Inorganic Chemistry · 2000 · 36 citations · 34 references
Natural SciencesChemistryMolecular RecognitionOrganic ChemistryStructure-activity RelationshipsBioinorganic ChemistryCoordination ChemistryHeterocyclic ChemistryLigand BindingStructural Basis Of RecognitionAqueous SolvationLigand ChemistryMolecular Recognition FeaturesMolecular Recognition MotifsMolecular Recognition ThermodynamicsPhosphate ChemistryPhosphate RecognitionPotentiometric Measurement
The host−guest interactions between ortho- (Ph), pyro- (Pp), and tripolyphosphate (Tr) anions together with ATP (At), ADP (Ad), and AMP (Am) nucleotides and the two hexaazamacrocyclic ligands 1,15-dioxa-4,8,12,18,22,26-hexaazacyclooctacosane (Pn) and 1,13-dioxa-4,7,10,16,20,24-hexaazacyclohexacosane (Op) have been investigated by potentiometric equilibrium methods. Ternary complexes are formed in aqueous solution as a result of hydrogen bond formation and Coulombic attraction between the host and the guest. Formation constants for all the species obtained are reported. The selectivity of the Pn and Op ligands with regard to the different phosphate and nucleotide substrates is discussed and illustrated with total species distribution diagrams. A comparison is also carried out, with the results obtained in this work and those obtained previously with three other closely related hexaazamacrocyclic ligands. This comparison manifests the importance of ligand basicity, rigidity, and π-stacking capability in order to understand their binding and selectivity.
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Mir Wais Hosseini, A. John Blacker, J.‐M. Lehn · Journal of the American Chemical Society · 1990 · 273 citations
Pharmacy, Biochemistry, Chemistry +17
Molecular recognition and biophysical organic chemistry
Julius Rebek · Accounts of Chemical Research · 1990 · 190 citations