Graduate School of Engineering, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522, Japan.
Department of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Knowledge City, Sector 81, S.A.S. Nagar, Manauli PO, Punjab 140306, India.
Nat Commun. 2017 May 10;8:15254. doi: 10.1038/ncomms15254.
Unlike classical covalent polymers, one-dimensionally (1D) elongated supramolecular polymers (SPs) can be encoded with high degrees of internal order by the cooperative aggregation of molecular subunits, which endows these SPs with extraordinary properties and functions. However, this internal order has not yet been exploited to generate and dynamically control well-defined higher-order (secondary) conformations of the SP backbone, which may induce functionality that is comparable to protein folding/unfolding. Herein, we report light-induced conformational changes of SPs based on the 1D exotic stacking of hydrogen-bonded azobenzene hexamers. The stacking causes a unique internal order that leads to spontaneous curvature, which allows accessing conformations that range from randomly folded to helically folded coils. The reversible photoisomerization of the azobenzene moiety destroys or recovers the curvature of the main chain, which demonstrates external control over the SP conformation that may ultimately lead to biological functions.
与经典的共价聚合物不同,一维(1D)拉长的超分子聚合物(SP)可以通过分子亚基的协同聚集来编码高度的内部有序性,这赋予了这些 SP 非凡的性质和功能。然而,这种内部有序性尚未被开发出来,以产生和动态控制 SP 主链的明确定义的更高阶(二级)构象,这可能会诱导与蛋白质折叠/去折叠相当的功能。在此,我们报道了基于氢键偶氮苯六聚体的一维奇特堆积的光诱导 SP 构象变化。堆积导致了独特的内部有序性,从而导致自发曲率,这使得可以获得从随机折叠到螺旋折叠线圈的构象。偶氮苯部分的可逆光异构化破坏或恢复了主链的曲率,这证明了对外界对 SP 构象的控制,这最终可能导致生物功能。