Ruffin Hervé, Fihey Arnaud, Boitrel Bernard, Le Gac Stéphane
Univ Rennes, CNRS, ISCR, Institut des Sciences Chimiques de Rennes)-UMR 6226, 35000, Rennes, France.
Angew Chem Int Ed Engl. 2022 Feb 1;61(6):e202113844. doi: 10.1002/anie.202113844. Epub 2021 Dec 20.
By their conformational flexibility, Möbius aromatic hexaphyrins provide a dynamic chirality attractive to develop stimuli responsive systems such as chiroptical switches. A regular [28]hexaphyrin has been equipped with a chiral coordinating arm to achieve transfer of chirality from a fix stereogenic element to the dynamic Möbius one. The arm allows straightforward formation of labile monometallic Zn complexes with an exogenous ligand, either a carboxylato or an amino with opposite inwards/outwards orientations relative to the Möbius ring. As a corollary, the chiral coordinating arm is constrained over the ring or laterally, inducing opposite P and M Möbius configurations with unprecedented high stereoselectivity (diast. excess greater than 95 %). By tuning the transfer of chirality, these achiral effectors generate electronic circular dichroism spectra with bisignate Cotton effect of opposite signs. Switching between distinct chiroptical states was ultimately achieved in mild conditions owing to ligand exchange, with high robustness (10 cycles).
由于其构象灵活性,莫比乌斯芳香六卟啉具有动态手性,这对于开发诸如手性光开关等刺激响应系统具有吸引力。一种规则的[28]六卟啉配备了一个手性配位臂,以实现手性从固定的立体异构元素向动态莫比乌斯元素的转移。该臂允许与外源性配体直接形成不稳定的单金属锌配合物,该配体可以是羧酸盐或氨基,相对于莫比乌斯环具有相反的向内/向外取向。因此,手性配位臂在环上或横向受到限制,以前所未有的高立体选择性(非对映体过量大于95%)诱导相反的P和M莫比乌斯构型。通过调节手性转移,这些非手性效应器产生具有相反符号的双符号科顿效应的电子圆二色光谱。由于配体交换,最终在温和条件下实现了不同手性光状态之间的切换,具有高稳定性(10个循环)。