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稀土多金属氧酸盐

Rare Earth Polyoxometalates.

机构信息

School of Chemistry, University of Melbourne , Parkville, Victoria 3010, Australia.

出版信息

Acc Chem Res. 2017 Sep 19;50(9):2205-2214. doi: 10.1021/acs.accounts.7b00197. Epub 2017 Sep 5.

Abstract

Longstanding and important applications make use of the chemical and physical properties of both rare earth metals and polyoxometalates of early transition metals. The catalytic, optical, and magnetic features of rare earth metal ions are well-known, as are the reversible multielectron redox and photoredox capabilities of polyoxomolybdates and polyoxotungstates. The combination of rare earth ions and polyoxometalates in discrete molecules and coordination polymers is of interest for the unique combination of chemical and physical properties that can arise. This Account surveys our efforts to synthesize and investigate compounds with rare earth ions and polyoxometalates (RE-POMs), sometimes with carboxylate-based organic coligands. Our general synthetic approach is "bottom-up", which affords well-defined nanoscale molecules, typically in crystalline form and amenable to single-crystal X-ray diffraction for structure determination. Our particular focus is on elucidation of the physical properties conferred by the different structural components with a view to ultimately being able to tune these properties chemically. For this purpose, we employ a variety of spectroscopic, magnetochemical, electrochemical, and scattering techniques in concert with theoretical modeling and computation. Studies of RE-POM single-molecule magnets (SMMs) have utilized magnetic susceptibility, inelastic neutron scattering, and ab initio calculations. These investigations have allowed characterization of the crystal field splitting of the rare earth(III) ions that is responsible for the SMM properties of slow magnetic relaxation and magnetization quantum tunneling. Such SMMs are promising for applications in quantum computing and molecular spintronics. Photophysical measurements of a family of hybrid RE-POMs with organic ligands have afforded insights into sensitization of Tb(III) and Eu(III) emission through both organic and polyoxometalate chromophores in the same molecule. Detailed variable-temperature studies have revealed the temperature dependence of the POM-based sensitization, which is relevant for potential applications in phosphor thermometry. Novel RE-POM coordination polymers demonstrate the promise of higher-dimensional materials for catalytic and sensing applications that can make use of either or both rare earth and polyoxometalate capabilities. Finally, structural, electrochemical, and density functional theory studies on a family of modular RE-POMs that incorporate molybdotungstates with amino acid coligands have revealed how closed Mo-oxo loops that are reduced preferentially can act as electron reservoirs in mixed-metal molybdotungstates. This has important implications for mixed-metal polyoxometalates in redox and photoredox catalysis. Notably, these hybrid RE-POMs are stable in solution and maintain the chirality induced by amino acid ligands. The RE-POMs surveyed in this Account provide a glimpse of possible structural features that are accessible with this family of compounds. The studies of the ensuing chemical and physical properties reveal the promise of RE-POMs for diverse and varied applications and lay an excellent foundation for the future development of this new class of functional materials.

摘要

稀土金属和早期过渡金属的多酸化合物在化学和物理性质上都有长期而重要的应用。稀土金属离子的催化、光学和磁性特征是众所周知的,多酸钼酸盐和多酸钨酸盐的可逆多电子氧化还原和光氧化还原能力也是如此。稀土离子和多酸化合物在离散分子和配位聚合物中的结合引起了人们的兴趣,因为它们可以产生独特的化学和物理性质组合。本报告调查了我们合成和研究具有稀土离子和多酸化合物(RE-POMs)的化合物的努力,有时还使用基于羧酸的有机共配体。我们的一般合成方法是“自下而上”的,它提供了定义良好的纳米级分子,通常以结晶形式存在,并且适合单晶 X 射线衍射来确定结构。我们特别关注不同结构成分赋予的物理性质,以期最终能够通过化学手段来调节这些性质。为此,我们结合理论建模和计算,采用了各种光谱、磁化学、电化学和散射技术。对 RE-POM 单分子磁体(SMMs)的研究利用了磁化率、非弹性中子散射和从头算计算。这些研究使得能够对负责稀土(III)离子 SMM 性质的慢磁弛豫和磁化量子隧道的晶体场分裂进行表征。这种 SMM 在量子计算和分子自旋电子学中有应用前景。具有有机配体的混合 RE-POM 家族的光物理测量提供了对 Tb(III)和 Eu(III)发射通过同一分子中的有机和多酸发色团敏化的见解。详细的变温研究揭示了基于 POM 的敏化的温度依赖性,这对于在磷温度计测中的潜在应用是相关的。新型 RE-POM 配位聚合物展示了更高维材料在催化和传感应用中的潜力,这些应用可以利用稀土和多酸化合物的能力。最后,对一系列包含氨基酸共配体的钼钨多酸模块 RE-POM 的结构、电化学和密度泛函理论研究表明,优先还原的封闭 Mo-氧环可以作为混合金属钼钨多酸中的电子储库。这对氧化还原和光氧化还原催化中的混合金属多酸化合物有重要意义。值得注意的是,这些混合 RE-POM 在溶液中稳定,并且保持氨基酸配体诱导的手性。本报告中调查的 RE-POM 提供了对该化合物家族中可能的结构特征的一瞥。对随之而来的化学和物理性质的研究揭示了 RE-POM 在各种不同应用中的潜力,并为这种新型功能材料的未来发展奠定了良好的基础。

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