Molecular rotor of Cs2([18]crown-6)3 in the solid state coupled with the magnetism of [Ni(dmit)2]

被引:116
作者
Akutagawa, T [1 ]
Shitagami, K
Nishihara, S
Takeda, S
Hasegawa, T
Nakamura, T
Hosokoshi, Y
Inoue, K
Ikeuchi, S
Miyazaki, Y
Saito, K
机构
[1] Hokkaido Univ, Res Inst Elect Sci, Sapporo, Hokkaido 0600812, Japan
[2] JST, CREST, Kawaguchi 3320012, Japan
[3] Hokkaido Univ, Grad Sch Environm Earth Sci, Sapporo, Hokkaido 0600810, Japan
[4] Hokkaido Univ, Grad Sch Sci, Sapporo, Hokkaido 0600810, Japan
[5] Inst Mol Sci, Okazaki, Aichi 4448585, Japan
[6] Osaka Univ, Grad Sch Sci, Res Ctr Mol Thermodynam, Toyonaka, Osaka 5600043, Japan
关键词
D O I
10.1021/ja043527a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanoscale molecular rotors that can be driven in the solid state have been realized in Cs-2([18]crown-6)(3)[Ni(dmit)(2)](2) crystals. To provide interactions between the molecular motion of the rotor and the electronic system, [Ni(dmit)(2)](-) ions, which bear one S = (1)/(2) spin on each molecule, were introduced into the crystal. Rotation of the [18]crown-6 molecules within a Cs-2([18]crown-6)(3) supramolecule above 220 K was confirmed using X-ray diffraction, NMR, and specific heat measurements. Strong correlations were observed between the magnetic behavior of the [Ni(dmit)(2)](-) ions and molecular rotation. Furthermore, braking of the molecular rotation within the crystal was achieved by the application of hydrostatic pressure.
引用
收藏
页码:4397 / 4402
页数:6
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