Stable silylenes with acyclic, cyclic, and unsaturated cyclic structures: Effects of heteroatoms and cyclopropyl α-substituents at DFT

The effects of alkyl, amino, phosphino, oxy, and thio moieties on the stability, multiplicity and reactivity of α-cyclopropylsilylenes with acyclic, cyclic, and unsaturated cyclic structures are compared and contrasted at B3LYP/AUG-cc-pVTZ//B3LYP/6-31G∗ level. The simultaneous stabilizing effects of heteroatom and cyclopropyl α-substituents on the above silylenes create the following trend of singlet–triplet energy gaps (∆ES–T): amino ≈ oxy > thio > alkyl > phosphino. The ΔES–T values for all the above silylenes increase through cyclization, because cyclization stabilizes singlet states of all our α-heteroatom substitued silylenes while destabilizes their corresponding triplet states. The ΔES–T values for all the heteroatom substituted cyclic silylenes decrease upon unsaturation, due to the higher stabilization of triplet compared to the singlet state. Interestingly, isodesmic reactions showed the phosphino substituents stabilize the triplet more than the corresponding singlet states, not only in the unsaturated form but also in the acyclic and cyclic structures. This is in contrast to cyclopropyl which stabilizes singlet considerably more than the corresponding triplet states. The reactivity of the above silylenes is discussed in terms of nucleophilicity, and electrophilicity; showing phosphino- and aminocyclopropylsilylenes more nucleophilic than oxy- and thiocyclopropylsilylenes.

The effects of alkyl, amino, phosphino, oxy, and thio moieties on the stability, multiplicity and reactivity of α-cyclopropylsilylenes are compared and contrasted at B3LYP/AUG-cc-pVTZ//B3LYP/6-31G∗ level. Generally, the studied acyclic, cyclic, and unsaturated cyclic silylenes show the following ∆ES–T trend: (amino ≈ oxy) > thio > alkyl > phosphino.Figure optionsDownload as PowerPoint slideHighlights
► Effects of alkyl, amino, phosphino, oxy, and thio moieties on the stability, multiplicity and reactivity of α-cyclopropylsilylenes.
► Cyclopropylsilylenes with acyclic, cyclic, and unsaturated cyclic structures and simultaneous stabilizing effects of heteroatom and cyclopropyl α-substituents on silylenes.
► Stability of the triplet state more than the corresponding singlet by phosphino substituents.