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A monometallic lanthanide bis(methanediide) single molecule magnet with a large energy barrier and complex spin relaxation behaviour

机译:具有大能垒和复杂自旋弛豫行为的单金属镧系双(甲烷二甲烷)单分子磁体

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摘要

We report a dysprosium(iii) bis(methanediide) single molecule magnet (SMM) where stabilisation of the highly magnetic states and suppression of mixing of opposite magnetic projections is imposed by a linear arrangement of negatively-charged donor atoms supported by weak neutral donors. Treatment of [Ln(BIPMTMS)(BIPMTMSH)] [Ln = Dy, >1Dy; Y, >1Y; BIPMTMS = {C(PPh2NSiMe3)2}2–; BIPMTMSH = {HC(PPh2NSiMe3)2}] with benzyl potassium/18-crown-6 ether (18C6) in THF afforded [Ln(BIPMTMS)2][K(18C6)(THF)2] [Ln = Dy, >2Dy; Y, >2Y]. AC magnetic measurements of >2Dy in zero DC field show temperature- and frequency-dependent SMM behaviour. Orbach relaxation dominates at high temperature, but at lower temperatures a second-order Raman process dominates. Complex >2Dy exhibits two thermally activated energy barriers (Ueff) of 721 and 813 K, the largest Ueff values for any monometallic dysprosium(iii) complex. Dilution experiments confirm the molecular origin of this phenomenon. Complex >2Dy has rich magnetic dynamics; field-cooled (FC)/zero-field cooled (ZFC) susceptibility measurements show a clear divergence at 16 K, meaning the magnetic observables are out-of-equilibrium below this temperature, however the maximum in ZFC, which conventionally defines the blocking temperature, TB, is found at 10 K. Magnetic hysteresis is also observed in 10% >2Dy@>2Y at these temperatures. Ab initio calculations suggest the lowest three Kramers doublets of the ground 6H15/2 multiplet of >2Dy are essentially pure, well-isolated |±15/2, |±13/2 and |±11/2 states quantised along the CDyC axis. Thermal relaxation occurs via the 4th and 5th doublets, verified experimentally for the first time, and calculated Ueff values of 742 and 810 K compare very well to experimental magnetism and luminescence data. This work validates a design strategy towards realising high-temperature SMMs and produces unusual spin relaxation behaviour where the magnetic observables are out-of-equilibrium some 6 K above the formal blocking temperature.
机译:我们报告了a(iii)双(甲烷二甲烷)单分子磁体(SMM),其中强磁态的稳定和相反磁投影的混合的抑制是由弱中性施主所支持的带负电荷的施主原子的线性排列施加的。 [Ln(BIPM TMS )(BIPM TMS H)]的治疗[Ln = Dy,> 1Dy ; Y,> 1Y ; BIPM TMS = {C(PPh2NSiMe3)2} 2 – ; BIPM TMS H = {HC(PPh2NSiMe3)2} ],用苄基钾/ 18-冠-6醚(18C6)在THF中制得[Ln(BIPM TMS )2] [K(18C6)(THF)2] [Ln = Dy,> 2Dy ;是,> 2Y ]。在零直流磁场中,> 2Dy 的交流磁测量显示出与温度和频率有关的SMM行为。奥尔巴赫弛豫在高温下占主导地位,但在较低温度下,二阶拉曼过程占主导地位。复合物> 2Dy 具有两个分别为721和813 K的热激活能垒(Ueff),这是任何单金属(iii)复合物的最大Ueff值。稀释实验证实了这种现象的分子起源。复杂的> 2Dy 具有丰富的磁性。场冷(FC)/零场冷(ZFC)的磁化率测量显示在16 K处有明显的发散度,这意味着在此温度以下,磁观测值不平衡,但是ZFC的最大值通常定义了阻塞温度TB在10 K下发现。在这些温度下,还有10%> 2Dy @ > 2Y 观察到磁滞现象。从头算计算表明,最低> 2Dy 的地面 6 H15 / 2多重峰的最低三个Kramers双峰本质上是纯净的,隔离良好的|±15/2,|±13 /沿C <!-private-char pc1-> Dy <!-private-char pc1-> C轴量化的2和|±11/2状态。热弛豫是通过第4个和第5个双峰发生的,这是首次进行实验验证,并且计算出的742和810 K的Ueff值与实验的磁性和发光非常吻合数据。这项工作验证了实现高温SMM的设计策略,并产生了异常的自旋弛豫行为,在这种情况下,磁观测值比正式的阻断温度高出约6K。

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