Programmable spin-state switching in a mixed-valence spin-crossover iron grid

被引:171
作者
Matsumoto, Takuto [1 ]
Newton, Graham N. [1 ]
Shiga, Takuya [1 ]
Hayami, Shinya [2 ]
Matsui, Yuta [3 ]
Okamoto, Hiroshi [3 ]
Kumai, Reiji [4 ]
Murakami, Youichi [4 ]
Oshio, Hiroki [1 ]
机构
[1] Univ Tsukuba, Dept Chem, Grad Sch Pure & Appl Sci, Tsukuba, Ibaraki 3058571, Japan
[2] Kumamoto Univ, Dept Chem, Grad Sch Sci & Technol, Kumamoto 8608555, Japan
[3] Univ Tokyo, Grad Sch Frontier Sci, Dept Adv Mat Sci, Chiba 2778561, Japan
[4] High Energy Accelerator Res Org KEK, Inst Mat Struct Sci, Photon Factory & Condensed Matter Res Ctr, Tsukuba, Ibaraki 3050801, Japan
基金
日本学术振兴会;
关键词
INTERSYSTEM CROSSING DYNAMICS; COORDINATION-COMPOUNDS; MOLECULAR MATERIALS; IRON(III) COMPOUNDS; MEMORY DEVICES; TRANSITION; COMPLEXES; TEMPERATURE; LIGHT; COMPOUND;
D O I
10.1038/ncomms4865
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Photo-switchable systems, such as discrete spin-crossover complexes and bulk iron-cobalt Prussian blue analogues, exhibit, at a given temperature, a bistability between low-and high-spin states, allowing the storage of binary data. Grouping different bistable chromophores in a molecular framework was postulated to generate a complex that could be site-selectively excited to access multiple electronic states under identical conditions. Here we report the synthesis and the thermal and light-induced phase transitions of a tetranuclear iron(II) grid-like complex and its two-electron oxidized equivalent. The heterovalent grid is thermally inactive but the spin states of its constituent metal ions are selectively switched using different laser stimuli, allowing the molecule to exist in three discrete phases. Site-selective photo-excitation, herein enabling one molecule to process ternary data, may have major ramifications in the development of future molecular memory storage technologies.
引用
收藏
页数:8
相关论文
共 47 条
[41]   Spin Transitions in Fe(II) Metallogrids Modulated by Substituents, Counteranions, and Solvents [J].
Wang, Yi-Tong ;
Li, Shu-Tao ;
Wu, Shu-Qi ;
Cui, Ai-Li ;
Shen, De-Zhong ;
Kou, Hui-Zhong .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (16) :5942-5945
[42]   CHIRAL HETEROCYCLIC LIGANDS .7. SYNTHESES OF SOME CHIRAL 2,6-DI-N-PYRAZOLYLPYRIDINES [J].
WATSON, AA ;
HOUSE, DA ;
STEEL, PJ .
JOURNAL OF ORGANIC CHEMISTRY, 1991, 56 (12) :4072-4074
[43]   Spin-Crossover Fe4II Squares: Two-Step Complete Spin Transition and Reversible Single-Crystal-to-Single-Crystal Transformation [J].
Wei, Rong-Jia ;
Huo, Qian ;
Tao, Jun ;
Huang, Rong-Bin ;
Zheng, Lan-Sun .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (38) :8940-8943
[44]   A Spin-Crossover Cluster of Iron(II) Exhibiting a Mixed-Spin Structure and Synergy between Spin Transition and Magnetic Interaction [J].
Wu, Da-Yu ;
Sato, Osamu ;
Einaga, Yasuaki ;
Duan, Chun-Ying .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (08) :1475-1478
[45]   Exceptionally efficient unsymmetrical ruthenium(II) NNN complex catalysts bearing a pyridyl-based pyrazolyl-imidazolyl ligand for transfer hydrogenation of ketones [J].
Zeng, Fanlong ;
Yu, Zhengkun .
ORGANOMETALLICS, 2008, 27 (13) :2898-2901
[46]   A novel magnetically coupled nonamanganese(II) 3 x 3 portcullis-like grid involving just oxygen bridges, generated by strict self assembly of the metal cation and a single heptadentate ligand [J].
Zhao, LA ;
Matthews, CJ ;
Thompson, LK ;
Heath, SL .
CHEMICAL COMMUNICATIONS, 2000, (04) :265-266
[47]   Theoretical Analysis of Spin Crossover in Iron(II) [2 x 2] Molecular Grids [J].
Zueva, Ekaterina M. ;
Ryabikh, Elmira R. ;
Borshch, Serguei A. .
INORGANIC CHEMISTRY, 2011, 50 (21) :11143-11151