CoChat
Sign Up
Cited by 593biodegradable polymer synthesis and propertiesCarbon dioxide utilization in catalysisAdvanced Polymer Synthesis and Characterization

Ring-opening copolymerization (ROCOP): synthesis and properties of polyesters and polycarbonates

Open access
Paul, Shyeni, Zhu, Yunqing, Romain, Charles, Brooks, Rachel, Saini, Prabhjot K., Williams, Charlotte K.·2015·Chemical Communications
DOI 10.1039/c4cc10113h
Open this paper in CoChat — free accountOpen PDF

Abstract

This feature article highlights the opportunities presented by ring-opening copolymerization (ROCOP) as a controlled route to prepare polyesters and polycarbonates.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1039/c4cc10113h

Cites

240 of 240 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

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?

  • While the field of epoxide/CO2 copolymerization is quite mature, with several technologies commercialized, the progress in epoxide/cyclic anhydride copolymerization is more recent.

    “While the field of epoxide/CO2 copolymerization is quite mature, with several technologies been commercialized, the progress in epoxide/cyclic anhydride copolymerization is more recent.211,343”

    From Catalysis as an Enabling Science for Sustainable Polymers (2018) · cites this paper as [343]

  • Because of the mechanistic similarities between epoxide/CO2 copolymerization and epoxide/cyclic anhydride copolymerization, the two can be mediated by a similar array of catalysts.

    “Because of the mechanistic similarities between epoxide/CO2 copolymerization and epoxide/cyclic anhydride copolymerization, the two can be mediated by a similar array of catalysts.343”

    From Catalysis as an Enabling Science for Sustainable Polymers (2018) · cites this paper as [343]

  • The development of single-site metal complexes with ancillary ligands has largely boosted the understanding and the scope of ROCP.

    “The development of single-site metal complexes with ancillary ligands has largely boosted the understanding and the scope of ROCP.343”

    From Catalysis as an Enabling Science for Sustainable Polymers (2018) · cites this paper as [343]

  • In most cases, a nucleophilic cocatalyst is used to increase the activity of the metal complexes, the most common ones being bis(triphenylphosphine) iminium salts and 4-dimethylaminopyridine.

    “In most cases, a nucleophilic cocatalyst is used to increase the activity of the metal complexes, the most common ones being bis(triphenylphosphine) iminium salts ([PPN]X) and 4-dimethylaminopyridine (DMAP).”

    From Catalysis as an Enabling Science for Sustainable Polymers (2018) · cites this paper as [343]

  • Terpolymerization of epoxide, cyclic anhydride, and CO2 is a facile strategy for the one-pot synthesis of poly(ester-carbonate), a class of biodegradable polymers that have garnered considerable interest due to their possible superior properties than pure polyesters and polycarbonates.

    “Terpolymerization of epoxide, cyclic anhydride, and CO2 is a facile strategy for the onepot synthesis of poly(ester-carbonate), 211,343 a class of biodegradable polymers that have garnered considerable interest due to their possible superior properties than pure polyesters and polycarbonates.”

    From Catalysis as an Enabling Science for Sustainable Polymers (2018) · cites this paper as [343]

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 234

  1. S. Inkinen, M. Hakkarainen, A. C. Albertsson and A. Sodergard, Biomacromolecules, 2011, 12, 523-532;
  2. R. H. Platel, L. M. Hodgson and C. K. Williams, Polym. Rev., 2008, 48, 11-63;
  3. M. J. L. Tschan, E. Brule, P. Haquette and C. M. Thomas, Polym. Chem., 2012, 3, 836-851;
  4. R. Auras, B. Harte and S. Selke, Macromol. Biosci., 2004, 4, 835-864.
  5. K. Sudesh, H. Abe and Y. Doi, Prog. Polym. Sci., 2000, 25, 1503-1555;
  6. H. M. Muller and D. Seebach, Angew. Chem., Int. Ed., 1993, 32, 477-502;
  7. R. W. Lenz and R. H. Marchessault, Biomacro- molecules, 2005, 6, 1-8.
  8. J. Langanke, A. Wolf, J. Hofmann, K. Bohm, M. A. Subhani, T. E. Muller, W. Leitner and C. Gurtler, Green Chem., 2014, 16, 1865-1870.
  9. N. v. d. Assen and A. Bardow, Green Chem., 2014, 16, 3272-3280.
  10. S. Inoue, J. Polym. Sci., Part A: Polym. Chem., 2000, 38, 2861-2871;
  11. C. J. Hawker, Acc. Chem. Res., 1997, 30, 373-382;
  12. G. W. Coates, Chem. Rev., 2000, 100, 1223-1252;
  13. M. Okada, Prog. Polym. Sci., 2002, 27, 87-133;
  14. T. P. Lodge, Macromol. Chem. Phys., 2003, 204, 265-273;
  15. N. Hadjichristidis, H. Iatrou, M. Pitsikalis and J. Mays, Prog. Polym. Sci., 2006, 31, 1068-1132;
  16. W. A. Braunecker and K. Matyjaszewski, Prog. Polym. Sci., 2007, 32, 93-146;
  17. G. J. Domski, J. M. Rose, G. W. Coates, A. D. Bolig and M. Brookhart, Prog. Polym. Sci., 2007, 32, 30-92;
  18. N. V. Tsarevsky and K. Matyjaszewski, Chem. Rev., 2007, 107, 2270-2299;
  19. G. Moad, E. Rizzardo and S. H. Thang, Acc. Chem. Res., 2008, 41, 1133-1142;
  20. R. R. Schrock, Acc. Chem. Res., 2014, 47, 2457-2466.
  21. T. Tang, M. Oshimura, S. Yamada, A. Takasu, X. Yang and Q. Cai, J. Polym. Sci., Part A: Polym. Chem., 2012, 50, 3171-3183;
  22. T. Tang, T. Moyori and A. Takasu, Macromolecules, 2013, 46, 5464-5472.
  23. M. Helou, O. Miserque, J.-M. Brusson, J.-F. Carpentier and S. M. Guillaume, Adv. Synth. Catal., 2009, 351, 1312-1324;
  24. C. K. Williams, Chem. Soc. Rev., 2007, 36, 1573-1580;
  25. C. M. Thomas and J. F. Lutz, Angew. Chem., Int. Ed., 2011, 50, 9244-9246;
  26. M. J. Stanford and A. P. Dove, Chem. Soc. Rev., 2010, 39, 486-494;
  27. N. Ajellal, J. F. Carpentier, C. Guillaume, S. M. Guillaume, M. Helou, V. Poirier, Y. Sarazin and A. Trifonov, Dalton Trans., 2010, 39, 8363-8376;
  28. O. Dechy-Cabaret, B. Martin-Vaca and D. Bourissou, Chem. Rev., 2004, 104, 6147-6176;
  29. P. J. Dijkstra, H. Z. Du and J. Feijen, Polym. Chem., 2011, 2, 520-527;
  30. C. G. Jaffredo and S. M. Guillaume, Polym. Chem., 2014, 5, 4168-4194;
  31. S. Tempelaar, L. Mespouille, O. Coulembier, P. Dubois and A. P. Dove, Chem. Soc. Rev., 2013, 42, 1312-1336;
  32. S. Dagorne, M. Normand, E. Kirillov and J.-F. Carpentier, Coord. Chem. Rev., 2013, 257, 1869-1886;
  33. H. A. Brown and R. M. Waymouth, Acc. Chem. Res., 2013, 46, 2585-2596;
  34. S. M. Guillaume and J.-F. Carpentier, Catal. Sci. Technol., 2012, 2, 898-906;
  35. S. Dutta, W.-C. Hung, B.-H. Huang and C.-C. Lin, in Synthetic Biodegradable Polymers, ed. B. Rieger, A. Kunkel, G. W. Coates, R. Reichardt, E. Dinjus and T. A. Zevaco, 2012, pp. 219-283;
  36. L. Mespouille, O. Coulembier, M. Kawalec, A. P. Dove and P. Dubois, Prog. Polym. Sci., 2014, 39, 1144-1164;
  37. M. A. Hillmyer and W. B. Tolman, Acc. Chem. Res., 2014, 47, 2390-2396; (
  38. K. Yao and C. Tang, Macromolecules, 2013, 46, 1689-1712;
  39. M. Labet and W. Thielemans, Chem. Soc. Rev., 2009, 38, 3484-3504;
  40. A. Arbaoui and C. Redshaw, Polym. Chem., 2010, 1, 801-826.
  41. M. R. Kember, A. Buchard and C. K. Williams, Chem. Commun., 2011, 47, 141-163.
  42. E. H. Nejad, A. Paoniasari, C. G. W. van Melis, C. E. Koning and R. Duchateau, Macromolecules, 2013, 46, 631-637;
  43. C. E. Koning, R. J. Sablong, E. H. Nejad, R. Duchateau and P. Buijsen, Prog. Org. Coat., 2013, 76, 1704-1711;
  44. E. H. Nejad, A. Paoniasari, C. E. Koning and R. Duchateau, Polym. Chem., 2012, 3, 1308-1313;
  45. S. Huijser, E. HosseiniNejad, R. l. Sablong, C. D. Jong, C. E. Koning and R. Duchateau, Macromolecules, 2011, 44, 1132-1139;
  46. D. J. Darensbourg and S. J. Wilson, Macromolecules, 2013, 46, 5929-5934;
  47. D. J. Darensbourg and S. J. Wilson, J. Am. Chem. Soc., 2011, 133, 18610-18613;
  48. R. C. Jeske, A. M. DiCiccio and G. W. Coates, J. Am. Chem. Soc., 2007, 129, 11330-11331.
  49. D. J. Darensbourg and A. D. Yeung, Polym. Chem., 2014, 5, 3949-3962;
  50. D. J. Darensbourg, in CO2 Chemistry, ed. M. Aresta and R. V. Eldik, 2014, pp. 1-23;
  51. D. J. Darensbourg and S. J. Wilson, Green Chem., 2012, 14, 2665-2671;
  52. D. J. Darensbourg, Inorg. Chem., 2010, 49, 10765-10780;
  53. D. J. Darensbourg, Chem. Rev., 2007, 107, 2388-2410;
  54. D. J. Darensbourg and M. W. Holtcamp, Coord. Chem. Rev., 1996, 153, 155-174;
  55. D. J. Darensbourg, in Synthetic Biodegradable Polymers, ed. B. Rieger, A. Kunkel, G. W. Coates, R. Reichardt, E. Dinjus and T. A. Zevaco, 2012, pp. 1-27;
  56. E. Brule, J. Guo, G. W. Coates and C. M. Thomas, Macromol. Rapid Commun., 2011, 32, 169-185;
  57. G. W. Coates and D. R. Moore, Angew. Chem., Int. Ed., 2004, 43, 6618-6639;
  58. S. Klaus, M. W. Lehenmeier, C. E. Anderson and B. Rieger, Coord. Chem. Rev., 2011, 255, 1460-1479;
  59. X.-B. Lu, W.-M. Ren and G.-P. Wu, Acc. Chem. Res., 2012, 45, 1721-1735;
  60. W. Kuran, Prog. Polym. Sci., 1998, 23, 919-992;
  61. H. Sugimoto and S. Inoue, J. Polym. Sci., Part A: Polym. Chem., 2004, 42, 5561-5573;
  62. G. A. Luinstra, Polym. Rev., 2008, 48, 192-219;
  63. R. Korashvili, B. Noernberg, N. Bornholdt, E. Borchardt and G. A. Luinstra, Chem. Ing. Tech., 2013, 85, 437-446.
  64. M. I. Childers, J. M. Longo, N. J. Van Zee, A. M. LaPointe and G. W. Coates, Chem. Rev., 2014, 114, 8129-8152.
  65. R. F. Fischer, J. Polym. Sci., 1960, 44, 155-172.
  66. V. E. Schwenk, K. Gulbins, M. Roth, G. Benzing, R. Maysenho ¨lder and K. Hamann, Macromol. Chem. Phys., 1962, 51, 53-69;
  67. T. Tsuruta, K. Matsuura and S. Inoue, Macromol. Chem. Phys., 1964, 75, 211-214;
  68. K. Matsuura, T. Tsuruta, Y. Terada and S. Inoue, Macromol. Chem. Phys., 1965, 81, 258-260;
  69. V. A. Hilt, K. H. Reichert and K. Hamann, Macromol. Chem. Phys., 1967, 101, 246-270;
  70. J. Schaefer, R. J. Katnik and R. J. Kern, J. Am. Chem. Soc., 1968, 90, 2476-2480;
  71. S. Inoue, K. Kitamura and T. Tsuruta, Macromol. Chem. Phys., 1969, 126, 250-265;
  72. H. L. Hsieh, J. Macromol. Sci., Part A, 1973, 7, 1525-1535;
  73. W. Kuran and A. Niestochowski, Polym. Bull., 1980, 2, 411-416.
  74. T. Aida and S. Inoue, J. Am. Chem. Soc., 1985, 107, 1358-1364;
  75. T. Aida, K. Sanuki and S. Inoue, Macromolecules, 1985, 18, 1049-1055.
  76. N. D. Harrold, Y. Li and M. H. Chisholm, Macromolecules, 2013, 46, 692-698;
  77. C. Chatterjee, M. H. Chisholm, A. El-Khaldy, R. D. McIntosh, J. T. Miller and T. Wu, Inorg. Chem., 2013, 52, 4547-4553;
  78. C. Chatterjee and M. H. Chisholm, Inorg. Chem., 2012, 51, 12041-12052;
  79. C. Chatterjee and M. H. Chisholm, Inorg. Chem., 2011, 50, 4481-4492;
  80. P. Chen, M. H. Chisholm, J. C. Gallucci, X. Zhang and Z. Zhou, Inorg. Chem., 2005, 44, 2588-2595;
  81. C. Chatterjee and M. H. Chisholm, Chem. Rec., 2013, 13, 549-560;
  82. H. Sugimoto, H. Ohshima and S. Inoue, J. Polym. Sci., Part A: Polym. Chem., 2003, 41, 3549-3555;
  83. N. Takeda and S. Inoue, Macromol. Chem. Phys., 1978, 179, 1377-1381;
  84. S. Mang, A. I. Cooper, M. E. Colclough, N. Chauhan and A. B. Holmes, Macro- molecules, 2000, 33, 303-308.
  85. A. M. DiCiccio and G. W. Coates, J. Am. Chem. Soc., 2011, 133, 10724-10727.
  86. A. Bernard, C. Chatterjee and M. H. Chisholm, Polymer, 2013, 54, 2639-2646.
  87. M. Cheng, E. B. Lobkovsky and G. W. Coates, J. Am. Chem. Soc., 1998, 120, 11018-11019;
  88. M. Cheng, D. R. Moore, J. J. Reczek, B. M. Chamberlain, E. B. Lobkovsky and G. W. Coates, J. Am. Chem. Soc., 2001, 123, 8738-8749;
  89. S. D. Allen, D. R. Moore, E. B. Lobkovsky and G. W. Coates, J. Am. Chem. Soc., 2002, 124, 14284-14285;
  90. D. R. Moore, M. Cheng, E. B. Lobkovsky and G. W. Coates, J. Am. Chem. Soc., 2003, 125, 11911-11924;
  91. D. R. Moore, M. Cheng, E. B. Lobkovsky and G. W. Coates, Angew. Chem., Int. Ed., 2002, 41, 2599-2602.
  92. M. Cheng, A. B. Attygalle, E. B. Lobkovsky and G. W. Coates, J. Am. Chem. Soc., 1999, 121, 11583-11584;
  93. B. M. Chamberlain, M. Cheng, D. R. Moore, T. M. Ovitt, E. B. Lobkovsky and G. W. Coates, J. Am. Chem. Soc., 2001, 123, 3229-3238;
  94. L. R. Rieth, D. R. Moore, E. B. Lobkovsky and G. W. Coates, J. Am. Chem. Soc., 2002, 124, 15239-15248.
  95. D. J. Darensbourg, R. R. Poland and C. Escobedo, Macromolecules, 2012, 45, 2242-2248.
  96. E. Hosseini Nejad, C. G. W. van Melis, T. J. Vermeer, C. E. Koning and R. Duchateau, Macromolecules, 2012, 45, 1770-1776.
  97. P. K. Saini, C. Romain and C. K. Williams, Chem. Commun., 2014, 50, 4164-4167;
  98. M. R. Kember and C. K. Williams, J. Am. Chem. Soc., 2012, 134, 15676-15679;
  99. M. R. Kember, F. Jutz, A. Buchard, A. J. P. White and C. K. Williams, Chem. Sci., 2012, 3, 1245-1255;
  100. A. Buchard, F. Jutz, M. R. Kember, A. J. P. White, H. S. Rzepa and C. K. Williams, Macromolecules, 2012, 45, 6781-6795; (
  101. F. Jutz, A. Buchard, M. R. Kember, S. B. Fredrickson and C. K. Williams, J. Am. Chem. Soc., 2011, 133, 17395-17405;
  102. A. Buchard, M. R. Kember, K. G. Sandeman and C. K. Williams, Chem. Commun., 2011, 47, 212-214;
  103. M. R. Kember, P. D. Knight, P. T. R. Reung and C. K. Williams, Angew. Chem., Int. Ed., 2009, 48, 931-933;
  104. M. R. Kember, A. J. P. White and C. K. Williams, Inorg. Chem., 2009, 48, 9535-9542;
  105. W. C. Ellis, Y. Jung, M. Mulzer, R. Di Girolamo, E. B. Lobkovsky and G. W. Coates, Chem. Sci., 2014, 5, 4004-4011;
  106. T. Ohkawara, K. Suzuki, K. Nakano, S. Mori and K. Nozaki, J. Am. Chem. Soc., 2014, 136, 10728-10735;
  107. K. Nakano, S. Hashimoto and K. Nozaki, Chem. Sci., 2010, 1, 369-373;
  108. E. K. Noh, S. J. Na, S. Sujith, S.-W. Kim and B. Y. Lee, J. Am. Chem. Soc., 2007, 129, 8082-8083;
  109. B. Y. Lee, H. Y. Kwon, S. Y. Lee, S. J. Na, S.-i. Han, H. Yun, H. Lee and Y.-W. Park, J. Am. Chem. Soc., 2005, 127, 3031-3037;
  110. Y. Liu, W.-M. Ren, J. Liu and X.-B. Lu, Angew. Chem., Int. Ed., 2013, 52, 11594-11598;
  111. C. E. Anderson, S. I. Vagin, M. Hammann, L. Zimmermann and B. Rieger, ChemCatChem, 2013, 5, 3269-3280;
  112. S. Klaus, S. I. Vagin, M. W. Lehenmeier, P. Deglmann, A. K. Brym and B. Rieger, Macromolecules, 2011, 44, 9508-9516;
  113. S. I. Vagin, R. Reichardt, S. Klaus and B. Rieger, J. Am. Chem. Soc., 2010, 132, 14367-14369.
  114. J. Liu, Y.-Y. Bao, Y. Liu, W.-M. Ren and X.-B. Lu, Polym. Chem., 2013, 4, 1439-1444.
  115. D.-F. Liu, L.-Y. Wu, W.-X. Feng, X.-M. Zhang, J. Wu, L.-Q. Zhu, D.-D. Fan, X.-Q. Lu ¨and Q. Shi, J. Mol. Catal. A: Chem., 2014, 382, 136-145;
  116. L. Zhu, D. Liu, L. Wu, W. Feng, X. Zhang, J. Wu, D. Fan, X. Lu ¨, R. Lu and Q. Shi, Inorg. Chem. Commun., 2013, 37, 182-185.
  117. P. K. Saini, C. Romain, Y. Zhu and C. K. Williams, Polym. Chem., 2014, 5, 6068-6075.
  118. L. Y. Wu, D. D. Fan, X.-Q. Lu ¨and R. Lu, Chin. J. Polym. Sci., 2014, 32, 768-777.
  119. Y. Liu, K. Huang, D. Peng and H. Wu, Polymer, 2006, 47, 8453-8461.
  120. R. C. Jeske, J. M. Rowley and G. W. Coates, Angew. Chem., Int. Ed., 2008, 47, 6041-6044.
  121. Z. Duan, X. Wang, Q. Gao, L. Zhang, B. Liu and I. Kim, J. Polym. Sci., Part A: Polym. Chem., 2014, 52, 789-795;
  122. Y. Liu, M. Xiao, S. Wang, L. Xia, D. Hang, G. Cui and Y. Meng, RSC Adv., 2014, 4, 9503-9508;
  123. X.-K. Sun, X.-H. Zhang, S. Chen, B.-Y. Du, Q. Wang, Z.-Q. Fan and G.-R. Qi, Polymer, 2010, 51, 5719-5725.
  124. L. Gu, Y. Qin, Y. Gao, X. Wang and F. Wang, Chin. J. Chem., 2012, 30, 2121-2125.
  125. Y. Hwang, J. Jung, M. Ree and H. Kim, Macromolecules, 2003, 36, 8210-8212;
  126. Y. Hwang, H. Kim and M. Ree, Macromol. Symp., 2005, 224, 227-238;
  127. S. Liu, J. Wang, K. Huang, Y. Liu and W. Wu, Polym. Bull., 2011, 66, 327-340.
  128. M. Kroger, C. Folli, O. Walter and M. Doring, Adv. Synth. Catal., 2006, 348, 1908-1918.
  129. P. K. Saini, C. Romain, Y. Zhu and C. K. Williams, Polym. Chem., 2014, 5, 6068-6075.
  130. C. Romain and C. K. Williams, Angew. Chem., Int. Ed., 2014, 53, 1607-1610.
  131. A. Cyriac, S. H. Lee, J. K. Varghese, E. S. Park, J. H. Park and B. Y. Lee, Macromolecules, 2010, 43, 7398-7401.
  132. G.-P. Wu, D. J. Darensbourg and X.-B. Lu, J. Am. Chem. Soc., 2012, 134, 17739-17745.
  133. D. J. Darensbourg and G.-P. Wu, Angew. Chem., Int. Ed., 2013, 52, 10602-10606.
  134. N. J. Van Zee and G. W. Coates, Chem. Commun., 2014, 50, 6322-6325.
  135. L. Feng, Y. Liu, J. Hao, C. Xiong and X. Deng, J. Polym. Sci., Part A: Polym. Chem., 2012, 50, 1812-1818.
  136. J. M. Longo, A. M. DiCiccio and G. W. Coates, J. Am. Chem. Soc., 2014, 136, 15897-15900.
  137. G. L. Baker, E. B. Vogel and M. R. Smith, Polym. Rev., 2008, 48, 64-84.
  138. A. Takasu, M. Ito, Y. Inai, T. Hirabayashi and Y. Nishimura, Polym. J., 1999, 31, 961-969.
  139. S. Takenouchi, A. Takasu, Y. Inai and T. Hirabayashi, Polym. J., 2002, 34, 36-42.
  140. E. S. Gil and S. M. Hudson, Prog. Polym. Sci., 2004, 29, 1173-1222;
  141. X. J. Loh, J. del Barrio, P. P. C. Toh, T. C. Lee, D. Z. Jiao, U. Rauwald, E. A. Appel and O. A. Scherman, Biomacromolecules, 2012, 13, 84-91;
  142. T. Rossow, S. Hackelbusch, P. van Assenbergh and S. Seiffert, Polym. Chem., 2013, 4, 2515-2527;
  143. Z. X. Zhang, K. L. Liu and J. Li, Macromolecules, 2011, 44, 1182-1193.
  144. H. Vihola, A. Laukkanen, L. Valtola, H. Tenhu and J. Hirvonen, Biomaterials, 2005, 26, 3055-3064.
  145. L. Feng, Y. Liu, J. Hao, X. Li, C. Xiong and X. Deng, Macromol. Chem. Phys., 2011, 212, 2626-2632.
  146. I. Nishimura, A. Kameyama, T. Sakurai and T. Nishikubo, Macro- molecules, 1996, 29, 3818-3825.
  147. I. Nishimura, A. Kameyama and T. Nishikubo, Macromolecules, 1998, 31, 2789-2796.
  148. Y. Ono, N. Kawashima, H. Kudo, T. Nishikubo and T. Nagai, J. Polym. Sci., Part A: Polym. Chem., 2005, 43, 4412-4421.
  149. D. X. Wang, G. J. Zhang, Y. C. Zhang, Y. J. Gao, Y. H. Zhao, C. Y. Zhou, Q. Y. Zhang and X. K. Wang, J. Appl. Polym. Sci., 2007, 103, 417-424.
  150. S. Inoue, J. Polym. Sci., Part B: Polym. Lett., 1969, 7, 287-292.
  151. T. Hirano, S. Inoue and T. Tsuruta, Makromol. Chem., 1976, 177, 3245-3253.
  152. T. Hirano, S. Inoue and T. Tsuruta, Makromol. Chem., 1976, 177, 3237-3243.
  153. S. Inoue, K. Matsumoto and Y. Yoshida, Makromol. Chem., 1980, 181, 2287-2292.
  154. M. Takanashi, Y. Nomura, Y. Yoshida and S. Inoue, Makromol. Chem., 1982, 183, 2085-2092.
  155. S. Inoue, J. Macromol. Sci., Chem., 1979, 13, 651-664;
  156. H. Koinuma, S. Inoue and T. Tsuruta, Makromol. Chem., 1970, 136, 65-71.
  157. D. J. Darensbourg, W.-C. Chung and S. J. Wilson, ACS Catal., 2013, 3, 3050-3057.
  158. D. J. Darensbourg, C. C. Fang and J. L. Rodgers, Organometallics, 2004, 23, 924-927.
  159. C. M. Byrne, S. D. Allen, E. B. Lobkovsky and G. W. Coates, J. Am. Chem. Soc., 2004, 126, 11404-11405.
  160. Y. Liu, M. Wang, W.-M. Ren, K.-K. He, Y.-C. Xu, J. Liu and X.-B. Lu, Macromolecules, 2014, 47, 1269-1276.
  161. W.-M. Ren, M.-W. Liang, Y.-C. Xu and X.-B. Lu, Polym. Chem., 2013, 4, 4425-4433;
  162. K. Nakano, K. Kobayashi, T. Ohkawara, H. Imoto and K. Nozaki, J. Am. Chem. Soc., 2013, 135, 8456-8459;
  163. R.-J. Wei, X.-H. Zhang, B.-Y. Du, X.-K. Sun, Z.-Q. Fan and G.-R. Qi, Macromolecules, 2013, 46, 3693-3697;
  164. R. M. Thomas, P. C. B. Widger, S. M. Ahmed, R. C. Jeske, W. Hirahata, E. B. Lobkovsky and G. W. Coates, J. Am. Chem. Soc., 2010, 132, 16520-16525;
  165. S. M. Ahmed, A. Poater, M. I. Childers, P. C. B. Widger, A. M. LaPointe, E. B. Lobkovsky, G. W. Coates and L. Cavallo, J. Am. Chem. Soc., 2013, 135, 18901-18911;
  166. Y.-Z. Hua, L.-J. Lu, P.-J. Huang, D.-H. Wei, M.-S. Tang, M.-C. Wang and J.-B. Chang, Chem. -Eur. J., 2014, 20, 12394-12398;
  167. G.-p. Wu, S.-d. Jiang, X.-b. Lu, W.-m. Ren and S.-k. Yan, Chin. J. Polym. Sci., 2012, 30, 487-492;
  168. K. Nakano, S. Hashimoto, M. Nakamura, T. Kamada and K. Nozaki, Angew. Chem., Int. Ed., 2011, 50, 4868-4871;
  169. L. Shi, X.-B. Lu, R. Zhang, X.-J. Peng, C.-Q. Zhang, J.-F. Li and X.-M. Peng, Macromolecules, 2006, 39, 5679-5685;
  170. B. Li, G. P. Wu, W. M. Ren, Y. M. Wang, D. Y. Rao and X. B. Lu, J. Polym. Sci., Part A: Polym. Chem., 2008, 46, 6102-6113;
  171. G.-P. Wu, W.-M. Ren, Y. Luo, B. Li, W.-Z. Zhang and X.-B. Lu, J. Am. Chem. Soc., 2012, 134, 5682-5688;
  172. M. Luo, X. H. Zhang, B. Y. Du, Q. Wang and Z. Q. Fan, Macromolecules, 2013, 46, 5899-5904.
  173. X.-B. Lu and D. J. Darensbourg, Chem. Soc. Rev., 2012, 41, 1462-1484;
  174. N. Kielland, C. J. Whiteoak and A. W. Kleij, Adv. Synth. Catal., 2013, 355, 2115-2138.
  175. K. Nozaki, K. Nakano and T. Hiyama, J. Am. Chem. Soc., 1999, 121, 11008-11009;
  176. K. Nakano, K. Nozaki and T. Hiyama, J. Am. Chem. Soc., 2003, 125, 5501-5510;
  177. Y. Xiao, Z. Wang and K. Ding, Chem. -Eur. J., 2005, 11, 3668-3678.
  178. B. Li, R. Zhang and X.-B. Lu, Macromolecules, 2007, 40, 2303-2307;
  179. K. Nakano, M. Nakamura and K. Nozaki, Macromolecules, 2009, 42, 6972-6980.
  180. W. Guerin, A. K. Diallo, E. Kirilov, M. Helou, M. Slawinski, J.-M. Brusson, J.-F. Carpentier and S. M. Guillaume, Macromolecules, 2014, 47, 4230-4235.
  181. X.-B. Lu, B. Liang, Y.-J. Zhang, Y.-Z. Tian, Y.-M. Wang, C.-X. Bai, H. Wang and R. Zhang, J. Am. Chem. Soc., 2004, 126, 3732-3733;
  182. C. T. Cohen, T. Chu and G. W. Coates, J. Am. Chem. Soc., 2005, 127, 10869-10878;
  183. C. T. Cohen and G. W. Coates, J. Polym. Sci., Part A: Polym. Chem., 2006, 44, 5182-5191;
  184. X.-B. Lu, L. Shi, Y.-M. Wang, R. Zhang, Y.-J. Zhang, X.-J. Peng, Z.-C. Zhang and B. Li, J. Am. Chem. Soc., 2006, 128, 1664-1674;
  185. R. L. Paddock and S. T. Nguyen, Macromolecules, 2005, 38, 6251-6253;
  186. W. M. Ren, W. Z. Zhang and X. B. Lu, Sci. China: Chem., 2010, 53, 1646-1652;
  187. W. M. Ren, Y. Liu, G. P. Wu, J. Liu and X. B. Lu, J. Polym. Sci., Part A: Polym. Chem., 2011, 49, 4894-4901;
  188. Z. Qin, C. M. Thomas, S. Lee and G. W. Coates, Angew. Chem., Int. Ed., 2003, 115, 5642-5645;
  189. X.-B. Lu and Y. Wang, Angew. Chem., Int. Ed., 2004, 43, 3574-3577;
  190. H. Sugimoto and K. Kuroda, Macromolecules, 2007, 41, 312-317.
  191. G.-P. Wu, S.-H. Wei, W.-M. Ren, X.-B. Lu, B. Li, Y.-P. Zu and D. J. Darensbourg, Energy Environ. Sci., 2011, 4, 5084-5092.
  192. G.-P. Wu, P.-X. Xu, X.-B. Lu, Y.-P. Zu, S.-H. Wei, W.-M. Ren and D. J. Darensbourg, Macromolecules, 2013, 46, 2128-2133.
  193. M. R. Kember, J. Copley, A. Buchard and C. K. Williams, Polym. Chem., 2012, 3, 1196-1201.
  194. J. Geschwind, F. Wurm and H. Frey, Macromol. Chem. Phys., 2013, 214, 892-901;
  195. A. Dag, M. Aydin, H. Durmaz, G. Hizal and U. Tunca, J. Polym. Sci., Part A: Polym. Chem., 2012, 50, 4476-4483;
  196. J.-F. Zhang, W.-M. Ren, X.-K. Sun, Y. Meng, B.-Y. Du and X.-H. Zhang, Macromolecules, 2011, 44, 9882-9886.
  197. H. Blattmann, M. Fleischer, M. Ba ¨hr and R. Mu ¨lhaupt, Macromol. Rapid Commun., 2014, 35, 1238-1254;
  198. L. Chen, Y. Qin, X. Wang, X. Zhao and F. Wang, Polymer, 2011, 52, 4873-4880;
  199. G. Ren, X. Sheng, Y. Qin, X. Chen, X. Wang and F. Wang, Polymer, 2014, 55, 5460-5468;
  200. Y. Hao, H. Ge, L. Han, H. Liang, H. Zhang and L. Dong, Polym. Bull., 2013, 70, 1991-2003.

200 of 234 shown

Cited by

Sorted by citations

Related

Authors
Paul, S., Zhu, Y., Romain, C., Brooks, R., Saini, P. K., & Williams, C. K.
Affiliations
Imperial College London (GB)
Corresponding author
Williams, Charlotte K.
ORCID
Venue
Chemical Communications
Publisher
Royal Society of Chemistry (RSC)
Published
2015
Volume
51
Issue
30
Pages
6459-6479
ISSN
  • 1359-7345 (ISSN-L)
  • 1364-548X
DOI
10.1039/c4cc10113h
OpenAlex
W2163986861
Cited by
593
References
240
Citations by year
2026: 32 · 2025: 39 · 2024: 56 · 2023: 55 · 2022: 63 · 2021: 66 · 2020: 63 · 2019: 49 · 2018: 67 · 2017: 49 · 2016: 32 · 2015: 22
FWCI
20.45
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • Chemical Communications (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Spiral (Imperial College London) (submittedVersion)
Funders
Engineering and Physical Sciences Research Council (EP/K014070/1, EP/K035274/1, EP/L017393/1)
Topics
  • Physical Sciences › Materials Science › Biomaterials › biodegradable polymer synthesis and properties
  • Physical Sciences › Chemical Engineering › Process Chemistry and Technology › Carbon dioxide utilization in catalysis
  • Physical Sciences › Chemistry › Organic Chemistry › Advanced Polymer Synthesis and Characterization
Keywords
ring-opening copolymerization, polyesters, polycarbonate, CO2 utilization, homogeneous catalysts, polymer properties

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