Ephritikhine Michel
Service de Chimie Moléculaire, DSM, DRECAM, Laboratoire Claude Fréjacques (CNRS URA 331), CEA/Saclay, 91191, Gif-sur-Yvette, France.
Dalton Trans. 2006 Jun 7(21):2501-16. doi: 10.1039/b603463b. Epub 2006 May 8.
The intent of this Dalton Perspective is to highlight the recent advances in uranium molecular chemistry, with the results reported during the 2000-2006 period. This discipline is currently witnessing an impressive development, together with the theoretical chemistry and solid-state chemistry of the f-elements, and its face has profoundly changed, revealing unsuspected structural and reactivity features. This progress required and was facilitated by the use of new precursors. Studies of low-valent compounds gave a better insight into lanthanide(III)/actinide(III) differentiation and led to the discovery of unusual reactions, including activation of small molecules. A number of tetravalent uranium complexes, in particular polynuclear compounds, have been synthesized, which exhibit exciting structures and physicochemical properties. The potential of uranium(III) and uranium(IV) complexes in catalysis has been confirmed. The uranyl complexes, from mononuclear species to supramolecular assemblies, reveal a variety of novel structures, changing the generally accepted ideas on the coordination geometry and the stability of the UO2(2+) ion.
这篇《道尔顿视角》文章的目的是突出2000年至2006年期间报道的铀分子化学的最新进展。这一学科目前正经历着令人瞩目的发展,与f元素的理论化学和固态化学一起,其面貌已发生了深刻变化,展现出了意想不到的结构和反应特性。这一进展得益于新前体的使用,同时也需要新前体的使用。低价化合物的研究使人们对镧系元素(III)/锕系元素(III)的差异有了更深入的了解,并导致了包括小分子活化在内的异常反应的发现。已经合成了许多四价铀配合物,特别是多核化合物,它们展现出令人兴奋的结构和物理化学性质。铀(III)和铀(IV)配合物在催化方面的潜力已得到证实。从单核物种到超分子组装体的铀酰配合物揭示了各种新颖的结构,改变了人们对UO2(2+)离子配位几何和稳定性的普遍看法。