Rodríguez Humberto A, Bickelhaupt F Matthias, Fernández Israel
Departamento de Química Orgánica and Centro de Innovación en Química Avanzada (ORFEO-CINQA), Facultad de Ciencias Químicas, Universidad Complutense de Madrid Ciudad Universitaria, 28040-, Madrid, Spain.
Instituto de Productos Naturales y Agrobiología (IPNA), Consejo Superior de Investigaciones Científicas (CSIC), 38206-, La Laguna, Tenerife, Spain.
Chemphyschem. 2023 Sep 1;24(17):e202300379. doi: 10.1002/cphc.202300379. Epub 2023 Jun 27.
The Bürgi-Dunitz (BD) angle plays a pivotal role in organic chemistry to rationalize the nucleophilic addition to carbonyl groups. Yet, the origin of the obtuse trajectory of the nucleophile remains incompletely understood. Herein, we quantify the importance of the underlying physical factors quantum chemically. The obtuse BD angle appears to originate from the concerted action of a reduced Pauli repulsion between the nucleophile HOMO and carbonyl π bond, a more stabilizing HOMO-π*-LUMO(C=O) interaction, as well as a more favorable electrostatic attraction.
Bürgi-Dunitz(BD)角在有机化学中对于合理化亲核试剂加成到羰基的过程起着关键作用。然而,亲核试剂钝角轨迹的起源仍未被完全理解。在此,我们通过量子化学方法量化了潜在物理因素的重要性。钝角的BD角似乎源于亲核试剂最高占据分子轨道(HOMO)与羰基π键之间降低的泡利排斥、更稳定的HOMO-π*-最低未占分子轨道(LUMO)(C=O)相互作用以及更有利的静电吸引的协同作用。