期刊
CHEMISTRY-A EUROPEAN JOURNAL
卷 22, 期 2, 页码 772-782出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201503583
关键词
cyclopentadienyl ligands; hydrides; oxidation states; reduction; uranium
资金
- National Science Foundation [CHE-1464841]
- Chemical Sciences, Geosciences, and Biosciences Division of the Office of Basic Energy Sciences of the Department of Energy [DE-SC0004739]
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [1464841] Funding Source: National Science Foundation
The synthesis of new molecular complexes of U2+ has been pursued to make comparisons in structure, physical properties, and reactivity with the first U2+ complex, [K(2.2.2-cryptand)][Cp'U-3], 1 (Cp'=C5H4SiMe3). Reduction of Cp '' U-3 [Cp ''=C5H3(SiMe3)(2)] with KC8 in the presence of 2.2.2-cryptand or 18-crown-6 generates [K(2.2.2-cryptand)][Cp '' U-3], 2-K(crypt), or [K(18-crown-6)(THF)(2)][Cp '' U-3], 2-K(18c6), respectively. The UV/Vis spectra of 2-K and 1 are similar, and they are much more intense than those of U3+ analogues. Variable temperature magnetic susceptibility data for 1 and 2-K(crypt) reveal lower room temperature cMT values relative to the experimental values for the 5f3 U3+ precursors. Stability studies monitored by UV/Vis spectroscopy show that 2-K(crypt) and 2-K(18c6) have t(1/2) values of 20 and 15 h at room temperature, respectively, vs. 1.5 h for 1. Complex 2-K(18c6) reacts with H-2 or PhSiH3 to form the uranium hydride, [K(18-crown-6)(THF) 2][Cp '' 3UH], 3. Complexes 1 and 2-K(18c6) both reduce cyclooctatetraene to form uranocene, (C8H8)(2)U, as well as the U3+ byproducts [K(2.2.2-cryptand)][Cp'U-4], 4, and Cp '' U-3, respectively.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据