3,6-Anhydrogalactal as a Single-Addition Monomer for Chain-End Functionalization of Metathesis Polymers

Controlling the structure and reactivity of the chain-end group is a central objective in modern polymer chemistry. Here we introduce 3,6-anhydrogalactal as a single-addition monomer that enables efficient and versatile chain-end functionalization of metathesis polymers. Readily synthesized from biomass-derived galactal, 3,6-anhydrogalactal exhibits excellent single-addition reactivity, allowing precise chain-end modifications even when introduced simultaneously with the propagating monomer. Theoretical calculations provide mechanistic insights into the unique reactivities governing its single-addition behavior. Its broad functional group compatibility facilitates diverse applications, including block copolymer synthesis, polymer-polymer coupling, and bioconjugation, demonstrating significant potential for advancing polymer materials and bioconjugation strategies.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-05-09
DOI
https://doi.org/10.1021/jacs.5c03379
Citations
3
Primary Topic
Synthetic Organic Chemistry Methods
Type
article
Field-Weighted Citation Impact
2.81

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article

3,6-Anhydrogalactal as a Single-Addition Monomer for Chain-End Functionalization of Metathesis Polymers

Zefeng Zhou, Quan Pham, Abhishek Chatterjee, Jia Niu et al.
3 citations
Journal of the American Chemical Society
Synthetic Organic Chemistry Methods
2.81
article

3,6-Anhydrogalactal as a Single-Addition Monomer for Chain-End Functionalization of Metathesis Polymers

Zefeng Zhou, Quan Pham, Abhishek Chatterjee, Jia Niu, Gavin J. Giardino
article en
3 citations

Abstract

Controlling the structure and reactivity of the chain-end group is a central objective in modern polymer chemistry. Here we introduce 3,6-anhydrogalactal as a single-addition monomer that enables efficient and versatile chain-end functionalization of metathesis polymers. Readily synthesized from biomass-derived galactal, 3,6-anhydrogalactal exhibits excellent single-addition reactivity, allowing precise chain-end modifications even when introduced simultaneously with the propagating monomer. Theoretical calculations provide mechanistic insights into the unique reactivities governing its single-addition behavior. Its broad functional group compatibility facilitates diverse applications, including block copolymer synthesis, polymer-polymer coupling, and bioconjugation, demonstrating significant potential for advancing polymer materials and bioconjugation strategies.

Journal of the American Chemical SocietyVol. 147(20)
Boston College (US)
Camille and Henry Dreyfus Foundation, Division of Chemistry
Openalex Percentile: Top 11%
Synthetic Organic Chemistry Methods
2.81
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