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Very Large Magnetic Anisotropy of Cage Cobalt(II)Complexes with a Rigid Cholesteryl Substituent from Paramagnetic NMRSpectroscopy

机译:笼状钴(II)的非常大的磁各向异性顺磁性NMR与刚性胆固醇取代基的配合物光谱学

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摘要

Variable-temperature NMR spectroscopy has recently emerged as a new alternative to the magnetometry methods for studying single molecule magnets. Its use is based on an accurate determination of magnetic susceptibility tensor anisotropy Δχ, which is not always achievable due to some contact contribution to NMR chemical shifts and possible conformational dynamics. Here, we applied this approach to cholesteryl-substituted cage cobalt(II) complexes featuring a very large magnetic anisotropy. Conformational rigidity and large size of the cholesteryl substituent with many magnetically nonequivalent nuclei resulted in an excellent convergence of experimental and calculated 1H and 13C chemical shifts, thus allowing for the determination of Δχ value for all of the synthesized cobalt(II) complexes with a very high accuracy and providing a more reliable zero-field splitting energy for further calculations.
机译:最近,变温NMR光谱学已成为研究单分子磁体的磁力测定方法的新替代品。它的使用基于对磁化率张量各向异性Δx的精确确定,由于对NMR化学位移和可能的构象动力学的某些接触贡献,因此并非总是可以实现的。在这里,我们将这种方法应用于具有很大的磁各向异性的胆固醇取代的笼状钴(II)配合物。具有许多磁性非等价核的胆固醇取代基的构象刚度和大尺寸导致实验和计算的 1 H和 13 C化学位移的出色收敛,因此可以确定所有合成的钴(II)配合物的Δχ值具有很高的精确度,并提供了更可靠的零场分裂能,以供进一步计算。

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