化学
旋转交叉
渡线
金属
贵金属
自旋(空气动力学)
结晶学
热力学
有机化学
计算机科学
物理
人工智能
作者
Sergii I. Shylin,Olesia I. Kucheriv,Sergiu Shova,Vadim Ksenofontov,Wolfgang Tremel,Il’ya A. Gural'skiy
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2020-04-17
卷期号:59 (9): 6541-6549
被引量:15
标识
DOI:10.1021/acs.inorgchem.0c00627
摘要
Hofmann-like cyanometalates constitute a large class of spin-crossover iron(II) complexes with variable switching properties. However, it is not yet clearly understood how the temperature and cooperativity of a spin transition are influenced by their structure. In this paper, we report the synthesis and crystal structures of the metal–organic coordination polymers {FeII(Mepz)[AuI(CN)2]2} ([Au]) and {FeII(Mepz)2[AgI(CN)2]2} ([Ag]), where Mepz = 2-methylpyrazine, along with characterization of their spin-state behavior by variable-temperature SQUID magnetometry and Mössbauer spectroscopy. The compounds are built of cyanoheterometallic layers, which are pillared by the bridging Mepz ligands in [Au] but separated in [Ag]. The complex [Au] exhibits an incomplete stepped spin transition as a function of the temperature with TSCO1 = 170 K and TSCO2 = 308 K for the two subsequent steps. In contrast, the complex [Ag] attains the high-spin state over the whole temperature range. In the crystal structure of [Ag], weak interlayer contacts (Ag−π, Me−π, and Ag–N) are found that may be responsible for an unusual axial elongation of the FeN6 polyhedra. We propose that this structural distortion contributes to the trapping of iron in its high-spin state.
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