Strong exchange and magnetic blocking in N23--radical-bridged lanthanide complexes

被引:984
作者
Rinehart, Jeffrey D. [2 ]
Fang, Ming [1 ]
Evans, William J. [1 ]
Long, Jeffrey R. [2 ]
机构
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
[2] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
基金
美国国家科学基金会;
关键词
SINGLE-MOLECULE MAGNET; ANISOTROPY BARRIER; RELAXATION; AGGREGATE; LEVEL; STATE;
D O I
10.1038/nchem.1063
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Single-molecule magnets approach the ultimate size limit for spin-based devices. These complexes can retain spin information over long periods of time at low temperature, suggesting possible applications in high-density information storage, quantum computing and spintronics. Notably, the success of most such applications hinges upon raising the inherent molecular spin-inversion barrier. Although recent advances have shown the viability of lanthanide-containing complexes in generating large barriers, weak or non-existent magnetic exchange coupling allows fast relaxation pathways that mitigate the full potential of these species. Here, we show that the diffuse spin of an N-2(3-) radical bridge can lead to exceptionally strong magnetic exchange in dinuclear Ln(II) (Ln = Gd, Dy) complexes. The Gd(III) congener exhibits the strongest magnetic coupling yet observed for that ion, while incorporation of the high-anisotropy Dy(III) ion gives rise to a molecule with a record magnetic blocking temperature of 8.3 K at a sweep rate of 0.08 T s(-1).
引用
收藏
页码:538 / 542
页数:5
相关论文
共 28 条
[11]  
Gatteschi D, 2006, MESOSCOPIC PHYS NANO, P1
[12]   Two-Step Relaxation in a Linear Tetranuclear Dysprosium(III) Aggregate Showing Single-Molecule Magnet Behavior [J].
Guo, Yun-Nan ;
Xu, Gong-Feng ;
Gamez, Patrick ;
Zhao, Lang ;
Lin, Shuang-Yan ;
Deng, Ruiping ;
Tang, Jinkui ;
Zhang, Hong-Jie .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (25) :8538-+
[13]   Coupling Dy3 Triangles Enhances Their Slow Magnetic Relaxation [J].
Hewitt, Ian J. ;
Tang, Jinkui ;
Madhu, N. T. ;
Anson, Christopher E. ;
Lan, Yanhua ;
Luzon, Javier ;
Etienne, Mael ;
Sessoli, Roberta ;
Powell, Annie K. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (36) :6352-6356
[14]   Lanthanide double-decker complexes functioning as magnets at the single-molecular level [J].
Ishikawa, N ;
Sugita, M ;
Ishikawa, T ;
Koshihara, S ;
Kaizu, Y .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (29) :8694-8695
[15]   Mononuclear lanthanide complexes with a long magnetization relaxation time at high temperatures: A new category of magnets at the single-molecular level [J].
Ishikawa, N ;
Sugita, M ;
Ishikawa, T ;
Koshihara, S ;
Kaizu, Y .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (31) :11265-11271
[16]   Effects of Chemically Induced Contraction of a Coordination Polyhedron on the Dynamical Magnetism of Bis(phthalocyaninato)disprosium, a Single-4f-Ionic Single-Molecule Magnet with a Kramers Ground State [J].
Ishikawa, Naoto ;
Mizuno, Yoshifumi ;
Takamatsu, Satoshi ;
Ishikawa, Tadahiko ;
Koshihara, Shin-ya .
INORGANIC CHEMISTRY, 2008, 47 (22) :10217-10219
[17]   Quantum computing in molecular magnets [J].
Leuenberger, MN ;
Loss, D .
NATURE, 2001, 410 (6830) :789-793
[18]   A Polynuclear Lanthanide Single-Molecule Magnet with a Record Anisotropic Barrier [J].
Lin, Po-Heng ;
Burchell, Tara J. ;
Ungur, Liviu ;
Chibotaru, Liviu F. ;
Wernsdorfer, Wolfgang ;
Murugesu, Muralee .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (50) :9489-9492
[19]   Quantifying Exchange Coupling in f-Ion Pairs Using the Diamagnetic Substitution Method [J].
Lukens, Wayne W. ;
Walter, Marc D. .
INORGANIC CHEMISTRY, 2010, 49 (10) :4458-4465
[20]  
Mannini M, 2009, NAT MATER, V8, P194, DOI [10.1038/NMAT2374, 10.1038/nmat2374]