P. Roy and Diana T. Vagelos Laboratories, Department of Chemistry, University of Pennsylvania , 231 South 34th Street, Philadelphia, Pennsylvania 19104, United States.
J Am Chem Soc. 2016 Jun 8;138(22):6928-31. doi: 10.1021/jacs.6b03293. Epub 2016 May 26.
Structurally authenticated, terminal lanthanide-ligand multiple bonds are rare and expected to be highly reactive. Even capped with an alkali metal cation, poor orbital energy matching and overlap of metal and ligand valence orbitals should result in strong charge polarization within such bonds. We expand on a new strategy for isolating terminal lanthanide-ligand multiple bonds using cerium(IV) complexes. In the current case, our tailored tris(hydroxylaminato) ligand framework, TriNOx(3-), provides steric protection against ligand scrambling and metal complex oligomerization and electronic protection against reduction. This strategy culminates in isolation of the first formal Ce═N bonded moiety in the complex [K(DME)2][Ce═N(3,5-(CF3)2C6H3)(TriNOx)], whose Ce═N bond is the shortest known at 2.119(3) Å.
结构认证的,末端镧系配体多重键是罕见的,预计具有高反应性。即使被碱金属阳离子封端,金属和配体价轨道的轨道能量匹配和重叠也应该导致这些键中强烈的电荷极化。我们扩展了使用铈 (IV) 配合物分离末端镧系配体多重键的新策略。在当前情况下,我们定制的三 (羟基氨基) 配体框架 TriNOx(3-),提供了对配体混乱和金属配合物齐聚的空间保护,以及对还原的电子保护。该策略最终分离出配合物 [K(DME)2][Ce═N(3,5-(CF3)2C6H3)(TriNOx)] 中第一个形式的 Ce═N 键合部分,其 Ce═N 键是目前已知最短的,为 2.119(3) Å。