Ecofriendly Multifunctional Monodisperse Spherical Polymer Colloids from Hyperbranched Poly(p-phenyl ester) Phenol
Source abstract
Abstract
Multifunctional, monodisperse, and hyperbranched poly(p-phenyl ester) phenol (HPPEP) colloids are prepared using commercially available inexpensive monomers (i.e., terephthaloyl chloride (A2) and phloroglucinol (B3)) via a simple condensation polymerization reaction (A2 + B3) at room temperature. Because of their symmetrical, rigid, highly branched, and cross-linked structure and the presence of the terminal phenolic units, the formation of highly monodisperse HPPEP colloids (coefficient of variation < 1.6%) can be realized under trimethylamine base conditions without any emulsifier (or surfactants) and expensive catalyst. Owing to their rigid aromatic and cross-linked structure, the HPPEP colloids exhibit excellent thermal, chemical, and mechanical resistances. Furthermore, the phenolic surface groups of HPPEP colloids enable the generation of highly negative surface charges (−60 mV) and catalytic protons (0.26 mmol H+/g) while enhancing surface functionality by chemically binding to red, green, and blue fluorescent dye molecules. Through carbonization, HPPEP colloids can be directly transformed into monodisperse porous carbon spheres with a large surface area (as,BET = 644.99 m2 g–1). Moreover, the HPPEP colloids can fully decompose into environmentally benign monomers after being exposed to an alkali environment.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Dendrimers and Hyperbranched Polymers · Advanced Polymer Synthesis and Characterization · Synthesis and properties of polymers
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, The Catholic University of Korea, 43 Jibong-ro, Wonmi-gu, Bucheon, Gyeonggi-do 14662, Korea
Funding
National Research Foundation of Korea
References (70)
Show source-provided references
1. DeFusco A. J. · 1997 · 68 · 37910.1007/978-94-011-5512-0_25 ↗
2. Urban D. · 200210.1002/3527600582 ↗
3. Daniels E. S. · 2002
4. Konno M. · 2002 · 16
5. Klier J. · 2020
6. 10.1002/mabi.20110025210.1002/mabi.201100252 ↗
7. 10.1039/c3cs60078e10.1039/c3cs60078e ↗
8. 10.1002/anie.20060130210.1002/anie.200601302 ↗
9. Tang C. · 2020
10. 10.1002/adma.20090376510.1002/adma.200903765 ↗
11. 10.1021/acsmaterialslett.9b0017910.1021/acsmaterialslett.9b00179 ↗
12. 10.1039/C8TA02353K10.1039/C8TA02353K ↗
13. 10.1002/adma.20200247510.1002/adma.202002475 ↗
14. 10.1002/anie.20200205110.1002/anie.202002051 ↗
15. 10.1002/anie.20211123910.1002/anie.202111239 ↗
16. 10.1002/anie.20210095410.1002/anie.202100954 ↗
17. 10.1002/anie.20201241610.1002/anie.202012416 ↗
18. 10.1007/s10965-019-1767-810.1007/s10965-019-1767-8 ↗
19. 10.1021/acs.biomac.0c0076910.1021/acs.biomac.0c00769 ↗
20. 10.1021/acs.chemrev.0c0081210.1021/acs.chemrev.0c00812 ↗
21. 10.1002/anie.20090072310.1002/anie.200900723 ↗
22. 10.1021/cr800242x10.1021/cr800242x ↗
23. 10.1021/ma048566l10.1021/ma048566l ↗
24. 10.1002/ceat.20100021010.1002/ceat.201000210 ↗
25. 10.1088/0957-4484/22/27/27571810.1088/0957-4484/22/27/275718 ↗
26. 10.1002/anie.20110201110.1002/anie.201102011 ↗
27. 10.1002/anie.20110351410.1002/anie.201103514 ↗
28. 10.1039/c2jm31678a10.1039/c2jm31678a ↗
29. 10.1021/ma302119t10.1021/ma302119t ↗
30. 10.1038/ncomms379810.1038/ncomms3798 ↗
31. 10.1007/s11356-017-9910-810.1007/s11356-017-9910-8 ↗
32. Chatterjee S. · Field Actions Sci. Rep. · 2019 · 19 · 54
33. 10.1038/s41598-020-64464-910.1038/s41598-020-64464-9 ↗
34. 10.1007/s10311-020-00983-110.1007/s10311-020-00983-1 ↗
35. 10.1016/j.ibiod.2013.12.01410.1016/j.ibiod.2013.12.014 ↗
36. 10.1186/s13765-020-00511-310.1186/s13765-020-00511-3 ↗
37. 10.1021/acssuschemeng.9b0663510.1021/acssuschemeng.9b06635 ↗
38. 10.5012/bkcs.2013.34.4.122510.5012/bkcs.2013.34.4.1225 ↗
39. 10.1016/j.polymer.2015.10.00410.1016/j.polymer.2015.10.004 ↗
40. Carey F. A. · 2010
41. 10.1002/mrc.126026060210.1002/mrc.1260260602 ↗
42. 10.1016/0167-7322(95)00909-410.1016/0167-7322(95)00909-4 ↗
43. 10.1039/b104409p10.1039/b104409p ↗
44. Skoog D. A. · 2014
45. Dekker M. · 1999
46. 10.1021/ma00125a00910.1021/ma00125a009 ↗
47. 10.1002/anie.20046105110.1002/anie.200461051 ↗
48. 10.1016/j.progpolymsci.2003.12.00210.1016/j.progpolymsci.2003.12.002 ↗
49. 10.1080/0360255990935159310.1080/03602559909351593 ↗
50. 10.1002/pol.2019026110.1002/pol.20190261 ↗
51. 10.1007/s10924-008-0106-710.1007/s10924-008-0106-7 ↗
52. 10.1016/j.jclepro.2015.09.11110.1016/j.jclepro.2015.09.111 ↗
53. 10.1016/j.marchem.2011.04.00210.1016/j.marchem.2011.04.002 ↗
54. Klein S. · 2018 · 58
55. 10.1016/j.marpolbul.2011.05.03010.1016/j.marpolbul.2011.05.030 ↗
56. 10.1038/s41467-020-14538-z10.1038/s41467-020-14538-z ↗
57. Zhu S. · 2012
58. 10.1039/c3cs35517a10.1039/c3cs35517a ↗
59. 10.1021/ma048566l10.1021/ma048566l ↗
60. 10.1021/ma981202710.1021/ma9812027 ↗
61. 10.1002/pola.2338910.1002/pola.23389 ↗
62. 10.1021/ma201038e10.1021/ma201038e ↗
63. 10.1021/cr010356910.1021/cr0103569 ↗
64. 10.1016/j.cattod.2019.07.02510.1016/j.cattod.2019.07.025 ↗
65. 10.15227/orgsyn.063.018310.15227/orgsyn.063.0183 ↗
66. Lakowicz J. R. · 2010
67. 10.1021/jacs.0c1216910.1021/jacs.0c12169 ↗
68. 10.1039/c0cs00204f10.1039/c0cs00204f ↗
69. 10.1002/marc.20090030910.1002/marc.200900309 ↗
70. 10.1002/cplu.20170018210.1002/cplu.201700182 ↗