Atypical stoichiometry for a 3D bimetallic oxalate-based long-range ordered magnet exhibiting high proton conductivity

被引:41
作者
Maxim, Catalin [1 ,2 ,3 ]
Ferlay, Sylvie [1 ,6 ]
Tokoro, Hiroko [4 ]
Ohkoshi, Shin-Ichi [4 ]
Train, Cyrille [2 ,5 ,6 ]
机构
[1] Univ Strasbourg, UMR UDS CNRS 7140, Mol Tecton Lab, Inst Le Bel, F-67000 Strasbourg, France
[2] CNRS, LNCMI, F-38042 Grenoble 9, France
[3] Univ Bucharest, Fac Chem, Inorgan Chem Lab, Bucharest 020464, Romania
[4] Univ Tokyo, Sch Sci, Dept Chem, Tokyo 1130033, Japan
[5] Univ Grenoble Alpes, LNCMI, F-38041 Grenoble 9, France
[6] Inst Univ France, F-75005 Paris, France
关键词
METAL-ORGANIC FRAMEWORKS; COORDINATION POLYMERS; MN-II; FERROMAGNETISM; CROSSOVER; DESIGN; FIELD; CR; OX;
D O I
10.1039/c4cc00607k
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
The reproducible formation of a 3D oxalate based coordination compound of formula (NH4)(5)[ (Mn2Cr3III)-Cr-II(ox)(9)]center dot 10H(2)O, with an unusual MnII/CrIII ratio, is presented. The original topology of the anionic network leads to antiferromagnetic long-range ordering whereas its guests favour high humidity-dependent proton conductivity.
引用
收藏
页码:5629 / 5632
页数:4
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