Binuclear trivalent and tetravalent uranium halides and cyanides supported by cyclooctatetraene ligands
文献类型：期刊论文
| 作者 | Wang, Cong-Zhi1,2; Wu, Qun-Yan1,2; Lan, Jian-Hui1,2; Chai, Zhi-Fang1,2,3,4; Gibson, John K.5; Shi, Wei-Qun1,2 |
| 刊名 | Radiochimica acta
 |
| 出版日期 | 2017 |
| 卷号 | 105期号:1页码:21-32 |
| 关键词 | Density functional calculations Binuclear uranium complexes Halides Cyanides Cyclooctatetraene |
| ISSN号 | 0033-8230 |
| DOI | 10.1515/ract-2016-2615 |
| 通讯作者 | Shi, wei-qun(shiwq@ihep.ac.cn) |
| 英文摘要 | Although the first organoactinide chloride cp3ucl (cp = eta(5)-c h-5(5)) was synthesized more than 50 years ago, binuclear uranium halides remain very rare in organoactinide chemistry. herein, a series of binuclear trivalent and tetravalent uranium halides and cyanides with cyclooctatetraene ligands, (cot)(2)u2xn (cot = eta(8)-c8h8; x = f, cl, cn; n = 2, 4), have been systematically studied using scalar-relativistic density functional theory (dft). the structures with bridging halide or cyanide ligands were predicted to be the most stable complexes of (cot)(2)u2x (n), and all the complexes show weak antiferromagnetic interactions between the uranium centers. however, for each species, there is no significant uranium-uranium bonding interaction. the bonding between the metal and the ligands shows some degree of covalent character, especially between the metal and terminal halide or cyanide ligands. the u-5f and 6d orbitals are predominantly involved in the metal-ligand bonding. all the (cot)(2)u2xn species were predicted to be more stable compared to the mononuclear half-sandwich complexes at room temperature in the gas phase such that (cot)(2)u2x4 might be accessible through the known (cot)(2)u complex. the tetravalent derivatives (cot)(2)u2x4 are more energetically favorable than the trivalent (cot)(2)u2x2 analogs, which may be attributed to the greater number of strong metal-ligand bonds in the former complexes. |
| WOS关键词 | TRANSITION-METAL-COMPLEXES ; SEGMENTED CONTRACTION SCHEME ; EXCHANGE COUPLING-CONSTANTS ; PSEUDOPOTENTIAL BASIS-SETS ; DENSITY-FUNCTIONAL THEORY ; ELECTRONIC-STRUCTURES ; M(CO)(6) M=CR ; MAGNETIC-PROPERTIES ; CORRELATION-ENERGY ; APPROXIMATION |
| WOS研究方向 | Chemistry ; Nuclear Science & Technology |
| WOS类目 | Chemistry, Inorganic & Nuclear ; Nuclear Science & Technology |
| 语种 | 英语 |
| WOS记录号 | WOS:000394245800002 |
| 出版者 | WALTER DE GRUYTER GMBH |
| URI标识 | http://www.irgrid.ac.cn/handle/1471x/2176785 |
| 专题 | 高能物理研究所 |
| 通讯作者 | Shi, Wei-Qun |
| 作者单位 | 1.Chinese Acad Sci, Inst High Energy Phys, Lab Nucl Energy Chem, Beijing 100049, Peoples R China 2.Chinese Acad Sci, Inst High Energy Phys, Key Lab Biomed Effects Nanomat & Nanosafety, Beijing 100049, Peoples R China 3.Soochow Univ, Sch Radiol & Interdisciplinary Sci RAD X, Suzhou 215123, Peoples R China 4.Soochow Univ, Collaborat Innovat Ctr Radiat Med Jiangsu Higher, Suzhou 215123, Peoples R China 5.Lawrence Berkeley Natl Lab, Div Chem Sci, Berkeley, CA 94720 USA |
| 推荐引用方式 GB/T 7714 | Wang, Cong-Zhi,Wu, Qun-Yan,Lan, Jian-Hui,et al. Binuclear trivalent and tetravalent uranium halides and cyanides supported by cyclooctatetraene ligands[J]. Radiochimica acta,2017,105(1):21-32. |
| APA | Wang, Cong-Zhi,Wu, Qun-Yan,Lan, Jian-Hui,Chai, Zhi-Fang,Gibson, John K.,&Shi, Wei-Qun.(2017).Binuclear trivalent and tetravalent uranium halides and cyanides supported by cyclooctatetraene ligands.Radiochimica acta,105(1),21-32. |
| MLA | Wang, Cong-Zhi,et al."Binuclear trivalent and tetravalent uranium halides and cyanides supported by cyclooctatetraene ligands".Radiochimica acta 105.1(2017):21-32. |
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