Otake Ken-ichi, Otsubo Kazuya, Sugimoto Kunihisa, Fujiwara Akihiko, Kitagawa Hiroshi
Division of Chemistry, Graduate School of Science, Kyoto University , Kitashirakawa-Oiwakecho, Sakyo-ku, Kyoto 606-8502, Japan.
Japan Synchrotron Radiation Research Institute (JASRI), SPring-8 , 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5198, Japan.
Inorg Chem. 2016 Mar 7;55(5):2620-6. doi: 10.1021/acs.inorgchem.5b02980. Epub 2016 Feb 22.
One-dimensional (1D) electronic systems have attracted significant attention for a long time because of their various physical properties. Among 1D electronic systems, 1D halogen-bridged mixed-valence transition-metal complexes (the so-called MX chains) have been thoroughly studied owing to designable structures and electronic states. Here, we report the syntheses, structures, and electronic properties of three kinds of novel neutral MX-chain complexes. The crystal structures consist of 1D chains of Pt-X repeating units with (1R,2R)-(-)-diaminocychlohexane and CN(-) in-plane ligands. Because of the absence of a counteranion, the neutral MX chains have short interchain distances, so that strong interchain electronic interaction is expected. Resonance Raman spectra and diffuse-reflectance UV-vis spectra indicate that their electronic states are mixed-valence states (charge-density-wave state: Pt(2+)···X-Pt(4+)-X···Pt(2+)···X-Pt(4+)-X···). In addition, the relationship between the intervalence charge-transfer (IVCT) band gap and the degree of distortion of the 1D chain shows that the neutral MX chains have a larger IVCT band gap than that of cationic MX-chain complexes. These results provide new insight into the physical and electronic properties of 1D chain compounds.
一维(1D)电子系统因其多样的物理性质长期以来备受关注。在一维电子系统中,一维卤素桥连混合价态过渡金属配合物(即所谓的MX链)由于其可设计的结构和电子态而得到了深入研究。在此,我们报道了三种新型中性MX链配合物的合成、结构及电子性质。晶体结构由Pt-X重复单元的一维链组成,带有(1R,2R)-(-)-二氨基环己烷和面内配体CN⁻。由于不存在抗衡阴离子,中性MX链具有较短的链间距离,因此有望产生强烈的链间电子相互作用。共振拉曼光谱和漫反射紫外可见光谱表明其电子态为混合价态(电荷密度波态:Pt(2+)···X-Pt(4+)-X···Pt(2+)···X-Pt(4+)-X···)。此外,价间电荷转移(IVCT)带隙与一维链的畸变程度之间的关系表明,中性MX链的IVCT带隙比阳离子MX链配合物的更大。这些结果为一维链化合物的物理和电子性质提供了新的见解。