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Absolute Configuration Determination of a New Chiral Rigid Bisetherketone Macrocycle Containing Binaphthyl and Thioether Moieties by Vibrational Circular Dichroism
11
Citations
15
References
2005
Year
Pseudo‐high Dilution TechniqueOrganic Material ChemistryEnantioselective SynthesisEngineeringMacromolecular EngineeringAbsolute Configuration DeterminationThioether MoietiesImage StructureHeterocyclicOrganic ChemistryChiral RecognitionVibrational Circular DichroismChemistryHeterocycle ChemistryMolecule-based MaterialAsymmetric CatalysisBiophysics
Abstract Summary: A new chiral rigid bisetherketone macrocycle containing binaphthyl and thioether moieties was synthesized successfully using a modified pseudo‐high dilution technique. The compound was characterized by means of infrared absorption (IR) and vibrational circular dichroism (VCD). The experimental IR and VCD spectra were compared with those computed based on density functional theory (DFT) calculations at B3LYP/6‐31G (d) level. Good agreement was observed between the experimental and calculated spectra and, therefore, the absolute configuration was determined. Knowledge of the absolute configuration is of great importance when exploring the mechanisms of chiral recognition based on the chiral macrocyclic molecules. Structure of the new chiral rigid bisetherketone macrocycle produced. image Structure of the new chiral rigid bisetherketone macrocycle produced.
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