Schweez Christopher, Shushkov Philip, Grimme Stefan, Höger Sigurd
Kekulé Institut für Organische Chemie und Biochemie, Rheinische Friedrich-Wilhelms-Universität Bonn, Gerhard-Domagk-Strasse 1, 53121, Bonn, Germany.
Mulliken Center for Theoretical Chemistry, Institut für Physikalische und Theoretische Chemie, Rheinische Friedrich-Wilhelms-Universität Bonn, Beringstrasse 4, 53115, Bonn, Germany.
Angew Chem Int Ed Engl. 2016 Mar 1;55(10):3328-33. doi: 10.1002/anie.201509702. Epub 2016 Feb 2.
Phenylacetylene-based [2]rotaxanes were synthesized by a covalent-template approach by aminolysis of the corresponding prerotaxanes. The wheel and the bulky stoppers are made of phenylene-ethynylene-butadiynylene macrocycles of the same size. The stoppers are large enough to enable the synthesis and purification of the rotaxane. However, the wheel unthreads from the axle at elevated temperatures. The deslipping kinetics and the activation parameters were determined. We described theoretically the unthreading by state-of-the-art DFT-based molecular-mechanics models and a string method for the simulation of rare events. This approach enabled us to characterize in detail the unthreading mechanism, which involves the folding of the stopper during its passage through the wheel opening, a process that defies intuitive geometrical considerations. The conformational and energetic features of the transition allowed us to infer the molecular residues controlling the disassembly timescale.
基于苯乙炔的[2]轮烷通过相应前体轮烷的氨解共价模板法合成。轮和庞大的封端剂由相同尺寸的亚苯基-乙炔基-丁二炔基大环制成。封端剂足够大,能够实现轮烷的合成和纯化。然而,在高温下轮会从轴上解扣。测定了解扣动力学和活化参数。我们用基于最先进密度泛函理论的分子力学模型和模拟罕见事件的弦方法从理论上描述了解扣过程。这种方法使我们能够详细表征解扣机制,该机制涉及封端剂在穿过轮孔时的折叠,这一过程违背了直观的几何考虑。过渡态的构象和能量特征使我们能够推断出控制拆卸时间尺度的分子残基。