Ninković Dragan B, Blagojević Filipović Jelena P, Hall Michael B, Brothers Edward N, Zarić Snežana D
Innovation Center of the Faculty of Chemistry in Belgrade, Studentski trg 12-16, Belgrade 11001, Serbia.
Department of Chemistry, Texas A&M University, College Station, Texas 77843-3255, United States.
ACS Cent Sci. 2020 Mar 25;6(3):420-425. doi: 10.1021/acscentsci.0c00005. Epub 2020 Mar 2.
High-level calculations show that the most stable stacking for benzene-cyclohexane is 17% stronger than that for benzene-benzene. However, as these systems are displaced horizontally the benzene-benzene attraction retains its strength. At a displacement of 5.0 Å, the benzene-benzene attraction is still ∼70% of its maximum strength, while benzene-cyclohexane attraction has fallen to ∼40% of its maximum strength. Alternatively, the radius of attraction (>2.0 kcal/mol) for benzene-benzene is 250% larger than that for benzene-cyclohexane. Thus, at relatively large distances aromatic rings can recognize each other, a phenomenon that helps explain their importance in protein folding and supramolecular structures.
高级计算表明,苯 - 环己烷最稳定的堆积比苯 - 苯的堆积强17%。然而,当这些体系水平位移时,苯 - 苯之间的吸引力保持其强度。在位移5.0 Å时,苯 - 苯之间的吸引力仍约为其最大强度的70%,而苯 - 环己烷之间的吸引力已降至其最大强度的约40%。或者说,苯 - 苯之间的吸引半径(>2.0千卡/摩尔)比苯 - 环己烷之间的吸引半径大250%。因此,在相对较大的距离时,芳香环能够相互识别,这一现象有助于解释它们在蛋白质折叠和超分子结构中的重要性。