首页> 外文期刊>Crystal growth & design >Syntheses, Structural Variation, and Characterization of a Series of Crystalline Coordination Compounds with 4-Benzene-1,2,4-triazole: Polymorph, Incomplete Spin Transition, and Single Crystal-to-Single Crystal Transformation
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Syntheses, Structural Variation, and Characterization of a Series of Crystalline Coordination Compounds with 4-Benzene-1,2,4-triazole: Polymorph, Incomplete Spin Transition, and Single Crystal-to-Single Crystal Transformation

机译:一系列与4-苯-1,2,4-三唑的结晶配位化合物的合成,结构变异和表征:多晶型,不完全自旋转变和单晶至单晶转变

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摘要

Based on the 4-substituted 1,2,4-triazole derivate ligand 4-benzene-1,2,4-triazole (L), a series of crystalline coordination complexes varying from mononuclear to trinuclear species, namely, [Zn(L)_2Br_2] (1), [Zn(L)_2Br_2] (2), [Fe(L)_4(NCS)_2]_2 (3), [Fe_2(μ_2-L)_3(L)_2(NCS)_4]·CH_3OH·CH_3CH_2OH (4), [Fe_2(μ_2-L)_3(L)_2(NCS)_4]·2CH_3CH_2OH (5), [Fe_2(μ_2-L)_3(L)_2(NCS)_4]·2CH_3CH_2OH·1.5H_2O (6), and [Ni_3(μ_2-L)6(L)_4(H_2O)_2](NO_3)_6·15.5H_2O (7), have been isolated. 1 and 2 present a temperature-induced polymorphic phenomenon of two zinc(II) coordination complexes with L. The solvent effect plays the key role for the self-assembly of these Fe(II) complexes 3-6: 3 contains mononuclear Fe(L)_4(NCS)_2 units without spin-transition behavior, whereas both 4 and 5 present binuclear Fe(II) complexes with three N_1,N_2-1,2,4-triazole bridges exhibiting incomplete spin-transition behavior. The low-temperature X-ray structural analysis (100 K) of 4 also confirms that one of the Fe(II) centers is located at the low-spin (LS) state and the other Fe(II) center is located at the high-spin (HS) state. Interestingly, when the binuclear Fe(II) complex 5 was exposed in the water atmosphere, solvent-induced single crystal-tosingle crystal transformation can be observed, and the binuclear Fe(II) complex 6 exhibiting antiferromagnetic interactions can be isolated. Further, a trinuclear crystalline compound is isolated when Ni(II) salts were used to react with L. Variabletemperature magnetic susceptibility measurement (2-300 K) reveals antiferromagnetic interactions in 7. The polymorphic phenomenon (1 and 2), incomplete spin-transition phenomenon (4 and 5), and single crystal-to-single crystal transformation (from 5 to 6) also reveal great potential in the construction of these novel functional materials with L.
机译:基于4-取代的1,2,4-三唑衍生物配体4-苯-1,2,4-三唑(L),从单核到三核的一系列晶体配位化合物,即[Zn(L) _2Br_2](1),[Zn(L)_2Br_2](2),[Fe(L)_4(NCS)_2] _2(3),[Fe_2(μ_2-L)_3(L)_2(NCS)_4] ·CH_3OH·CH_3CH_2OH(4),[Fe_2(μ_2-L)_3(L)_2(NCS)_4]·2CH_3CH_2OH(5),[Fe_2(μ_2-L)_3(L)_2(NCS)_4]·2CH_3CH_2OH分离出·1.5H_2O(6)和[Ni_3(μ_2-L)6(L)_4(H_2O)_2](NO_3)_6·15.5H_2O(7)。图1和图2显示了两个与L配合的锌(II)配合物的温度诱导多态现象。溶剂效应在这些Fe(II)配合物的自组装中起关键作用3-6:3包含单核Fe(L) )_4(NCS)_2单元没有自旋转变行为,而4和5都存在具有三个N_1,N_2-1,2,4-三唑桥的双核Fe(II)配合物,表现出不完全的自旋转变行为。 X的低温X射线结构分析(100 K)也证实了一个Fe(II)中心位于低自旋(LS)状态,另一个Fe(II)中心位于高自旋状态旋转(HS)状态。有趣的是,当双核Fe(II)络合物5暴露于水气氛中时,可以观察到溶剂诱导的单晶-单晶转变,并且可以分离出显示反铁磁相互作用的双核Fe(II)络合物6。此外,当使用Ni(II)盐与L反应时,分离出三核结晶化合物。可变磁化率测量值(2-300 K)显示7中存在反铁磁相互作用。多晶现象(1和2),自旋转变不完全现象(4和5),以及单晶到单晶的转变(从5到6)也显示出在用L构建这些新型功能材料方面的巨大潜力。

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