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Two-Step Spin-Transition lron(Hl) Compound with a Wide [High Spin-Low Spin] Plateau

机译:具有高[高自旋-低自旋]平稳期的两步自旋转变lron(Hl)化合物

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摘要

A new iron(lll) coordination compound exhibiting a two-step spin-transition behavior with a remarkably wide [HS-LS] plateau of about 45 K has been synthesized from a hydrazino Schiff-base ligand with an N,N,O donor set, namely 2-methoxy-6-(pyridine-2-ylhydrazonomethyl)phenol (Hmph). The single-crystal X-ray structure of the coordination compound {[Fe(mph)_2](ClO_4)(MeOH)_0.5(H_20)_0.5}_2 (1) determined at 150 K reveals the presence of two slightly different iron(lIl) centers in pseudo-octahedral environments generated by two deprotonated tridentate mph ligands. The presence of hydrogen bonding interactions, instigated by the well-designed ligand, may justify the occurrence of the abrupt transitions. 1 has been characterized by temperature-dependent magnetic susceptibility measurements, EPR spectroscopy, differential scanning calorimetry, and ~57Fe M_ssbauer spectroscopy, which all confirm the occurrence of a two-step transition. ln.addition, the iron(lll) species in the high-spin state has been trapped and characterized by rapid cooling EPR studies
机译:从具有N,N,O供体组的肼基席夫碱配体合成了一种新的铁(III)配位化合物,该化合物具有两步自旋转变行为,具有约45 K的[HS-LS]平稳期,即2-甲氧基-6-(吡啶-2-基肼基甲基)苯酚(Hmph)。在150 K下测定的配位化合物{[Fe(mph)_2](ClO_4)(MeOH)_0.5(H_20)_0.5} _2(1)的单晶X射线结构显示存在两个由两个去质子化的三齿mph配体生成的伪八面体环境中的不同铁(III)中心。通过精心设计的配体引起的氢键相互作用的存在可以证明突变的发生是合理的。图1的特征是依赖于温度的磁化率测量,EPR光谱,差示扫描量热法和〜57Fe M_ssbauer光谱,这些都证实了两步过渡的发生。另外,高自旋态的铁(III)被捕获并通过快速冷却EPR研究进行了表征

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