USc<sub>2</sub>C<sub>2</sub> and USc<sub>2</sub>NC Clusters with U–C Triple Bond Character Stabilized Inside Fullerene Cages
Hongjie Jiang, Xiaojuan Yu, Min Guo, Yang‐Rong Yao, Qingyu Meng, Luís Echegoyen, Jochen Autschbach, Ning Chen
Abstract
The chemistry of f-block metal–carbon multiple bonds is underdeveloped compared to well-established carbene complexes of the d-block transition metals. Herein, we report two new actinide-rare earth mixed metal carbides and nitrogen carbide cluster fullerenes, USc 2 C 2 @ D 5h (6)-C 80 and USc 2 NC@ D 5h (6)-C 80, which contain U–C bonds with triple bond character and were successfully synthesized and characterized by mass spectrometry, UV–vis–NIR spectroscopy, Fourier transform infrared spectroscopy, single crystal X-ray diffraction, and DFT calculations. Crystallographic studies show that the two previously unreported clusters, USc 2 C 2 and USc 2 NC, are stabilized in the D 5h (6)-C 80 carbon cage and adopt unique trifoliate configurations, in which C 2 /NC units are almost vertically inserted into the plane defined by the U and two Sc atoms. Combined experimental and theoretical studies further reveal the bonding structure of USc 2 C 2 and USc 2 NC, which contain C═U(VI)═C and C═U(V)═N bonding motifs. The electronic structures of the two compounds are determined as U 6+ (Sc 2 ) 6+ (C 4– ) 2 @ D 5h (6)-C 80 4– and U 5+ (Sc 2 ) 6+ (N) 3– (C) 4– @ D 5h (6)-C 80 4–, respectively. Quantum-chemical studies confirm that the U–C bonds in both molecules show unprecedented multicenter triple-bond character. The discovery of this unique U–C multiple bond offers a deeper understanding of the fundamentals of uranium chemistry.