Photomagnetism in Cyano-Bridged Bimetal Assemblies

被引:258
作者
Ohkoshi, Shin-Ichi [1 ,2 ]
Tokoro, Hiroko [1 ,3 ]
机构
[1] Univ Tokyo, Sch Sci, Dept Chem, Bunkyo Ku, Tokyo 1730033, Japan
[2] JST, CREST, Chiyoda Ku, Tokyo 7020076, Japan
[3] JSPS, NEXT, Chiyoda Ku, Tokyo 7028472, Japan
关键词
MAGNETIC-POLE INVERSION; PRUSSIAN BLUE ANALOGS; TRANSFER PHASE-TRANSITION; HIGH CURIE-TEMPERATURE; MOLECULE-BASED MAGNETS; PHOTOINDUCED MAGNETIZATION; SPIN-CROSSOVER; ELECTRON-TRANSFER; MIXED-VALENCE; ELECTROCHEMICAL SYNTHESIS;
D O I
10.1021/ar300068k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The study of photoinduced phase-transition materials has implications for the fields of Inorganic chemistry, solid-state chemistry, and materials science. Cyano-bridged bimetal assemblies are promising photomagnetic materials. Because cyano-bridged bimetal assemblies possess various absorption bands in the visible light region, their electronic and spin states can be controlled by visible light irradiation. Moreover, the selection of magnetic metal ions and organic ligands provide a way of controlling spin spin interactions through a cyano bridge. In this Account, we describe cyano-bridged bimetal assemblies developed in our laboratory. Cu-2(II)[Mo-IV(CN)(8)]center dot 8H(2)O (CuMo), (RbMnII)-Mn-I[Fe-III(CN)(6)] (RbMnFe), and Co-3(II)[W-V(CN)(8)](2)center dot(pyrimidine)(4)center dot 6H(2)O (CoW) induce photomagnetism via photoinduced metal-to-metal charge transfers (MM'CT), while Fe-2(II)[Nb-IV(CN)(8)]center dot(4-pyridinealdoxime)(8)center dot 2H(2)O (FeNb) exhibits a photoinduced magnetization via a photoinduced spin crossover. Irradiation with 473 nm light causes the CuMo system to exhibit a spontaneous magnetization with a Curie temperature (T-C) of 25 K, but irradiation with 532, 785, and 840 nm light reduces the magnetization. In this reversible photomagnetic process, excitation of the MM'CT from Mo-IV to Cu-II produces a ferromagnetic mixed-valence isomer of (CuCuII)-Cu-I[Mo-V(CN)(8)]center dot 8H(2)O (CuMo'). CuMo' returns to CuMo upon irradiation in the reverse-M'MCT band. RbMnFe shows a charge transfer (CT)-Induced phase transition from the Mn-II-Fe-III phase to the Mn-III-Fe-II phase. Irradiation with 532 nm light converts the Mn-III-Fe-II phase into the Mn-II-Fe-III phase, and we observe photodemagnetization. In contrast, irradiation of the Mn-II-Fe-III phase with 410 nm light causes the reverse phase transition. A CT-induced Jahn-Teller distortion Is responsible for this visible light-induced reversible photomagnetic effect. In the CoW system, a CT-induced spin transition causes the thermal phase transition from the Co-II-W-V phase to the Co-III-W-IV phase. Irradiation of the Co-III-W-IV phase with 840 nm light causes ferromagnetism with a T-C of 40 K and magnetic coercive field (H-c) of 12 000 Oe, but excitation of the back M'MCT (Co-II -> W-V) with 532 nm light leads to the reverse phase transition. These examples of the photomagnetic effect have occurred by exciting MM'CT bands. In the fields of inorganic chemistry and materials science, researchers have studied extensively the photoinduced phase transitions between low-spin (LS) and high-spin (HS) transition metal ions. Recently, we have observed the first example of photoinduced spin crossover ferromagnetism with a FeNb system (T-C = 20 K and H-c = 240 Oe), in which a strong superexchange interaction between photoproduced Fe-II(HS) and neighboring paramagnetic Nb-IV operates through a CN bridge. The optical switching magnets described in this Account may lead to novel optical recording technologies such as optomagnetic memories and optical computers.
引用
收藏
页码:1749 / 1758
页数:10
相关论文
共 95 条
[41]   HIGH-T(C) MOLECULAR-BASED MAGNETS - FERRIMAGNETIC MIXED-VALENCE CHROMIUM(III)-CHROMIUM(II) CYANIDES WITH T(C) AT 240-KELVIN AND 190-KELVIN [J].
MALLAH, T ;
THIEBAUT, S ;
VERDAGUER, M ;
VEILLET, P .
SCIENCE, 1993, 262 (5139) :1554-1557
[42]   Large lattice responses in a mixed-valence Prussian blue analogue owing to electronic and spin transitions induced by X-ray irradiation [J].
Margadonna, S ;
Prassides, K ;
Fitch, AN .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (46) :6316-6319
[43]  
MEINDERS ER, 2006, OPTICAL DATA STRAGE
[44]   Nanoporous magnets of chiral and racemic [{Mn(HL)}2Mn{Mo(CN)7}2] with switchable ordering temperatures (TC=85 K ⇆ 106 K) driven by H2O sorption (L = N,N-dimethylalaninol) [J].
Milon, Julie ;
Daniel, Marie-Christine ;
Kaiba, Abdellah ;
Guionneau, Philippe ;
Brandes, Stephane ;
Sutter, Jean-Pascal .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (45) :13872-13878
[45]   Structures of metastable states in phase transitions with a high-spin low-spin degree of freedom [J].
Miyashita, S ;
Konishi, Y ;
Tokoro, H ;
Nishino, M ;
Boukheddaden, K ;
Varret, F .
PROGRESS OF THEORETICAL PHYSICS, 2005, 114 (04) :719-735
[46]  
Miyashita S., 2009, PHYS REV B, V80, P1
[47]  
Mizuno M, 2000, ADV MATER, V12, P1955, DOI 10.1002/1521-4095(200012)12:24<1955::AID-ADMA1955>3.0.CO
[48]  
2-I
[49]   Transparent, superparamagnetic KxICoyII[FeIII(CN)6]1 -: Silica nanocomposites with tunable photomagnetism [J].
Moore, JG ;
Lochner, EJ ;
Ramsey, C ;
Dalal, NS ;
Stiegman, AE .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (24) :2741-2743
[50]   Coordination Assemblies of [Mn4] Single-Molecule Magnets Linked by Photochromic Ligands: Photochemical Control of the Magnetic Properties [J].
Morimoto, Masakazu ;
Miyasaka, Hitoshi ;
Yamashita, Masahiro ;
Irie, Masahiro .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (28) :9823-9835