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二维铁(II)酞嗪氰基金属配合物中的自旋交叉现象。

Spin crossover in 2D iron(ii) phthalazine cyanometallic complexes.

作者信息

Hiiuk Volodymyr M, Shova Sergiu, Rotaru Aurelian, Golub Alexander A, Fritsky Igor O, Gural'skiy Il'ya A

机构信息

Department of Chemistry, Taras Shevchenko National University of Kyiv, 64 Volodymyrska St., 01601 Kyiv, Ukraine.

"Petru Poni" Institute of Macromolecular Chemistry, 41A Aleea Gr. Ghica Voda, 700487 Iasi, Romania.

出版信息

Dalton Trans. 2020 Apr 28;49(16):5302-5311. doi: 10.1039/d0dt00783h.

Abstract

Two new 2D spin-crossover (SCO) analogues of Hofmann clathrates of composition [Fe(phth)2MII(CN)4] (where phth = phthalazine; MII = Pd, Pt) have been synthesized and their structures and switchable behaviour have been characterized. Single-crystal X-ray analysis reveals that the Pt and Pd derivatives contain FeII centres equatorially surrounded by four equivalent μ4-[MII(CN)4]2- groups. Two crystallographically equivalent phthalazine (phth) ligands occupy the axial positions of each FeII site, completing its octahedral coordination environment. The stabilization of these structures is realized via supramolecular C-HM interactions and π-π stacking. Temperature-dependent magnetic susceptibility measurements showed that Pt (T1/2↓ = 211 K and T1/2↑ = 218 K) and Pd (T1/2↓ = 202 K and T1/2↑ = 207 K) derivatives display cooperative spin crossover with narrow thermal hysteresis loops. In addition, spin crossover in these complexes was characterized by optical measurements, differential scanning calorimetry, and IR and Raman spectroscopy. This research shows that the use of phthalazine leads to the production of new SCO systems with attractive transition characteristics and opens up new perspectives for the design of switchable complexes based on fused bicyclic azine ligands.

摘要

合成了两种新的组成为[Fe(酞嗪)₂MII(CN)₄](其中酞嗪 = phthalazine;MII = Pd、Pt)的霍夫曼包合物二维自旋交叉(SCO)类似物,并对其结构和可切换行为进行了表征。单晶X射线分析表明,Pt和Pd衍生物中的FeII中心在赤道平面上被四个等效的μ₄-[MII(CN)₄]²⁻基团包围。两个晶体学上等效的酞嗪(phth)配体占据每个FeII位点的轴向位置,完成其八面体配位环境。这些结构的稳定是通过超分子C-H…M相互作用和π-π堆积实现的。变温磁化率测量表明,Pt(T₁/₂↓ = 211 K,T₁/₂↑ = 218 K)和Pd(T₁/₂↓ = 202 K,T₁/₂↑ = 207 K)衍生物表现出具有窄热滞回线的协同自旋交叉。此外,通过光学测量、差示扫描量热法以及红外和拉曼光谱对这些配合物中的自旋交叉进行了表征。该研究表明,酞嗪的使用导致产生具有吸引人的转变特性的新型SCO体系,并为基于稠合双环嗪配体的可切换配合物的设计开辟了新的前景。

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