Not Carbon s–p Hybridization, but Coordination Number Determines C−H and C−C Bond Length
Pascal Vermeeren, Willem‐Jan van Zeist, Trevor A. Hamlin, Célia Fonseca Guerra, F. Matthias Bickelhaupt
Abstract
Abstract A fundamental and ubiquitous phenomenon in chemistry is the contraction of both C−H and C−C bonds as the carbon atoms involved vary, in s–p hybridization, along sp 3 to sp 2 to sp. Our quantum chemical bonding analyses based on Kohn–Sham molecular orbital theory show that the generally accepted rationale behind this trend is incorrect. Inspection of the molecular orbitals and their corresponding orbital overlaps reveals that the above‐mentioned shortening in C−H and C−C bonds is not determined by an increasing amount of s ‐character at the carbon atom in these bonds. Instead, we establish that this structural trend is caused by a diminishing steric (Pauli) repulsion between substituents around the pertinent carbon atom, as the coordination number decreases along sp 3 to sp 2 to sp.