scholarly journals Identification of a uranium–rhodium triple bond in a heterometallic cluster

2019 ◽  
Vol 116 (36) ◽  
pp. 17654-17658 ◽  
Author(s):  
Genfeng Feng ◽  
Mingxing Zhang ◽  
Penglong Wang ◽  
Shuao Wang ◽  
Laurent Maron ◽  
...  

The chemistry of d-block metal–metal multiple bonds has been extensively investigated in the past 5 decades. However, the synthesis and characterization of species with f-block metal–metal multiple bonds are significantly more challenging and such species remain extremely rare. Here, we report the identification of a uranium–rhodium triple bond in a heterometallic cluster, which was synthesized under routine conditions. The uranium–rhodium triple-bond length of 2.31 Å in this cluster is only 3% longer than the sum of the covalent triple-bond radii of uranium and rhodium (2.24 Å). Computational studies reveal that the nature of this uranium–rhodium triple bond is 1 covalent bond with 2 rhodium-to-uranium dative bonds. This heterometallic cluster represents a species with f-block metal–metal triple bond structurally authenticated by X-ray diffraction. These studies not only demonstrate the authenticity of the uranium–metal triple bond, but also provide a possibility for the synthesis of other f-block metal–metal multiple bonds. We expect that this work may further our understanding of the bonding between uranium and transition metals, which may help to design new d-f heterometallic catalysts with uranium–metal bonds for small-molecule activation and to promote the utilization of abundant depleted uranium resources.

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Jiaxin Zhuang ◽  
Roser Morales-Martínez ◽  
Jiangwei Zhang ◽  
Yaofeng Wang ◽  
Yang-Rong Yao ◽  
...  

AbstractThe nature of the actinide-actinide bonds is of fundamental importance to understand the electronic structure of the 5f elements. It has attracted considerable theoretical attention, but little is known experimentally as the synthesis of these chemical bonds remains extremely challenging. Herein, we report a strong covalent Th-Th bond formed between two rarely accessible Th3+ ions, stabilized inside a fullerene cage nanocontainer as Th2@Ih(7)-C80. This compound is synthesized using the arc-discharge method and fully characterized using several techniques. The single-crystal X-Ray diffraction analysis determines that the two Th atoms are separated by 3.816 Å. Both experimental and quantum-chemical results show that the two Th atoms have formal charges of +3 and confirm the presence of a strong covalent Th-Th bond inside Ih(7)-C80. Moreover, density functional theory and ab initio multireference calculations suggest that the overlap between the 7s/6d hybrid thorium orbitals is so large that the bond still exists at Th-Th separations larger than 6 Å. This work demonstrates the authenticity of covalent actinide metal-metal bonds in a stable compound and deepens our fundamental understanding of f element metal bonds.


2006 ◽  
Vol 45 (11) ◽  
pp. 4526-4536 ◽  
Author(s):  
Wanzhi Chen ◽  
Fenghui Liu ◽  
Kazuko Matsumoto ◽  
Jochen Autschbach ◽  
Boris Le Guennic ◽  
...  

2019 ◽  
Vol 48 (34) ◽  
pp. 12867-12879 ◽  
Author(s):  
Shu-Xian Hu ◽  
Erli Lu ◽  
Stephen T. Liddle

A relativistic quantum chemical study on hypothetical but potentially experimentally realisable TM–actinide and –neodymium complexes reveals the similarity in their structures but the differences in the multiplicity of the metal–metal bonds.


Sign in / Sign up

Export Citation Format

Share Document