Spectroscopic Signature of the Carbon–Carbon Coupling Reaction between Carbon Monoxide and Nickel Carbide

• Published in: The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Vol. 127; no. 49; pp. 10450 - 10456
• Main Authors: Yang, Jianpeng, Du, Shihu, Ju, Bangmin, Zhang, Ziheng, Li, Gang, Zou, Jinghan, Cao, Juntao, Jing, Qiangshan, Xie, Hua, Jiang, Ling
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 14.12.2023
• Subjects: A: Structure, Spectroscopy, and Reactivity of Molecules and Clusters
• ISSN: 1089-5639; 1520-5215
• DOI: 10.1021/acs.jpca.3c06197

Spectroscopic characterization of ketenylidene complexes is of essential importance for understanding the structure–reactivity relationships of the catalytic sites. Here, we report a size-specific photoelectron velocity map imaging spectroscopic study of the reactions of carbon monoxide with nickel carbide. Quantum chemical calculations have been conducted to search for the energetically favorable isomers and to recognize the experimental spectra. The target products with the chemical formula of NiC­(CO) n – (n = 3–5) are characterized to have an intriguing ketenylidene CCO unit. The evolution from NiC­(CO)3 – to NiC­(CO)4 – involves the breaking and formation of the Ni–C bond and the coordination conversion between the terminal and bridging carbonyls. Experimental and theoretical analyses reveal an efficient C–C bond formation process within the reactions of carbon monoxide and laser-vaporized nickel carbide. This work highlights the pivotal roles played by metal carbides in the C–C bond formation and also proposes new ideas for the design and chemical control of a broad class of complexes with unique physical and chemical properties.