Slow relaxation of the magnetization in high-nuclearity Ln-complexes

被引:40
作者
Gu, Xiaojun [2 ]
Clerac, Rodolphe [1 ]
Houri, Ahmad [1 ]
Xue, Dongfeng [2 ]
机构
[1] Univ Bordeaux 1, CNRS, Ctr Rech Paul Pascal, UPR8641, F-33600 Pessac, France
[2] Dalian Univ Technol, State Key Lab Fine Chem, Dept Mat Sci & Chem Engn, Dalian 116012, Peoples R China
基金
中国国家自然科学基金;
关键词
surface modification; lanthanide; cluster; slow relaxation; magnetization;
D O I
10.1016/j.ica.2008.02.051
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
By the surface modi. cation strategy, a novel high-nuclearity lanthanide complex with a discrete structure, Er26I(mu(3)-OH)(20)(mu(3)-O)(6)(NO3)(9)(IN)(33)(OH)(3)(H2O)(33) (noted Er-26, HIN = isonicotinic acid), has been prepared under hydrothermal conditions. The magnetic properties of Er26 and two analogue dysprosium assemblies Dy30I(mu(3)-OH)(24)(mu(3)-O)(6)(NO3)(9)(IN)(41)(OH)(3)(H2O)(38) (noted Dy-26-I) and Dy26I(mu(3)-OH)(20)(mu(3)-O) (6)(NO3)(9)(IN)(31.25)(OH)(4.75)(H2O)(41.75) (noted Dy-26-II) have been studied. The results show that the slow relaxation of the magnetization is newly found in Dy-26-I constructed from {Dy-26} and {Dy-4} cluster units. The {Dy-4} units in Dy-26-I, the relative orientation of the complex or the inter-molecular interactions between {Dy26} cores might play an important role in the origin of this magnetic behavior. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:3873 / 3876
页数:4
相关论文
共 30 条
[11]   3D coordination framework [Ln4(μ3-OH)2Cu6I5(IN)8(OAc)3] (IN = isonicotinate):: Employing 2D layers of lanthanide wheel clusters and 1D chains of copper halide clusters [J].
Gu, Xiaojun ;
Xue, Dongfeng .
INORGANIC CHEMISTRY, 2007, 46 (13) :5349-5353
[12]   Surface modification of high-nuclearity lanthanide clusters:: Two tetramers constructed by cage-shaped {Dy26} clusters and isonicotinate linkers [J].
Gu, Xiaojun ;
Xue, Dongfeng .
INORGANIC CHEMISTRY, 2007, 46 (08) :3212-3216
[13]   Lanthanide clusters with internal Ln ions: Highly emissive molecules with solid-state cores [J].
Kornienko, A ;
Emge, TJ ;
Kumar, GA ;
Riman, RE ;
Brennan, JG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (10) :3501-3505
[14]   Slow relaxation in a one-dimensional rational assembly of antiferromagnetically coupled [Mn4] single-molecule magnets [J].
Lecren, L ;
Roubeau, O ;
Coulon, C ;
Li, YG ;
Le Goff, XF ;
Wernsdorfer, W ;
Miyasaka, H ;
Clérac, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (49) :17353-17363
[15]   Quantum tunneling and quantum phase interference in a [MnII2MnIII2] single-molecule magnet [J].
Lecren, L ;
Wernsdorfer, W ;
Li, YG ;
Roubeau, O ;
Miyasaka, H ;
Clérac, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (32) :11311-11317
[16]   One-dimensional supramolecular organization of single-molecule magnets [J].
Lecren, Lollita ;
Wernsdorfer, Wolfgang ;
Li, Yang-Guang ;
Vindigni, Alessandro ;
Miyasaka, Hitoshi ;
Clerac, Rodolphe .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (16) :5045-5051
[17]   Quantum computing in molecular magnets [J].
Leuenberger, MN ;
Loss, D .
NATURE, 2001, 410 (6830) :789-793
[18]   An S=6 cyanide-bridged octanuclear FeIII4NiII4 complex that exhibits slow relaxation of the magnetization [J].
Li, DF ;
Parkin, S ;
Wang, GB ;
Yee, GT ;
Clerac, R ;
Wernsdorfer, W ;
Holmes, SM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (13) :4214-4215
[19]  
Ma BQ, 2000, ANGEW CHEM INT EDIT, V39, P3644, DOI 10.1002/1521-3773(20001016)39:20<3644::AID-ANIE3644>3.0.CO
[20]  
2-1