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Issue 19, 2016
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Octanuclear Ni(II) cubes based on halogen-substituted pyrazolates: synthesis, structure, electrochemistry and magnetism

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Abstract

The employment of halogen-substituted pyrazole ligands in nickel(II) clusters afforded three anionic Ni(II) cubes, (HNEt3)2[Ni8(Xpz)12(OH)6] (X = Cl, 1·2CH3CN; X = Br, 2·2CH3CN; X = I, 3·12CH3CN; pz = pyrazolate). Clusters 1–3 are isolated as dianionic compounds which have similar cube geometry with each vertex occupied by a Ni(II) atom and eight μ4-OH capped on eight square faces. The Xpz ligands adopt a bidentate mode to bind paired Ni(II) atoms on the edge of the cube. Interestingly, the three Ni8 cubes have similar symmetry, size and shape but pack together to form different lattice symmetry, which should be dictated by the halogen-related supramolecular interactions (C–X⋯H, C–X⋯π and X⋯X halogen bonding) in different crystals. The electrochemistry of 1–3 showed a Ni(II)/Ni(I) redox couple with E1/2 at ca. 900 mV and the oxidization potential order is 1 > 3 > 2 depending on the halogen substituents. 1–3 exhibit excellent electrocatalytic performances toward the oxidation of nitrite. The different packing of Ni8 cubes in 1–3 also has an important influence on their magnetic behaviors. Complex 2 showed antiferromagnetic couplings between the Ni(II) ions within the cubes, whereas 1 and 3 exclusively exhibited mixed ferromagnetic and antiferromagnetic properties, leading to frustration and typical spin glass behavior.

Graphical abstract: Octanuclear Ni(ii) cubes based on halogen-substituted pyrazolates: synthesis, structure, electrochemistry and magnetism

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Publication details

The article was received on 07 Mar 2016, accepted on 09 Apr 2016 and first published on 11 Apr 2016


Article type: Paper
DOI: 10.1039/C6CE00528D
Citation: CrystEngComm, 2016,18, 3462-3471
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    Octanuclear Ni(II) cubes based on halogen-substituted pyrazolates: synthesis, structure, electrochemistry and magnetism

    Z. Wang, Z. Jagličić, L. Han, G. Zhuang, G. Luo, S. Zeng, C. Tung and D. Sun, CrystEngComm, 2016, 18, 3462
    DOI: 10.1039/C6CE00528D

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