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Abstract

Local energy decomposition (LED) analysis decomposes the interaction energy between two fragments calculated at the domain-based local pair natural orbital CCSD(T) (DLPNO-CCSD(T)) level of theory into a number of chemically meaningful contributions. Herein, this scheme is applied to the interaction between the transition metal (TM) and the alkane in σ-complexes. It is demonstrated that the often-neglected London dispersion (LD) energy is a fundamental component of the TM–alkane interaction for a wide range of experimentally characterized σ-complexes. LD effects determine the structure and the thermodynamic stability of σ-complexes and influence the selectivity of CH activation reactions. The magnitude of the LD energy can be modulated by increasing the size of the alkane and of the ancillary ligands on the TM. These results provide further evidence on the fundamental role that London dispersion plays in organometallic chemistry.