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100th Anniversary of Macromolecular Science Viewpoint: Degradable Polymers from Radical Ring-Opening Polymerization: Latest Advances, New Directions, and Ongoing Challenges
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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.
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“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]
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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
Warren, N. J., & Armes, S. P. (2014) · Journal of the American Chemical Society · doi:10.1021/ja502843f · Cited by 1,119
Cross-linked block copolymer micelles: functional nanostructures of great potential and versatility
O’Reilly, R. K., Hawker, C. J., & Wooley, K. L. (2006) · Chemical Society Reviews · doi:10.1039/b514858h · Cited by 949
Charleux, B., Delaittre, G., Rieger, J., & D’Agosto, F. (2012) · Macromolecules · doi:10.1021/ma300713f · Cited by 837
Tardy, A., Nicolas, J., Gigmes, D., Lefay, C., & Guillaneuf, Y. (2017) · Chemical Reviews · doi:10.1021/acs.chemrev.6b00319 · Cited by 469
Self-citationThermoresponsive polymer nanocarriers for biomedical applications
Bordat, A., Boissenot, T., Nicolas, J., & Tsapis, N. (2018) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2018.10.005 · Cited by 439
Self-citationChemical Vapor Deposition of Conformal, Functional, and Responsive Polymer Films
Alf, M. E., Asatekin, A., Barr, M. C., Baxamusa, S. H., Chelawat, H., İnce, G. Ö., Petruczok, C. D., Sreenivasan, R., Tenhaeff, W. E., Trujillo, N. J., et al. (2009) · Advanced Materials · doi:10.1002/adma.200902765 · Cited by 400
Degradable vinyl polymers for biomedical applications
Delplace, V., & Nicolas, J. (2015) · Nature Chemistry · doi:10.1038/nchem.2343 · Cited by 400
Self-citationLiving Radical Polymerization as a Tool for the Synthesis of Polymer‐Protein/Peptide Bioconjugates
Nicolas, J., Mantovani, G., & Haddleton, D. M. (2007) · Macromolecular Rapid Communications · doi:10.1002/marc.200700112 · Cited by 327
Self-citationRecent trends in the design of anticancer polymer prodrug nanocarriers
Delplace, V., Couvreur, P., & Nicolas, J. (2013) · Polymer Chemistry · doi:10.1039/c3py01384g · Cited by 291
Self-citationSynthetic Biodegradable Polymers
Rieger, B., Zevaco, T. A., Dinjus, E., Reichardt, R., Coates, G. W., & Künkel, A. (2012) · Advances in polymer science · doi:10.1007/978-3-642-27154-0 · Cited by 269
Agarwal, S. (2010) · Polymer Chemistry · doi:10.1039/c0py00040j · Cited by 263
Bailey, W. J., Ni, Z., & Wu, S. (1982) · Journal of Polymer Science Polymer Chemistry Edition · doi:10.1002/pol.1982.170201101 · Cited by 259
Radical Approach to Thioester-Containing Polymers
Smith, R. A., Fu, G., McAteer, O., Xu, M., & Gutekunst, W. R. (2019) · Journal of the American Chemical Society · doi:10.1021/jacs.8b12154 · Cited by 248
Recent advances in the design of bioconjugates from controlled/living radical polymerization
Droumaguet, B. L., & Nicolas, J. (2010) · Polymer Chemistry · doi:10.1039/b9py00363k · Cited by 233
Self-citationDegradable vinyl copolymers through thiocarbonyl addition–ring-opening (TARO) polymerization
Bingham, N. M., & Roth, P. J. (2019) · Chemical Communications · doi:10.1039/c8cc08287a · Cited by 176
Free Radical Polymers with Tunable and Selective Bio- and Chemical Degradability
Paulusse, J. M. J., Amir, R. J., Evans, R. A., & Hawker, C. J. (2009) · Journal of the American Chemical Society · doi:10.1021/ja903245p · Cited by 149
Synthesis and free radical ring‐opening polymerization of 2‐methylene‐4‐phenyl‐1,3‐dioxolane
Bailey, W. J., Wu, S., & Ni, Z. (1982) · Die Makromolekulare Chemie · doi:10.1002/macp.1982.021830811 · Cited by 139
Ketene Acetals. XIX. 2-Methylene-1,3-dioxolanes and 1,3-Dioxanes
McElvain, S. M., & Curry, M. J. (1948) · Journal of the American Chemical Society · doi:10.1021/ja01191a071 · Cited by 128
Drug-Initiated Synthesis of Polymer Prodrugs: Combining Simplicity and Efficacy in Drug Delivery
Nicolas, J. (2016) · Chemistry of Materials · doi:10.1021/acs.chemmater.5b04281 · Cited by 119
Self-citationTardy, A., Honore, J., Tran, J., Siri, D., Delplace, V., Bataille, I., Letourneur, D., Perrier, J., Nicoletti, C., Maresca, M., et al. (2017) · Angewandte Chemie International Edition · doi:10.1002/anie.201707043 · Cited by 118
Self-citationNew Free-Radical Ring-Opening Acrylate Monomers
Evans, R. A., Moad, G., Rizzardo, E., & Thang, S. H. (1994) · Macromolecules · doi:10.1021/ma00104a062 · Cited by 112
Methylenations of heteroatom-substituted carbonyls with dimethyl titanocene
Petasis, N. A., & Lu, S.-P. (1995) · Tetrahedron Letters · doi:10.1016/0040-4039(95)00320-c · Cited by 110
Free-Radical ring-opening polymerization of cyclic allylic sulfides
Evans, R. A., & Rizzardo, E. (1996) · Macromolecules · doi:10.1021/ma960573p · Cited by 110
Delplace, V., Tardy, A., Harrisson, S., Mura, S., Gigmès, D., Guillaneuf, Y., & Nicolas, J. (2013) · Biomacromolecules · doi:10.1021/bm401157g · Cited by 109
Self-citationHill, M. R., Guégain, E., Tran, J., Figg, C. A., Turner, A. C., Nicolas, J., & Sumerlin, B. S. (2017) · ACS Macro Letters · doi:10.1021/acsmacrolett.7b00572 · Cited by 109
Self-citationBiodegradable Polymer with Hydrolysis-Induced Zwitterions for Antibiofouling
Xie, Q., Xie, Q., Pan, J., Ma, C., & Zhang, G. (2018) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.8b00962 · Cited by 106
Harrisson, S., Nicolas, J., Maksimenko, A., Bui, D. T., Mougin, J., & Couvreur, P. (2012) · Angewandte Chemie International Edition · doi:10.1002/anie.201207297 · Cited by 103
Self-citationHill, M. R., Kubo, T., Goodrich, S. L., Figg, C. A., & Sumerlin, B. S. (2018) · Macromolecules · doi:10.1021/acs.macromol.8b00889 · Cited by 99
Undin, J., Illanes, T., Finne-Wistrand, A., & Albertsson, A.-C. (2012) · Polymer Chemistry · doi:10.1039/c2py20034a · Cited by 97
Synthesis and Characterization of Copolymers of 5,6-Benzo-2-methylene-1,3-dioxepane and Styrene
Wickel, H., & Agarwal, S. (2003) · Macromolecules · doi:10.1021/ma034551w · Cited by 97
Hedir, G. G., Bell, C. A., O’Reilly, R. K., & Dove, A. P. (2015) · Biomacromolecules · doi:10.1021/acs.biomac.5b00476 · Cited by 95
Ganda, S., Dulle, M., Drechsler, M., Förster, B., Förster, S., & Stenzel, M. H. (2017) · Macromolecules · doi:10.1021/acs.macromol.7b01453 · Cited by 94
Functional Degradable Polymers by Xanthate-Mediated Polymerization
Hedir, G. G., Bell, C. A., Ieong, N. S., Chapman, E., Collins, I. R., O’Reilly, R. K., & Dove, A. P. (2014) · Macromolecules · doi:10.1021/ma500428e · Cited by 93
Reversible-deactivation radical polymerization of cyclic ketene acetals
Jackson, A. W. (2020) · Polymer Chemistry · doi:10.1039/d0py00446d · Cited by 89
Spick, M. P., Bingham, N. M., Li, Y., de Jesus, J., Costa, C., Bailey, M. J., & Roth, P. J. (2020) · Macromolecules · doi:10.1021/acs.macromol.9b02497 · Cited by 88
Biodegradable Poly(ester- co -acrylate) with Antifoulant Pendant Groups for Marine Anti-Biofouling
Dai, G., Xie, Q., Ma, C., & Zhang, G. (2019) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.9b01247 · Cited by 87
Zhang, Y., Chu, D., Zheng, M., Kissel, T., & Agarwal, S. (2012) · Polymer Chemistry · doi:10.1039/c2py20403g · Cited by 86
Radical Cascade-Triggered Controlled Ring-Opening Polymerization of Macrocyclic Monomers
Huang, H., Sun, B., Huang, Y., & Niu, J. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b05365 · Cited by 85
Radical Ring-Opening Copolymerization-Induced Self-Assembly (rROPISA)
Guégain, E., Zhu, C., Giovanardi, E., & Nicolas, J. (2019) · Macromolecules · doi:10.1021/acs.macromol.9b00161 · Cited by 84
Self-citationChenal, M., Mura, S., Marchal, C., Gigmès, D., Charleux, B., Fattal, E., Couvreur, P., & Nicolas, J. (2010) · Macromolecules · doi:10.1021/ma101880m · Cited by 83
Self-citationAgarwal, S., Kumar, R., Kissel, T., & Reul, R. (2009) · Polymer Journal · doi:10.1295/polymj.pj2009091 · Cited by 83
Bingham, N. M., Nisa, Q. U., Chua, S. H. L., Fontugne, L., Spick, M. P., & Roth, P. J. (2020) · ACS Applied Polymer Materials · doi:10.1021/acsapm.0c00503 · Cited by 82
Siegwart, D. J., Bencherif, S. A., Srinivasan, A., Hollinger, J. O., & Matyjaszewski, K. A. (2008) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.31708 · Cited by 78
Synthesis and enzymatic degradation of 2‐methylene‐1,3‐dioxepane and methyl acrylate copolymers
Sun, L., Zhuo, R. ‐., & Liu, Z. (2003) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.10868 · Cited by 77
Radical Ring-Closing/Ring-Opening Cascade Polymerization
Huang, H., Wang, W., Zhou, Z., Sun, B., An, M., Hæffner, F., & Niu, J. (2019) · Journal of the American Chemical Society · doi:10.1021/jacs.9b05568 · Cited by 77
Zeng, T., You, W., Chen, G., Nie, X., Zhang, Z., Xia, L., Hong, C., Chen, C., & You, Y. (2020) · iScience · doi:10.1016/j.isci.2020.100904 · Cited by 75
Huang, J., Gil, R. R., & Matyjaszewski, K. A. (2005) · Polymer · doi:10.1016/j.polymer.2005.09.048 · Cited by 72
Guégain, E., Michel, J., Boissenot, T., & Nicolas, J. (2018) · Macromolecules · doi:10.1021/acs.macromol.7b02655 · Cited by 72
Self-citationGuégain, E., Guillaneuf, Y., & Nicolas, J. (2015) · Macromolecular Rapid Communications · doi:10.1002/marc.201500042 · Cited by 71
Self-citationSmit, K. D., Marien, Y. W., Geem, K. M. V., Steenberge, P. H. M. V., & D’hooge, D. (2020) · Reaction Chemistry & Engineering · doi:10.1039/d0re00266f · Cited by 71
Controlling the synthesis of degradable vinyl polymers by xanthate-mediated polymerization
Bell, C. A., Hedir, G. G., O’Reilly, R. K., & Dove, A. P. (2015) · Polymer Chemistry · doi:10.1039/c5py01156f · Cited by 70
Hedir, G. G., Stubbs, C., Aston, P., Dove, A. P., & Gibson, M. I. (2017) · ACS Macro Letters · doi:10.1021/acsmacrolett.7b00905 · Cited by 70
Tran, J., Guégain, E., Ibrahim, N., Harrisson, S., & Nicolas, J. (2016) · Polymer Chemistry · doi:10.1039/c6py00778c · Cited by 69
Self-citationYuan, J.-Y., Pan, C.-Y., & Tang, B. Z. (2001) · Macromolecules · doi:10.1021/ma0004099 · Cited by 68
Xiao, N., Liang, H., & Lu, J. (2011) · Soft Matter · doi:10.1039/c1sm06181j · Cited by 67
Ratcliffe, L. P. D., Couchon, C., Armes, S. P., & Paulusse, J. M. J. (2016) · Biomacromolecules · doi:10.1021/acs.biomac.6b00540 · Cited by 67
Gigmès, D., Steenberge, P. H. M. V., Siri, D., D’hooge, D., Guillaneuf, Y., & Lefay, C. (2018) · Macromolecular Rapid Communications · doi:10.1002/marc.201800193 · Cited by 66
Nicolas, J., Couvreur, P., & Charleux, B. (2008) · Macromolecules · doi:10.1021/ma800609b · Cited by 65
Self-citationDelplace, V., Guégain, E., Harrisson, S., Gigmès, D., Guillaneuf, Y., & Nicolas, J. (2015) · Chemical Communications · doi:10.1039/c5cc04610f · Cited by 64
Self-citationGanda, S., Jiang, Y., Thomas, D. S., Eliezar, J., & Stenzel, M. H. (2016) · Macromolecules · doi:10.1021/acs.macromol.6b00266 · Cited by 64
Hedir, G. G., Arno, M. C., Langlais, M., Husband, J. T., O’Reilly, R. K., & Dove, A. P. (2017) · Angewandte Chemie International Edition · doi:10.1002/anie.201703763 · Cited by 64
Lena, J.-B., Jackson, A. W., Chennamaneni, L. R., Wong, C. T., Lim, F. C. H., Andriani, Y., Thoniyot, P., & van Herk, A. M. (2020) · Macromolecules · doi:10.1021/acs.macromol.0c00207 · Cited by 64
Polyesters by a Radical Pathway: Rationalization of the Cyclic Ketene Acetal Efficiency
Tardy, A., Gil, N., Plummer, C. M., Siri, D., Gigmès, D., Lefay, C., & Guillaneuf, Y. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.202005114 · Cited by 61
Tardy, A., Delplace, V., Siri, D., Lefay, C., Harrisson, S., Pereira, B. D. F. A., Charles, L., Gigmès, D., Nicolas, J., & Guillaneuf, Y. (2013) · Polymer Chemistry · doi:10.1039/c3py00719g · Cited by 60
Self-citationRen, L., & Agarwal, S. (2007) · Macromolecular Chemistry and Physics · doi:10.1002/macp.200600484 · Cited by 60
Studies on the Synthesis and Properties of Temperature Responsive and Biodegradable Hydrogels
Sun, L., Zhuo, R., & Liu, Z. (2003) · Macromolecular Bioscience · doi:10.1002/mabi.200300012 · Cited by 58
Delplace, V., Harrisson, S., Tardy, A., Gigmès, D., Guillaneuf, Y., & Nicolas, J. (2013) · Macromolecular Rapid Communications · doi:10.1002/marc.201300809 · Cited by 57
Self-citationLena, J.-B., & van Herk, A. M. (2019) · Industrial & Engineering Chemistry Research · doi:10.1021/acs.iecr.9b02375 · Cited by 56
Biodegradable poly(ester)-poly(methyl methacrylate) copolymer for marine anti-biofouling
Dai, G., Xie, Q., Chen, S., Ma, C., & Zhang, G. (2018) · Progress in Organic Coatings · doi:10.1016/j.porgcoat.2018.08.003 · Cited by 55
Guégain, E., Tran, J., Deguettes, Q., & Nicolas, J. (2018) · Chemical Science · doi:10.1039/c8sc02256a · Cited by 55
Self-citationUpdating radical ring-opening polymerisation of cyclic ketene acetals from synthesis to degradation
Folini, J., Murad, W., Mehner, F., Meier, W. P., & Gaitzsch, J. (2020) · European Polymer Journal · doi:10.1016/j.eurpolymj.2020.109851 · Cited by 55
Tardy, A., Honore, J., Siri, D., Nicolas, J., Gigmès, D., Lefay, C., & Guillaneuf, Y. (2017) · Polymer Chemistry · doi:10.1039/c7py00337d · Cited by 52
Self-citationTran, J., Pesenti, T., Cressonnier, J., Lefay, C., Gigmès, D., Guillaneuf, Y., & Nicolas, J. (2018) · Biomacromolecules · doi:10.1021/acs.biomac.8b01500 · Cited by 52
Self-citationPoly(ester)–poly(silyl methacrylate) copolymers: synthesis and hydrolytic degradation kinetics
Xie, Q., Ma, C., Zhang, G., & Bressy, C. (2018) · Polymer Chemistry · doi:10.1039/c8py00052b · Cited by 48
He, T., Zou, Y.-F., & Pan, C.-Y. (2002) · Polymer Journal · doi:10.1295/polymj.34.138 · Cited by 47
Degradable PEGylated protein conjugates utilizing RAFT polymerization
Decker, C. G., & Maynard, H. D. (2015) · European Polymer Journal · doi:10.1016/j.eurpolymj.2015.01.025 · Cited by 47
Ding, D., Pan, X., Zhang, Z., Li, N., Zhu, J., & Zhu, X. (2016) · Polymer Chemistry · doi:10.1039/c6py01061j · Cited by 47
Yuan, J., & Pan, C. (2002) · European Polymer Journal · doi:10.1016/s0014-3057(02)00085-x · Cited by 45
Hiracuri, Y., & Tokiwa, Y. (1993) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.1993.080311233 · Cited by 45
Komatsu, S., Asoh, T., Ishihara, R., & Kikuchi, A. (2017) · Polymer · doi:10.1016/j.polymer.2017.09.073 · Cited by 45
Cascade Reactions in Chain-Growth Polymerization
Yuan, J., Wang, W., Zhou, Z., & Niu, J. (2020) · Macromolecules · doi:10.1021/acs.macromol.0c00417 · Cited by 44
Wais, U., Chennamaneni, L. R., Thoniyot, P., Zhang, H., & Jackson, A. W. (2018) · Polymer Chemistry · doi:10.1039/c8py01113c · Cited by 43
Undin, J., Plikk, P., Finne‐Wistrand, A., & Albertsson, A. (2010) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.24292 · Cited by 42
Functional Degradable Polymers via Radical Ring‐Opening Polymerization and Click Chemistry
Maji, S., Zheng, M., & Agarwal, S. (2011) · Macromolecular Chemistry and Physics · doi:10.1002/macp.201100375 · Cited by 41
Main-chain degradable single-chain cyclized polymers as gene delivery vectors
Gao, Y., Böhmer, V. I., Zhou, D., Zhao, T., Wang, W., & Paulusse, J. M. J. (2016) · Journal of Controlled Release · doi:10.1016/j.jconrel.2016.07.046 · Cited by 41
Synthesis and Characterization of Backbone Degradable Azlactone-Functionalized Polymers
Carter, M. C. D., Jennings, J., Appadoo, V., & Lynn, D. M. (2016) · Macromolecules · doi:10.1021/acs.macromol.6b01212 · Cited by 40
Ko, J. H., Terashima, T., Sawamoto, M., & Maynard, H. D. (2017) · Macromolecules · doi:10.1021/acs.macromol.7b01973 · Cited by 40
Folini, J., Huang, C.-H., Anderson, J. C., Meier, W. P., & Gaitzsch, J. (2019) · Polymer Chemistry · doi:10.1039/c9py01103j · Cited by 40
Biodegradable phosphorylcholine copolymer for cardiovascular stent coating
Liu, J., Wang, J., Xue, Y., Chen, T., Huang, D., Wang, Y., Ren, K., Wang, Y., Fu, G., & Ji, J. (2020) · Journal of Materials Chemistry B · doi:10.1039/d0tb00813c · Cited by 40
Mothe, S. R., Tan, J. S. J., Chennamaneni, L. R., Aidil, F., Su, Y., Kang, H. C., Lim, F. C. H., & Thoniyot, P. (2020) · Journal of Polymer Science · doi:10.1002/pol.20200210 · Cited by 39
Degradable pH and redox dual responsive nanoparticles for efficient covalent drug delivery
Du, J., Choi, B., Liu, Y., Feng, A., & Thang, S. H. (2019) · Polymer Chemistry · doi:10.1039/c8py01583j · Cited by 38
Pan, C., & Lou, X. (2000) · Macromolecular Chemistry and Physics · doi:10.1002/1521-3935(20000701)201:11 · Cited by 37
Backbone‐Degradable Polymers Prepared by Chemical Vapor Deposition
Xie, F., Deng, X., Kratzer, D., Cheng, K., Friedmann, C., Qi, S., Solorio, L., & Lahann, J. (2016) · Angewandte Chemie International Edition · doi:10.1002/anie.201609307 · Cited by 37
Wei, Y., CONNORS, E. J., Jia, X., & Wang, B. (1996) · Chemistry of Materials · doi:10.1021/cm950487o · Cited by 35
Self-Cross-Linking Degradable Polymers for Antifouling Coatings
Xie, Q., Zhou, X. C., Ma, C., & Zhang, G. (2017) · Industrial & Engineering Chemistry Research · doi:10.1021/acs.iecr.7b00557 · Cited by 33
A new elimination with phase-transfer catalysis for cyclic ketene acetals
Bailey, W. J., & Zhou, L. (1991) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)74266-3 · Cited by 32
Hyperbranched Polycaprolactone through RAFT Polymerization of 2-Methylene-1,3-dioxepane
Xu, P., Huang, X., Pan, X., Li, N., Zhu, J., & Zhu, X. (2019) · Polymers · doi:10.3390/polym11020318 · Cited by 31
Komatsu, S., Asoh, T., Ishihara, R., & Kikuchi, A. (2019) · Polymer · doi:10.1016/j.polymer.2019.121633 · Cited by 31
Agarwal, S. (2006) · Journal of Polymer Research · doi:10.1007/s10965-006-9058-6 · Cited by 30
Shi, Y., & Agarwal, S. (2015) · e-Polymers · doi:10.1515/epoly-2015-0096 · Cited by 29
Gaitzsch, J., Welsch, P. C., Folini, J., Schoenenberger, C., Anderson, J. C., & Meier, W. P. (2018) · European Polymer Journal · doi:10.1016/j.eurpolymj.2018.02.015 · Cited by 29
Jackson, A. W., Mothe, S. R., Chennamaneni, L. R., van Herk, A. M., & Thoniyot, P. (2020) · Materials · doi:10.3390/ma13102325 · Cited by 29
Lau, U. Y., Pelegri-O’Day, E. M., & Maynard, H. D. (2017) · Macromolecular Rapid Communications · doi:10.1002/marc.201700652 · Cited by 27
Jackson, A. W., Chennamaneni, L. R., & Thoniyot, P. (2019) · European Polymer Journal · doi:10.1016/j.eurpolymj.2019.109391 · Cited by 25
Investigations on free radical polymerization of phenyl‐substituted 2‐methylene‐1,3‐dioxanes
Schulze, T. G., & Klemm, E. (1995) · Die Angewandte Makromolekulare Chemie · doi:10.1002/apmc.1995.052290108 · Cited by 23
Turturicǎ, G., Andrei, M., Stãnescu, P. O., Draghici, C. C., Vuluga, D. M., Zaharia, A., Sârbu, A., & Teodorescu, M. (2016) · Colloid & Polymer Science · doi:10.1007/s00396-016-3831-9 · Cited by 18
Kertsomboon, T., Agarwal, S., & Chirachanchai, S. (2020) · Macromolecular Rapid Communications · doi:10.1002/marc.202000243 · Cited by 18
Joubert, F., & Pasparakis, G. (2020) · Journal of Polymer Science · doi:10.1002/pol.20200303 · Cited by 13
Andrei, M., Stãnescu, P. O., Draghici, C. C., Butac, L. M., & Teodorescu, M. (2018) · Colloid & Polymer Science · doi:10.1007/s00396-018-4414-8 · Cited by 11
Synthesis of Polyspiroketals Containing Five-, Six-, Seven-, and Eight-Membered Rings
Bailey, W. J., Beam, C. F., Cappuccilli, E. D., HADDAD, I., & Volpe, A. A. (1982) · ACS symposium series · doi:10.1021/bk-1982-0195.ch030 · Cited by 10
Zhao, K., Pi, B., Zhao, L., Tian, S., Ge, J., Yang, H., Sha, W., & Wang, L. (2019) · RSC Advances · doi:10.1039/c9ra01638d · Cited by 10
Andrei, M., Stãnescu, P. O., Draghici, C. C., & Teodorescu, M. (2017) · Colloid & Polymer Science · doi:10.1007/s00396-017-4161-2 · Cited by 9
Jackson, A. W., Chennamaneni, L. R., Mothe, S. R., & Thoniyot, P. (2020) · Chemical Communications · doi:10.1039/d0cc03792c · Cited by 9
Battisti, U. M., Sorbi, C., Franchini, S., Tait, A., & Brasili, L. (2014) · Synthesis · doi:10.1055/s-0033-1340662 · Cited by 7
Chaumont, P. R., Asgarzadeh, F., Colombani, D., Arotçaréna, M., & Baudouin, A. (1998) · Macromolecular Chemistry and Physics · doi:10.1002/macp.1998.021991128 · Cited by 6
Controlled free radical ring-opening polymerization and chain extension of the living polymer
Wei, Y., Connors, E. J., Jia, X., & Wang, C. (1998) · Journal of Polymer Science Part A: Polymer Chemistry · doi:10.1002/(sici)1099-0518(19980415)36:5
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
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
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