铀
分子
氮化物
齿合度
化学
铀酰
结晶学
三嗪
冠醚
晶体结构
无机化学
材料科学
有机化学
冶金
离子
图层(电子)
作者
David M. King,Floriana Tuna,Eric J. L. McInnes,Jonathan McMaster,William Lewis,Alexander J. Blake,Stephen T. Liddle
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2012-06-29
卷期号:337 (6095): 717-720
被引量:342
标识
DOI:10.1126/science.1223488
摘要
The terminal uranium nitride linkage is a fundamental target in the study of f-orbital participation in metal-ligand multiple bonding but has previously eluded characterization in an isolable molecule. Here, we report the preparation of the terminal uranium(V) nitride complex [UN(Tren(TIPS))][Na(12-crown-4)(2)] {in which Tren(TIPS) = [N(CH(2)CH(2)NSiPr(i)(3))(3)](3-) and Pr(i) = CH(CH(3))(2)} by reaction of the uranium(III) complex [U(Tren(TIPS))] with sodium azide followed by abstraction and encapsulation of the sodium cation by the polydentate crown ether 12-crown-4. Single-crystal x-ray diffraction reveals a uranium-terminal nitride bond length of 1.825(15) angstroms (where 15 is the standard uncertainty). The structural assignment is supported by means of (15)N-isotopic labeling, electronic absorption spectroscopy, magnetometry, electronic structure calculations, elemental analyses, and liberation of ammonia after treatment with water.
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