Effects of intercluster coupling in high spin molecular magnets

被引:11
作者
Affronte, A
Sessoli, R
Gatteschi, D
Wernsdorfer, W
Lasjaunias, JC
Heath, SL
Powell, AK
Fort, A
Rettori, A
机构
[1] Univ Modena, INFM S, Natl Res Ctr Nanostruct & Biosyst Surfaces, I-41100 Modena, Italy
[2] Univ Modena, Dipartimento Fis, I-41100 Modena, Italy
[3] Univ Florence, INSTM, I-50019 Sesto Fiorentino, Italy
[4] Univ Florence, Dipartimento Chim, I-50019 Sesto Fiorentino, Italy
[5] CNRS, Lab Louis Neel, F-38042 Grenoble, France
[6] CNRS, Ctr Rech Tres Basses Temp, F-38042 Grenoble, France
[7] Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
[8] Univ Karlsruhe, Inst Inorgan Chem, D-76131 Karlsruhe, Germany
[9] Univ Florence, INFM, I-50019 Sesto Fiorentino, Italy
[10] Univ Florence, Dipartimento Fis, I-50019 Sesto Fiorentino, Italy
关键词
D O I
10.1016/j.jpcs.2003.11.009
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report evidences for long-range antiferromagnetic (AF) order in iron oxyhydroxides Fe(19)metheidi and (enH(2))(2)Fe-6 clusters that at low temperature behave like single molecule magnets with total spin S = 33/2 and S = 5, respectively. Anomalies are clearly observed at 1.19 K in the heat capacity and in the low-field magnetization of Fe(19)metheidi while for (enH(2))(2)Fe-6 a broad gimel-peak is found at 0.99 K in the heat capacity. Since dipolar interactions are estimated to be similar to190 mK and similar to40 mK for Fe(19)metheidi and (enH(2))(2)Fe-6, respectively, the origin of the A-F ordering is due to super-exchange in these cases. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:745 / 748
页数:4
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