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Improved pseudorotaxane and catenane formation from a derivative of bis(m-phenylene)-32-crown-10

机译:改进的双(间亚苯基)-32-crown-10衍生物的拟轮烷和链烷形成

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摘要

2,2'-Dihydroxy-bis(m-phenylene)-32-crown-10 (2,2'-dihydroxy-BMP32C10, 1a) was synthesized and used to prepare the [2]catenane 4 in an unexpected yield of 68 %, three times the corresponding value for the case in which BMP32C10 (1b) was used and close to the corresponding value for the case in which bis(p-phenylene)-34-crown-10 was used. This indicated that 1a and paraquat derivatives formed pseudorotaxanes rather than the previously reported "taco complexes" between BMP32C10 and paraquat derivatives. Another unique feature of 1a in relation to other previously reported BMP32C10 derivatives was that its binding to paraquat derivatives in solution could be switched off and back on by addition of K+ and then dibenzo-18-crown-6. In the solid state, a 2:1 [3]pseudorotaxane of 1a with a paraquat derivative was formed. A bis(m-phenylene)-32-crown-10 derivative formed pseudorotaxanes and not the previously reported "taco complexes" with paraquat derivatives both in solution and in the solid state, as seen in the efficient formation of a [2]catenane and its crystal structure with a paraquat derivative. Another unique feature was that its binding to paraquat derivatives could be switched off and back on.
机译:合成了2,2'-二羟基-双(间亚苯基)-32-crown-10(2,2'-二羟基-BMP32C10,1a),并以68%的意外产率制备了[2] catenane 4 ,是使用BMP32C10(1b)时对应值的三倍,接近使用双(对亚苯基)-34-crown-10时对应的值。这表明1a和百草枯衍生物形成假轮烷,而不是先前报道的BMP32C10和百草枯衍生物之间的“ taco络合物”。 1a相对于其他先前报道的BMP32C10衍生物的另一个独特特征是,可以先添加K +,然后再添加dibenzo-18-crown-6,将其与溶液中百草枯衍生物的结合关闭并重新打开。在固态下,形成具有百草枯衍生物的1a的2:1 [3]假轮烷。双(间-亚苯基)-32-冠-10衍生物在溶液和固态下均能形成假轮烷,而不是先前报道的与百草枯衍生物形成的“ taco络合物”,如有效形成[2]邻苯二酚和其晶体结构具有百草枯衍生物。另一个独特的功能是它与百草枯衍生物的结合作用可以关闭然后再打开。

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