Chem. J. Chinese Universities ›› 2005, Vol. 26 ›› Issue (3): 471.

• Articles • Previous Articles     Next Articles

Coordination Chemistry of Calix[4]arene-biscrown-6 with Cs~+ in Solution

GAO Jian-Xun1,3, WANG Bing-Wu2, ZHANG Lin3, WANG Jian-Chen3, SONG Chong-Li LIU Tao3, HU Tian-Dou4, XIE Ya-Ning4, ZHANG Jing4   

  1. 1. Institute of Polymer Material, Beijing University of Science and Technology, Beijing 100083, China;
    2. College of Chemistry and Molecular Engineering, Peiking University, Beijing 100871, China;
    3. Institute of Nuclear Energy and Technology, Tsinghua University, Beijing 100084, China;
    4. Institute of High Energy Physics, Academy of Chinese Sciences, Beijing 100039, China
  • Received:2004-09-13 Online:2005-03-10 Published:2005-03-10

Abstract: The coordination chemistry of Calix[4]arene-biscrown-6(BisC6) with Cs+ was studied in solution. The extraction experiments demonstrated that Cs+ extracting percentage at the single stage was 99.36% in o-nitrophenyl methyl ether(NPME) at room temperature. In simulated HLLW, the separation factor of Cs+/Na+ and Cs+/K2+ is 3.92×104 and 2.21×104 respectively. The local structure model of the complex showed that HNO3 or H2O might be located in the complexes. ESI-MS showed that the cesium ion complex with BisC6 might form both 1:1 (mononuclear) and 2:1 (bisnuclear) Cs+: ligand species and [BisC6·H2O], [BisC6·Cs+]+, [BisC6·2Cs+·H2O]2+, [BisC6·2Cs+·NO-3]+ etc. might exist in BisC6/NPME/HNO3 system. The EXAFS results indicated that the coordination number of cesium in BisC6 was seven and the complex structure with seven-oxygen coordination was stable. ADF computation verified the EXAFS results.

Key words: Calix[4]arene-biscrown-6, Coordination chemistry, Cs+

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