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Ring-Opening Copolymerization of Epoxides and Cyclic Anhydrides with Discrete Metal Complexes: Structure–Property Relationships
Abstract
Polyesters synthesized through the alternating copolymerization of epoxides and cyclic anhydrides compose a growing class of polymers that exhibit an impressive array of chemical and physical properties. Because they are synthesized through the chain-growth polymerization of two variable monomers, their syntheses can be controlled by discrete metal complexes, and the resulting materials vary widely in their functionality and physical properties. This polymer-focused review gives a perspective on the current state of the field of epoxide/anhydride copolymerization mediated by discrete catalysts and the relationships between the structures and properties of these polyesters.
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“While the field of epoxide/CO2 copolymerization is quite mature, with several technologies been commercialized, the progress in epoxide/cyclic anhydride copolymerization is more recent.211,343”
From Catalysis as an Enabling Science for Sustainable Polymers (2018) · cites this paper as [211]
In the citing paper
“Terpolymerization of epoxide, cyclic anhydride, and CO2 is a facile strategy for the onepot synthesis of poly(ester-carbonate), 211,343 a class of biodegradable polymers that have garnered considerable interest due to their possible superior properties than pure polyesters and polycarbonates.”
From Catalysis as an Enabling Science for Sustainable Polymers (2018) · cites this paper as [211]
In the citing paper
“Additionally, many epoxides and cyclic anhydrides contain unsaturated moieties that can be utilized for post-polymerization modifications and crosslinking, 211 which increases the range of architectures and functionalities that can be achieved through the ROCP method.”
From Catalysis as an Enabling Science for Sustainable Polymers (2018) · cites this paper as [211]
In the citing paper
“By using a different combination of epoxide and cyclic anhydride, Tg of polyesters can be tuned to almost any value from -44 to 184 °C.211”
From Catalysis as an Enabling Science for Sustainable Polymers (2018) · cites this paper as [211]
Citations
Cites
Odian, G. (2004) · doi:10.1002/047147875x · Cited by 7,158
The Path Forward for Biofuels and Biomaterials
Ragauskas, A. J., Williams, C. K., Davison, B. H., Britovsek, G., Cairney, J., Eckert, C. A., Frederick, W. J., Hallett, J. P., Leak, D. J., Liotta, C. L., et al. (2006) · Science · doi:10.1126/science.1114736 · Cited by 5,741
An Overview of Polylactides as Packaging Materials
Auras, R., Harte, B., & Selke, S. (2004) · Macromolecular Bioscience · doi:10.1002/mabi.200400043 · Cited by 3,454
Biodegradable Polymers for the Environment
Gross, R. A., & Kalra, B. (2002) · Science · doi:10.1126/science.297.5582.803 · Cited by 2,029
Biodegradable polyesters for medical and ecological applications
Ikada, Y., & Tsuji, H. (2000) · Macromolecular Rapid Communications · doi:10.1002/(sici)1521-3927(20000201)21:3 · Cited by 1,538
Polyurethanes: Versatile Materials and Sustainable Problem Solvers for Today’s Challenges
Engels, H., Pirkl, H., Albers, R., Albach, R. W., Krause, J., Hoffmann, A., Casselmann, H., & Dormish, J. (2013) · Angewandte Chemie International Edition · doi:10.1002/anie.201302766 · Cited by 1,236
Applications of life cycle assessment to NatureWorks™ polylactide (PLA) production
Vink, E. T. H., Rábago, K. R., Glassner, D. A., & Gruber, P. R. (2003) · Polymer Degradation and Stability · doi:10.1016/s0141-3910(02)00372-5 · Cited by 1,093
Amass, W., Amass, A. J., & Tighe, B. J. (1998) · Polymer International · doi:10.1002/(sici)1097-0126(1998100)47:2 · Cited by 1,015
Lactic acid: recent advances in products, processes and technologies — a review
Datta, R., & Henry, M. P. (2006) · Journal of Chemical Technology & Biotechnology · doi:10.1002/jctb.1486 · Cited by 973
New emerging trends in synthetic biodegradable polymers—Polylactide: A critique
Gupta, A. P., & Kumar, V. (2007) · European Polymer Journal · doi:10.1016/j.eurpolymj.2007.06.045 · Cited by 941
Research works printed but not linked: 1
- 2006, The Merck Index
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Items 101–200 of 598
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Borane catalysis for epoxide (co)polymerization
Naumann, S. (2023) · Polymer Chemistry · doi:10.1039/d3py00018d · Cited by 53
Zhang, H., Hu, S., Zhao, J., & Zhang, G. (2017) · Macromolecules · doi:10.1021/acs.macromol.7b00599 · Cited by 54
Orthogonal functionalization of alternating polyesters: selective patterning of (AB) n sequences
Yi, N., Chen, T. T. D., Unruangsri, J., Zhu, Y., & Williams, C. K. (2019) · Chemical Science · doi:10.1039/c9sc03756j · Cited by 53
Popowski, Y., Lu, Y., Coates, G. W., & Tolman, W. B. (2022) · Journal of the American Chemical Society · doi:10.1021/jacs.2c02981 · Cited by 52
Self-citationCobalt-Catalyzed Trifluoromethoxylation of Epoxides
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Xu, J., & Hadjichristidis, N. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.202015339 · Cited by 50
The versatile, functional polyether, polyepichlorohydrin: History, synthesis, and applications
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Isnard, F., Carratù, M., Lamberti, M., Venditto, V., & Mazzeo, M. (2018) · Catalysis Science & Technology · doi:10.1039/c8cy01174e · Cited by 49
Chen, X.-L., Wang, B., Song, D., Pan, L., & Li, Y. (2022) · Macromolecules · doi:10.1021/acs.macromol.1c02303 · Cited by 48
Zhang, X., Guo, W., Zhang, C., & Zhang, X. (2023) · Nature Communications · doi:10.1038/s41467-023-41136-6 · Cited by 49
Chang, C., Tsai, C., Lin, W., Su, Y., Chuang, H., Liu, W., Chen, C., Chen, C.-K., & Ko, B. (2018) · Polymer · doi:10.1016/j.polymer.2018.02.063 · Cited by 49
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Zhang, H., Zhou, G., Jiang, M. Y., Zhang, H., Wang, H., Wu, Y., & Wang, R. (2020) · Macromolecules · doi:10.1021/acs.macromol.0c00344 · Cited by 48
Xue, L., Tan, F., & Zhu, Y. (2021) · Frontiers in Chemistry · doi:10.3389/fchem.2021.647245 · Cited by 48
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Shaik, M., Peterson, J., & Du, G. (2018) · Macromolecules · doi:10.1021/acs.macromol.8b02096 · Cited by 46
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Tran, D. K., Braaksma, A. N., Andras, A. M., Boopathi, S. K., Darensbourg, D. J., & Wooley, K. L. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.3c05529 · Cited by 42
Wang, L., Zhang, J., Zhao, N., Ren, C., Liu, S., & Li, Z. (2020) · ACS Macro Letters · doi:10.1021/acsmacrolett.0c00564 · Cited by 42
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Metadata
- Authors
- Longo, J. M., Sanford, M. J., & Coates, G. W.
- Affiliations
- Cornell University (US)
- Corresponding author
- Coates, Geoffrey W.
- Venue
- Chemical Reviews
- Publisher
- American Chemical Society (ACS)
- Published
- 2016-12-12
- Volume
- 116
- Issue
- 24
- Pages
- 15167-15197
- ISSN
- 0009-2665 (ISSN-L)
- 1520-6890
- OpenAlex
- W2563186293
- Cited by
- 596
- References
- 86
- Citations by year
- 2026: 43 · 2025: 71 · 2024: 73 · 2023: 82 · 2022: 85 · 2021: 72 · 2020: 56 · 2019: 40 · 2018: 48 · 2017: 26
- FWCI
- 2.04
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Chemical Reviews (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Division of Chemistry (CHE-1413862)
- Topics
- Physical Sciences › Materials Science › Biomaterials › biodegradable polymer synthesis and properties
- Physical Sciences › Chemistry › Organic Chemistry › Advanced Polymer Synthesis and Characterization
- Physical Sciences › Chemical Engineering › Process Chemistry and Technology › Carbon dioxide utilization in catalysis
- Keywords
- ring-opening copolymerization, epoxides, cyclic anhydrides, polyester synthesis, alternating copolymerization, chain-growth polymerization, structure-property relationships
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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