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BiMn6PO12, a new bismuth manganese II/III oxyphosphate with an original manganese-oxygen cubic network

机译:BiMn6PO12,一种具有原始锰氧立方网络的新型铋锰II / III氧磷酸盐

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A new bismuth manganese oxyphosphate, BiMn6PO12, with an original cubic structure has been synthesized by solid state reaction from Bi2O3, MnO2, and (NH4)(2)HPO4 or BiPO4 and Mn3O4 mixtures. Its crystal structure has been determined from single-crystal X-ray diffraction data, It crystallizes in the cubic system with space group Fm (3) over barm and unit cell parameter a = 9.626(1) Angstrom, Z = 4. A full-matrix least-squares refinement yielded R = 0.044 and R-w = 0.045 for 131 independent reflections with I > 2 sigma (I) collected on a Philips PW100 diffractometer (MoK alpha radiation). The structure of BiMn6PO12 is characterized by a three-dimensional network of manganese-oxygen bonds. The oxygen atoms form a rhombicuboctahedron. The manganese atoms occupy two-thirds of the square faces of this polyhedron and are at the vertices of cuboctahedra, Manganese and oxygen atoms form a Mn12O24 cage, which constitute the strong basic element of the global building. The PO4 tetrahedron is located within this cage and can be moved between two equivalent orientations. The connection between Mn12O24 entities created little cubic holes occupied by bismuth atoms. In this compound all the manganese atoms are crystallographically equivalent and the mean oxidation state of manganese is +2.67. A superstructure, which could be due to PO4 orientations ordering, was evidenced by an electronic diffraction study. BiMn6PO12 exhibits complicated magnetic behavior with several magnetic transitions both in the paramagnetic state and in the low-temperature ordered state. (C) 2001 Academic Press. [References: 33]
机译:通过固相反应从Bi2O3,MnO2和(NH4)(2)HPO4或BiPO4和Mn3O4混合物固相反应合成了一种具有原始立方结构的新型氧化铋锰铋BiMn6PO12。它的晶体结构是根据单晶X射线衍射数据确定的,它在立方系统中以Barm的空间群Fm(3)和晶胞参数a = 9.626(1)埃,Z = 4进行结晶。在飞利浦PW100衍射仪上收集的I> 2σ(I)的131个独立反射的最小二乘矩阵精化结果分别为R = 0.044和Rw = 0.045(MoK alpha辐射)。 BiMn6PO12的结构特征在于锰-氧键的三维网络。氧原子形成菱形八面体。锰原子占据了该多面体正方形表面的三分之二,并且位于立方八面体的顶点,锰和氧原子形成了Mn12O24笼,构成了全球建筑的强大基础元素。 PO4四面体位于此笼中,可以在两个等效方向之间移动。 Mn12O24实体之间的连接产生了由铋原子占据的小立方孔。在该化合物中,所有锰原子在晶体学上均等价,并且锰的平均氧化态为+2.67。通过电子衍射研究证明了可能是由于PO4取向有序的上层建筑。 BiMn6PO12表现出复杂的磁行为,在顺磁态和低温有序态均具有多个磁跃迁。 (C)2001学术出版社。 [参考:33]

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