Department of Chemistry, Taras Shevchenko National University of Kyiv, 64 Volodymyrska Street, 01601 Kiev, Ukraine.
Institute of Inorganic Chemistry and Analytical Chemistry, Johannes Gutenberg-University of Mainz, Duesbergweg 10-14, 55128 Mainz, Germany.
Nat Commun. 2017 Jan 19;8:14099. doi: 10.1038/ncomms14099.
In nature, iron, the fourth most abundant element of the Earth's crust, occurs in its stable forms either as the native metal or in its compounds in the +2 or +3 (low-valent) oxidation states. High-valent iron (+4, +5, +6) compounds are not formed spontaneously at ambient conditions, and the ones obtained synthetically appear to be unstable in polar organic solvents, especially aqueous solutions, and this is what limits their studies and use. Here we describe unprecedented iron(IV) hexahydrazide clathrochelate complexes that are assembled in alkaline aqueous media from iron(III) salts, oxalodihydrazide and formaldehyde in the course of a metal-templated reaction accompanied by air oxidation. The complexes can exist indefinitely at ambient conditions without any sign of decomposition in water, nonaqueous solutions and in the solid state. We anticipate that our findings may open a way to aqueous solution and polynuclear high-valent iron chemistry that remains underexplored and presents an important challenge.
在自然界中,铁是地壳中第四丰富的元素,以稳定的形式存在,要么是单质,要么是以+2 或+3(低价)氧化态的化合物形式存在。高价铁(+4、+5、+6)化合物不会在环境条件下自发形成,而通过合成获得的化合物在极性有机溶剂中,特别是在水溶液中,似乎不稳定,这限制了它们的研究和应用。在这里,我们描述了前所未有的铁(IV)六氨合笼形配合物,它们是在碱性水介质中由铁(III)盐、草酸二酰二肼和甲醛在金属模板反应过程中组装而成的,反应伴随着空气氧化。在环境条件下,这些配合物可以无限期存在,在水中、非水溶剂中和固态中都没有任何分解的迹象。我们预计,我们的发现可能为水溶液和多核高价铁化学开辟一条道路,这些领域仍未得到充分探索,是一个重要的挑战。