Abstract
A variety of armed cyclens were prepared in which ester, amide, nitrile, and pyridine moieties were attached as cation-ligating side arms to a 12-membered ring. Ester-, amide-, and pyridine-armed cyclens nicely accommodated a Na+ ion in a three-dimensional fashion and clearly discriminated the cation from Li+ and K+ ions. They extracted Na+ ion more efficiently and selectively than common Na+ ion-selective ligands. X-ray diffraction, FAB-MS, 23Na NMR binding studies, and computer modeling experiments demonstrated that the cyclens having ester-, amide-, and pyridine-functionalized side arms formed highly selective encapsulated Na + complexes Via a cooperative action of parent cyclen and side arms.
| Original language | English |
|---|---|
| Pages (from-to) | 3506-3512 |
| Number of pages | 7 |
| Journal | Inorganic Chemistry |
| Volume | 38 |
| Issue number | 15 |
| DOIs | |
| Publication status | Published - 1999 |
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