The DOI matches its Crossref record; 126 of the 127 references it cites were found in a registry or an index.
100th Anniversary of Macromolecular Science Viewpoint: Degradable Polymers from Radical Ring-Opening Polymerization: Latest Advances, New Directions, and Ongoing Challenges
Open accessAbstract
Radical ring-opening polymerization (rROP) allows facile incorporation of labile groups (e.g., ester) into the main chain of vinyl polymers to obtain (bio)degradable materials. rROP has focused a lot of attention especially since the advent of reversible deactivation radical polymerization (RDRP) techniques and is still incredibly moving forward, as attested by the numerous achievements in terms of monomer synthesis, macromolecular engineering, and potential biomedical applications of the resulting degradable polymers. In the present Viewpoint, we will cover the latest progress made in rROP in the last ∼5 years, such as its recent directions, its remaining limitations, and the ongoing challenges. More specifically, this will be achieved through the three different classes of monomers that recently caught most of the attention: cyclic ketene acetals (CKA), thionolactones, and macrocyclic monomers.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“However, the rROP approach requires delicate design of the cyclic monomer to achieve high reactivity and to control the ratio of ring-opened and cyclic structures.”
From Direct Radical Copolymerizations of Thioamides To Generate Vinyl Polymers with Degradable Thioether Bonds in the Backbones (2023) · cites this paper as [22]
Citations
Cites
Atom Transfer Radical Polymerization
Matyjaszewski, K. A., & Xia, J. (2001) · Chemical Reviews · doi:10.1021/cr940534g · Cited by 7,751
Stimuli-responsive nanocarriers for drug delivery
Mura, S., Nicolas, J., & Couvreur, P. (2013) · Nature Materials · doi:10.1038/nmat3776 · Cited by 6,289
Self-citationMetal-Catalyzed Living Radical Polymerization
Kamigaito, M., Ando, T., & Sawamoto, M. (2001) · Chemical Reviews · doi:10.1021/cr9901182 · Cited by 3,277
Living Radical Polymerization by the RAFT Process
Moad, G., Rizzardo, E., & Thang, S. H. (2005) · Australian Journal of Chemistry · doi:10.1071/ch05072 · Cited by 2,286
Design of polymeric nanoparticles for biomedical delivery applications
Elsabahy, M., & Wooley, K. L. (2012) · Chemical Society Reviews · doi:10.1039/c2cs15327k · Cited by 1,717
Recent Developments in Ring Opening Polymerization of Lactones for Biomedical Applications
Albertsson, A.-C., & Varma, I. K. (2003) · Biomacromolecules · doi:10.1021/bm034247a · Cited by 1,582
Living ring-opening metathesis polymerization
Bielawski, C. W., & Grubbs, R. H. (2006) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2006.08.006 · Cited by 1,522
50th Anniversary Perspective : RAFT Polymerization─A User Guide
Perrier, S. (2017) · Macromolecules · doi:10.1021/acs.macromol.7b00767 · Cited by 1,514
Nitroxide-mediated polymerization
Nicolas, J., Guillaneuf, Y., Lefay, C., Bertin, D., Gigmes, D., & Charleux, B. (2013) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2012.06.002 · Cited by 1,380
Self-citationPerrier, S., & Takolpuckdee, P. (2005) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.20986 · Cited by 1,157
Research works printed but not linked: 2
- 10.1295/kobunshi.30.331 · DOI
- Bailey W. J., 1982, Proc. IUPAC, IUPAC, Macromol. Symp., 214
Cited by
Sorted by citations
Jung, K., Corrigan, N. A., Wong, E. H. H., & Boyer, C. A. (2021) · Advanced Materials · doi:10.1002/adma.202105063 · Cited by 193
Controlled-Radical Polymerization of α-Lipoic Acid: A General Route to Degradable Vinyl Copolymers
Albanese, K. R., Morris, P. T., de Alaniz, J. R., Bates, C. M., & Hawker, C. J. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.3c08248 · Cited by 184
Kiel, G. R., Lundberg, D. J., Prince, E., Husted, K. E. L., Johnson, A. M., Lensch, V., Li, S., Shieh, P., & Johnson, J. A. (2022) · Journal of the American Chemical Society · doi:10.1021/jacs.2c05374 · Cited by 151
Degradable Vinyl Polymers for Combating Marine Biofouling
Pan, J., Ai, X., Ma, C., & Zhang, G. (2022) · Accounts of Chemical Research · doi:10.1021/acs.accounts.2c00187 · Cited by 139
Polymer Colloids: Current Challenges, Emerging Applications, and New Developments
Aguirre, M., Ballard, N., González, E., Hamzehlou, S., Sardón, H., Calderón, M., Paulis, M., Tomovská, R., Dupin, D., Bean, R. H., et al. (2023) · Macromolecules · doi:10.1021/acs.macromol.3c00108 · Cited by 134
Building Tunable Degradation into High-Performance Poly(acrylate) Pressure-Sensitive Adhesives
Albanese, K. R., Okayama, Y., Morris, P. T., Gerst, M., Gupta, R., Speros, J. C., Hawker, C. J., Choi, C., de Alaniz, J. R., & Bates, C. M. (2023) · ACS Macro Letters · doi:10.1021/acsmacrolett.3c00204 · Cited by 130
Degradable polymers via olefin metathesis polymerization
Sun, H. R., Liang, Y., Thompson, M. P., & Gianneschi, N. C. (2021) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2021.101427 · Cited by 116
Martinez, M. R., Bossa, F. D. L., Olszewski, M., & Matyjaszewski, K. A. (2021) · Macromolecules · doi:10.1021/acs.macromol.1c02246 · Cited by 106
Lefay, C., & Guillaneuf, Y. (2023) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2023.101764 · Cited by 102
Recent advances in the ring-opening polymerization of sulfur-containing monomers
Purohit, V. B., Pięta, M., Pietrasik, J., & Plummer, C. M. (2022) · Polymer Chemistry · doi:10.1039/d2py00831a · Cited by 90
Wang, W., Zhou, Z., Sathe, D., Tang, X., Moran, S., Jin, J., Hæffner, F., Wang, J., & Niu, J. (2021) · Angewandte Chemie International Edition · doi:10.1002/anie.202113302 · Cited by 86
Recent Advances in Antifouling Surface Polymer Brushes
Xu, X., Chang, Y.-X., Gong, Y., Zhang, Y., Yu, Y., Peng, H., & Fu, C. (2023) · ACS Applied Polymer Materials · doi:10.1021/acsapm.3c02150 · Cited by 81
Galanopoulo, P., Gil, N., Gigmes, D., Lefay, C., Guillaneuf, Y., Lages, M., Nicolas, J., Lansalot, M., & D'Agosto, F. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202117498 · Cited by 73
Self-citationYang, Y., Shi, K., Yu, K., Xing, F., Lai, H., Zhou, Y., & Xiao, P. (2021) · Advanced Healthcare Materials · doi:10.1002/adhm.202101504 · Cited by 79
Current status and outlook for ATRP
Matyjaszewski, K. A. (2024) · European Polymer Journal · doi:10.1016/j.eurpolymj.2024.113001 · Cited by 76
Polythioesters Prepared by Ring‐Opening Polymerization of Cyclic Thioesters and Related Monomers
Li, H., Guillaume, S. M., & Carpentier, J. (2022) · Chemistry - An Asian Journal · doi:10.1002/asia.202200641 · Cited by 70
Bossion, A., Zhu, C., Guerassimoff, L., Mougin, J., & Nicolas, J. (2022) · Nature Communications · doi:10.1038/s41467-022-30220-y · Cited by 63
Self-citationZhu, C., & Nicolas, J. (2022) · Biomacromolecules · doi:10.1021/acs.biomac.2c00230 · Cited by 64
Self-citationDeng, Y., Mehner, F., & Gaitzsch, J. (2023) · Macromolecular Rapid Communications · doi:10.1002/marc.202200941 · Cited by 62
Elliss, H., Dawson, F., Nisa, Q. U., Bingham, N. M., Roth, P. J., & Kopeć, M. (2022) · Macromolecules · doi:10.1021/acs.macromol.2c01140 · Cited by 60
Mechanically triggered on-demand degradation of polymers synthesized by radical polymerizations
Liu, P., Jimaja, S., Immel, S., Thomas, C., Mayer, M., Weder, C., & Bruns, N. (2024) · Nature Chemistry · doi:10.1038/s41557-024-01508-x · Cited by 70
Tunable backbone-degradable robust tissue adhesives via in situ radical ring-opening polymerization
Yang, R., Zhang, X., Chen, B., Yan, Q., Yin, J., & Luan, S. (2023) · Nature Communications · doi:10.1038/s41467-023-41610-1 · Cited by 61
Albanese, K. R., de Alaniz, J. R., Hawker, C. J., & Bates, C. M. (2024) · Polymer · doi:10.1016/j.polymer.2024.127167 · Cited by 60
Lages, M., Gil, N., Galanopoulo, P., Mougin, J., Lefay, C., Guillaneuf, Y., Lansalot, M., D’Agosto, F., & Nicolas, J. (2022) · Macromolecules · doi:10.1021/acs.macromol.2c01734 · Cited by 55
Self-citationDegradable Block Copolymer Nanoparticles Synthesized by Polymerization‐Induced Self‐Assembly
Zhang, S., Li, R., & An, Z. (2023) · Angewandte Chemie International Edition · doi:10.1002/anie.202315849 · Cited by 55
Braun, O., Coquery, C., Kieffer, J., Blondel, F., Favero, C., Besset, C., Mesnager, J., Voelker, F., Delorme, C., & Matioszek, D. (2021) · Molecules · doi:10.3390/molecules27010042 · Cited by 54
Watanabe, H., & Kamigaito, M. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.3c01796 · Cited by 51
Stimuli-sensitive polymer prodrug nanocarriers by reversible-deactivation radical polymerization
Guerassimoff, L., Ferrere, M., Bossion, A., & Nicolas, J. (2024) · Chemical Society Reviews · doi:10.1039/d2cs01060g · Cited by 58
Self-citationSustainable and degradable plastics
Guillaume, S. M. (2022) · Nature Chemistry · doi:10.1038/s41557-022-00901-8 · Cited by 50
Galanopoulo, P., Gil, N., Gigmès, D., Lefay, C., Guillaneuf, Y., Lages, M., Nicolas, J., D’Agosto, F., & Lansalot, M. (2023) · Angewandte Chemie International Edition · doi:10.1002/anie.202302093 · Cited by 47
Self-citationZhang, S., Fang, H., & Tian, H. (2024) · Biomacromolecules · doi:10.1021/acs.biomac.4c01193 · Cited by 48
Plummer, C. M., Gil, N., Dufils, P.-E., Wilson, D. J., Lefay, C., Gigmes, D., & Guillaneuf, Y. (2021) · ACS Applied Polymer Materials · doi:10.1021/acsapm.1c00569 · Cited by 45
Ko, K., Lundberg, D. J., Johnson, A. M., & Johnson, J. A. (2024) · Journal of the American Chemical Society · doi:10.1021/jacs.3c14554 · Cited by 45
Zhu, C., & Nicolas, J. (2021) · Polymer Chemistry · doi:10.1039/d0py01425g · Cited by 42
Self-citationZhu, C., Denis, S., & Nicolas, J. (2022) · Chemistry of Materials · doi:10.1021/acs.chemmater.1c04151 · Cited by 44
Self-citationBackbone-Degradable Vinyl Acetate Latex: Coatings for Single-Use Paper Products
Carter, M. C. D., Hejl, A., Woodfin, S., Einsla, B. R., Jančo, M., DeFelippis, J., Cooper, R. J., & Even, R. C. (2021) · ACS Macro Letters · doi:10.1021/acsmacrolett.1c00172 · Cited by 41
Zhao, W., Li, C., Chang, J., Zhou, H., Wang, D., Sun, J., Liu, T., Peng, H., Wang, Q., Li, Y., et al. (2023) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2023.101739 · Cited by 42
Jiang, N., Zhou, Z., & Niu, J. (2024) · Journal of the American Chemical Society · doi:10.1021/jacs.3c14244 · Cited by 41
AlFaraj, Y. S., Mohapatra, S., Shieh, P., Husted, K. E. L., Ivanoff, D. G., Lloyd, E. M., Cooper, J. C., Dai, Y., Singhal, A. P., Moore, J. S., et al. (2023) · ACS Central Science · doi:10.1021/acscentsci.3c00502 · Cited by 39
Uchiyama, M., Murakami, Y., Satoh, K., & Kamigaito, M. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202215021 · Cited by 39
Kimura, T., & Ouchi, M. (2023) · Angewandte Chemie International Edition · doi:10.1002/anie.202305252 · Cited by 37
Lages, M., Pesenti, T., Zhu, C., Lê, D., Mougin, J., Guillaneuf, Y., & Nicolas, J. (2023) · Chemical Science · doi:10.1039/d2sc05316k · Cited by 38
Self-citationEmbedding Peptides into Synthetic Polymers: Radical Ring-Opening Copolymerization of Cyclic Peptides
Sbordone, F., Veskova, J., Richardson, B., Thi, P., Micallef, A. S., & Frisch, H. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.2c12517 · Cited by 37
A General Strategy for Radical Ring-Opening Polymerization of Macrocyclic Allylic Sulfides
Zhang, S., Cao, C., Jiang, S., & Huang, H. (2022) · Macromolecules · doi:10.1021/acs.macromol.2c01636 · Cited by 36
Lipoic acid/ethyl lipoate as cleavable comonomers for synthesis of degradable polymer networks
Dawson, F., Irvine, G., & Kopeć, M. (2025) · Polymer Chemistry · doi:10.1039/d5py00379b · Cited by 34
Programming Photodegradability into Vinylic Polymers via Radical Ring‐Opening Polymerization
Do, P. T., Poad, B. L. J., & Frisch, H. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202213511 · Cited by 35
Rix, M. F. I., Collins, K., Higgs, S. J., Dodd, E. M., Coles, S. J., Bingham, N. M., & Roth, P. J. (2023) · Macromolecules · doi:10.1021/acs.macromol.3c01811 · Cited by 46
Nisa, Q. U., Theobald, W., Hepburn, K. S., Riddlestone, I. M., Bingham, N. M., Kopeć, M., & Roth, P. J. (2022) · Macromolecules · doi:10.1021/acs.macromol.2c01317 · Cited by 33
Radical Homopolymerization of Linear α‐Olefins Enabled by 1,4‐Cyano Group Migration
An, B., Zhou, L., Liu, S., Zheng, Y., Li, C., Cui, F., Yue, C., Liu, H., Sui, Y., Ji, C., et al. (2024) · Angewandte Chemie International Edition · doi:10.1002/anie.202402511 · Cited by 31
Lages, M., & Nicolas, J. (2022) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2022.101637 · Cited by 30
Self-citationWang, W., Rondon, B., Wang, Z., Wang, J., & Niu, J. (2023) · Macromolecules · doi:10.1021/acs.macromol.2c02025 · Cited by 28
Pesenti, T., Gillon, É., Ishii, S., Messaoudi, S., Guillaneuf, Y., Imberty, A., & Nicolas, J. (2023) · Biomacromolecules · doi:10.1021/acs.biomac.2c01419 · Cited by 27
Self-citationDeng, Y., Frezel, A., Mehner, F., Friedel, P., & Gaitzsch, J. (2023) · Polymer Chemistry · doi:10.1039/d3py00929g · Cited by 26
Oh, X. Y., Ge, Y., & Goto, A. (2021) · Chemical Science · doi:10.1039/d1sc03560f · Cited by 26
Summating potential and action potential ratio in Meniere's disease before and after treatment.
Orchik, D. J., Shea, J. J., & Ge, N. N. (1998) · PubMed · Cited by 26
Han, S., Lee, K., Morris, P. T., Michelas, M., Moad, G., Bates, C. M., Hawker, C. J., & Boyer, C. A. (2025) · Macromolecules · doi:10.1021/acs.macromol.5c02734 · Cited by 25
Pesenti, T., Zhu, C., Gonzalez-Martinez, N., Tomás, R. M. F., Gibson, M. I., & Nicolas, J. (2022) · ACS Macro Letters · doi:10.1021/acsmacrolett.2c00298 · Cited by 25
Self-citationZhang, Z., Sun, Y., Rajeshkumar, T., Li, Y., Maron, L., & Hong, M. (2025) · Nature Chemistry · doi:10.1038/s41557-025-01751-w · Cited by 28
Georgiou, P. G., Neal, T. J., Newell, M. A., Hepburn, K. S., Tyler, J. J. S., Farmer, M. A. H., Chohan, P., Roth, P. J., Nicolas, J., & Armes, S. P. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.5c03744 · Cited by 25
Self-citationGao, P., Jiang, X. M., Li, J., Nicolas, J., & Ha‐Duong, T. (2025) · Advanced Healthcare Materials · doi:10.1002/adhm.202503503 · Cited by 28
Self-citationAi, X., Pan, J., Xie, Q., Ma, C., & Zhang, G. (2021) · Polymer Chemistry · doi:10.1039/d1py00810b · Cited by 22
Mehner, F., Geisler, M., Arnhold, K., Komber, H., & Gaitzsch, J. (2022) · ACS Applied Polymer Materials · doi:10.1021/acsapm.2c01483 · Cited by 23
Lages, M., Gil, N., Galanopoulo, P., Mougin, J., Lefay, C., Guillaneuf, Y., Lansalot, M., D’Agosto, F., & Nicolas, J. (2023) · Macromolecules · doi:10.1021/acs.macromol.3c01478 · Cited by 22
Self-citationPlenty of Space in the Backbone: Radical Ring‐Opening Polymerization
Sbordone, F., & Frisch, H. (2024) · Chemistry - A European Journal · doi:10.1002/chem.202401547 · Cited by 21
A Strategy for Controlling the Polymerizations of Thiyl Radical Propagation by RAFT Agents
Zhang, S., Wang, Y., Huang, H., & Cao, D. (2023) · Angewandte Chemie International Edition · doi:10.1002/anie.202308524 · Cited by 21
Uchiyama, M., Imai, M., & Kamigaito, M. (2024) · Polymer Journal · doi:10.1038/s41428-023-00869-3 · Cited by 23
100th Anniversary of Macromolecular Science Viewpoints
Rowan, S. J. (2021) · ACS Macro Letters · doi:10.1021/acsmacrolett.1c00175 · Cited by 21
Du, Y., Du, Y., Lazzari, S., Reimers, T., Konradi, R., Holcombe, T. W., & Coughlin, E. B. (2022) · Polymer Chemistry · doi:10.1039/d2py00986b · Cited by 20
Reversible Thiyl Radical Addition−Fragmentation Chain Transfer Polymerization
Wang, Y., Du, J., & Huang, H. (2024) · Angewandte Chemie International Edition · doi:10.1002/anie.202318898 · Cited by 20
Visible Light Photoiniferter Polymerization for the Synthesis of Degradable Lipoate Copolymers
Jiang, H., & An, Z. (2025) · ACS Macro Letters · doi:10.1021/acsmacrolett.5c00583 · Cited by 18
Radical Ring Opening Polymerization of Cyclic Ketene Acetals Derived From d -Glucal
Hardy, C., Levere, M. E., Kociok-Köhn, G. I., & Buchard, A. (2023) · ACS Macro Letters · doi:10.1021/acsmacrolett.3c00397 · Cited by 18
Kuroda, K., & Ouchi, M. (2023) · Angewandte Chemie International Edition · doi:10.1002/anie.202316875 · Cited by 18
Towards the optimal design of optically clear adhesives for flexible display
Park, Y., Kim, J., Kim, D., Lee, S., Hwang, D., & Kwon, M. S. (2024) · Soft Science · doi:10.20517/ss.2024.22 · Cited by 17
Ghorbani, M., & Prince, E. (2024) · Biomacromolecules · doi:10.1021/acs.biomac.4c01116 · Cited by 17
Chen, Y., Ye, H., Zhao, X., Li, P., Chen, H., Liu, H., Zhang, H., & Li, W. (2025) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.4c19192 · Cited by 17
Degradable polymer films: RAFT-mediated emulsion copolymerization of lipoic acid with vinyl monomers
Thompson, S. W., Fadil, Y., Chan, N. J.-A., Moad, G., Perrier, S., & Zetterlund, P. B. (2025) · Green Chemistry · doi:10.1039/d5gc04609b · Cited by 16
Mousa, M., Jonsson, M., Wilson, O. R., Geerts, R., Bergenudd, H., Bengtsson, C., Kron, A. L., & Malmström, E. (2023) · Polymer Chemistry · doi:10.1039/d3py00630a · Cited by 16
Deng, Y., Schäfer, S., Kronstein, D., Atabay, A., Susewind, M., Krieg, E., Seiffert, S., & Gaitzsch, J. (2023) · Biomacromolecules · doi:10.1021/acs.biomac.3c00992 · Cited by 16
Barquero, A., Zanoni, A., Gabirondo, E., Román, E. G. D. S., Hamzehlou, S., Ximenis, M., Moscatelli, D., Sardón, H., & Leiza, J. R. (2024) · ACS Macro Letters · doi:10.1021/acsmacrolett.4c00101 · Cited by 15
Jiang, S., & Huang, H. (2024) · Polymer · doi:10.1016/j.polymer.2024.127106 · Cited by 15
Cvek, M., Jazani, A. M., Bossa, F. D. L., Bernat, R., Kapil, K., & Matyjaszewski, K. A. (2024) · European Polymer Journal · doi:10.1016/j.eurpolymj.2024.113429 · Cited by 15
Ring‐Opening Polymerization Strategies for Degradable Polyesters
Narmon, A. S., Jenisch, L. M., Pitet, L. M., & Dusselier, M. (2022) · Wiley eBooks · doi:10.1002/9783527827589.ch7 · Cited by 15
Wang, W., Zhou, Z., Sathe, D., Tang, X., Moran, S., Jin, J., Hæffner, F., Wang, J., & Niu, J. (2021) · Angewandte Chemie · doi:10.1002/ange.202113302 · Cited by 14
Mothe, S. R., Zhao, W., van Herk, A. M., & Thoniyot, P. (2024) · Macromolecules · doi:10.1021/acs.macromol.3c02474 · Cited by 14
Controlling Molecular Aggregation-Induced Emission by Controlled Polymerization
Bao, Y. (2021) · Molecules · doi:10.3390/molecules26206267 · Cited by 14
Degradable Glycopolyester-like Nanoparticles by Radical Ring-Opening Polymerization
Pesenti, T., Domingo‐Lopez, D. A., Gillon, É., Ibrahim, N., Messaoudi, S., Imberty, A., & Nicolas, J. (2022) · Biomacromolecules · doi:10.1021/acs.biomac.2c00851 · Cited by 14
Self-citationMorris, P. T., Olsen, S. C., Santiago, M., Wang, H. M., Denton, E. H., Read de Alaniz, J., Bates, C. M., Albanese, K. R., & Hawker, C. J. (2026) · Journal of the American Chemical Society · doi:10.1021/jacs.5c20808 · Cited by 17
Xiong, Y., Lu, Z.-B., Zhao, Y., Xia, L., Hong, C., Zhang, Z., & You, Y. (2025) · Polymer science & technology. · doi:10.1021/polymscitech.5c00017 · Cited by 14
Main chain selective polymer degradation: controlled by the wavelength and assembly
Do, P. T., Sbordone, F., Kalmer, H., Sokolova, A. V., Zhang, C., Thai, L. D., Golberg, D. V., Chapman, R., Poad, B. L. J., & Frisch, H. (2024) · Chemical Science · doi:10.1039/d4sc02172j · Cited by 13
Dardé, T., Diomar, E., Schultze, X., & Taton, D. (2024) · Angewandte Chemie International Edition · doi:10.1002/anie.202411249 · Cited by 13
pH‐Controlled Reversible Folding of Copolymers via Formation of β‐sheet Secondary Structures
Sbordone, F., Micallef, A. S., & Frisch, H. (2024) · Angewandte Chemie International Edition · doi:10.1002/anie.202319839 · Cited by 13
Insertion of Degradable Thioester Linkages into Styrene and Methacrylate PolymersPreprint
Rix, M. F. I., Higgs, S. J., Dodd, E. M., Coles, S. J., Bingham, N. M., & Roth, P. J. (2022) · ChemRxiv · doi:10.26434/chemrxiv-2022-cdt52 · Cited by 13
Stimuli-Responsive Main-Chain Degradable Polymers: Synthesis, Applications, and Future Perspectives
Bag, S., Ghosh, D., Banerjee, S., & De, P. (2025) · ACS Applied Polymer Materials · doi:10.1021/acsapm.5c03009 · Cited by 13
A Versatile Comonomer Additive for Radically Recyclable Vinyl‐derived Polymers
Mineo, A. M., & Katsumata, R. (2023) · Angewandte Chemie International Edition · doi:10.1002/anie.202316248 · Cited by 12
Synthesis of Degradable Vinyl Copolymers Based on Lipoic Acid via Ab Initio Emulsion Polymerization
Fadil, Y., Fan, D., Thompson, S. W., & Zetterlund, P. B. (2025) · ACS Sustainable Chemistry & Engineering · doi:10.1021/acssuschemeng.5c06894 · Cited by 11
Decarboxylation-Triggered Polymer Deconstruction
Gitter, S. R., Eades, C. B., Lott, M. E., Hughes, R. W., Evans, A. M., & Sumerlin, B. S. (2025) · ACS Polymers Au · doi:10.1021/acspolymersau.5c00146 · Cited by 14
Degradable Vinyl-Based Polymers by Radical Ring-Opening Polymerization: A User Guide
Luzel, B., Kouider, S., D’Agosto, F., Gigmès, D., Lansalot, M., Bates, C. M., Ackerman, E., Labalme, S., Johnson, J. A., Niu, J., et al. (2026) · ACS Polymers Au · doi:10.1021/acspolymersau.5c00191 · Cited by 12
Self-citationMothe, S. R., Chennamaneni, L. R., Tan, J. S. J., Lim, F. C. H., Zhao, W., & Thoniyot, P. (2023) · Macromolecular Chemistry and Physics · doi:10.1002/macp.202300221 · Cited by 11
Degradable Block Copolymer Nanoparticles Synthesized by Polymerization‐Induced Self‐Assembly
Zhang, S., Li, R., & An, Z. (2023) · Angewandte Chemie · doi:10.1002/ange.202315849 · Cited by 12
Degradable polymer bone adhesives
Bao, Z., Yang, R., Chen, B., & Luan, S. (2024) · Fundamental Research · doi:10.1016/j.fmre.2023.11.023 · Cited by 11
Metadata
- Authors
- Pesenti, T., & Nicolas, J.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- Corresponding author
- Nicolas, Julien
- Venue
- ACS Macro Letters
- Publisher
- American Chemical Society (ACS)
- Published
- 2020-12-02
- Volume
- 9
- Issue
- 12
- Pages
- 1812-1835
- ISSN
- 2161-1653 (ISSN-L)
- OpenAlex
- W3110095379
- Cited by
- 214
- References
- 127
- Citations by year
- 2026: 38 · 2025: 38 · 2024: 45 · 2023: 42 · 2022: 32 · 2021: 18
- Type
- journal article
- Language
- en
- Open access
- green
- hal.science
- Licence
- Locations
- ACS Macro Letters (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion, other-oa)
- Funders
- Agence Nationale de la Recherche (ANR-11-JS08-0005, ANR-15-CE08-0019)
- Centre National de la Recherche Scientifique
- Ministre de l'Enseignement sup?rieur, de la Recherche et de l'Innovation
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Advanced Polymer Synthesis and Characterization
- Physical Sciences › Materials Science › Biomaterials › biodegradable polymer synthesis and properties
- Physical Sciences › Materials Science › Polymers and Plastics › Polymer composites and self-healing
- Keywords
- radical ring-opening polymerization, degradable polymers, bio-based polymers, controlled radical polymerization, cyclic ketene acetals, thionolactones, macrocyclic monomers, macromolecular engineering, biomedical applications, monomer synthesis
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 ›
Are you an author, or do you see a problem with this page? Request a review