Structure and stability of the heteroannulated [8-10]circulenes: A quantum-chemical studyстатья
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Дата последнего поиска статьи во внешних источниках: 18 июля 2013 г.
Аннотация:The structure and stability of a new family of heterocyclic [n]circulenes C(n)N(n)Y(n) (n = 8-10; Y = N, P, As, BF(2), AlF(2), GaF(2)) have been computationally studied using density functional theory (DFT) B3LYP/6-311G* calculations. The geometry of the compounds is determined by the balance of steric factors and effects of aromatic pi-electron delocalization depending on the electronegativity of heteroatoms. An increase in the bulkiness of peripheral atoms Y and enlargement of the inner C(n) cycle leads to the gradual transformation of the bowl-shaped circulene structure (Y = N, BF(2)) to planar and then saddle-shaped forms (Y = P, As, AlF(2), GaF(2)). The calculations performed manifest stabilization of the heteroannulated circulenes ensured by the strong aromatic character of the conjugated five-membered rings fringing the central non-aromatic or antiaromatic [8-10] annulene rings.