School of Chemistry, University of Nottingham, University Park, Nottingham NG7 2RD, United Kingdom.
Proc Natl Acad Sci U S A. 2012 Jun 12;109(24):9265-70. doi: 10.1073/pnas.1203417109. Epub 2012 May 31.
Carbon monoxide (CO) is in principle an excellent resource from which to produce industrial hydrocarbon feedstocks as alternatives to crude oil; however, CO has proven remarkably resistant to selective homologation, and the few complexes that can effect this transformation cannot be recycled because liberation of the homologated product destroys the complexes or they are substitutionally inert. Here, we show that under mild conditions a simple triamidoamine uranium(III) complex can reductively homologate CO and be recycled for reuse. Following treatment with organosilyl halides, bis(organosiloxy)acetylenes, which readily convert to furanones, are produced, and this was confirmed by the use of isotopically (13)C-labeled CO. The precursor to the triamido uranium(III) complex is formed concomitantly. These findings establish that, under appropriate conditions, uranium(III) can mediate a complete synthetic cycle for the homologation of CO to higher derivatives. This work may prove useful in spurring wider efforts in CO homologation, and the simplicity of this system suggests that catalytic CO functionalization may soon be within reach.
一氧化碳(CO)原则上是一种极好的资源,可以用来生产替代原油的工业碳氢化合物原料;然而,CO 被证明对选择性同系化具有很强的抗性,并且能够实现这种转化的少数配合物不能被回收,因为同系化产物的释放会破坏配合物或它们是取代惰性的。在这里,我们表明在温和的条件下,一种简单的三氨基胺铀(III)配合物可以还原同系化 CO 并可回收再利用。用有机硅卤化物处理后,很容易转化为呋喃酮的双(有机硅氧基)乙炔生成,这通过使用同位素(13)C 标记的 CO 得到了证实。三氨基铀(III)配合物的前体同时形成。这些发现表明,在适当的条件下,铀(III)可以介导 CO 向更高衍生物同系化的完整合成循环。这项工作可能有助于推动 CO 同系化的更广泛努力,并且该系统的简单性表明催化 CO 功能化可能很快就会实现。