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A novel molecule tetra-N-alkylation of cyclen (1,4,7,10-tetraazacyclododecane), 1,4,7,10-tetrakis(2-((4-hydroxy)phenoxy)ethyl)-1,4,7,10-tetraazacyclododecane 2, was synthesized and structurally characterized by single-crystal X-ray diffraction. The molecule turned into chiral helical compound crystals grown from EtOH by slow diffusion at room temperature and three of the four hydroquinone groups of the benzene ring formed a g-electron-rich cavity by C-H…π stacking interaction. The crystal belongs to the monoclinic system, space group P21/C with a = 13.9192(9), b = 13.2871(6), c = 22.1894(15)A^°, β = 91.4600(10)°, V = 4102.5(4)A^°3, Z = 4, Dc = 1.219 g/cm^3, C40H52N4O8, Mr = 752.89, F(000) = 1616,μ = 0.088 mm^-1, MoKa radiation (λ = 0.71073), R = 0.0578 and wR = 0.1389 for 5588 observed reflections with I 〉 2σ(I). Moreover, compound 2 was characterized with ^1H NMR, ^13C NMR, IR spectra and MS. 相似文献
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含丁三醇端基富电子醚链与阳离子环蕃超分子准轮烷的表征和性能研究 总被引:1,自引:0,他引:1
以4-(2-(4-(苄氧基)苯氧基)乙氧基)-1,2,3-丁三醇(C)为富电子供体的醚链,与缺电子联吡啶大环化合物环双(百草枯-亚苯基)四阳离子环蕃(CPQT)和四氟取代环蕃(4FCPQT)自组装形成超分子准轮烷C(CPQT)和C(4FCPQT),并利用1HNMR的化学位移变化来研究两种不同准轮烷在温度变化时它们的相互作用。实验结果表明,由于富电子供体的一端含有3个羟基,易和缺电子联吡啶大环形成氢键,因此醚链的丁三醇端不能进入大环;缺电子联吡啶大环的一个苯环上的氢被氟取代后,由于电场力的作用,使富电子供体进入大环的概率相对降低,并使富电子醚链供体穿入大环的位置发生"偏心"作用。 相似文献
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利用π-π堆积作用,富电子4,4′-二氨基二苯醚(A)和4,4′-二羟基二苯醚(B)分别与缺电子联吡啶大环(CPQT)自组装成准轮烷A-CPQT和B-CPQT;利用酸碱调控准轮烷A-CPQT的“开”与“关”,此过程可利用体系的核磁共振氢谱的化学位移变化进行跟踪. 相似文献