Open shell versus closed shell bonding interaction in cyclopropane derivatives: EDA‐NOCV analyses

Abstract

Cyclopropane ring is a very common motif in organic/bio‐organic compounds. The chemical bonding of this strained ring is taught to all chemistry students. This three‐membered cyclic, C3 ring is quite reactive which has attracted both, synthetic and theoretical chemists to rationalize/correlate its stability and bonding with its reactivity and physical properties over a century. There are a few bonding models (mainly the Bent–Bond model and Walsh model) of this C3 ring that are debated to date. Herein, we have carried out energy decomposition analysis coupled with natural orbital for chemical valence (EDA‐NOCV) to study the two most reactive bonds of cyclopropane rings of 49 different organic compounds containing different functional groups to obtain a much deeper bonding insight toward a more general bonding model of this class of compounds. The EDA‐NOCV analyses of fragment orbitals and susequent bond formation revealed that the nature of the CC bond of the cyclopropane (splitting two bonds at a time out of three CC bonds) ring is preferred to form two dative covalent CC bonds (between a singlet olefin‐fragment and an excited singlet carbene‐fragment with a vacant sp2 orbital and a filled p‐orbital) for the majority (37/49) of compounds over two covalent electron sharing bonds in some (7/49) compounds (between an excited triplet olefin and triplet carbene), while a few (5/49) compounds show flexibility to adopt either the electron sharing or dative covalent bond as both are equally possible. The effects of functional groups on the nature of chemical bond in cyclopropane rings have been studied in detail. Our bonding analyses are in line with the QTAIM analyses which produce small negative values of the Laplacian, significantly positive values of bond ellipticity, and accumulation of electron densities around the ring critical point of C3‐rings. These corresponding QTAIM parameters of C3‐rings are quite different for CC single bonds of normal hydrocarbons as expected. The chemical bonding in the majority of cyclopropane rings can be very similar to those of metal–olefin systems.