Cited by 258biodegradable polymer synthesis and propertiesCarbon dioxide utilization in catalysisAdvanced Polymer Synthesis and Characterization

Chemoselective Polymerizations from Mixtures of Epoxide, Lactone, Anhydride, and Carbon Dioxide

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Romain, Charles, Zhu, Yunqing, Dingwall, Paul, Paul, Shyeni, Rzepa, Henry S., Buchard, Antoine, Williams, Charlotte K.·2016·Journal of the American Chemical Society

Abstract

Controlling polymer composition starting from mixtures of monomers is an important, but rarely achieved, target. Here a single switchable catalyst for both ring-opening polymerization (ROP) of lactones and ring-opening copolymerization (ROCOP) of epoxides, anhydrides, and CO2 is investigated, using both experimental and theoretical methods. Different combinations of four model monomers-ε-caprolactone, cyclohexene oxide, phthalic anhydride, and carbon dioxide-are investigated using a single dizinc catalyst. The catalyst switches between the distinct polymerization cycles and shows high monomer selectivity, resulting in block sequence control and predictable compositions (esters and carbonates) in the polymer chain. The understanding gained of the orthogonal reactivity of monomers, specifically controlled by the nature of the metal-chain end group, opens the way to engineer polymer block sequences.

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  • This approach was extended to a monomer mixture of epoxide, lactone, anhydride, and CO2 to synthesize a variety of block copolymers with great sequence control and predictable compositions in the polymer chains.

    “Recently, this approach was extended to a monomer mixture of epoxide, lactone, anhydride, and CO2 to synthesize a variety of block copolymers with great sequence control and predictable compositions in the polymer chains.323”

    From Catalysis as an Enabling Science for Sustainable Polymers (2018) · cites this paper as [323]

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Authors
Romain, C., Zhu, Y., Dingwall, P., Paul, S., Rzepa, H. S., Buchard, A., & Williams, C. K.
Affiliations
  • Imperial College London (GB)
  • University of Bath (GB)
Corresponding author
  • Romain, Charles
  • Williams, Charlotte K.
Venue
Journal of the American Chemical Society
Published
2016-03-22
Volume
138
Issue
12
Pages
4120-4131
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2309157060
Cited by
258
References
73
Citations by year
2026: 12 · 2025: 22 · 2024: 23 · 2023: 24 · 2022: 32 · 2021: 35 · 2020: 29 · 2019: 16 · 2018: 34 · 2017: 25 · 2016: 6
FWCI
12.56
Type
journal article
Language
en
Open access
Locations
  • Journal of the American Chemical Society (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • The University of Bath Online Publications Store (The University of Bath) (submittedVersion, cc-by)
  • Research Portal (Queen's University Belfast) (submittedVersion, cc-by)
  • Spiral (Imperial College London) (submittedVersion, cc-by)
Funders
  • Engineering and Physical Sciences Research Council (EP/K014070/1, EP/K014668/1, EP/K035274/1, EP/L017393/1)
  • China Scholarship Council
Topics
  • Physical Sciences › Materials Science › Biomaterials › biodegradable polymer synthesis and properties
  • Physical Sciences › Chemical Engineering › Process Chemistry and Technology › Carbon dioxide utilization in catalysis
  • Physical Sciences › Chemistry › Organic Chemistry › Advanced Polymer Synthesis and Characterization
Keywords
ring-opening polymerization, ring-opening copolymerization, switchable catalysts, epoxides, lactones, phthalic anhydride, carbon dioxide, ε-caprolactone, cyclohexene oxide, block copolymers, monomer selectivity

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