Dipartimento di Chimica, Università di Roma La Sapienza, Piazzale Aldo Moro 5, 00185 Roma, Italy.
J Phys Chem B. 2013 Jun 27;117(25):7806-18. doi: 10.1021/jp403103w. Epub 2013 Jun 12.
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.
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。