Departamento de Química and Centro de Investigacións Científicas Avanzadas (CICA). Facultade de Ciencias , Universidade da Coruña , 15071 , A Coruña , Spain.
Departamento de Química Orgánica, Facultad de Ciencias , Universidad de Granada , Campus Fuentenueva S/N, 18071 Granada , Spain.
J Am Chem Soc. 2019 Mar 6;141(9):3959-3964. doi: 10.1021/jacs.8b12599. Epub 2019 Feb 19.
We present herein the development of a new polycationic molecular receptor, inspired by the ubiquitous cyclobis(paraquat- p-phenylene)cyclophane ("blue box"). Our analogue, the "white box", has been easily self-assembled on a preparative scale in water, using a template-assisted process by acyl hydrazone bonding of complementary bis(pyridinium)xylylene tweezers, followed by kinetic trapping of the empty receptor. The obtained macrocycle was found to display a marked pH responsiveness in water, because of an abnormal acidity of the amide protons within its structure. Consequently, and because of the concurrence of rotational isomerism under acidic conditions (fixed at higher pH values), the compound was found to display a dual behavior as a conformationally locked/flexible molecular host, being able to recognize appropriate aromatic substrates, in a lock and key or induced fit fashion, by a conjunction of π-π, C-H···π, and, crucially, the hydrophobic effect.
我们在此提出了一种新的聚阳离子分子受体的发展,该受体受到无处不在的环双(paraquat-p-亚苯基)环笼(“蓝盒”)的启发。我们的类似物“白盒”已通过酰肼键合互补的双(吡啶鎓)二甲苯镊子,在水相中使用模板辅助过程,在制备规模上轻松地自组装,然后通过动力学捕获空受体。发现所得大环在水中表现出明显的 pH 响应性,因为其结构内酰胺质子的异常酸度。因此,并且由于在酸性条件下(在较高 pH 值下固定)旋转异构的并发,该化合物被发现表现出作为构象锁定/灵活分子主体的双重行为,能够以锁和键或诱导契合的方式识别适当的芳香底物,通过π-π、C-H···π 的结合,以及至关重要的疏水作用。