Related Experiment Video
Updated: May 20, 2025

Fabricating Reactive Surfaces with Brush-like and Crosslinked Films of Azlactone-Functionalized Block Co-Polymers
Published on: June 30, 2018
α-Methoxy Benzaldehyde Based Photopolymers as a Promising Toolbox for Architected Carbon
Kjetil Baglo1, Laurent Remy2, Kai Mundsinger2
1Chair of Materials Science, Department of Materials Engineering, School of Engineering and Design, Technical University of Munich (TUM), Boltzmannstr. 15, 85748, Garching, Germany.
Stable carbonized microspheres with high char yields (~60%) are produced from Diels-Alder photopolymers. These materials show promise for advanced additively manufactured carbon precursors due to their excellent charring properties and low shrinkage.
Area of Science:
- Polymer Chemistry
- Materials Science
- Organic Chemistry
Background:
- Photopolymers offer tunable properties for advanced material applications.
- Diels-Alder reactions provide efficient polymerization pathways.
- Additive manufacturing requires precursors with specific thermal and mechanical properties.
Purpose of the Study:
- To investigate the pyrolysis of novel photopolymers for carbonized microsphere production.
- To elucidate the chemical decomposition pathways during thermal treatment.
- To evaluate the suitability of these photopolymers as precursors for additively manufactured carbon.
Main Methods:
- Synthesis of photopolymers using α-methoxy benzaldehyde and bismaleimide precursors.
- Photo-induced Diels-Alder step-growth polymerization.
- Thermogravimetric analysis (TGA) to determine char yield.
- Infrared (IR) spectroscopy to analyze decomposition products.
Main Results:
- Achieved high char yields close to 60% from the photopolymers.
- Observed low shrinkage of approximately 33% during carbonization.
- Identified specific chemical decomposition pathways contributing to high char formation.
Conclusions:
- Diels-Alder-type photopolymers are excellent precursors for stable carbonized microspheres.
- The high char yield and low shrinkage are advantageous for additive manufacturing.
- These findings position the photopolymers as promising materials for next-generation AMcarbon applications.
Related Concept Videos
Anionic Chain-Growth Polymerization: Overview
Free-Radical Chain Reaction and Polymerization of Alkenes
Cycloaddition Reactions: MO Requirements for Photochemical Activation
Electrophilic Aromatic Substitution: Friedel–Crafts Acylation of Benzene
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)

