Carbon-hydrogen bond activation in bridging cyclobutadiene ligands in unsaturated binuclear vanadium carbonyl derivatives

• Published in: Journal of molecular modeling 2022-02, Vol.28 (2), p.39-39, Article 39
• Main Authors: Song, Chongyao, Liu, Qifa, Chen, Wenqian, Chen, Xiaohong, Jin, Rong, Du, Quan, Xie, Yaoming, King, R. Bruce
• Format: Article
• Language: English
• Subjects: Carbon monoxide; Carbonyls; Characterization and Evaluation of Materials; Chemical bonds; Chemistry; Chemistry and Materials Science; Computer Appl. in Life Sciences; Computer Applications in Chemistry; Configurations; Density functional theory; Electrons; Hydrogen bonds; Molecular Medicine; Original Paper; Theoretical and Computational Chemistry; Vanadium
• ISSN: 1610-2940; 0948-5023
• DOI: 10.1007/s00894-021-05009-3

The structures and energetics of the binuclear cyclobutadiene vanadium carbonyls (C 4 H 4 ) 2 V 2 (CO) n ( n  = 8, 7, 6, 5, 4, 3, 2) have been investigated by density functional theory (DFT). The lowest energy (C 4 H 4 ) 2 V 2 (CO) 8 structure consists of two C 4 H 4 V(CO) 4 units linked by a V-V single bond of length 3.4 Å. The two lowest energy (C 4 H 4 ) 2 V 2 (CO) 7 structures also have formal V-V single bonds. The “extra” two electrons to give each vanadium atom in these heptacarbonyls the favored 18-electron configuration can come from either an agostic C-H-V interaction activating a hydrogen atom from one of the cyclobutadiene rings or from a four-electron donor bridging η 2 -µ-CO group with a short V–O distance. The lowest energy (C 4 H 4 ) 2 V 2 (CO) 6 structure has a formal V≡V triple bond of length 2.52 Å similar to the V≡V triple bond of length 2.46 Å found in the experimentally known cyclopentadienyl derivative (η 5 -C 5 H 5 ) 2 V 2 (CO) 5 . The lowest energy structures for the more highly unsaturated (C 4 H 4 ) 2 V 2 (CO) n ( n  = 5, 4, 3, 2) have at least two four-electron donor bridging η 2 -µ-CO groups and a vanadium-vanadium bond order sufficient to give each vanadium atom at least a 16-electron configuration. Graphical abstract The structures and energetics of the binuclear cyclobutadiene vanadium carbonyls (C 4 H 4 ) 2 V 2 (CO) n ( n  = 8, 7, 6, 5, 4, 3, 2) have been investigated by density functional theory. The two lowest energy (C 4 H 4 ) 2 V 2 (CO) 7 structures include one with an agostic C-H-V interaction activating a hydrogen atom from one of the cyclobutadiene rings and another with a four-electron donor bridging η 2 -µ-CO group with a short V–O bonding distance.