Photo-responsive liquid crystalline polymer from a renewable furfural derivative of dimethyl 2,5-furandicarboxylate via catalytic carbonylative esterification
Source abstract
Abstract
A main chain liquid crystalline polymer has been prepared via melting polycondensation of a bifunctionalized furan monomer (DMFD) from inedible biomass with a photo-responsive azobenzene unit, which can be used in information storage.
Only a short abstract or summary was supplied by the source.
Source: crossref · Quality: short
Research context
OpenAlex topics: Catalysis for Biomass Conversion · Synthesis and Properties of Aromatic Compounds · Cyclopropane Reaction Mechanisms
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education, Hubei Engineering Research Center for Biomaterials and Medical Protective Materials, Hubei Key Laboratory of Materials Chemistry and Service Failure, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan, 430074, China
State Key Laboratory of Material Processing and Die & Mould Technology, Huazhong University of Science and Technology, Wuhan, 430074, China
Funding
National Natural Science Foundation of China
References (55)
Show source-provided references
1. Vilela · Polym. Chem. · 2014 · 5 · 311910.1039/C3PY01213A ↗
2. Delidovich · Chem. Rev. · 2016 · 116 · 154010.1021/acs.chemrev.5b00354 ↗
3. Llevot · Chem. – Eur. J. · 2016 · 22 · 1151010.1002/chem.201602068 ↗
4. Bozell · Green Chem. · 2010 · 12 · 53910.1039/b922014c ↗
5. De Jong · ACS Symp. Ser. · 2012 · 1105 · 110.1021/bk-2012-1105.ch001 ↗
6. Sousa · Polym. Chem. · 2015 · 6 · 596110.1039/C5PY00686D ↗
7. Y. T.Huang , J. J.Wong , C. J.Huang , C. L.Li and G. W. B.Jang , in Chemicals and Fuels from Bio-based Buildingblocks , ed. F. Cavani , S. Albonetti , F. Basile and A. Gandini , Wiley-VCH , 2016 , pp. 191–21510.1002/9783527698202.ch8 ↗
8. Zhang · ACS Catal. · 2015 · 5 · 652910.1021/acscatal.5b01491 ↗
9. Sajid · Green Chem. · 2018 · 20 · 542710.1039/C8GC02680G ↗
10. Wang · Sci. China: Chem. · 2017 · 60 · 87010.1007/s11426-016-9035-1 ↗
11. Thoma · ChemSusChem · 2020 · 13 · 354410.1002/cssc.202000581 ↗
12. Li · Chem. Eng. J. · 2001 · 81 · 33810.1016/S1385-8947(00)00182-0 ↗
13. Zhu · ACS Catal. · 2021 · 11 · 1005810.1021/acscatal.1c01989 ↗
14. Shi · Catal. Commun. · 2011 · 2 · 73110.1016/j.catcom.2010.12.033 ↗
15. Guo · J. Phys. Chem. · 2011 · 115 · 17516
16. Zhang · ACS Sustainable Chem. Eng. · 2017 · 5 · 936010.1021/acssuschemeng.7b02396 ↗
17. Zhang · ACS Sustainable Chem. Eng. · 2018 · 6 · 1319210.1021/acssuschemeng.8b02780 ↗
18. Shen · Mol. Catal. · 2018 · 455 · 20410.1016/j.mcat.2018.06.015 ↗
19. Shen · Ind. Eng. Chem. Res. · 2019 · 58 · 2295110.1021/acs.iecr.9b05134 ↗
20. Shen · ChemistrySelect · 2017 · 2 · 709610.1002/slct.201701263 ↗
21. Shen · Mol. Catal. · 2019 · 463 · 9410.1016/j.mcat.2018.11.021 ↗
22. Lei · Ind. Eng. Chem. Res. · 2020 · 59 · 1987610.1021/acs.iecr.0c04203 ↗
23. Zhu · Mol. Catal. · 2021 · 513 · 11181410.1016/j.mcat.2021.111814 ↗
24. Roux · Polymers · 2021 · 13 · 388310.3390/polym13223883 ↗
25. Tachibana · ACS Omega · 2018 · 3 · 533610.1021/acsomega.8b00466 ↗
26. Lalanne · Biotechnol. Adv. · 2021 · 48 · 10770710.1016/j.biotechadv.2021.107707 ↗
27. Burgess · Macromolecules · 2014 · 47 · 138310.1021/ma5000199 ↗
28. Zhang · ACS Sustainable Chem. Eng. · 2017 · 5 · 936010.1021/acssuschemeng.7b02396 ↗
29. Ahmed · Ind. Eng. Chem. Res. · 2021 · 60 · 749510.1021/acs.iecr.1c00629 ↗
30. Cheng · Soft Matter · 2018 · 14 · 521310.1039/C8SM00639C ↗
31. Zhao · Langmuir · 2018 · 34 · 751910.1021/acs.langmuir.8b01031 ↗
32. Zhao · Langmuir · 2018 · 34 · 70010.1021/acs.langmuir.7b03786 ↗
33. Hu · Macromol. Rapid Commun. · 2019 · 40 · 180062910.1002/marc.201800629 ↗
34. Tong · Soft Matter · 2019 · 15 · 641110.1039/C9SM01310E ↗
35. Tong · Langmuir · 2020 · 36 · 1187310.1021/acs.langmuir.0c01901 ↗
36. Wang · Langmuir · 2015 · 31 · 545610.1021/acs.langmuir.5b01180 ↗
37. Yan · Polymer · 2021 · 221 · 12361710.1016/j.polymer.2021.123617 ↗
38. Yan · Langmuir · 2020 · 36 · 740810.1021/acs.langmuir.0c00964 ↗
39. Zhang · J. Mater. Chem. C · 2021 · 9 · 97510.1039/D0TC05131D ↗
40. Zhao · Macromol. Rapid Commun. · 2019 · 40 · 190003710.1002/marc.201900037 ↗
41. Zhao · Chin. J. Polym. Sci. · 2021 · 39 · 161710.1007/s10118-021-2618-8 ↗
42. Wang · J. Therm. Anal. Calorim. · 2010 · 102 · 73910.1007/s10973-010-0772-2 ↗
43. Wang · RSC Adv. · 2020 · 10 · 372610.1039/C9RA10161F ↗
44. G.Cervi , E.Felder , G. M. E.Papeo , A.Vulpetti , C. L. F.Gennari , Barbara , F.Nicotra and M.Riccaboni , Italy Pat. , EP2003129-A1, 2008
45. P. S.Hoffman , R. L.Guerrant , T. L.Macdonald and T. E.Ballard Jr. , US Pat. , WO2010107736-A2, 2010
46. Li · Chem. Soc. Rev. · 2018 · 47 · 17210.1039/C7CS00529F ↗
47. Quesnel · J. Am. Chem. Soc. · 2013 · 135 · 1684110.1021/ja4098093 ↗
48. Grigg · Tetrahedron · 2010 · 66 · 551510.1016/j.tet.2010.03.090 ↗
49. Gadge · RSC Adv. · 2014 · 4 · 1036710.1039/c3ra46273k ↗
50. Lei · J. Mol. Catal. A: Chem. · 2014 · 392 · 10510.1016/j.molcata.2014.05.006 ↗
51. Vybornyi · Angew. Chem., Int. Ed. · 2021 · 60 · 587210.1002/anie.202108745 ↗
52. Kainulainen · Polym. Degrad. Stab. · 2022 · 200 · 10996010.1016/j.polymdegradstab.2022.109960 ↗
53. Sousa · Polymer · 2013 · 54 · 51310.1016/j.polymer.2012.11.081 ↗
54. Zhou · Polym. Degrad. Stab. · 2021 · 189 · 10959110.1016/j.polymdegradstab.2021.109591 ↗
55. Haines · Thermochim. Acta · 1989 · 148 · 36510.1016/0040-6031(89)85236-0 ↗