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Ni-Centered Coordination-Induced Spin-State Switching Triggered by Electrical Stimulation
被引:12
|作者:
Al Shehimy, Shaymaa
[1
]
Baydoun, Orsola
[1
]
Denis-Quanquin, Sandrine
[1
]
Mulatier, Jean-Christophe
[1
]
Khrouz, Lhoussain
[1
]
Frath, Denis
[1
]
Dumont, Elise
[1
,2
]
Murugesu, Muralee
[3
,4
]
Chevallier, Floris
[1
]
Bucher, Christophe
[1
]
机构:
[1] CNRS, ENSL, Lab Chim UMR 5182, F-69342 Lyon, France
[2] Inst Univ France, F-75005 Paris, France
[3] Univ Ottawa, Dept Chem & Biomol Sci, Ottawa, ON K1N 6N5, Canada
[4] Univ Ottawa, Ctr Catalysis Res & Innovat, Ottawa, ON K1N 6N5, Canada
关键词:
MAGNETIC-PROPERTIES;
ELECTRONIC-STRUCTURE;
ROOM-TEMPERATURE;
PHASE-TRANSITION;
RATIONAL DESIGN;
CROSSOVER;
PORPHYRINS;
NICKEL(II);
COMPLEXES;
METAMORPHISM;
D O I:
10.1021/jacs.2c07196
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
We herein report the synthesis and magnetic properties of a Ni(II)-porphyrin tethered to an imidazole ligand through a flexible electron-responsive mechanical hinge. The latter is capable of undergoing a large amplitude and fully reversible folding motion under the effect of electrical stimulation. This redox-triggered movement is exploited to force the axial coordination of the appended imidazole ligand onto the square-planar Ni(II) center, resulting in a change in its spin state from low spin (S = 0) to high spin (S = 1) proceeding with an 80% switching efficiency. The driving force of this reversible folding motion is the pi -dimerization between two electrogenerated viologen cation radicals. The folding motion and the associated spin state switching are demonstrated on the grounds of NMR, (spectro)electrochemical, and magnetic data supported by quantum calculations.
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页码:17955 / 17965
页数:11
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