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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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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:我们报道了a( III )双(甲烷二甲烷)单分子磁体(SMM),其中高磁性态的稳定化和对相反磁性投影的混合的抑制是由带负电荷的供体的线性排列施加的弱的中性供体支持的原子。 [Ln(BIPM TMS )(BIPM TMS H)的处理] [Ln = Dy,1Dy; Y,1Y; BIPM TMS = {C(PPh 2 NSiMe 3 2 } 2? ; BIPM TMS H = {HC(PPh 2 NSiMe 3 < / small>) 2 } ]和苄基钾/ 18-冠-6醚(18C6), THF得到[Ln(BIPM TMS 2 ] [K(18C6)(THF) < sub> 2 ] [Ln = Dy,2Dy; Y,2Y]。零直流磁场中2Dy的交流磁测量表明,温度和频率取决于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。复杂2Dy具有两个热活化能垒( U eff ),分别为721和813 K,最大的 U <任何单金属( III )配合物的small> eff 值。稀释实验证实了这种现象的分子起源。复杂的2Dy具有丰富的磁动力学。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在10 K下发现 T B 。在这些温度下,在10%2Dy @ 2Y中也观察到磁滞现象。 从头算起计算表明,地面 6 H 15/2 的最低三个Kramers双峰2Dy的small>多重峰基本上是纯的,完全隔离的|±15/2〉,|±13/2〉和|±11/2〉状态,沿着CDyC轴量化。热弛豫是通过第4个 th 和5 th 双重峰发生的。首次计算出的742和810 K的 U eff 值与实验磁性和发光数据相比非常好。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,磁观测值与正式的阻断温度相比,存在约6 K的不平衡。

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