Abstract
AbstractExperimental binding energies for 24 ammonium ion ligands, derived from amines of type (I), for the synthetic receptor cucurbituril (a novel nonadecacyclic cage compound formed by acid‐catalyzed condensation of urea, glyoxal, and HCHO) are adjusted for ligand solvation and then are factored by regression analysis into contributions from various fragments of the ligands in their inclusion complexes.
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