Enthalpies of solution of C-alkylresorcin[4]arenes in alcohols at T= 298.15 K

Riveros, Diana C.; Vargas, Édgar F.

doi:10.1016/j.jct.2015.08.037

Cited by 2 publications

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References 29 publications

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“…While some physicochemical properties of C -ARAs have been reported, − rather little is known about their enthalpies of solution (Δ sln H ) in either aqueous or nonaqueous solvents. , Such properties are not only of intrinsic interest but can also provide fundamental insight into the behavior of C -ARAs in solution and, by analogy, of other classes of macrocyclic compounds. However, apart from the previous work by our group, , to the best of our knowledge there are no thermodynamic data on related systems from which worthwhile conclusions can be drawn at the present time.…”

Section: Introductionmentioning

confidence: 99%

Enthalpies of Solution of C-Alkylresorcin[4]arenes in Water and Acetonitrile: Hydrophilic and Hydrophobic Effects

2019

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Enthalpies of solution, Δ sln H, of six Calkylresorcin[4]arene (C-ARA) solids, with alkyl substituents varying systematically from methyl (Me) to hexyl (Hx), have been measured in water, using solubility data, and in acetonitrile, by direct calorimetry. For all of the C-ARAs studied, the values of Δ sln H were highly favorable (exothermic) for dissolution into water but were strongly unfavorable (endothermic) for dissolution into acetonitrile (ACN). The differences between the two solvents varied systematically with increasing carbon chain length, from about 100 kJ•mol −1 (for Me) to 140 kJ•mol −1 (for Hx). These extraordinary variances can be attributed to the loss of hydrophilic hydration of the eight −OH groups on the rim of the C-ARAs and also by the loss of (enthalpically favorable) hydrophobic hydration of the alkyl chains upon transfer from the highly structured, strongly Hbonding water to the aprotic, relatively weak donor/acceptor ACN. Although Δ sln H values for the present C-ARAs in H 2 O are strongly favorable, they are more than counteracted by even larger negative changes in the entropy of dissolution, Δ sln S. This enthalpy/entropy compensation effect is consistent with the low aqueous solubilities (<10 −3 mol•kg −1 ) of the C-ARAs and their slight increase with increasing carbon chain length, which is opposite to typical behavior of the homologous series of organic molecules.

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