首页> 外文期刊>Chemistry: A European journal >A new basic motif in cyanometallate coordination polymers: Structure and magnetic behavior of M(mu-OH2)(2)[Au(CN)(2)](2) (M = Cu, Ni)
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A new basic motif in cyanometallate coordination polymers: Structure and magnetic behavior of M(mu-OH2)(2)[Au(CN)(2)](2) (M = Cu, Ni)

机译:氰基金属盐配位聚合物中的一个新的基本图案:M(mu-OH2)(2)[Au(CN)(2)](2)(M = Cu,Ni)的结构和磁行为

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摘要

The structures of two cyanoaurate-based coordination polymers, M(mu-OH2)(2)[Au(CN)(2)](2) (M=Cu, Ni), were determined by using a combination of powder and single-crystal X-ray diffraction techniques. The basic structural motif for both polymers contains rarely observed M(mu-OH2)(2)M double aqua-bridges, which generate an infinite chain; two trans [Au(CN)(2)](-) units also dangle from each metal center. The chains form ribbons that interact three dimensionally through (CNH)-H-... hydrogen bonding. The magnetic properties of both compounds and of the dehydrated analogue Cu[Au(CN)(2)](2) were investigated by direct current (dc) and alternating current (ac) magnetometry; muon spin-relaxation data was also obtained to probe their magnetic properties in zero-field. In M(mu OH2)(2)[Au(CN)(2)](2), ferromagnetic chains of M(mu-OH2)(2)M are present below 20 K. Interchain magnetic interactions mediated through hydrogen bonding, involving water and cyanoaurate units, yield a long-range magnetically ordered system in Cu(mu-OH2)(2)[Au(CN)(2)](2) below 0.20 K, as indicated by precession in the muon spin polarization decay. Ni(mu-OH2)(2)[Au(CN)(2)](2) undergoes a transition to a spin-glass state in zero-field at 3.6 K, as indicated by a combination of muon spin-relaxation and ac-susceptibility data. This transition is probably due to competing interactions that lead to spin frustration. A phase transition to a paramagnetic state is possible for Ni(mu OH2)(2)[Au(CN)(2)](2) upon application of an external field; the critical field was determined to be 700 Oe at 1.8 K. The dehydrated compound Cu[Au(CN)(2)](2) shows weak antiferromagnetic interactions at low temperatures.
机译:两种粉末型氰基金酸酯配位聚合物M(mu-OH2)(2)[Au(CN)(2)](2)(M = Cu,Ni)的结构通过粉末和单晶体X射线衍射技术。两种聚合物的基本结构基序均包含很少观察到的M(mu-OH2)(2)M双水桥,可产生无限链。每个金属中心也悬挂了两个反式[Au(CN)(2)](-)单元。链形成通过(CNH)-H -...氢键在三维上相互作用的带。通过直流(dc)和交流(ac)磁力分析法研究了这两种化合物和脱水类似物Cu [Au(CN)(2)](2)的磁性。还获得了μ子自旋弛豫数据以探测其在零场下的磁性能。在M(mu OH2)(2)[Au(CN)(2)](2)中,M(mu-OH2)(2)M的铁磁链存在于20 K以下。通过氢键介导的链间磁相互作用涉及水和氰基金酸酯单元在0.20 K以下产生Cu(mu-OH2)(2)[Au(CN)(2)](2)中的长程磁有序系统,如μ子自旋极化衰变的进动所示。 Ni(mu-OH2)(2)[Au(CN)(2)](2)在3.6 K的零场下经历了自旋玻璃态的转变,这是由μon自旋弛豫和ac的结合所表明的敏感性数据。这种过渡可能是由于竞争相互作用导致旋转受挫。 Ni(mu OH2)(2)[Au(CN)(2)](2)在施加外场时可能会发生顺磁态相变;临界场在1.8 K下确定为700 Oe。脱水的化合物Cu [Au(CN)(2)](2)在低温下显示弱的反铁磁相互作用。

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