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Encapsulation-induced remarkable stability of a hydrogen-bonded heterocapsule

机译:包封诱导的氢键杂胶囊的显着稳定性

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Remarkably enhanced stability of the self-assembled hydrogen-bonded heterocapsule 1×2 by the encapsulation of 1,4-bis(1-propynyl)benzene 3 a was found with K_a=1.14×10~9 M~(-1) in CDCl_3 and K_(a2)=1.59×10~8 M~(-2) in CD_3OD/CDCl_3 (10 % v/v) at 298 K. The formation of 3 a(1×2) was enthalpically driven (ΔH°<0 and ΔS°<0) and there was a unique inflection point in the correlation between ΔH° versus ΔS° as a function of polar solvent content. The ab initio calculations revealed that favorable guest-capsule dispersion and electrostatic interactions between the acetylenic parts (triple bonds) of 3 a and the aromatic inner space of 1×2, as well as less structural deformation of 1×2 upon encapsulation of 3 a, play important roles in the remarkable stability of 3 a(1×2).
机译:通过在CDCl_3中K_a = 1.14×10〜9 M〜(-1)包封1,4-双(1-丙炔基)苯3a可以显着提高自组装氢键杂胶囊1×2的稳定性。 CD_3OD / CDCl_3(10%v / v)中的K_(a2)= 1.59×10〜8 M〜(-2)(298%)。3 a(1×2)的形成被焓驱动(ΔH°<0并且ΔS°<0),并且在ΔH°与ΔS°之间的相关性中作为极性溶剂含量的函数存在独特的拐点。从头算计算表明,3a的炔属部分(三键)与1×2的芳族内部空间之间的良好客体-胶囊分散和静电相互作用,以及封装3a时1×2的结构变形较小,在3 a(1×2)的出色稳定性中起重要作用。

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