參考文獻 |
[1]Robert F. T. Stepto,"Dispersity in polymer science (IUPAC Recommendations 2009)"Pure Appl. Chem., 81, 2009, 351-353.
[2]Energy, M.,“Plastic bags were created to save the planet, inventor’s son says.”Independent TV, 2019.
[3]Dechy-Cabaret, O.; Martin-Vaca, B.; Bourissou, D.,
“Controlled ring-opening polymerization of lactide and glycolide.”Chem. Rev., 104 (12), 2004, 6147-6176.
[4]Jadrich, C. N.; Pane, V. E.; Lin, B.; Jones, G. O.; Hedrick, J. L.; Park, N. H.; Waymouth, R. M.,“A Cation-Dependent Dual Activation Motif for Anionic Ring-Opening Polymerization of Cyclic Esters.”JACS, 144 (19), 2022, 8439-8443.
[5]Wang, X.; Xu, J.; Li, Z.; Liu, J.; Sun, J.; Hadjichristidis, N.; Guo, K.,“Non-metal with metal behavior: metal-free coordination-insertion ring-opening polymerization.”Chem. Sci., 12 (32), 2021, 10732-10741.
[6]Tschan, M. J. L.; Gauvin, R. M.; Thomas, C. M.,“Controlling polymer stereochemistry in ring-opening polymerization: a decade of advances shaping the future of biodegradable polyesters.”Chem. Soc. Rev., 50 (24), 2021, 13587-13608.
[7]Bińczak, J.; Szelwicka, A.; Siewniak, A.; Dziuba, K.; Chrobok,“Oxidation of Cyclohexanone with Peracids—A Straight Path to the Synthesis of ε-Caprolactone Oligomers.”Materials., 15 (19), 2022, 6608
[8]Goldberg, D.,“A review of the biodegradability and utility of poly(caprolactone).” J Polym Environ., 3 (2), 1995, 61-67.
[9]Kruliš, Z.,“Structure Characterization and Biodegradation Rate of Poly(εcaprolactone)/Starch Blends.”Front. Mater., 7, 2020, 1-14.
[10] Reddy, M. M.; Vivekanandhan, S.; Misra, M.; Bhatia, S. K.; Mohanty, A. K.,“Biobased plastics and bionanocomposites: Current status and future opportunities.” Prog. Polym. Sci., 38 (10), 2013, 1653-1689.
[11] Yuan, P.; Sun, Y.; Xu, X.; Luo, Y.; Hong, M.,“Towards high-performance sustainable polymers via isomerization-driven irreversible ring-opening polymerization of five-membered thionolactones.”Nat. Chem., 14 (3), 2022, 294-303.
[12] Zhou, J.; Schmidt, A. M.; Ritter, H.,“Bicomponent Transparent Polyester Networks with Shape Memory Effect.”Macromolecules, 43 (2), 2010, 939-942.
[13] Hong, M.; Chen, E. Y. X., “Coordination Ring-Opening Copolymerization of Naturally Renewable α-Methylene-γ-butyrolactone into Unsaturated Polyesters.”
Macromolecules, 47 (11), 2014, 3614-3624.
[14] Tang, X.; Hong, M.; Falivene, L.; Caporaso, L.; Cavallo, L.; Chen, E. Y. X.,“The Quest for Converting Biorenewable Bifunctional α-Methylene-γ-butyrolactone into Degradable and Recyclable Polyester: Controlling Vinyl-Addition/Ring-Opening/Cross-Linking Pathways.” JACS, 138 (43), 2016, 14326-14337.
[15] Cywar, R. M.; Zhu, J.-B.; Chen, E. Y. X., “Selective or living organopolymerization of a six-five bicyclic lactone to produce fully recyclable polyesters.” Polymer Chemistry, 10 (23), 2019, 3097-3106.
[16] J.-B. Zhu, E. M. W., J. Tang, E. Y.-X. Chen, “A synthetic polymer system with repeatable chemical recyclability.” Science, 360, 2018, 398–403.
[17] Zhu, J.-B. C., E. Y.-X.,“Catalyst-Sidearm-Induced Stereoselectivity Switching in Polymerization of a Racemic Lactone for Stereocomplexed Crystalline Polymer with a Circular Life Cycle.” Angew. Chem., Int. Ed., 58, 2019, 1178−1182.
[18] Cui, Y.; Jiang, J.; Mao, X.; Wu, J.,“Mononuclear Salen–Sodium Ion Pairs as Catalysts for Isoselective Polymerization of rac-Lactide.” Inorg. Chem., 58 (1), 2019, 218-227.
[19] Ou, H.-W.; Lo, K.-H.; Du, W.-T.; Lu, W.-Y.; Chuang, W.-J.; Huang, B.-H.; Chen, H.-Y.; Lin, C.-C.,“Synthesis of Sodium Complexes Supported with NNO-Tridentate Schiff Base Ligands and Their Applications in the Ring-Opening Polymerization of l-Lactide.” Inorg. Chem., 55 (4), 2016, 1423-1432.
[20] Lin, B.; Waymouth, R. M.,“Urea Anions: Simple, Fast, and Selective Catalysts for Ring-Opening Polymerizations.”JACS, 139 (4), 2017, 1645-1652.
[21] Frkanec, L.; Žinić, M.,“Chiral bis(amino acid)- and bis(amino alcohol)-oxalamide gelators. Gelation properties, self-assembly motifs and chirality effects.” Chem. Commun., 46 (4), 2010, 522-537.
[22] Ma, P.; Xu, Y.; Wang, D.; Dong, W.; Chen, M.,“Rapid Crystallization of Poly(lactic acid) by Using Tailor-Made Oxalamide Derivatives as Novel Soluble-Type Nucleating Agents.” Ind. Eng. Chem. Res., 53 (32), 2014, 12888-12892.
[23] Shen, T.; Xu, Y.; Cai, X.; Ma, P.; Dong, W.; Chen, M.,“Enhanced crystallization kinetics of poly(lactide) with oxalamide compounds as nucleators: effect of spacer length between the oxalamide moieties.” RSC Advances, 6 (54), 2016, 48365-48374.
[24] Manna, C. M.; Kaur, A.; Yablon, L. M.; Haeffner, F.; Li, B.; Byers,
J. A.,“Stereoselective Catalysis Achieved through in Situ Desymmetrization of an Achiral Iron Catalyst Precursor.” JACS, 137 (45), 2015, 14232-14235.
[25] Zhang, Q.; Zhang, W.; Wang, S.; Solan, G. A.; Liang, T.; Rajendran, N. M.; Sun, W.-H.,“Sodium iminoquinolates with cubic and hexagonal prismatic motifs: synthesis, characterization and their catalytic behavior toward the ROP of rac-lactide.” Inorg. Chem. Front. 3 (9), 2016, 1178-1189.
[26]楊長安 (1R,2R)-反式環己烷二甲酸的合成工藝 精細化工. 2013, 30 ,1046-1051, DOI:10.13550/J.jxhg.2013.09.016.
[27] Eric M. B. Moos, S. G.-G., Michael Radius, Frank Brehe,“Rhodium(I) Complexes of N-Aryl-Substituted Mono- and Bis(amidinates) Derived from Their Alkali Metal Salts.” Eur. J. Inorg. Chem., 2018, 3022-3035.
[28] process for preparing conjugated diene (co)polymers in the presence of a catalytic system comprising a pyridyl iron (iii) complexinternational WO 2018/073795, 2018.04.26.
[29] Save, M.; Schappacher, M.; Soum, A.,“Controlled Ring-Opening Polymerization of Lactones and Lactides Initiated by Lanthanum Isopropoxide, 1. General Aspects and Kinetics.” Macromol. Chem. Phys., 203 (5-6), 2002, 889-899. |