Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, PR China.
Inorg Chem. 2009 Dec 7;48(23):11209-14. doi: 10.1021/ic9016867.
The first layered iron borate, Fe(5)O(5)[B(6)O(10)(OH)(3)] x nH(2)O, has been prepared by the boric acid flux method. Its structure, determined by single crystal X-ray diffraction, contains a double FeO(6)-octahedral layer and an unusual [B(6)O(13)] chain. The rigid and cambered [B(6)O(13)] chains bend the octahedral layers, resulting in a wave-like and sandwiched structure. Crystallographic study indicates the structural modulation is mainly from the [B(6)O(13)] chains because of the insertion of water molecules in between. Nevertheless, FeO(6) layers in the average structure, which are well separated by borate chains, is still a reasonable model to understand the two-dimensional magnetism. The strong antiferromagnetic interactions and the complex Fe(3+)-net suggest a possible geometrically magnetic frustration, which may be the reason for the second-order temperature-induced magnetic transition at approximately 125 K. The condensed Fe(3+) layers and the relatively low redox potential at about 1.25 V versus Li(+)/Li show its potentials as an anodic material.
首例层状铁硼酸盐 Fe(5)O(5)[B(6)O(10)(OH)(3)] x nH(2)O 采用硼酸助熔剂法制备。通过单晶 X 射线衍射确定其结构包含双层 FeO(6)-八面体层和独特的[B(6)O(13)]链。刚性和弯曲的[B(6)O(13)]链使八面体层弯曲,形成波浪状和夹层结构。晶体结构研究表明,结构的调制主要来自[B(6)O(13)]链,因为水分子插入其中。然而,在平均结构中,由硼酸盐链隔开的 FeO(6)层仍然是理解二维磁性的合理模型。强烈的反铁磁相互作用和复杂的 Fe(3+)-网络表明可能存在几何磁阻,这可能是在大约 125 K 时发生二级温度诱导磁转变的原因。密集的 Fe(3+)层和大约 1.25 V 相对于 Li(+)/Li 的较低氧化还原电位表明其具有作为阳极材料的潜力。