Olvera Angeles, Pérez-Casas Silvia, Costas Miguel
Laboratorio de Biofisicoquímica, Departamento de Fisicoquímica, Facultad de Química, Universidad Nacional Autónoma de México, Cd. Universitaria, México D. F. 04510, México.
J Phys Chem B. 2007 Oct 4;111(39):11497-505. doi: 10.1021/jp072098a. Epub 2007 Sep 13.
An analysis scheme for the formation of the inclusion complexes in water is presented. It is exemplified for the case where the host is alpha-cyclodextrin and the guest is a linear alcohol (1-propanol to 1-octanol) or the isomers of 1-pentanol. Eight transfer isobaric heat capacities, DeltatCp, involving different initial and final states are evaluated at infinite dilution of the guest using both data determined in this work and from the literature. Apart from the usual definition for the inclusion heat capacity change, three inclusion transfers are used. The sign of each DeltatCp indicates if the transfer is an order-formation or an order-destruction process. From the DeltatCp data, the main contributions to the heat capacity of cyclodextrin complexation, namely, those due to dehydration of the hydrophobic section of the guest molecule, H-bond formation, formation of hydrophobic interactions, and release of water molecules from the cyclodextrin cavity, are estimated. The relative weight of each of these contributions to the DeltatCp values is discussed, providing a better characterization of the molecular recognition process involved in the inclusion phenomena.
本文提出了一种在水中形成包合物的分析方案。以主体为α-环糊精、客体为直链醇(1-丙醇至1-辛醇)或1-戊醇异构体的情况为例进行说明。利用本工作中测定的数据和文献数据,在客体无限稀释的条件下,评估了涉及不同初始和终态的八个转移等压热容ΔtCp。除了包合热容变化的常用定义外,还使用了三种包合转移。每个ΔtCp的符号表明该转移是有序形成过程还是有序破坏过程。根据ΔtCp数据,估算了环糊精络合热容的主要贡献,即客体分子疏水部分的脱水、氢键形成、疏水相互作用的形成以及水分子从环糊精腔中释放所导致的贡献。讨论了这些贡献对ΔtCp值的相对权重,从而更好地描述了包合现象中涉及的分子识别过程。