Abstract
It is shown that complementary positioning of recognition sites (particularly hydrogen bonding, stacking and hydrophobic groups) into a macrocyclic structure can lead to very strong and specific complexation of uncharged organic molecules.
Original language | English (US) |
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Pages (from-to) | 27-38 |
Number of pages | 12 |
Journal | Journal of Inclusion Phenomena and Molecular Recognition in Chemistry |
Volume | 7 |
Issue number | 1 |
DOIs | |
State | Published - Feb 1989 |
Keywords
- Molecular recognition
- barbiturate
- guanine
- nucleotide
- thymine
ASJC Scopus subject areas
- Food Science
- General Chemistry
- Condensed Matter Physics