Electronic interaction in an outer-sphere mixed-valence double salt:: A polarized neutron diffraction study of K3(MnO4)2

被引:4
作者
Cannon, RD
Jayasooriya, UA
Tilford, C
Anson, CE
Sowrey, FE [1 ]
Rosseinsky, DR
Stride, JA
Tasset, F
Ressouche, E
White, RP
Ballou, R
机构
[1] Univ Kent, Sch Phys Sci, Canterbury CT2 7NR, Kent, England
[2] Univ Karlsruhe, Inst Anorgan Chem 2, D-76128 Karlsruhe, Germany
[3] Univ E Anglia, Sch Chem Sci, Norwich NR4 7TJ, Norfolk, England
[4] Univ Exeter, Sch Chem, Exeter EX4 4QD, Devon, England
[5] Inst Max Von Laue Paul Langevin, F-38042 Grenoble 9, France
[6] CNRS, Lab Louis Neel, F-38042 Grenoble 9, France
关键词
D O I
10.1021/ic0492340
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The mixed-valence double salt K-3(MnO4)(2) crystallizes in space group P2(1)/m with Z = 2. The manganese centers Mn1 and Mn2 constitute discrete "permanganate", [Mn(VII)O4](-), and "manganate", [(MnO4)-O-VI](2-), ions, respectively. There is a spin-ordering transition to an antiferromagnetic state at ca. T = 5 K. The spin-density distribution in the paramagnetic phase at T= 10 K has been determined by polarized neutron diffraction, confirming that unpaired spin is largely confined to the nominal manganate ion Mn2. Through use of both Fourier refinement and maximum entropy methods, the spin on Mn1 is estimated as 1.75+/-1% of one unpaired electron with an upper limit of 2.5%.
引用
收藏
页码:7061 / 7067
页数:7
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