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含铜配位聚合物中跨越磁量子相变的自旋-晶格耦合

Spin-Lattice Coupling Across the Magnetic Quantum-Phase Transition in Copper-Containing Coordination Polymers.

作者信息

Hughey Kendall D, Harms Nathan C, O'Neal Kenneth R, Clune Amanda J, Monroe Jeffrey C, Blockmon Avery L, Landee Christopher P, Liu Zhenxian, Ozerov Mykhaylo, Musfeldt Janice L

机构信息

Department of Chemistry , University of Tennessee , Knoxville , Tennessee 37996 , United States.

Carlson School of Chemistry and Biochemistry , Clark University , Worcester , Massachusetts 01610 , United States.

出版信息

Inorg Chem. 2020 Feb 17;59(4):2127-2135. doi: 10.1021/acs.inorgchem.9b02394. Epub 2020 Feb 3.

DOI:10.1021/acs.inorgchem.9b02394
PMID:32009403
Abstract

We measured the infrared vibrational properties of two copper-containing coordination polymers, Cu(pyz)(2-HOpy) and Cu(pyz)(4-HOpy), under different external stimuli in order to explore the microscopic aspects of spin-lattice coupling. While the temperature and pressure control hydrogen bonding, an applied field drives these materials from the antiferromagnetic → fully saturated state. Analysis of the pyrazine (pyz)-related vibrational modes across the magnetic quantum-phase transition provides a superb local probe of magnetoelastic coupling because the pyz ligand functions as the primary exchange pathway and is present in both systems. Strikingly, the PF compound employs several pyz-related distortions in support of the magnetically driven transition, whereas the ClO system requires only a single out-of-plane pyz bending mode. Bringing these findings together with magnetoinfrared spectra from other copper complexes reveals spin-lattice coupling across the magnetic quantum-phase transition as a function of the structural and magnetic dimensionality. Coupling is maximized in Cu(pyz)(4-HOpy) because of its ladderlike character. Although spin-lattice interactions can also be explored under compression, differences in the local structure and dimensionality drive these materials to unique high-pressure phases. Symmetry analysis suggests that the high-pressure phase of the ClO compound may be ferroelectric.

摘要

我们测量了两种含铜配位聚合物Cu(pyz)(2-HOpy)和Cu(pyz)(4-HOpy)在不同外部刺激下的红外振动特性,以探究自旋-晶格耦合的微观方面。虽然温度和压力控制着氢键,但外加磁场会驱使这些材料从反铁磁态转变为完全饱和态。对跨越磁量子相变的吡嗪(pyz)相关振动模式进行分析,可提供磁弹耦合的极佳局部探针,因为pyz配体是主要的交换途径,且在两个体系中均存在。引人注目的是,PF化合物利用了几种与pyz相关的畸变来支持磁驱动转变,而ClO体系仅需要一种平面外的pyz弯曲模式。将这些发现与其他铜配合物的磁红外光谱结合起来,揭示了跨越磁量子相变的自旋-晶格耦合是结构和磁维度的函数。由于其梯状结构,Cu(pyz)(4-HOpy)中的耦合最大化。虽然在压缩条件下也可以探究自旋-晶格相互作用,但局部结构和维度的差异会驱使这些材料进入独特的高压相。对称性分析表明,ClO化合物的高压相可能是铁电的。

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