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
Department of Chemistry , University of Tennessee , Knoxville , Tennessee 37996 , United States.
Carlson School of Chemistry and Biochemistry , Clark University , Worcester , Massachusetts 01610 , United States.
Inorg Chem. 2020 Feb 17;59(4):2127-2135. doi: 10.1021/acs.inorgchem.9b02394. Epub 2020 Feb 3.
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.
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。