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Updated: Jun 14, 2025

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
The Mechanism of Boron-Carbon Bond Formation in the DA Reaction of the Pyridine Adduct of Borabenzene with Acetylene:
1Faculty of Chemistry, University of Wroclaw, 14 F. Joliot-Curie, 50-383 Wroclaw, Poland.
Abstract:
The mechanism of the DA cycloaddition reaction between the pyridine adduct of borabenzene and acetylene has been investigated using topological analysis of the electron localization function (ELF) and catastrophe theory (bonding evolution theory, BET). The study focuses on the differences in the electronic structures of C-C and C-B bonds during their formation. Additionally, the influence of electron density functionals with different constructions (B3LYP, CAM-B3LYP, B2PLYP, M06, M062X, and M052X) on the BET results was examined. The reaction proceeds through ten distinct phases. The B-C bond forms first, followed by the C-C bond. Significant differences were observed in the behavior of the non-bonding basins V(C) and V(B) compared to the V(C), V(C) basins, which precede the formation of the bonding basins V(B,C) and V(C,C). The use of different functionals results in quantitative variations in the lengths and positions of the reaction phases-for example, relative to the transition state structure. A possible qualitative influence on the overall picture of the reaction mechanism is suggested by the results obtained using the CAM-B3LYP and B2PLYP functionals, particularly in phases VI and VII.
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