Abstract
Previously studied disubstituted 4,13-diaza-18-crown-6 derivatives, R < N18N > R, in which the substituents were cyanomethyl or propargyl did not show intramolecular, lariat-type cation solvation. The ring-bound cation in the propargyl derivative is solvated by the six macroring heteroatoms and apically by a bifurcated interaction of the type F···K+···F. In contrast, when the sidearm is cyanoethyl, an extended intermolecular network forms when the bound cation is either Na+ or K+.
Original language | English (US) |
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Pages (from-to) | 121-126 |
Number of pages | 6 |
Journal | Inorganica Chimica Acta |
Volume | 317 |
Issue number | 1-2 |
DOIs | |
State | Published - May 28 2001 |
Funding
We thank the NIH (GM-36262) and the NSF (CHE-9805840) for grants that supported this work.
Keywords
- Aza macrocycles
- Crown ethers
- Supramolecular network
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Inorganic Chemistry
- Materials Chemistry