Unexpected Roles of Alkali-Metal Cations in the Assembly of Low-Valent Uranium Sulfate Molecular Complexes
文献类型：期刊论文
| 作者 | Yue, ZH; Guo, XF; Feng, ML; Lin, YJ; Ju, Y; Lin, X; Zhang, ZH; Guo, XJ; Lin, J; Huang, YY |
| 刊名 | INORGANIC CHEMISTRY
 |
| 出版日期 | 2020 |
| 卷号 | 59期号:4页码:2348-2357 |
| 关键词 | STATE STRUCTURAL CHEMISTRY DIMENSIONAL REDUCTION CRYSTAL-STRUCTURE FISSION-PRODUCTS CLUSTER HEXANUCLEAR COORDINATION SPECIATION HYDROLYSIS SELENITES |
| ISSN号 | 0020-1669 |
| DOI | 10.1021/acs.inorgchem.9b03182 |
| 文献子类 | 期刊论文 |
| 英文摘要 | The directing effect of coordinating ligands in the formation of uranium molecular complexes has been well established, but the role of counterions in metal-ligand interactions remains ambiguous and requires further investigation. In this work, we describe the targeted isolation, through the choice of alkali-metal ions, of a family of tetravalent uranium sulfates, showing the influence of the overall topology and, unexpectedly, the U-IV nuclearity upon the inclusion of such countercations. Analyses of the structures of uranium(IV) oxo/hydroxosulfate oligomeric species isolated from consistent synthetic conditions reveal that the incorporation of Na+ and Rb+ promotes the crystallization of OD discrete clusters with a hexanuclear [U6O4(OH)(4)(H2O)(4)](12+) core, whereas the larger Cs+ ion allows for the isolation of a 2D-layered oligomer with a less condensed trinuclear [U-3(O)](10+) center. This finding expands the prevalent view that counterions play an innocent role in molecular complex synthesis, affecting only the overall packing but not the local oligomerization. Interestingly, trends in nuclearity appear to correlate with the hydration enthalpies of alkali-metal cations, such that the alkali-metal cations with larger hydration enthalpies correspond to more hydrated complexes and cluster cores. These findings afford new insights into the mechanism of nucleation of U-IV, and they also open a new path for the rational design and synthesis of targeted molecular complexes. |
| 语种 | 英语 |
| 源URL | [http://ir.sinap.ac.cn/handle/331007/33252]  |
| 专题 | 上海应用物理研究所_中科院上海应用物理研究所2011-2017年 |
| 作者单位 | 1.Chinese Acad Sci, Shanghai Inst Appl Phys, Key Lab Interfacial Phys & Technol, Shanghai 201800, Peoples R China 2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China 3.Chinese Acad Sci, Shanghai Adv Res Inst, Shanghai 201210, Peoples R China 4.Washington State Univ, Dept Chem, Pullman, WA 99164 USA 5.Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China 6.Fudan Univ, Dept Chem, Shanghai 200433, Peoples R China 7.Changzhou Univ, Jiangsu Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Jiangsu, Peoples R China 8.Shanghai Normal Univ, Educ Minist, Key Lab Resource Chem, Shanghai 200234, Peoples R China 9.Shanghai Normal Univ, Dept Chem & Chem Engn, Shanghai Key Lab Rare Earth Funct Mat, Shanghai 200234, Peoples R China |
| 推荐引用方式 GB/T 7714 | Yue, ZH,Guo, XF,Feng, ML,et al. Unexpected Roles of Alkali-Metal Cations in the Assembly of Low-Valent Uranium Sulfate Molecular Complexes[J]. INORGANIC CHEMISTRY,2020,59(4):2348-2357. |
| APA | Yue, ZH.,Guo, XF.,Feng, ML.,Lin, YJ.,Ju, Y.,...&Wang, JQ.(2020).Unexpected Roles of Alkali-Metal Cations in the Assembly of Low-Valent Uranium Sulfate Molecular Complexes.INORGANIC CHEMISTRY,59(4),2348-2357. |
| MLA | Yue, ZH,et al."Unexpected Roles of Alkali-Metal Cations in the Assembly of Low-Valent Uranium Sulfate Molecular Complexes".INORGANIC CHEMISTRY 59.4(2020):2348-2357. |
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来源：上海应用物理研究所
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