In chemistry, the term supramolecular chirality is used to describe supramolecular assemblies that are non-superposable on their mirror images.
Chirality in supramolecular chemistry implies the non-symmetric arrangement of molecular components in a non-covalent assembly. Chirality may arise in a supramolecular system if one of its component is chiral or if achiral components arrange in a non symmetrical way to produce a supermolecule that is chiral.[1]
References
- ↑ "Supramolecular Chirality: Chiral hydrogen-bonded supermolecules from achiral molecular components". Helvetica Chimica Acta 81: 1–13. 1998. doi:10.1002/hlca.19980810102.
Concepts in enantioselective synthesis |
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| Chirality types |
- Chirality
- Stereocenter
- Planar chirality
- C2-Symmetric ligands
- Axial chirality
- Supramolecular chirality
- Inherent chirality
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| Chiral molecules |
- Stereoisomer
- Enantiomer
- Diastereomer
- Meso compound
- Racemic mixture
- Enantiomeric excess (ee)
- Diastereomeric excess (de)
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| Analysis |
- Optical rotation
- Chiral derivatizing agents
- NMR spectroscopy of stereoisomers
- Ultraviolet–visible spectroscopy of stereoisomers
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| Chiral resolution |
- Recrystallization
- Kinetic resolution
- Chiral column chromatography
- Diastereomeric recrystallization
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| Reactions |
- Asymmetric induction
- Chiral pool synthesis
- Chiral auxiliaries
- Asymmetric catalysis
- Organocatalysis
- Biocatalysis
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 | Original source: https://en.wikipedia.org/wiki/Supramolecular chirality. Read more |