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Subphthalocyanine-Stoppered [2]Rotaxanes: Synthesis and Size/Energy Threshold of Slippage.
Organic Letters ( IF 5.2 ) Pub Date : 2020-01-16 , DOI: 10.1021/acs.orglett.9b04620 Yuto Kage 1 , Soji Shimizu 1, 2 , Gabriele Kociok-Köhn 3 , Hiroyuki Furuta 1, 2 , G Dan Pantoş 3
Organic Letters ( IF 5.2 ) Pub Date : 2020-01-16 , DOI: 10.1021/acs.orglett.9b04620 Yuto Kage 1 , Soji Shimizu 1, 2 , Gabriele Kociok-Köhn 3 , Hiroyuki Furuta 1, 2 , G Dan Pantoş 3
Affiliation
Subphthalocyanine (SubPc)-stoppered [2]rotaxanes were synthesized for the first time. The rotaxane bearing unsubstituted SubPc as a stopper exhibited an equilibrium of slipping-on and slipping-off, whereas a perfluorinated SubPc stopper completely blocked slippage of the ring due to its slightly larger size. Kinetic studies revealed the Gibbs free energy of activation for the slipping-on and slipping-off processes. The optical properties of the rotaxanes, including photoinduced electron transfer, were also revealed.
中文翻译:
不足酞菁的[2]轮烷:滑移的合成和尺寸/能量阈值。
首次合成了亚酞菁(SubPc)封端的[2]轮烷。带有轮烷的未取代的SubPc作为塞子表现出滑移和滑脱的平衡,而全氟化的SubPc塞子由于其尺寸稍大而完全阻止了环的滑动。动力学研究揭示了吉布斯活化自由能在滑移和滑移过程中的作用。还揭示了轮烷的光学性质,包括光致电子转移。
更新日期:2020-01-16
中文翻译:
不足酞菁的[2]轮烷:滑移的合成和尺寸/能量阈值。
首次合成了亚酞菁(SubPc)封端的[2]轮烷。带有轮烷的未取代的SubPc作为塞子表现出滑移和滑脱的平衡,而全氟化的SubPc塞子由于其尺寸稍大而完全阻止了环的滑动。动力学研究揭示了吉布斯活化自由能在滑移和滑移过程中的作用。还揭示了轮烷的光学性质,包括光致电子转移。