Related Experiment Video
Updated: Jul 17, 2026

Discovery and Synthesis Optimization of Isoreticular Al(III) Phosphonate-Based Metal-Organic Framework Compounds Using High-Throughput Methods
Published on: October 6, 2023
Orthogonal assembly of hetero-porous structures by reversible adaptation for efficient isomeric separation
Qi Mou1, Changpin Chen1, Xin Li1
1PCFM, GTRCSSTC and GD HPPC Lab, School of Chemistry Sun Yat-sen University, Guangzhou, China.
Researchers developed a novel membrane for isomer separation using dynamic chemistry. This highly oriented, multi-porous membrane achieves efficient separation of isomers and enantiomers with high selectivity.
Area of Science:
- Materials Science
- Chemical Engineering
- Separation Science
Background:
- Isomer separation is critical in chemical and biological processes.
- Mixed-matrix membranes (MMMs) offer potential but face compatibility issues.
- Efficient separation requires high permeability and selectivity.
Purpose of the Study:
- To design and construct a highly oriented multi-porous membrane for efficient isomer separation.
- To overcome the limitations of traditional mixed-matrix membranes.
- To create a versatile platform for energy-efficient separations.
Main Methods:
- Orthogonal assembly of hydrogen-bonded macrocycle amphiphiles via dynamic adaptation.
- Formation of lyotropic liquid crystal gels with helical propagation.
- Simultaneous control of immiscible pores for creating aligned chiral nanochannels.
Main Results:
- Achieved precise molecular sieving with a separation factor of 11.46 for constitutional isomers.
- Obtained 92% enantiomeric excess (ee) for enantiomer separation.
- Demonstrated a versatile platform for energy-efficient separations.
Conclusions:
- The developed membrane strategy enables precise molecular sieving.
- This approach provides a versatile platform for chiral resolution and fine chemical purification.
- The dynamic chemistry principle offers a new avenue for biomimetic transport systems.
Related Concept Videos
Heterogeneous Catalysis
Ion Exchange
Optimizing Chromatographic Separations
Band broadening refers to spreading solute bands as they travel through the column. This broadening can impact resolution. Plate height (H) represents the length required for one theoretical plate. A lower plate height corresponds to...
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn stereochemistry.
