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Updated: Jun 23, 2025

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
Published on: April 22, 2016
Porous organic crystals crosslinked by free-radical reactions
Krishanu Samanta1, Jiashan Mi2,3, Albert D Chen1
1Department of Chemistry, Dartmouth College, 41 College Street, Hanover, NH 03755, USA. cke@wustl.edu.
Researchers synthesized two hydrogen-bonded crosslinked organic frameworks (HCOFs) using butadiene and isoprene. One framework was chemically modified to a hydroxylated structure, preserving its crystalline nature.
Area of Science:
- Materials Science
- Organic Chemistry
- Crystallography
Background:
- Hydrogen-bonded crosslinked organic frameworks (HCOFs) offer tunable properties for advanced applications.
- Achieving high crystallinity in HCOFs is crucial for detailed structural analysis and property prediction.
Purpose of the Study:
- To synthesize novel HCOFs with high crystallinity.
- To explore the chemical modification of HCOFs while preserving their structural integrity.
Main Methods:
- Free radical polymerization using butadiene and isoprene as crosslinkers.
- Single-crystal X-ray diffraction for structural characterization.
- Hydroboration-oxidation reaction for framework functionalization.
Main Results:
- Two crystalline HCOFs were successfully synthesized.
- Detailed structural information was obtained via X-ray diffraction.
- An olefin-rich HCOF was converted to a hydroxylated framework, retaining high crystallinity.
Conclusions:
- The synthesis of crystalline HCOFs is feasible using readily available monomers.
- Chemical modification of HCOFs can be achieved without compromising crystallinity.
- These findings open avenues for designing functional porous materials.
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