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TETRAHEDRON LETTERS
卷 43, 期 9, 页码 1629-1631出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0040-4039(02)00096-5
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Two 1.3-alternate calix[4]arene-biscrowns with one proton-ionizable group and two dibenzocrown-6-ether units are synthesized. The compounds exhibit high Cs+ extraction efficiency and selectivity. Cs+/Na+ and Cs+/K+ selectivities for the new N-(trifluoromethylsulfonyl)carbamoyl-substituted calix[4]arene-bis(dibenzocrown-6) are found to be higher than those for an analog with no benzo group substituents in the crown ether units. (C) 2002 Elsevier Science Ltd. All rights reserved.
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