4.5 Article

[n]Pseudorotaxanes (n=2, 3) from Self-Assembly of Two Cryptands and a 1,2-Bis(4-pyridinium)ethane Derivative

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2012, 期 32, 页码 6351-6356

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201200964

关键词

Macrocycles; Cryptands; Rotaxanes; Supramolecular chemistry; Self-assembly

资金

  1. National Natural Science Foundation of China (NSFC) [20834004, 91027006, 21125417]
  2. Fundamental Research Funds for the Central Universities [2012QNA3013]
  3. Program for New Century Excellent Talents in University
  4. Zhejiang Provincial Natural Science Foundation of China [R4100009]

向作者/读者索取更多资源

Efficient hostguest complexation and interesting self-assembled structures formed between two crown ether-based cryptands and a 1,2-bis(4-pyridinium)ethane derivative 3 are reported. By self-assembly of cis-dibenzo-24-crown-8-based cryptand 1 and guest 3, a [3]pseudorotaxane was formed in solution, which further formed a supramolecular poly[3]pseudorotaxane structure in the solid state driven by pi-pi stacking interactions. Meanwhile, a [2]pseudorotaxane, obtained from self-assembly of a bis(m-phenylene)-32-crown-10-based cryptand 2 and guest 3, can form a supramolecular poly[2]pseudorotaxane structure in the solid state. This difference in the binding model reflects the diversity of hostguest chemistry of crown ether-based cryptands. Furthermore, these hostguest recognition processes and self-assembled structures were fully characterized by H-1 NMR, UV/Vis spectroscopy, electrospray ionization mass spectrometry, and single-crystal X-ray analysis. Interestingly, formation of the [3]pseudorotaxane between cryptand 1 and guest 3 can be reversibly controlled by adding and removing potassium cations in acetone. This reversible complexation process provides a simple on/off mechanism that can be used in the construction of controllable molecular switches.

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