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首页> 外文期刊>Angewandte Chemie >Two-Electron Reductive Carbonylation of Terminal Uranium(V) and Uranium(VI) Nitrides to Cyanate by Carbon Monoxide
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Two-Electron Reductive Carbonylation of Terminal Uranium(V) and Uranium(VI) Nitrides to Cyanate by Carbon Monoxide

机译:一氧化碳将末端铀(V)和铀(VI)的两电子还原羰基化为氰酸盐

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摘要

Two-electron reductive carbonylation of the ura-nium(VI) nitride [U(Tren~(TIPS))(N)] (2, Tren~(TIPS) = N(CH2CH2NSiiPr3)3) with CO gave the uranium(IV) cyanate [U(Tren~(TIPS))(NCO)J (3). KC8 reduction of 3 resulted in cyanate dissociation to give [U(Tren~(TIPS))] (4) and KNCO, or cyanate retention in [U(Tren~(TIPS))(NCO)][K(B15C5)2] (5, B15C5 = benzo-15-crown-5 ether) with B15C5. Complexes 5 and 4 and KNCO were also prepared from CO and the uranium(V) nitride [{U(Tren~(TIPS))(N)K}2] (6), with or without B15C5, respectively. Complex 5 can be prepared directly from CO and [U(Tren~(TIPS))(N)][K(B15C5)2] (7). Notably, 7 reacts with CO much faster than 2. This unprecedented f-block reactivity was modeled theoretically, revealing nucleophilic attack of the π* orbital of CO by the nitride with activation energy barriers of 24.7 and 11.3 kcalmol~(-1) for uranium(VI) and uranium(V), respectively. A remarkably simple two-step, two-electron cycle for the conversion of azide to nitride to cyanate using 4, NaN3 and CO is presented.
机译:用CO对氮化铀(VI)进行两电子还原羰基化[U(Tren〜(TIPS))(N)](2,Tren〜(TIPS)= N(CH2CH2NSiiPr3)3)得到铀(IV)氰酸盐[U(Tren〜(TIPS))(NCO)J(3)。 KC8减少3导致氰酸盐解离,生成[U(Tren〜(TIPS))(4)和KNCO,或氰酸盐保留在[U(Tren〜(TIPS))(NCO)] [K(B15C5)2]中(5,B15C5 =苯并15-冠-5醚)与B15C5。配合物5和4以及KNCO分别由具有或不具有B15C5的CO和氮化铀(V)氮化物[{U(Tren〜(TIPS))(N)K} 2](6)制备。络合物5可以直接从CO和[U(Tren〜(TIPS))(N)] [K(B15C5)2](7)制备。值得注意的是,7与CO的反应要比2快得多。从理论上对这种前所未有的f嵌段反应性进行了建模,揭示了氮化物对CO的π*轨道的亲核攻击,铀的活化能垒为24.7和11.3 kcalmol〜(-1)。 (VI)和铀(V)。提出了一种非常简单的两步,两电子循环,用于使用4,NaN3和CO将叠氮化物转化为氮化物以生成氰酸盐。

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