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RESEARCH PRODUCT

Monoester copillar[5]arenes: synthesis, unusual self-inclusion behavior, and molecular recognition.

Minqing HeHerbert MeierYu ChenDerong CaoLixia ZhouDieter SchollmeyerLingyun Wang

subject

Models MolecularMagnetic Resonance SpectroscopyMolecular StructureChemistryStereochemistryOrganic ChemistryMolecular ConformationGeneral ChemistryNuclear magnetic resonance spectroscopyAcetatesCrystallography X-RayCombinatorial chemistryCatalysisMolecular conformationMolecular recognitionMoleculePolycyclic CompoundsHost–guest chemistrySelectivity

description

The self-inclusion behavior of monoester copillar[5]arenes depends on the position of the ester group, which causes different guest selectivities. Monoester copillar[5]arenes bearing an acetate chain can form stable self-inclusion complexes in low- and high-concentration solution and exhibit high guest selectivity. However, a monoester copillar[5]arene bearing a butyrate chain can not form a self-inclusion complex and exhibits low guest selectivity. Thus, a new class of stable self-inclusion complexes of copillar[5]arenes was explored to improve the selectivity of molecular recognition.

10.1002/chem.201204628https://pubmed.ncbi.nlm.nih.gov/23568621