appears in going from the primary to secondary alcohols. The effective shielding of the OH group in the linear alcohols is achieved when on both sides of the OH group are ethyl or longer substituents, while the shielding by methyl groups is less efficient. Water is much better soluble in the cyclic alcohols as compared with the linear ones due to better accessibility of the OH group. The soft confinement of water in aliphatic alcohols allows for flexible structural arrangements and interactions. Even at low water content, we did not observe free molecules of water. At these conditions, the molecules of water are singly or doubly bonded to the OH groups from the alcohol. Increasing solubility of water reduces the number of the free OH groups and leads to formation of water clusters. Obtained results allow concluding that in alcohols with sizable aliphatic part the molecules of water are confined in the vicinity of the OH groups.

Association and solubility of chlorophenols in CCl4: MIR/NIR spectroscopic and DFT study.

This work provides new information on the effect of position and number of substituents on association and solubility of chlorophenols in CCl4. Using MIR and NIR spectroscopy we examined solutions of 12 chlorophenols at several concentrations. In addition, we calculated (DFT) theoretical spectra and structures of monomers and associates of chlorophenols from dimer to tetramer. The number of substituents at positions 2 and 6 allows to divide studied chlorophenols into three Groups: I (3; 4; 3,4; 3,5), II (2; 2,3; 2,4; 2,5; 2,4,5), and III (2,6; 2,4,6; 2,3,4,5,6). An equilibrium between intermolecular OH⋅⋅⋅OH and intramolecular OH⋅⋅⋅Cl hydrogen bonding depends on position and number of substituents. The extent of association decreases in going from Group I to Group III due to growing steric hindrance near the OH group and the resonance effect from Cl. In chlorophenols of Group I, Cl at positions 3 or 5 weakens the OH⋅⋅⋅OH intermolecular hydrogen bonding, while for Group II it strengthens the OH⋅⋅⋅⋅Cl intramolecular bonding. In contrast, Cl at position 4 has minor effect on association. In the case of Group I, increasing concentration shifts the equilibrium towards solute-solute interactions, whereas for Groups II and III dominate the species with intramolecular OH⋅⋅⋅Cl bonding. The theoretical calculations predict that for monosubstituted chlorophenols of Group I the most stable are non-planar cyclic tetramers, while for disubstituted ones, the non-planar cyclic tetramers and linear trimers have similar binding energies. Chlorophenols of Group II prefer the cyclic non-planar trimers, whereas those of Group III form the planar dimers with an antiparallel orientation of the OH groups. Our study reveals that chlorophenols creating the cyclic associates are better soluble in CCl4 as compared with those forming the linear ones. Hence, one can conclude that in an inert or weakly interacting solvents the solubility is closely related to the structure of the solute associates.