Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, 3663 N. Zhongshan Road, Shanghai 200062, China.
Anhui Province Key Laboratory of Optoelectronic Material Science and Technology, School of Physics and Electronic Information, Anhui Normal University, Wuhu 241002, China.
Molecules. 2021 Jan 30;26(3):716. doi: 10.3390/molecules26030716.
The precise operation of molecular motion for constructing complicated mechanically interlocked molecules has received considerable attention and is still an energetic field of supramolecular chemistry. Herein, we reported the construction of two tris[2]pseudorotaxanes metallacycles with acid-base controllable molecular motion through self-sorting strategy and host-guest interaction. Firstly, two hexagonal Pt(II) metallacycles and decorated with different host-guest recognition sites have been constructed via coordination-driven self-assembly strategy. The binding of metallacycles and with dibenzo-24-crown-8 (DB24C8) to form tris[2]pseudorotaxanes complexes and have been investigated. Furthermore, by taking advantage of the strong binding affinity between the protonated metallacycle and DB24C8, the addition of trifluoroacetic acid (TFA) as a stimulus successfully induces an acid-activated motion switching of DB24C8 between the discrete metallacycles and . This research not only affords a highly efficient way to construct stimuli-responsive smart supramolecular systems but also offers prospects for precisely control multicomponent cooperative motion.
构建复杂机械互锁分子的分子运动的精确操作受到了相当多的关注,并且仍然是超分子化学的一个充满活力的领域。在此,我们通过自组装策略和主客体相互作用,报道了两种具有酸碱可控分子运动的三[2]伪轮烷金属环的构建。首先,通过配位驱动自组装策略构建了两个带有不同主客体识别位点的六配位 Pt(II)金属环 和 。研究了金属环 和 与二苯并-24-冠-8(DB24C8)形成三[2]伪轮烷配合物 和 的结合。此外,利用质子化金属环 和 DB24C8 之间的强结合亲和力,加入三氟乙酸(TFA)作为刺激物,成功地诱导了 DB24C8 在离散金属环 和 之间的酸激活运动切换。这项研究不仅提供了一种构建刺激响应智能超分子系统的高效方法,而且为精确控制多组分协同运动提供了前景。