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A Microcalorimetric Study of Host–Guest Complexes of α-Cyclodextrin with Alkyl Trimethyl Ammonium Bromides in Aqueous Solutions

机译:水溶液中α-环糊精与烷基三甲基溴化铵的客体-客体配合物的量热法研究

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摘要

Interactions between α-CD and three alkyl trimethyl ammonium bromides, a homologues series of surfactants, in aqueous solutions have been investigated with titration microcalorimetry at 298.15 K. The results are discussed in the light of the amphiphilic interaction and the iceberg structure of water molecules existing around the hydrophobic tail of the surfactant. The stoichiometry of the host–guest complex changes from 1:1 to 2:1, as the number of carbon atoms (n) in the hydrophobic chain, C n H2 n +1, increases from 8 to 14. All the complexes are quite stable, with the apparent experiential stability constants being β1 = 2.65 × 103 dm3-mol−1, β2 = 4.85 × 106 dm6-mol−2, β2 = 6.50 × 106 dm6-mol−2, respectively for n = 8, 12, 14. All the complexation processes are shown to be enthalpy driven, and the standard enthalpy effect (−ΔH 0) increases while standard entropy change (ΔS 0) decreases with elongation of the hydrophobic chain.
机译:α-CD与三种烷基三甲基溴化铵(一种表面活性剂的同系物系列)在水溶液中的相互作用已通过298.15 K的滴定微量热法进行了研究。根据两亲相互作用和存在的水分子的冰山结构对结果进行了讨论在表面活性剂的疏水尾部附近。主客体复合物的化学计量从1:1变为2:1,这是因为疏水链中的碳原子数(n)C n H2 n +1 从8增加到14。所有配合物都相当稳定,表观经验稳定性常数为β1 = 2.65×103 dm3 -mol−1 ,β2 = 4.85×106 dm6 -mol−2 ,β2 = 6.50×106 dm6 -mol− n = 8、12、14分别为2 。所有络合过程均显示为焓驱动,标准焓变(-ΔH0 )增大,而标准熵变(ΔS0 <随疏水链的延长而降低。

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