Clayton Jessica A, Keller Katharina, Qi Mian, Wegner Julia, Koch Vanessa, Hintz Henrik, Godt Adelheid, Han Songi, Jeschke Gunnar, Sherwin Mark S, Yulikov Maxim
University of California, Santa Barbara, Department of Physics, Santa Barbara, CA, USA.
Phys Chem Chem Phys. 2018 Apr 18;20(15):10470-10492. doi: 10.1039/c7cp08507a.
The magnetic properties of paramagnetic species with spin S > 1/2 are parameterized by the familiar g tensor as well as "zero-field splitting" (ZFS) terms that break the degeneracy between spin states even in the absence of a magnetic field. In this work, we determine the mean values and distributions of the ZFS parameters D and E for six Gd(iii) complexes (S = 7/2) and critically discuss the accuracy of such determination. EPR spectra of the Gd(iii) complexes were recorded in glassy frozen solutions at 10 K or below at Q-band (∼34 GHz), W-band (∼94 GHz) and G-band (240 GHz) frequencies, and simulated with two widely used models for the form of the distributions of the ZFS parameters D and E. We find that the form of the distribution of the ZFS parameter D is bimodal, consisting roughly of two Gaussians centered at D and -D with unequal amplitudes. The extracted values of D (σD) for the six complexes are, in MHz: Gd-NO3Pic, 485 ± 20 (155 ± 37); Gd-DOTA/Gd-maleimide-DOTA, -714 ± 43 (328 ± 99); iodo-(Gd-PyMTA)/MOMethynyl-(Gd-PyMTA), 1213 ± 60 (418 ± 141); Gd-TAHA, 1361 ± 69 (457 ± 178); iodo-Gd-PCTA-[12], 1861 ± 135 (467 ± 292); and Gd-PyDTTA, 1830 ± 105 (390 ± 242). The sign of D was adjusted based on the Gaussian component with larger amplitude. We relate the extracted P(D) distributions to the structure of the individual Gd(iii) complexes by fitting them to a model that superposes the contribution to the D tensor from each coordinating atom of the ligand. Using this model, we predict D, σD, and E values for several additional Gd(iii) complexes that were not measured in this work. The results of this paper may be useful as benchmarks for the verification of quantum chemical calculations of ZFS parameters, and point the way to designing Gd(iii) complexes for particular applications and estimating their magnetic properties a priori.
自旋(S > 1/2)的顺磁物种的磁性由常见的(g)张量以及“零场分裂”(ZFS)项参数化,即使在没有磁场的情况下,这些项也会打破自旋态之间的简并性。在这项工作中,我们确定了六种钆(III)配合物((S = 7/2))的ZFS参数(D)和(E)的平均值和分布,并严格讨论了这种确定的准确性。在10 K或更低温度下,于玻璃态冷冻溶液中在Q波段(约34 GHz)、W波段(约94 GHz)和G波段(240 GHz)频率下记录了钆(III)配合物的电子顺磁共振(EPR)光谱,并用两种广泛使用的ZFS参数(D)和(E)分布形式的模型进行了模拟。我们发现ZFS参数(D)的分布形式是双峰的,大致由两个以(D)和(-D)为中心、幅度不等的高斯分布组成。六种配合物的(D)((\sigma_D))提取值(单位为MHz)为:钆 - 硝酸根吡啶,(485 ± 20)((155 ± 37));钆 - DOTA/钆 - 马来酰亚胺 - DOTA,(-714 ± 43)((328 ± 99));碘代 - (钆 - PyMTA)/甲炔基 - (钆 - PyMTA),(1213 ± 60)((418 ± 141));钆 - TAHA,(1361 ± 69)((457 ± 178));碘代 - 钆 - PCTA - [12],(1861 ± 135)((467 ± 292));以及钆 - PyDTTA,(1830 ± 105)((390 ± 242))。根据幅度较大的高斯分量调整了(D)的符号。通过将提取的(P(D))分布拟合到一个叠加配体每个配位原子对(D)张量贡献的模型,我们将其与各个钆(III)配合物的结构相关联。使用该模型,我们预测了在本工作中未测量的几种其他钆(III)配合物的(D)、(\sigma_D)和(E)值。本文的结果可能作为验证ZFS参数量子化学计算的基准有用,并为设计用于特定应用并先验估计其磁性的钆(III)配合物指明方向。