Molecular magnets

被引:51
作者
Blundell, Stephen J. [1 ]
机构
[1] Univ Oxford, Dept Phys, Clarendon Lab, Oxford OX1 3PU, England
关键词
D O I
10.1080/00107510801967415
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Magnetic materials in which the fundamental building block is molecular have attracted a great deal of interest because they capitalize on the flexibility inherent in carbon chemistry. Some compounds incorporating chemically stable free radicals are purely organic and show long-range magnetic order at very low temperatures, but the most useful molecular magnets incorporate transition metal or lanthanide ions, with the molecular groups providing a bridge to mediate exchange interactions between the ions. Some of these materials exhibit a spin crossover effect between low-spin and high-spin states. Other molecular magnets form model low-dimensional magnetic compounds that can be used to test models of quantum spin systems. Molecular nanomagnets are complex molecules containing a number of metal ions whose individual moments conspire to create a giant magnetic moment associated with the entire molecule. These systems can be used to exhibit quantum tunnelling of magnetization and are also candidate systems for quantum computing applications.
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收藏
页码:275 / 290
页数:16
相关论文
共 124 条
[1]   A ring cycle: studies of heterometallic wheels [J].
Affronte, Marco ;
Carretta, Stefano ;
Timco, Grigore A. ;
Winpenny, Richard E. P. .
CHEMICAL COMMUNICATIONS, 2007, (18) :1789-1797
[2]   A ferromagnetically coupled Mn19 aggregate with a record S=83/2 ground spin state [J].
Ako, Ayuk M. ;
Hewitt, Ian J. ;
Mereacre, Valeritt ;
Clerac, Rodolphe ;
Wernsdorfer, Wolfgang ;
Anson, Christopher E. ;
Powell, Annie K. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (30) :4926-4929
[3]   ORGANIC MOLECULAR SOFT FERROMAGNETISM IN A FULLERENE-C60 [J].
ALLEMAND, PM ;
KHEMANI, KC ;
KOCH, A ;
WUDL, F ;
HOLCZER, K ;
DONOVAN, S ;
GRUNER, G ;
THOMPSON, JD .
SCIENCE, 1991, 253 (5017) :301-303
[4]   MAGNETIC-SUSCEPTIBILITY AND LOW-TEMPERATURE STRUCTURE OF THE LINEAR-CHAIN CUPRATE SR2CUO3 [J].
AMI, T ;
CRAWFORD, MK ;
HARLOW, RL ;
WANG, ZR ;
JOHNSTON, DC ;
HUANG, Q ;
ERWIN, RW .
PHYSICAL REVIEW B, 1995, 51 (09) :5994-6001
[5]   AN APPROXIMATE QUANTUM THEORY OF THE ANTIFERROMAGNETIC GROUND STATE [J].
ANDERSON, PW .
PHYSICAL REVIEW, 1952, 86 (05) :694-701
[6]  
Andres H, 2002, CHEM-EUR J, V8, P4867, DOI 10.1002/1521-3765(20021104)8:21<4867::AID-CHEM4867>3.0.CO
[7]  
2-R
[8]   Will spin-relaxation times in molecular magnets permit quantum information processing? [J].
Ardavan, Arzhang ;
Rival, Olivier ;
Morton, John J. L. ;
Blundell, Stephen J. ;
Tyryshkin, Alexei M. ;
Timco, Grigore A. ;
Winpenny, Richard E. P. .
PHYSICAL REVIEW LETTERS, 2007, 98 (05)
[9]   FERROMAGNETIC INTERMOLECULAR INTERACTION IN THE GALVINOXYL RADICAL - COOPERATION OF SPIN POLARIZATION AND CHARGE-TRANSFER INTERACTION [J].
AWAGA, K ;
SUGANO, T ;
KINOSHITA, M .
CHEMICAL PHYSICS LETTERS, 1987, 141 (06) :540-544
[10]  
Bean C. P., 1959, J APPL PHYS, V30, pS120, DOI [10.1063/1.2185850, DOI 10.1063/1.2185850]