Chemical and Materials Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 99354, USA.
J Am Chem Soc. 2010 Sep 15;132(36):12597-604. doi: 10.1021/ja1014458.
A comprehensive analysis of the H(3)O(+) and H(2)O structure in the first solvation shell about Cl(-) in aqueous HCl solutions is reported from X-ray absorption fine structure (XAFS) measurements. Results show increasing degree of contact ion pairing between Cl(-) and H(3)O(+) as the HCl concentration increases from 6.0 m, 10.0 m, and finally 16.1 m HCl (acid concentrations are expressed as molality or mole HCl/1000 g water). At the highest acid concentration there are on average, approximately 1.6 H(3)O(+) ions and 4.2 H(2)O's in the first shell about Cl(-). The structure of the Cl(-)/H(3)O(+) contact ion pair is distinctly different from that of the H(2)O structure about Cl(-). The Cl-O bond length (2.98 A) for Cl(-)/H(3)O(+) is approximately 0.16 A shorter than the Cl(-)/H(2)O bond. The bridging proton resides at an intermediate position between Cl and O at 1.60 A from the Cl(-) and approximately 1.37 A from the O of the H(3)O(+). The bridging-proton structure of this contact ion pair, (Cl-H-OH(2)), is similar to the structure of the water Zundel ion, (H(2)O-H-OH(2)(+)). In both cases there is a shortened Cl-O or O-O bond, and the intervening proton bond distances are substantially longer than for the covalent bonds of either HCl or H(2)O. A detailed structural analysis of the aqueous chloride species, Cl(-)/(H(2)O)(n), was also completed as part of this study in order to understand the relative importance of various XAFS photoelectron scattering paths. For aqueous Cl(-) the measured Cl-O and Cl-H distances of 3.14 A and 2.23 A, respectively, are in excellent agreement with earlier neutron and X-ray diffraction results. Overall, these results significantly improve our understanding of the interaction of H(3)O(+) with Cl(-). The results are of interest to fundamental physical chemistry and they have important consequences in biochemical, geochemical, and atmospheric processes.
从 X 射线吸收精细结构(XAFS)测量结果报告了在盐酸水溶液中 Cl^-的第一溶剂化壳中 H(3)O(+)和 H(2)O 结构的综合分析。结果表明,随着 HCl 浓度从 6.0m、10.0m 增加到 16.1mHCl(酸浓度表示为质量摩尔浓度或每 1000g 水中的摩尔 HCl),Cl^-和 H(3)O^+之间的接触离子对的程度逐渐增加。在最高酸浓度下,Cl^-的第一壳层中平均有大约 1.6 个 H(3)O^+离子和 4.2 个 H(2)O。Cl^-/H(3)O^+接触离子对的结构明显不同于 Cl^-/H(2)O 的结构。Cl-O 键长(2.98Å)为 Cl^-/H(3)O^+比 Cl^-/H(2)O 键短约 0.16Å。桥接质子位于 Cl 和 O 之间的中间位置,距离 Cl^-为 1.60Å,距离 H(3)O^+的 O 约为 1.37Å。这种接触离子对的桥接质子结构(Cl-H-OH(2))类似于水 Zundel 离子(H(2)O-H-OH(2)(+))的结构。在这两种情况下,Cl-O 或 O-O 键都缩短了,而中间质子键的距离都远远长于 HCl 或 H(2)O 的共价键。作为这项研究的一部分,还完成了对水合氯化物物种 Cl^-/(H(2)O)(n)的详细结构分析,以了解各种 XAFS 光电子散射路径的相对重要性。对于水合 Cl^-,测量得到的 Cl-O 和 Cl-H 距离分别为 3.14Å 和 2.23Å,与早期的中子和 X 射线衍射结果非常吻合。总的来说,这些结果大大提高了我们对 H(3)O^+与 Cl^-相互作用的理解。这些结果对基础物理化学有意义,并且在生化、地球化学和大气过程中具有重要意义。