Stevens Matthew P, Liu Yu, Alexopoulos Elias, Xec Daudo Shifaa S A, Hawker Rebecca R, Khan Adam, Lezama Luis, Reta Daniel, Ortu Fabrizio
School of Chemistry, University of Leicester, University Road, Leicester, UK.
Departamento de Química Orgánica e Inorgánica, Facultad de Ciencia y Tecnología, Universidad del País Vasco, B° Sarriena s/n, Leioa, Spain.
Commun Chem. 2025 Jun 5;8(1):175. doi: 10.1038/s42004-025-01572-5.
There is a great demand from the synthetic community for readily accessible organometallic alkaline earth and rare earth compounds that can be used as synthons for the preparation of new complexes and materials. Here we report the use of the methanide ligand {CH(SiMe)P(Ph) = NSiMe} (NPC-H) in the stabilization of alkaline earth and rare earth organometallics and their potential use as synthetic precursors. Bis- and tris-methanide complexes were obtained following two methods: (1) deprotonation of the proligand with organometallic precursors; (2) salt elimination reactivity between potassium methanide and metal iodides. All compounds were characterised by multinuclear nuclear magnetic resonance, infra-red spectroscopy, elemental analysis, ultraviolet-visible spectroscopy and single crystal X-ray diffraction. Additionally, selected rare earth methanides were tested as synthetic precursors for the preparation of solvent-free rare earth complexes. Finally, the electronic structures of open-shell divalent rare earth methanides were probed using electron paramagnetic resonance, magnetometry studies and ab initio calculations.
合成化学领域对易于获得的有机金属碱土和稀土化合物有很大需求,这些化合物可用作合成新配合物和材料的合成子。在此,我们报道了甲硅烷基配体{CH(SiMe)P(Ph) = NSiMe}(NPC-H)在稳定碱土和稀土有机金属化合物方面的应用及其作为合成前体的潜在用途。通过两种方法获得了双甲硅烷基和三甲硅烷基配合物:(1)用有机金属前体使前体配体去质子化;(2)甲硅烷基钾与金属碘化物之间的盐消除反应。所有化合物均通过多核核磁共振、红外光谱、元素分析、紫外可见光谱和单晶X射线衍射进行了表征。此外,对选定的稀土甲硅烷基化合物作为制备无溶剂稀土配合物的合成前体进行了测试。最后,使用电子顺磁共振、磁学研究和从头算计算对开壳二价稀土甲硅烷基化合物的电子结构进行了探究。