0000000000620449

AUTHOR

Lixia Zhou

showing 2 related works from this author

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

2012

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.

Models MolecularMagnetic Resonance SpectroscopyMolecular StructureChemistryStereochemistryOrganic ChemistryMolecular ConformationGeneral ChemistryNuclear magnetic resonance spectroscopyAcetatesCrystallography X-RayCombinatorial chemistryCatalysisMolecular conformationMolecular recognitionMoleculePolycyclic CompoundsHost–guest chemistrySelectivityChemistry (Weinheim an der Bergstrasse, Germany)
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CCDC 902683: Experimental Crystal Structure Determination

2013

Related Article: Yu Chen, Derong Cao, Lingyun Wang, Minqing He, Lixia Zhou, Dieter Schollmeyer, Herbert Meier|2013|Chem.-Eur.J.|19|7064|doi:10.1002/chem.201204628

Ethyl ((91419242628303234-nonamethoxyhexacyclo[21.2.2.2^36^.2^811^.2^1316^.2^1821^]pentatriaconta-1(25)3581013151820232628303234-pentadecaen-4-yl)oxy)acetateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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