Chemical Research in Chinese Universities ›› 2013, Vol. 29 ›› Issue (6): 1094-1097.doi: 10.1007/s40242-013-3218-0

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Synthesis and Characterization of Two [2]Catenanes Based on Phenylene-diacetylene Crown Ethers

CHEN Mu-juan, ZHOU Song-gen, LI Mei, LEI Chun-yan, XIAO Rui, JIANG La-sheng   

  1. School of Chemistry and Environment, South China Normal University, Guangzhou 510006, P. R. China
  • Received:2013-05-15 Revised:2013-06-13 Online:2013-12-01 Published:2013-07-10
  • Contact: JIANG La-sheng E-mail:jianglsh@scnu.edu.cn
  • Supported by:

    Supported by the National Natural Science Foundation of China(No.21072066) and the Natural Science Foundation of Guangdong Province of China(No.8151063101000015).

Abstract:

Two charged donor-acceptor [2]catenanes were synthesized by the cyclization of the π-acceptor 1,1'-[1,4-phenylenebis-(methylene)]bis(4,4'-bipyridinium)bis(hexafluorophosphate)(2) and bis(bromomethyl)benzene with the templates of the π-donor phenylene-diacetylene crown ethers 1a and 1b in the yields of 31%, 35%, respectively. The mass spectra, 1H and 13C NMR spectra confirm that the phenylene-diacetylene crown ethers, with a nonaromatic π-system, successfully template the cyclization of CBPQT4+. The X-ray crystallography analysis shows that the CBPQT4+ ring encircles around the phenylene motif of the crown ethers, leaving the 1,3-butadiyne fragment out of the cavity of CBPQT4+ ring. The mechanically interlocked structure of [2]catenanes was stabilized by the cooperative effects of π-stacking and hydrogen bonding interactions.

Key words: [2]Catenane, Crystal structure, Crown ether