Puts, D. R.; Sogah, D. Y. Universal Multifunctional Initiator Containing Orthogonal Reactive Sites. Synthesis of Macromonomers and Comb Polymers Using Consecutive Controlled Free Radical and Cationic Ring-Opening Polymerizations. Macromolecules 1997, 30, 7050-7055, 10.1021/ma970329d
Mecerreyes, D.; Moineau, G.; Dubois, P.; Jerome, R.; Hedrick, J. L.; Hawker, C. J.; Malmstrom, E. E.; Trollsas, M. Simultaneous Dual Living Polymerizations: A Novel One-Step Approach to Block and Graft Copolymers. Angew. Chem., Int. Ed. 1998, 37, 1274-1276, 10.1002/(SICI)1521-3773(19980518)37:9<1274::AID-ANIE1274>3.0.CO;2-J
Duxbury, Ch. J.; Wang, W.; de Geus, M.; Heise, A.; Howdle, S. M. Can Block Copolymers Be Synthesized by a Single-Step Chemoenzymatic Route in Supercritical Carbon Dioxide?. J. Am. Chem. Soc. 2005, 127, 2384-2385, 10.1021/ja042903o
Nasser-Eddine, M.; Delaite, C.; Hurtrez, G.; Dumas, P. Controlled one-step synthesis of a deblock copolymer. Eur. Polym. J. 2005, 41, 313-318, 10.1016/j.eurpolymj.2004.09.006
Huang, C.-F.; Kuo, S.-W.; Lee, H.-F.; Chang, F.-C. A new strategy for the one-step synthesis of block copolymers through simultaneous free radical and ring opening polymerizations using a dual-functional initiator. Polymer 2005, 46, 1561-1565, 10.1016/j.polymer.2004.12.013
Zou, P.; Yang, L.-P.; Pan, C.-Y. One-Pot Synthesis of Linear-Hyperbranched Diblock Copolymers via Self-Condensing Vinyl Polymerization and Ring Opening Polymerization. J. Polym. Sci., Part A: Polym. Chem. 2008, 46, 7628-7636, 10.1002/pola.23063
Song, J.; Xu, J.; Pispas, S.; Zhang, G. One-pot synthesis of poly(L-lactide)-b-poly(methylmethacrylate) block copolymers. RSC Adv. 2015, 5, 38243-38247, 10.1039/C4RA17202G
Kannan, M.-B.; Lessard, B.-H. Copolymerization of 2,3,4,5,6-Pentafluorostyrene and Methacrylic Acid by Nitroxide-Mediated Polymerization: The Importance of Reactivity Ratios. Macromol. React. Eng. 2016, 10, 600-610, 10.1002/mren.201600052
Gleede, T.; Rieger, E.; Blankenburg, J.; Klein, K.; Wurm, F. R. Fast Access to Amphiphilic Multiblock Architectures by the Anionic Copolymerization of Aziridines and Ethylene Oxide. J. Am. Chem. Soc. 2018, 140, 13407-13412, 10.1021/jacs.8b08054
Endo, T. In Handbook of Ring-Opening Polymerization; Dubois, Ph., Raquez, J.-M., Coulembier, O., Eds.; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, 2009; p 53.
Sosnowski, S.; Slomkowski, S.; Penczek, S. On the Ambident Reactivity of;-Lactones in Their Reactions with Alcoholates Initiating Polymerization. Macromolecules 1993, 26, 5526-5527, 10.1021/ma00072a034
Coulembier, O.; Dubois, Ph. In Handbook of Ring-Opening Polymerization; Dubois, Ph., Raquez, J.-M., Coulembier, O., Eds.; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, 2009; p 227.
Khalil, A.; Cammas-Marion, S.; Coulembier, O. Organocatalysis Applied to the Ring-Opening Polymerization of b-Lactones: A Brief Overview. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 657-672, 10.1002/pola.29322
Coulembier, O.; Degée, Ph; Cammas-Marion, S.; Guérin, Ph; Dubois, Ph New Amphiphilic Poly[(R,S)-N-malic acid-b - -caprolactone] Diblock Copolymers by Combining Anionic and Coordination-Insertion Ring-Opening Polymerization. Macromolecules 2002, 35, 9896-9903, 10.1021/ma0209500
Saito, T.; Aizawa, Y.; Yamamoto, T.; Tajima, K.; Isono, T.; Satoh, T. Alkali Metal Carboxylate as an Efficient and Simple Catalyst for Ring-Opening Polymerization of Cyclic Esters. Macromolecules 2018, 51, 689-696, 10.1021/acs.macromol.7b02566
Coady, D. J.; Fukushima, K.; Horn, H. W.; Rice, J. L.; Hedrick, J. L. Catalytic insights into acid/base conjugates: highly selective bifunctional catalysts for the ring-opening polymerization of lactide. Chem. Commun. 2011, 47, 3105-3107, 10.1039/c0cc03987j
De Winter, J.; Coulembier, O.; Gerbaux, P.; Dubois, Ph High Molecular Weight Poly(H,','-trisubstituted - lactones) As Generated by Metal-Free Phosphazene Catalysts. Macromolecules 2010, 43, 10291-10296, 10.1021/ma102123b
Kawalec, M.; Coulembier, O.; Gerbaux, P.; Sobota, M.; De Winter, J.; Dubois, Ph; Kowalczuk, M.; Kurcok, P. Traces do matter-Purity of 4-methyl-2-oxetanone and its effect on anionic ring-opening polymerization as evidenced by phosphazene superbase catalysis. React. Funct. Polym. 2012, 72, 509-520, 10.1016/j.reactfunctpolym.2012.04.013
Moins, S.; Henoumont, C.; De Winter, J.; Khalil, A.; Laurent, S.; Cammas-Marion, S.; Coulembier, O. Reinvestigation of the mechanism of polymerization of r-butyrolactone from 1,5,7-triazabicyclo[4.4.0]dec-5-ene. Polym. Chem. 2018, 9, 1840-1847, 10.1039/C8PY00206A
Schuchardt, U.; Sercheli, R.; Vargas, R. M. Transesterification of Vegetable Oils: a Review. J. Braz. Chem. Soc. 1998, 9, 199-210, 10.1590/S0103-50531998000300002
Timofeev, O.; Zhu, M. M; Gross, M. L Information for proteomics: ESI-MS titration by sodium ions gives the number of carboxylate groups in peptides. Int. J. Mass Spectrom. 2004, 231, 113-117, 10.1016/j.ijms.2003.09.015
Hall, H. K., Jr. The nucleophile-initiated polymerization of HHH-disubstituted - lactones. Macromolecules 1969, 2, 488-497, 10.1021/ma60011a008
Eisenbach, C. D.; Lenz, R. W. Solvent and counterion effects in the anionic polymerization of nnn-disubstituted - propiolactone. Makromol. Chem. 1976, 177, 2539-2545, 10.1002/macp.1976.021770822
Bigdeli, E.; Lenz, R. W. Polymerization of BBB-disubstituted - propiolactones and lactams. 14. Substituent, solvent, and counterion effects in the anionic polymerization of lactones. Macromolecules 1978, 11, 493-496, 10.1021/ma60063a013
Slomkowski, S.; Penczek, S. Macroions and Macroion Pairs in the Anionic Polymerization of β-Propiolactone (β-PL). Macromolecules 1980, 13, 229-233, 10.1021/ma60074a005
Kawalec, M.; Smiga-Matuszowicz, M.; Kurcok, P. Counterion and solvent effects on the anionic polymerization of b-butyrolactone initiated with acetic acid salts. Eur. Polym. J. 2008, 44, 3556-3563, 10.1016/j.eurpolymj.2008.09.008
Malmstroem, E.; Johansson, M.; Hult, A. Hyperbranched Aliphatic Polyesters. Macromolecules 1995, 28, 1698-1703, 10.1021/ma00109a049
Coulembier, O.; Dove, A. P.; Pratt, R. C.; Sentman, A. C.; Culkin, D. A.; Mespouille, L.; Dubois, P.; Waymouth, R. M.; Hedrick, J. L. Latent, Thermally Activated Organic Catalysts for the On-Demand Living Polymerization of Lactide. Angew. Chem., Int. Ed. 2005, 44, 4964-4968, 10.1002/anie.200500723
Florczak, M.; Libiszowski, J.; Mosnacek, J.; Duda, A.; Penczek, S. L,L-Lactide and;-Caprolactone Block Copolymers by a "Poly(L,L-lactide) Block First" Route. Macromol. Rapid Commun. 2007, 28, 1385-1391, 10.1002/marc.200700160
Xiao, Y.; Coulembier, O.; Koning, C. E.; Heise, A.; Dubois, Ph Cumulated advantages of enzymatic and carbene chemistry for the non-organometallic synthesis of (co)polyesters. Chem. Commun. 2009, 2472-2474, 10.1039/b819624a
Ajellal, N.; Carpentier, J.-F.; Guillaume, C.; Guillaume, S. M.; Helou, M.; Poirier, V.; Sarazin, Y.; Trifonov, A. Metal-catalyzed immortal ring-opening polymerization of lactones, lactides and cyclic carbonates. Dalton Trans 2010, 39, 8363-8376, 10.1039/c001226b
Jaffredo, C. G.; Carpentier, J.-F.; Guillaume, S. M. Poly(hydroxyalkanoate) Block or Random Copolymers of β-Butyrolactone and Benzyl β-Malolactone: A Matter of Catalytic Tuning. Macromolecules 2013, 46, 6765-6776, 10.1021/ma401332k
Basko, M.; Duda, A.; Kazmierski, S.; Kubisa, P. Cationic copolymerization of racemic - -butyrolactone with L,L-lactide: One-pot synthesis of block copolymers. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 4873-4884, 10.1002/pola.26916
Bouyahyi, M.; Duchateau, R. Metal-Based Catalysts for Controlled Ring-Opening Polymerization of Macrolactones: High Molecular Weight and Well-Defined Copolymer Architectures. Macromolecules 2014, 47, 517-524, 10.1021/ma402072t
Wang, X.; Thevenon, A.; Brosmer, J. L.; Yu, I.; Khan, S. I.; Mehrkhodavandi, P.; Diaconescu, P. L. Redox Control of Group 4 Metal Ring-Opening Activity toward L-Lactide and,-Caprolactone. J. Am. Chem. Soc. 2014, 136, 11264-11267, 10.1021/ja505883u
Ladelta, V.; Kim, J. D.; Bilalis, P.; Gnanou, Y.; Hadjichristidis, N. Block Copolymers of Macrolactones/Small Lactones by a "Catalyst-Switch" Organocatalytic Strategy. Thermal Properties and Phase Behavior. Macromolecules 2018, 51 (7), 2428-2436, 10.1021/acs.macromol.8b00153
