Molecular Boron-Phosphides: From Stable Monomers to Aromaticity-Tunable Smallest Neutral Metallacycles

Unlike the conventional polymeric boron-phosphide-based (BP) semiconductors, which exhibit limited reactivity, the neutral monomeric BP motif ( 1 ) is extremely reactive and nonexistent under ambient conditions. Herein, we depict the ligand-engineering strategies for stabilizing the elusive species 1, initially by employing stereoelectronically tuned donor-based ligands, followed by their successive incorporation into the smallest metallacycles with induced aromaticity, and hence excellent stability. The electron density distribution and chemical bonding of homo- and heterobileptic ligand-stabilized monomers [(L′)BP(L)] ( 2 – 7 ) [L′, L = singlet carbenes], and the corresponding neutral 3-membered metal(II)dihalide complexes [BP(MX 2 )] ( 8 – 9′ ) and [((L′)BP(L))(MX 2 )] ( 10 – 17 ) [M = Pd/Pt, X = Cl, Br], are investigated by various quantum chemical methods. The remarkable ligand-switched σ and π aromaticity in the unprecedented mixed d- and p-block planar metallacycles is unambiguously confirmed by NICS zz calculations, ELF, AdNDP, GIMIC, and EDDB analyses.