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固体辛基和癸基氯化铵及其水溶液的理论与实验综合研究。

A combined theoretical and experimental study of solid octyl and decylammonium chlorides and of their aqueous solutions.

机构信息

Dipartimento di Chimica, Università di Roma La Sapienza, Piazzale Aldo Moro 5, 00185 Roma, Italy.

出版信息

J Phys Chem B. 2013 Jun 27;117(25):7806-18. doi: 10.1021/jp403103w. Epub 2013 Jun 12.

Abstract

The analysis of the thermal behavior of octyl- (OAC) and decylammonium chloride (DAC) has provided relevant new information. OAC shows a polymorphic phase transition that starts at 308 K and is completed at 313 K, between a monoclinic and a tetragonal structure, which belongs to a space group different from what was observed for other alkylammonium chlorides. At the melting temperature (463 K), the growing of a strong first sharp diffraction peak (FSDP) occurring at a d-spacing of ca. 21.0 Å was observed. DAC is characterized by two phase transitions at 318 (T(d1)) and 323 K (T(d2)). At T(d1), the LT polymorph coexists with a new-formed phase. At T(d2) the LT polymorph is replaced by a further polymorphic modification of DAC that becomes the only one at 328 K. This second phase transition signals the occurrence of a phase, closely related to the LT polymorph of HeAC, that crystallizes in the tetragonal crystal system a = ca. 5.00 Å and c = ca. 28.5 Å, P4/nmm space group. DAC melting starts at 458 K and is accompanied, as in the case of OAC, by the growing of a strong FSDP at a d-spacing of ca. 24.8 Å. A parallel DSC study confirmed the above-mentioned transitions. In addition, the structural properties of OAC/water and DAC/water mixtures were studied using an integrated approach, which combines X-ray diffraction and molecular dynamics (MD) techniques. A very good agreement between theoretical and experimental diffraction patterns has been obtained for both investigated mixtures. A thorough analysis of the MD trajectories shows that strong anion-water interactions are present in the mixtures, where Cl(-) forms a rather unstructured first hydration shell of water molecules bound to the anion in a linear Cl···H-O configuration. Moreover, cations and anions were found to interact with each other, and to form "solvent-shared ion pairs", in which one or more water molecules are shared between Cl(-) and the alkylammonium cation.

摘要

对辛基氯化铵(OAC)和癸基氯化铵(DAC)的热行为分析提供了相关的新信息。OAC 显示出一种多晶型相变,起始于 308 K,在 313 K 完成,从单斜晶系转变为四方晶系,属于与其他烷基氯化铵观察到的不同的空间群。在熔点(463 K)下,观察到一个强烈的第一尖锐衍射峰(FSDP)在约 21.0 Å 的 d 间距处生长。DAC 的特点是在 318(T(d1)) 和 323 K(T(d2)) 处有两个相变。在 T(d1) 时,LT 多晶型与新形成的相共存。在 T(d2) 时,LT 多晶型被 DAC 的另一种多晶型变体取代,在 328 K 时成为唯一的变体。第二次相变表明出现了一种与 HeAC 的 LT 多晶型密切相关的相,该相在四方晶系中结晶,a = ca. 5.00 Å,c = ca. 28.5 Å,P4/nmm 空间群。DAC 的熔融始于 458 K,与 OAC 一样,在约 24.8 Å 的 d 间距处产生强烈的 FSDP。DSC 平行研究证实了上述转变。此外,还使用结合 X 射线衍射和分子动力学(MD)技术的综合方法研究了 OAC/水和 DAC/水混合物的结构性质。对于两种研究混合物,理论和实验衍射图谱之间都取得了非常好的一致性。对 MD 轨迹的深入分析表明,混合物中存在强阴离子-水相互作用,其中 Cl(-) 形成了一个相当无序的第一水合壳,水分子以线性 Cl···H-O 构型结合在阴离子上。此外,还发现阳离子和阴离子相互作用,并形成“溶剂共享离子对”,其中一个或多个水分子在 Cl(-) 和烷基铵阳离子之间共享。

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