The first study about the relationship between the extractability of thiacalix[4]arene derivatives and the position of the coordination binding sites
Three organic ionophores (2–4) based on the p-tert-butylthiacalix[4]arene backbone, blocked in the 1,3- alternate conformation, bearing two pyridyl coordinating moieties (ortho for 2, meta for 3 and para for 4), have been synthesized and characterized in the solid state. The solvent extraction exper...
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| Main Authors: | , , , , , , , , , |
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| Format: | Default Article |
| Published: |
2015
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| Subjects: | |
| Online Access: | https://hdl.handle.net/2134/18137 |
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