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一种基于 pH 敏感的套索轮烷分子开关。

A pH-sensitive lasso-based rotaxane molecular switch.

机构信息

Supramolecular Machines and Architectures Team, Institut des Biomolécules Max Mousseron-UMR CNRS 5247, Université Montpellier 2 et 1, place Eugène Bataillon, case courrier 1706, 34095 Montpellier Cedex 5, France.

出版信息

Chemistry. 2013 Feb 25;19(9):2982-9. doi: 10.1002/chem.201203597. Epub 2013 Jan 23.

Abstract

The synthesis of a pH-sensitive two-station [1]rotaxane molecular switch by self-entanglement of a non-interlocked hermaphrodite molecule, containing an anilinium and triazole moieties, is reported. The anilinium was chosen as the best template for the macrocycle benzometaphenylene[25]crown-8 (BMP25C8) and allowed the self-entanglement of the molecule. The equilibrium between the hermaphrodite molecule and the pseudo[1]rotaxane was studied by (1)H NMR spectroscopy: the best conditions of self-entanglement were found in the less polar solvent CD(2)Cl(2) and at high dilution. The triazole moiety was then benzylated to afford a benzyltriazolium moiety, which then played a dual role. On one hand, it acts as a bulky gate to trap the BMP25C8, thus to avoid any self-disentanglement of the molecular architecture. On another hand, it acts as a second molecular station for the macrocycle. At acidic pH, the BMP25C8 resides around the best anilinium molecular station, displaying the lasso [1]rotaxane in a loosened conformation. The deprotonation of the anilinium molecular station triggers the shuttling of the BMP25C8 around the triazolium moiety, therefore tightening the lasso.

摘要

报告了一种通过非互锁两性分子的自缠结合成 pH 敏感的双工位[1]轮烷分子开关,该两性分子含有苯胺基和三唑部分。选择苯胺基作为大环苯并间苯并[25]冠-8(BMP25C8)的最佳模板,并允许分子自缠结。通过(1)H NMR 光谱研究了两性分子和伪[1]轮烷之间的平衡:在极性较小的溶剂 CD(2)Cl(2)和高稀释度下找到了最佳的自缠结条件。然后将三唑部分苄基化得到苄基三唑部分,它起到双重作用。一方面,它作为一个庞大的门来捕获 BMP25C8,从而避免分子结构的任何自解缠。另一方面,它作为大环的第二个分子站。在酸性 pH 下,BMP25C8 位于最佳苯胺分子站周围,呈现松弛构象的套索[1]轮烷。苯胺分子站的去质子化触发 BMP25C8 在三唑部分周围的穿梭,从而收紧套索。

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