等结构
化学
镧系元素
氮化物
结晶学
配体(生物化学)
金属环
苯
金属
芯(光纤)
二聚体
立体化学
路易斯酸
锂(药物)
桥接(联网)
咪唑酯
小型化
碱金属
分子
部分
桥联配体
复分解
无机化学
作者
Zhou Wu,Yan Tang,Chenyan Cao,Siyu Zhao,X L,Chenhao Cai,Junru Ding,X James Li,Tingting Li,Weiguo Zhu,Haijun Li,Lijie Liu,Hongnan Jia,Laurent Maron,Jingzhen Du
摘要
Lanthanide nitrides remain rare, being restricted to the singular example with a CeN(Li 2 )Ce core stabilized by two Lewis acidic lithium ions. Here, we introduce a new cyclohexyltriamide ligand [Tach DMBS ] to lanthanide chemistry, which enables us to isolate a lanthanide nitride complex [{(Tach DMBS )Ce} 2 (μ–N)][Na(12–crown–4) 2 ] ( 6 ) with a linear CeNCe core without any alkali metal interaction. Complex 6 was prepared by the reaction of a rare dinuclear tuck-in–tuck-over cerium(IV) metallacycle [{(CH 2 CHNSiMe 2 t Bu) 2 (CHNSiMe t Bu(μ–CH 2 )Ce} 2 ] ( 4 ) with one equivalent of NaNH 2 in benzene in the presence of two equivalents of 12–crown–4, yielding 48%. The Ce–N(nitride) bond distances in 6 (2.051(19) Å) are close to the shortest Ce–N bonds reported so far, and a linear Ce–N–Ce bond angle in 6 (180.00°) is disclosed. The isostructural oxo analogue [{(Tach DMBS )Ce} 2 (μ–O)] ( 7 ) was prepared for comparison. Computational analysis of 6 and 7 reveals Ce═N multiple-bonding character consisting of two 2c–2e σ-bonds and two orthogonal 3c–2e π-bonds in 6, showing a similar bonding trend to that in the known CeN(Li 2 )Ce linkage, but single bonds for Ce–O in 7, confirming the stronger donating capability of N 3– vs O 2– in the bridging mode and highlighting the importance of supporting ligands in stabilizing the unsupported CeNCe core.
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