Effects of nitrogen atoms on the stability and reactivity of tricyclic boracarbenes by DFT

Following our quest for novel carbenes, effects of substituting 1 to 5 nitrogen atoms on the stability and reactivity of singlet (s) and triplet (t) forms of 7-boratricyclo[1,1,1,0,0,0]hexa-2-carbylenes (1–20) are compared and contrasted, at B3LYP/aug-cc-pvtz level of theory. All species appear as ground state minima on their energy surface, for showing no negative force constant. Singlets (1–20) are ground states and more stable than their corresponding triplets (1–20). Reactivity of the species (1–20 vs. 1–20) is discussed in terms of isodesmic reactions, considering nucleophilicity (N), electrophilicity (ω), and heat of hydrogenation. As well as, the addition of nitrogen atoms decreased nucleophilicity (N), while increasing electrophilicity (ω). Despite the enormous steric strain involved in their cubic structures, the most stable scrutinized carbenes appear to be singlet 1,4,5-triaza-7-boratricyclo[1,1,1,0,0,0]hexa-2-carbylene (13) for showing the highest value of ΔE. Such higher stabilization is attributed to a coordinate covalent bond observed between the carbenic center and the boron atom. This study offers new insights into the chemistry of these exotic tricyclic shaped carbenes.