Mixed H2S and H2O Clusters─New Insights into Dispersion-Dominated Hydrogen Bonding.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-11-07 Epub Date: 2024-10-24 DOI:10.1021/acs.jpca.4c05510
Philipp Meyer, Svenja Jäger, Jai Khatri, Stefan Henkel, Gerhard Schwaab, Martina Havenith
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Abstract

Here, we report the results of an IR spectroscopy study on heteroclusters of H2S and H2O and several of their isotopomers using mass-selective IR spectroscopy in superfluid helium nanodroplets in the range of 2560-2800 cm-1. Based on DFT calculations on the B3LYP-D3/6-311++G(d,p) level of theory, we were able to assign the experimentally observed O-D stretching bands to heterodimer and heterotrimer clusters. Since no bands of the S-H-bound conformer HSH···OH2 could be observed, we were able to determine the O-H-bound conformer HOH···SH2 to be the global minimum structure. A trapping of the local minima in helium nanodroplets was not observed. This is in line with the weaker hydrogen bond expected for H2S complexes. In these clusters, the interaction energy is expected to be more dominated by dispersion and less dictated by highly directional electrostatic forces.

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混合 H2S 和 H2O 簇--对分散主导型氢键的新认识。
在此,我们报告了在超流体纳米氦液滴中使用质量选择性红外光谱对 H2S 和 H2O 的杂簇及其几种同素异形体在 2560-2800 cm-1 范围内进行红外光谱研究的结果。基于 B3LYP-D3/6-311++G(d,p) 理论水平的 DFT 计算,我们将实验观察到的 O-D 伸展带归属于杂二聚体和杂三聚体簇。由于没有观察到 S-H 结合构象 HSH-OH2 的带,我们确定 O-H 结合构象 HOH-SH2 是全局最小结构。在氦纳米液滴中没有观察到局部最小结构的捕获。这与 H2S 复合物氢键较弱的预期相符。在这些团簇中,相互作用能预计将更多地由分散作用所主导,而较少由高度定向的静电力所决定。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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