Valence-Electron Control of Mono-, Di-, and Tri-Noble-Gas (He–Kr) Binding to Electron-Deficient Main-Group Centers

The interactions of noble gases (Ng = He, Ne, Ar, Kr) with highly electron-deficient main-group fragments are systematically investigated by using high-level CCSD and CCSD(T) calculations. A broad set of electrophilic acceptors is considered, spanning six-electron (O, S, F +, Cl +, Br +, OH +, SH +, NH 2 + ), four-electron (BF 2 +, AlF 2 + ), and two-electron (BeF +, MgF + ) centers. Optimized geometries, interaction energies, and electronic descriptors reveal a continuous evolution of Ng binding behavior across the series from weak polarization-dominated interactions for He and Ne, to donor–acceptor bonding for Ar, and to strongly covalent-like coordination in Kr complexes. The analysis, supported by natural bond orbital (NBO), quantum theory of atoms in molecules (QTAIM), symmetry-adapted perturbation theory (SAPT), and molecular electrostatic potential (MESP) descriptors, demonstrates that the strength and multiplicity of Ng binding are governed primarily by the electrophilicity and valence-electron deficiency of the acceptor fragment with noble-gas polarizability modulating the interaction strength. Within this context, a unified 2e–4e–6e valence-electron framework is employed as a descriptive tool to rationalize why six-electron centers preferentially bind one Ng atom, four-electron centers stabilize two Ng atoms, and highly electron-deficient two-electron centers accommodate three Ng atoms. Among the multi-noble-gas complexes examined, BeF + and MgF + are found to stabilize tri-noble-gas adducts across the He–Kr series, with Kr 3 BeF + exhibiting the strongest overall binding. Trihelium coordination to BeF +, with interaction energies of several kcal mol –1 per He atom, highlights the remarkable stabilization that can arise in extreme electron-deficient environments. Overall, the results provide a unified and internally consistent framework for organizing mono-, di-, and tri-noble-gas binding motifs across the noble-gas series, clarifying the electronic factors that govern noble-gas coordination in highly electrophilic chemical regimes.