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二维(2D)霍夫曼型配位聚合物中的滞后自旋交叉

Hysteretic Spin Crossover in Two-Dimensional (2D) Hofmann-Type Coordination Polymers.

作者信息

Liu Wei, Wang Lu, Su Yu-Jun, Chen Yan-Cong, Tucek Jiri, Zboril Radek, Ni Zhao-Ping, Tong Ming-Liang

机构信息

Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education, School of Chemistry and Chemical Engineering, Sun Yat-Sen University , Guangzhou 510275, People's Republic of China.

Regional Centre of Advanced Technologies and Materials, Departments of Physical Chemistry and Experimental Physics, Faculty of Science, Palacky University , Slechtitelu 27, 783 71 Olomouc, Czech Republic.

出版信息

Inorg Chem. 2015 Sep 8;54(17):8711-6. doi: 10.1021/acs.inorgchem.5b01341. Epub 2015 Aug 10.

Abstract

Three new two-dimensional (2D) Hofmann-type coordination polymers with general formula [Fe(3-NH2py)2M(CN)4] (3-NH2py = 3-aminopyridine, M = Ni (1), Pd (2), Pt (3)) have been synthesized. Magnetic susceptibility measurements show that they exhibited cooperative spin crossover (SCO) with remarkable hysteretic behaviors. Their hysteresis widths are 25, 37, and 30 K for 1-3, respectively. The single-crystal structure of 1 suggest that the pseudo-octahedral Fe sites are equatorially bridged by M(CN)4 to form 2D grids and axially coordinated by 3-NH2py ligands. The intermolecular interactions between layers (the offset face-to-face π···π interactions, hydrogen bonds, and weak N(amino)···Ni(II) contacts) together with the covalent bonds bridged by M(CN)4 units are responsible to the significant cooperativity.

摘要

合成了三种通式为[Fe(3-NH₂py)₂M(CN)₄](3-NH₂py = 3-氨基吡啶,M = Ni (1)、Pd (2)、Pt (3))的新型二维(2D)霍夫曼型配位聚合物。磁化率测量表明,它们表现出具有显著滞后行为的协同自旋交叉(SCO)。对于1 - 3,其滞后宽度分别为25、37和30 K。1的单晶结构表明,伪八面体铁位点通过M(CN)₄在赤道面桥连形成二维网格,并由3-氨基吡啶配体轴向配位。层间的分子间相互作用(错位面对面π···π相互作用、氢键和弱N(氨基)···Ni(II)接触)以及由M(CN)₄单元桥连的共价键导致了显著的协同性。

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