The DOI matches its Crossref record.
Handbook of Ring‐Opening Polymerization
Abstract
THERMODYNAMICS AND KINETICS OF RING-OPENING POLYMERIZATION Introduction Thermodynamics of the Ring-Opening Polymerization Kinetics of Ring-Opening Polymerization GENERAL MECHANISMS IN RING-OPENING POLYMERIZATION Introduction Anionic Ring-Opening Polymerization Cationic Ring-Opening Polymerization Radical Ring-Opening Polymerization SILOXANE-CONTAINING POLYMERS Introduction Polydimethylsiloxanes Functional Silicones Polycarbosiloxanes SULFUR-NITROGEN-PHOSPHOROUS-CONTAINING POLYMERS Introduction Mechanism and Methods in Ring-Opening Polymerization (ROP) of Halogenated Cyclotriphosphazanes Ring-Opening Polymerization and Chemistry of Nonhalogenated Phosphazane Rings Incorporation of Sulfur into Phosphazane Ring Systems and Their Polymerization Chemistry POLYMERIZATION OF CYCLIC DEPSIPEPTIDES, UREAS AND URETHANES Introduction Polydepsipeptides Monomers Ring-Opening Polymerization Enzymatic Polymerization Ring Expansion Polyureas Polyurethanes POLYETHERS AND POLYOXAZOLINES Introduction Polyethers Polyoxazolines POLYAMIDES Introduction Mechanism of the Anionic Polymerization of Lactams Initiators for the Anionic Polymerization of Lactams Activators for Anionic Polymerization of Lactams Nonactivated Polymerization Cyclic Oligomers of Epsilon-Caprolactam Block Copolymers of Lactams Anionic Copolymerization of Epsilon-Caprolactam with Omega-Laurolactam Copolymerization of Lactams with Lactones (Epsilon-Caprolactone) Powdered Polyamide Nanocomposites Anionic Polymerization of 2-Pyrrolidone RING-OPENING METATHESIS POLYMERIZATION General Introduction Introduction to Ring-Opening Metathesis Polymerization (ROMP) Well-Defined Catalysts for ROMP 'Living? ROMP Selected Recent Applications and Developments POLYESTERS FROM BETA-LACTONES Introduction Beta-Lactones Preparation Ionic Polymerization Coordination Process Carbene-Based Polymerization Enzymatic Polymerization Illustrative Experimental Section POLYESTERS FROM DILACTONES Introduction General Concepts and ROP Promoted by Metallic Recent Advances in ROP Macromolecular Engineering Applications POLYESTERS FROM LARGE LACTONES Introduction Controlled Synthesis of Linear Polyesters Physical Properties of Polymers POLYCARBONATES Introduction Polymerization of Cyclic Carbonates: Homopolymers and Block Copolymers POLYMERIZATION OF CYCLOALKANES Introduction General Overview and Thermodynamic Requirements Structure-Reactivity Relationships Based on a Comprehensive Survey of the Current Literature METAL-FREE CATALYSIS IN RING-OPENING POLYMERIZATION Introduction Nucleophilic ROP Metal-Free Ionic ROP ENZYME-MEDIATED RING-OPENING POLYMERIZATION Introduction Characteristics of Enzymatic ROP Classes of Monomer Polymer Architectures Employing Enzymatic ROP
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
“for most ROP the driving force is the ring strain and associated steric considerations.”
From Ring-Opening Polymerization—An Introductory Review (2013) · cites this paper as [1]
In the citing paper
“there is the consideration of the ring chain equilibrium, which leads to the considerable influence of the initial monomer concentration and temperature on the microstructure of the products.”
From Ring-Opening Polymerization—An Introductory Review (2013) · cites this paper as [1]
In the citing paper
“RROP offers novel routes to polyesters and polyketones particularly using vinyl substituted cyclic monomers (see Section 2.2) [6].”
From Ring-Opening Polymerization—An Introductory Review (2013) · cites this paper as [6]
In the citing paper
“For the propagation step the Δ H p ≈ 0 kJ mol -1 , but due to the increased rotational freedom of the side chains the Δ S p = +6.7 J mol -1 polymerization does occur.”
From Ring-Opening Polymerization—An Introductory Review (2013) · cites this paper as [119]
In the citing paper
“Cyclic siloxanes can also undergo ROP via anionic intermediates employing alkali metal oxides or hydroxides as initiators [119].”
From Ring-Opening Polymerization—An Introductory Review (2013) · cites this paper as [119]
In the citing paper
“If other siloxanes with different (e.g., phenyl or methyl) substituents are mixed with D4 statistical copolymers are obtained [119].”
From Ring-Opening Polymerization—An Introductory Review (2013) · cites this paper as [119]
Citations
Cited by
Sorted by citations
Items 301–400 of 546
Dencheva, N. V., & Denchev, Z. Z. (2013) · Journal of Applied Polymer Science · doi:10.1002/app.39274 · Cited by 15
Ring-opening polymerization of donor–acceptor cyclopropanes catalyzed by Lewis acids
Hayakawa, K., Matsuoka, S., & Suzuki, M. (2017) · Polymer Chemistry · doi:10.1039/c7py00794a · Cited by 15
Controlled polymerization for lithium-ion batteries
Singh, R., & Rhee, H. (2022) · Energy storage materials · doi:10.1016/j.ensm.2022.08.029 · Cited by 16
Chen, W., Guo, C., Ding, H., et al. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.3c10765 · Cited by 15
Digital Polymers Based on Cyclic Monomers
Ren, X., Ding, H., Li, S., & Zhang, K. (2024) · Macromolecules · doi:10.1021/acs.macromol.3c02405 · Cited by 15
Kostova, B., Ivanova, S., Balashev, K., Rachev, D., & Christova, D. (2014) · AAPS PharmSciTech · doi:10.1208/s12249-014-0120-0 · Cited by 15
New approaches in silicon production and recycling for sustainable future
Muzafarov, A. M., Bystrova, A. V., Vasilenko, N. G., et al. (2013) · Russian Chemical Reviews · doi:10.1070/rc2013v082n07abeh004406 · Cited by 15
Alonso‐Moreno, C., Antiñolo, A., García-Martínez, J. C., García-Yuste, S., López-Solera, I., Otero, A., Pérez‐Flores, J. C., & Tercero-Morales, M. T. (2012) · European Journal of Inorganic Chemistry · doi:10.1002/ejic.201101263 · Cited by 15
Synthesis and Biodegradation of Poly(l-lactide-co-β-propiolactone)
Nakayama, Y., Aihara, K., Cai, Z., Shiono, T., & Tsutsumi, C. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18061312 · Cited by 15
Peng, X., Behl, M., Zhang, P., Mazurek‐Budzyńska, M., Feng, Y., & Lendlein, A. (2018) · Macromolecular Bioscience · doi:10.1002/mabi.201800257 · Cited by 14
Meduri, A., Mazzeo, M., Lamberti, M., Capacchione, C., & Milione, S. (2019) · Molecular Catalysis · doi:10.1016/j.mcat.2019.04.007 · Cited by 14
Li, M., Zhang, S., Zhang, X., Wang, Y., Chen, J., Tao, Y., & Wang, X. (2020) · Angewandte Chemie · doi:10.1002/ange.202011352 · Cited by 14
Johnson, J. D., & Zhukhovitskiy, A. V. (2023) · ACS Catalysis · doi:10.1021/acscatal.3c04135 · Cited by 14
Fodor, C., Bozi, J., Blazsó, M., & Iván, B. (2015) · RSC Advances · doi:10.1039/c4ra16881j · Cited by 15
Ein Katalysator für die Tandem‐Ringöffnungsmetathesepolymerisation/Vinylinsertionspolymerisation
Buchmeiser, M. R., Camadanlı, Ş., Wang, D., et al. (2011) · Angewandte Chemie · doi:10.1002/ange.201004125 · Cited by 14
Dietrich, A., & Mejía, E. (2019) · European Polymer Journal · doi:10.1016/j.eurpolymj.2019.109377 · Cited by 15
Sebai, A., Ruśkowski, P., Bijak, V., et al. (2017) · Organic Process Research & Development · doi:10.1021/acs.oprd.7b00266 · Cited by 14
Caovilla, A., Penning, J. S., Pinheiro, A. C., Hild, F., Stieler, R., Dagorne, S., Casagrande, O. L., & Gil, M. (2018) · Journal of Organometallic Chemistry · doi:10.1016/j.jorganchem.2018.03.040 · Cited by 13
Polyoxazoline associated with cardanol for bio‐based linear alkyl benzene surfactants
Delage, B., Briou, B., Brossier, T., Catrouillet, S., Robin, J., & Lapinte, V. (2019) · Polymer International · doi:10.1002/pi.5763 · Cited by 14
Raeskinet, B., Moins, S., Harvey, L., Winter, J. D., Henoumont, C., Laurent, S., & Coulembier, O. (2019) · Macromolecules · doi:10.1021/acs.macromol.9b01282 · Cited by 14
Osváth, Z., Szőke, A., Pásztor, S., et al. (2020) · Processes · doi:10.3390/pr8070856 · Cited by 14
Accelerating effect of crown ethers on the lactide polymerization catalysed by potassium acetate
Moins, S., Henoumont, C., Roover, Q. D., Laurent, S., Winter, J. D., & Coulembier, O. (2021) · Catalysis Science & Technology · doi:10.1039/d1cy00756d · Cited by 13
Polyamides Derived from Terpenes: Advances in Their Synthesis, Characterization and Applications
Winnacker, M. (2023) · European Journal of Lipid Science and Technology · doi:10.1002/ejlt.202300014 · Cited by 14
He, Y., Li, Z., Zhao, D., Shen, Y., Fu, W., & Li, Z. (2024) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2024.101921 · Cited by 14
Valentini, M., de Almeida, O., Kakkonen, M., et al. (2024) · Composites Part A Applied Science and Manufacturing · doi:10.1016/j.compositesa.2024.108681 · Cited by 13
Resonance promoted ring-opening metathesis polymerization of twisted amides
Xu, M., Bullard, K. K., Nicely, A. M., & Gutekunst, W. R. (2019) · Chemical Science · doi:10.1039/c9sc03602d · Cited by 12
Novák, M., Turek, J., Milasheuskaya, Y., Růžičková, Z., Podzimek, Š., & Jambor, R. (2021) · Dalton Transactions · doi:10.1039/d1dt02658e · Cited by 12
Scoponi, G., Francini, N., Paradiso, V., Donno, R., Gennari, A., d’Arcy, R., Capacchione, C., Athanassiou, A., & Tirelli, N. (2021) · Macromolecules · doi:10.1021/acs.macromol.1c01503 · Cited by 13
Marchetti, F., & Pampaloni, G. (2011) · Inorganica Chimica Acta · doi:10.1016/j.ica.2011.06.006 · Cited by 13
Nanoscale Control of Polymer Assembly on a Synthetic Catalyst–Bilayer System
Gorgoll, R. M., Harano, K., & Nakamura, E. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b05414 · Cited by 13
Ring-Opening Polymerization of Cyclic Esters
Raquez, J., Mincheva, R., Coulembier, O., & Dúbois, P. (2012) · Elsevier eBooks · doi:10.1016/b978-0-444-53349-4.00105-9 · Cited by 15
Silicones with enhanced permittivity for dielectric elastomer actuators
Dünki, S. J., Dascălu, M., Nüesch, F. A., et al. (2016) · Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE · doi:10.1117/12.2218881 · Cited by 13
Tohidi, S. D., Dencheva, N. V., Denchev, Z. Z., et al. (2020) · Materials Today Communications · doi:10.1016/j.mtcomm.2020.100912 · Cited by 13
Rad’kova, N. Y., Kovylina, T. A., Shavyrin, A. S., Cherkasov, A. V., Fukin, G. K., Lyssenko, K. A., & Trifonov, A. A. (2020) · New Journal of Chemistry · doi:10.1039/d0nj00042f · Cited by 13
A cascade strategy towards the direct synthesis of green polyesters with versatile functional groups
Wan, X.-T., Jiang, J. M., Tu, Y., Xu, S., Li, J., Lu, H., Li, Z., Xiong, L., Li, X., Zhao, Y., et al. (2021) · Polymer Chemistry · doi:10.1039/d1py01124c · Cited by 13
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
Piskun, Y. A., Vasilenko, I. V., Gaponik, L. V., et al. (2011) · Polymer Bulletin · doi:10.1007/s00289-011-0621-x · Cited by 13
Thermodynamic and Kinetic Polymerizability
Penczek, S., & Kałużyński, K. (2012) · Elsevier eBooks · doi:10.1016/b978-0-444-53349-4.00090-x · Cited by 12
Kalamiotis, A., Ilchev, A., Irvine, D. J., et al. (2019) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2019.03.120 · Cited by 12
Duez, Q., Hoyas, S., Josse, T., Cornil, J., Gerbaux, P., & Winter, J. D. (2021) · Mass Spectrometry Reviews · doi:10.1002/mas.21745 · Cited by 13
Tang, J., & Chen, E. Y. ‐. (2015) · Organic Chemistry Frontiers · doi:10.1039/c5qo00262a · Cited by 14
Peng, X., Behl, M., Zhang, P., et al. (2016) · Polymer · doi:10.1016/j.polymer.2016.10.033 · Cited by 12
Tohidi, S. D., Rocha, A. M., Dencheva, N. V., et al. (2018) · Polymer Composites · doi:10.1002/pc.25075 · Cited by 12
Anionic Polymerization of Nonpolar Monomers
Quirk, R. P. (2012) · Elsevier eBooks · doi:10.1016/b978-0-444-53349-4.00076-5 · Cited by 14
Polycarbosilanes Based on Silicon-Carbon Cyclic Monomers
Finkelshtein, E. S., Ushakov, N. V., & Gringolts, M. L. (2010) · Advances in polymer science · doi:10.1007/12_2009_39 · Cited by 12
Anionic copolymerization of nylon 6/12: A comprehensive review
Mohammadi, M., Ahmadi, S., Ghasemi, I., & Rahnama, M. (2019) · Polymer Engineering and Science · doi:10.1002/pen.25171 · Cited by 10
Formation of cyclic structures in the cationic ring-opening polymerization of 1,3-dioxolane
Coenen, A. M. J., Harings, J., Ghazanfari, S., Jockenhoevel, S., & Bernaerts, K. V. (2020) · RSC Advances · doi:10.1039/d0ra00904k · Cited by 11
Xie, T., Chen, S., Li, Y., & Chen, D. (2024) · Angewandte Chemie International Edition · doi:10.1002/anie.202405408 · Cited by 12
Zárate-Saldaña, D., Landeros‐Rivera, B., Cruz‐Morales, J. A., et al. (2020) · Journal of Organometallic Chemistry · doi:10.1016/j.jorganchem.2020.121206 · Cited by 11
Pascouau, C., Wirotius, A., Carlotti, S., Cramail, H., & Peruch, F. (2022) · European Polymer Journal · doi:10.1016/j.eurpolymj.2022.111793 · Cited by 13
Terpene-based polyamides: A sustainable polymer class with huge potential
Winnacker, M. (2023) · Current Opinion in Green and Sustainable Chemistry · doi:10.1016/j.cogsc.2023.100819 · Cited by 12
Fuoco, T., Meduri, A., Lamberti, M., Pellecchia, C., & Pappalardo, D. (2015) · Journal of Applied Polymer Science · doi:10.1002/app.42567 · Cited by 11
Ogden, M. D., Orme, C. J., & Stewart, F. F. (2011) · Polymer · doi:10.1016/j.polymer.2011.07.010 · Cited by 11
Illy, N., Taylan, E., Brissault, B., Wojno, J., Boileau, S., Barbier, V., & Penelle, J. (2013) · European Polymer Journal · doi:10.1016/j.eurpolymj.2013.09.014 · Cited by 11
Ruengdechawiwat, S., Siripitayananon, J., Molloy, R., Somsunan, R., Topham, P. D., & Tighe, B. J. (2016) · International Journal of Polymeric Materials · doi:10.1080/00914037.2015.1119683 · Cited by 11
Synthetic and semi-synthetic polymers for pharmaceutical applications
Macchione, M. A., Bedoya, D. A., Figueroa, F. N., et al. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-820043-8.00005-0 · Cited by 11
Duchiron, S., Pollet, É., Givry, S., et al. (2018) · Molecules · doi:10.3390/molecules23020290 · Cited by 11
Progress in Catalytic Ring-Opening Polymerization of Biobased Lactones
Al-Shok, L., Haddleton, D. M., & Adams, F. (2022) · Advances in Polymer Science · doi:10.1007/12_2021_111 · Cited by 10
Qian, X., Wang, M., Ding, Z., Liu, X., & Wang, B. (2024) · Giant · doi:10.1016/j.giant.2024.100268 · Cited by 9
Adams, F. (2024) · Macromolecular Rapid Communications · doi:10.1002/marc.202400122 · Cited by 10
Fredi, G., Broggio, L., Valentini, M., et al. (2024) · Polymer · doi:10.1016/j.polymer.2024.127562 · Cited by 10
Predicting Chemical Recyclability Thermodynamics via Molecular Simulations
Nieboer, V., Olsén, P., Odelius, K., & Wohlert, J. (2024) · Macromolecules · doi:10.1021/acs.macromol.4c01469 · Cited by 11
Efficient Bulky Organo-Zinc Scorpionates for the Stereoselective Production of Poly(rac-lactide)s
Navarro, M., Garcés, A., Sánchez‐Barba, L. F., de la Cruz‐Martínez, F., Fernández‐Baeza, J., & Lara‐Sánchez, A. (2021) · Polymers · doi:10.3390/polym13142356 · Cited by 10
Niemczyk, E. M., Gomez‐Lopez, A., Haler, J. R. N., Frache, G., Sardón, H., & Quintana, R. (2021) · Polymers · doi:10.3390/polym13172856 · Cited by 12
Ultrasound-Assisted Enzymatic Synthesis of Poly-ε-Caprolactone: Kinetic Behavior and ReactorDesign
Gumel, A. M., Annuar, M. S. M., & Yusuf Chisti, B. (2014) · International Journal of Chemical Reactor Engineering · doi:10.1515/ijcre-2013-0115 · Cited by 10
Ring-Opening Polymerization of Cyclic Phosphorus Monomers
Łapienis, G. (2012) · Elsevier eBooks · doi:10.1016/b978-0-444-53349-4.00113-8 · Cited by 11
Herzog, B., Kohan, M. I., Mestemacher, S. A., et al. (2020) · Ullmann's Encyclopedia of Industrial Chemistry · doi:10.1002/14356007.a21_179.pub4 · Cited by 10
Schwarz, W., Schossig, J., Rossbacher, R., Pinkos, R., & Höke, H. (2019) · Ullmann's Encyclopedia of Industrial Chemistry · doi:10.1002/14356007.a04_495.pub2 · Cited by 10
Minyaev, M. E., Nifant'ev, I. E., Shlyakhtin, A. V., Ivchenko, P. V., & Lyssenko, K. A. (2018) · Acta Crystallographica Section C Structural Chemistry · doi:10.1107/s2053229618005090 · Cited by 9
Barouti, G., Jaffredo, C. G., & Guillaume, S. M. (2015) · Polymer Chemistry · doi:10.1039/c5py00724k · Cited by 9
Synthesis and properties of new polymeric surfactant with quaternary ammonium salt
Zhang, L., Lv, X., Zhu, Y., et al. (2011) · Colloid & Polymer Science · doi:10.1007/s00396-011-2482-0 · Cited by 9
Zhou, T., Guo, Y.-T., Du, F., & Li, Z. (2022) · Chinese Journal of Polymer Science · doi:10.1007/s10118-022-2725-1 · Cited by 9
Yu, L., Cao, Y., He, W., et al. (2017) · Chemical Engineering Journal · doi:10.1016/j.cej.2017.06.065 · Cited by 9
Humphry, J., Yang, N., Vandi, L., et al. (2020) · Materials Today Communications · doi:10.1016/j.mtcomm.2020.101473 · Cited by 9
Kimura, A., Takahashi, S., Kawauchi, S., et al. (2013) · The Journal of Organic Chemistry · doi:10.1021/jo400058f · Cited by 9
Anionic ring-opening polymerization of cyclic 1,3-dithiocarbonate and thermal depolymerization
Jeon, S. J., Jung, M.-Y., & Yun, J. (2016) · Reactive and Functional Polymers · doi:10.1016/j.reactfunctpolym.2016.01.005 · Cited by 9
Rajendran, N. M., Xi, Y., Zhang, W., Braunstein, P., Liang, T., & Sun, W. (2016) · Inorganic Chemistry Frontiers · doi:10.1039/c6qi00177g · Cited by 9
Jaffredo, C. G., Schmid, M., del Rosal, I., Mevel, T., Roesky, P. W., Maron, L., & Guillaume, S. M. (2014) · Chemistry – A European Journal · doi:10.1002/chem.201403545 · Cited by 9
Ding, Z., Wang, M., Wang, B., Pan, L., & Li, Y. (2023) · Macromolecules · doi:10.1021/acs.macromol.3c01899 · Cited by 7
Illy, N., Fu, H.-Q., & Mongkhoun, E. (2024) · ChemCatChem · doi:10.1002/cctc.202401032 · Cited by 8
Macías, A. H., Román-Aguirre, M., Talamantes, R. P., Soto, K. M., Araiza, J. L. R., Lozano, N. E. M., Apátiga-Castro, M., Pineda-Piñón, J., Gasca-Tirado, J. R., López-Romero, J. M., et al. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e39415 · Cited by 8
Guo, X.-Y., Li, Z., Li, Z., et al. (2025) · Macromolecules · doi:10.1021/acs.macromol.4c02388 · Cited by 8
Photo-Triggerable Polymerization and Depolymerization of Stiff-Stilbene Lactones
Su, Y.-L., Xiong, W., Hunter, T. M., Engle, K. S., & Gutekunst, W. R. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.5c10480 · Cited by 9
More than ring-strain: revisiting the definition of enthalpy in ring-opening polymerization
Nieboer, V., Wohlert, J., Olsén, P., & Odelius, K. (2025) · Faraday Discussions · doi:10.1039/d5fd00060b · Cited by 8
Narita, M., Yoneyama, H., Matsunaga, T., et al. (2019) · Polymer Journal · doi:10.1038/s41428-019-0262-8 · Cited by 8
Hornberger, L.-S., Weingarten, P., Lange, P. L., Schleid, T., & Adams, F. (2023) · European Polymer Journal · doi:10.1016/j.eurpolymj.2023.112449 · Cited by 9
Çetinkaya, S., Özker, T., & Bayram, R. (2010) · Applied Catalysis A General · doi:10.1016/j.apcata.2010.11.021 · Cited by 8
Xiang, Y., Burrill, D. J., Bullard, K. K., Albrecht, B. J., Tragesser, L. E., McCaffrey, J., Lambrecht, D. S., & Pentzer, E. (2017) · Polymer Chemistry · doi:10.1039/c7py00858a · Cited by 8
Reactive Extrusion and Magnesium (II) N-Heterocyclic Carbene Catalyst in Continuous PLA Production
Mincheva, R., Chilla, S. N. M., Todd, R., Guillerm, B., Winter, J. D., Gerbaux, P., Coulembier, O., Dúbois, P., & Raquez, J. (2019) · Polymers · doi:10.3390/polym11121987 · Cited by 7
Mohammadi, M., Ahmadi, S., & Ghasemi, I. (2019) · Polymer · doi:10.1016/j.polymer.2019.122093 · Cited by 7
Tohidi, S. D., Denchev, Z. Z., Dencheva, N. V., et al. (2020) · Materials Today Communications · doi:10.1016/j.mtcomm.2020.101068 · Cited by 8
Ring opening polymerization of β-acetoxy-δ-methylvalerolactone, a triacetic acid lactone derivative
Sajjad, H., Prebihalo, E. A., Tolman, W. B., & Reineke, T. M. (2021) · Polymer Chemistry · doi:10.1039/d1py00561h · Cited by 9
Jin, M., & Hoye, T. R. (2023) · Macromolecules · doi:10.1021/acs.macromol.2c01141 · Cited by 9
Li, X., Clarke, R. W., An, H., Gowda, R. R., Jiang, J., Xu, T., & Chen, E. Y. ‐. (2023) · Angewandte Chemie · doi:10.1002/ange.202303791 · Cited by 8
Synthesis and characterization of a poly(ethylene glycol)–poly(simvastatin) diblock copolymer
Asafo-Adjei, T. A., Dziubla, T. D., & Puleo, D. A. (2014) · RSC Advances · doi:10.1039/c4ra10310f · Cited by 8
Zorn, A. M., & Barner‐Kowollik, C. (2012) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.26011 · Cited by 8
Cho, J., Chun, M. K., Nayab, S., & Jeong, J. H. (2018) · Transition Metal Chemistry · doi:10.1007/s11243-018-0282-9 · Cited by 8
Superparamagnetic Nanocomposites Templated with Pyrazole-Containing Diblock Copolymers
Biswas, S., Belfield, K. D., Das, R. K., Ghosh, S. S., & Hebard, A. F. (2012) · Polymers · doi:10.3390/polym4021211 · Cited by 8
Cationic Polymerization of Hexamethylcyclotrisiloxane in Excess Water
Barnes, Q., Longuet, C., & Ganachaud, F. (2021) · Molecules · doi:10.3390/molecules26154402 · Cited by 7
Nieboer, V., Fanjul‐Mosteirín, N., Olsén, P., & Odelius, K. (2023) · Polymer Chemistry · doi:10.1039/d3py00310h · Cited by 8
Metadata
- Venue
- Wiley eBooks
- Publisher
- Wiley
- Published
- 2009-01-28
- OpenAlex
- W600467921
- Cited by
- 544
- References
- 0
- Citations by year
- 2026: 11 · 2025: 20 · 2024: 33 · 2023: 20 · 2022: 30 · 2021: 34 · 2020: 38 · 2019: 43 · 2018: 48 · 2017: 40 · 2016: 42 · 2015: 38 · 2014: 35 · 2013: 35 · 2012: 29
- FWCI
- 15.15
- Type
- book
- Language
- en
- Open access
- closed
- Locations
- Wiley eBooks (publishedVersion)
- PolyPublie (École Polytechnique de Montréal) (submittedVersion)
- Topics
- Physical Sciences › Materials Science › Biomaterials › biodegradable polymer synthesis and properties
- Physical Sciences › Chemistry › Organic Chemistry › Advanced Polymer Synthesis and Characterization
- Physical Sciences › Materials Science › Polymers and Plastics › Polymer crystallization and properties
- Keywords
- ring-opening polymerization, ring-opening metathesis polymerization, anionic polymerization, cationic polymerization, radical polymerization, lactam polymerization, caprolactam, cyclic depsipeptides, urethane, polyesters, β-lactones, dilactones, cyclic carbonates, polyoxazoline, polyethers, siloxane-containing polymers, enzymatic polymerization, block copolymers, macromolecular engineering
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