Wang Yue, Shi Xin, Wu Wenbin, Deng Xianhong, Xin Kai, Zhou Ziqing, Tang Lihong, Ning Zhiyuan
School of Chemical Science and Technology, Yunnan University, Yunnan Province, Kunming650091, People's Republic of China.
Langmuir. 2022 Nov 29;38(47):14485-14496. doi: 10.1021/acs.langmuir.2c02600. Epub 2022 Nov 15.
A peculiar heterogeneous metal sandwich fragment {(Ge)[η-Ge(PdPPh)]} anion cluster was synthesized for the first time by Xu et al. (Xu, H. L.; Tkachenko, N. V.; Wang, Z. C.; Chen, W. X.; Qiao, L.; Munoz-Castro, A.; Boldyrev, A. I.; Sun, Z. M. , , 5286). In this work, novel analogous sandwich compounds ({(E)[η-E(PdPH)]} (E = Si (), Ge (), Sn ()) were studied using quantum chemical calculations and wave function analysis to determine the geometry, bonding nature, aromaticity, active sites, and hydrogen storage. Structural analysis revealed that the clusters were compounds formed by the coordination of two E (E = Si, Ge, Sn) Zintl clusters with a central E@Pd (E = Si, Ge, Sn) interlayer. The steric hindrance at both ends is small, facilitating facile attachment to other molecules. The valence states of the central atom E (E = Si, Ge, Sn) are close to zero, indicating that they are stable novel heterometallic sandwich compounds, and the Zintl ligands at both ends are negative, thus they can react with Lewis acids. Bonding analysis showed that the E (E = Si, Ge, Sn) cluster has a delocalized framework bonding mode. For aromaticity analysis, we used AdNDP, ELF, LOL, ICSS, and NICS to qualitatively and quantitatively clarify that these clusters possess the characteristics of overall delocalization, σ aromaticity, and remarkable stability. By analyzing the unique structure and predicting the reaction sites, we concluded that the E ligand reacts with Lewis acids. Finally, through the adsorption of hydrogen molecules, the average adsorption energies of - were 0.387, 0.374, and 0.325 eV per H molecule, respectively, meeting the physical adsorption standard, with the adsorption effect of being slightly more superior than that of and . Our study represents a substantial step forward in the study of high-density materials for volumetric H storage applications.
徐等人首次合成了一种特殊的异质金属夹心片段{(Ge)[η-Ge(PdPPh)]}阴离子簇(徐,H.L.;特卡琴科,N.V.;王,Z.C.;陈,W.X.;乔,L.;穆尼奥斯-卡斯特罗,A.;博尔迪列夫,A.I.;孙,Z.M.,,5286)。在这项工作中,使用量子化学计算和波函数分析研究了新型类似夹心化合物({(E)[η-E(PdPH)]} (E = Si (), Ge (), Sn ()),以确定其几何结构、键合性质、芳香性、活性位点和储氢性能。结构分析表明,这些簇是由两个E(E = Si、Ge、Sn)津特耳簇与一个中心E@Pd(E = Si、Ge、Sn)夹层配位形成的化合物。两端的空间位阻较小,便于与其他分子轻松连接。中心原子E(E = Si、Ge、Sn)的价态接近零,表明它们是稳定的新型异金属夹心化合物,两端的津特耳配体为负,因此它们可以与路易斯酸反应。键合分析表明,E(E = Si、Ge、Sn)簇具有离域骨架键合模式。对于芳香性分析,我们使用AdNDP、ELF、LOL、ICSS和NICS定性和定量地阐明这些簇具有整体离域、σ芳香性和显著稳定性的特征。通过分析独特结构并预测反应位点,我们得出E配体与路易斯酸反应的结论。最后,通过氢分子吸附,每H分子的平均吸附能分别为0.387、0.374和0.325 eV,符合物理吸附标准, 的吸附效果略优于 和 。我们的研究在用于体积储氢应用的高密度材料研究方面迈出了重要一步。