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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)氮化物进行双电子还原羰基化为氰酸盐

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摘要

Two-electron reductive carbonylation of the uranium(VI) nitride [U(TrenTIPS)(N)] (2, TrenTIPS=N(CH2CH2NSiiPr3)3) with CO gave the uranium(IV) cyanate [U(TrenTIPS)(NCO)] (3). KC8 reduction of 3 resulted in cyanate dissociation to give [U(TrenTIPS)] (4) and KNCO, or cyanate retention in [U(TrenTIPS)(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(TrenTIPS)(N)K}2] (6), with or without B15C5, respectively. Complex 5 can be prepared directly from CO and [U(TrenTIPS)(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 kcal mol−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:氮化铀(VI)的两电子还原羰基化[U(TrenTIPS)(N)](2,TrenTIPS = N(CH2CH2NSiiPr3)3)与CO生成氰酸铀(IV)[U(TrenTIPS)(NCO)] (3)。 KC8减少3导致氰酸盐解离,生成[U(TrenTIPS)](4)和KNCO,或氰酸盐保留在[U(TrenTIPS)(NCO)] [K(B15C5)2](5,B15C5 = benzo-15 -cro-5醚)与B15C5。配合物5和4以及KNCO分别由CO和氮化铀[{U(TrenTIPS)(N)K} 2](6)制成,分别含或不含B15C5。配合物5可以直接从CO和[U(TrenTIPS)(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。从理论上模拟了这种前所未有的f嵌段反应性,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 cal mol-1。 )和铀(V)。提出了一个非常简单的两步,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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