journal article·2022

Cu 2 O nanoparticle-catalyzed tandem reactions for the synthesis of robust polybenzoxazole

Huanqin Guan, Mengqi Shen, Cooro Harris, Honghong Lin, Kecheng Wei, Michael Morales, Noah Bronowich, Shouheng Sun

Nanoscale· Volume 14· Issue 16
Publisher page

Abstract

We report the synthesis of Cu2O nanoparticles (NPs) by controlled oxidation of Cu NPs and the study of these NPs as a robust catalyst for ammonia borane dehydrogenation, nitroarene hydrogenation, and amine/aldehyde condensation into Schiff-base compounds. Upon investigation of the size-dependent catalysis for ammonia borane dehydrogenation and nitroarene hydrogenation using 8-18 nm Cu2O NPs, we found 13 nm Cu2O NPs to be especially active with quantitative conversion of nitro groups to amines. The 13 nm Cu2O NPs also efficiently catalyze tandem reactions of ammonia borane, diisopropoxy-dinitrobenzene, and terephthalaldehyde, leading to a controlled polymerization and the facile synthesis of polybenzoxazole (PBO). The highly pure PBO (Mw = 19 kDa) shows much enhanced chemical stability than the commercial PBO against hydrolysis in boiling water or simulated seawater, demonstrating a great potential of using noble metal-free catalysts for green chemistry synthesis of PBO as a robust lightweight structural material for thermally and mechanically demanding applications.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Carbon dioxide utilization in catalysis · Multicomponent Synthesis of Heterocycles · Nanomaterials for catalytic reactions

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry, Brown University, Providence, RI, 02912, USA

Funding

Brown University

References (43)

Show source-provided references
1. Polshettiwar · Green Chem. · 2010 · 12 · 74310.1039/b921171c ↗
2. Sheldon · Chem. Soc. Rev. · 2012 · 41 · 143710.1039/C1CS15219J ↗
3. Astruc · Chem. Rev. · 2020 · 120 · 46110.1021/acs.chemrev.8b00696 ↗
4. Kalidindi · ChemSusChem · 2012 · 5 · 6510.1002/cssc.201100377 ↗
5. Sordakis · Chem. Rev. · 2018 · 118 · 37210.1021/acs.chemrev.7b00182 ↗
6. Wang · Chem. Soc. Rev. · 2021 · 50 · 343710.1039/D0CS00515K ↗
7. Graetz · Chem. Soc. Rev. · 2009 · 38 · 7310.1039/B718842K ↗
8. Huang · Energy Environ. Sci. · 2012 · 5 · 925710.1039/c2ee23039a ↗
9. Mboyi · Small · 2021 · 17 · 210275910.1002/smll.202102759 ↗
10. Muzzio · Nanoscale · 2019 · 11 · 1894610.1039/C9NR06080D ↗
11. Li · Acc. Chem. Res. · 2017 · 50 · 144910.1021/acs.accounts.7b00132 ↗
12. Zhan · ACS Catal. · 2016 · 6 · 689210.1021/acscatal.6b02209 ↗
13. Nie · ACS Catal. · 2021 · 11 · 107110.1021/acscatal.0c04939 ↗
14. Göksu · ACS Catal. · 2014 · 4 · 177710.1021/cs500167k ↗
15. Fu · J. Am. Chem. Soc. · 2018 · 140 · 1003410.1021/jacs.8b06511 ↗
16. Cui · Green Chem. · 2018 · 20 · 112110.1039/C7GC03710D ↗
17. Carrales-Alvarado · Chem. Commun. · 2021 · 57 · 647910.1039/D1CC01954F ↗
18. Li · ACS Catal. · 2020 · 10 · 775310.1021/acscatal.0c00177 ↗
19. Yu · J. Am. Chem. Soc. · 2017 · 139 · 571210.1021/jacs.7b01983 ↗
20. Yu · Matter · 2019 · 1 · 163110.1016/j.matt.2019.09.001 ↗
21. Shen · J. Am. Chem. Soc. · 2021 · 143 · 211510.1021/jacs.0c12488 ↗
22. Afshari · Polym. Rev. · 2008 · 48 · 23010.1080/15583720802020129 ↗
23. Chae · J. Appl. Polym. Sci. · 2006 · 100 · 79110.1002/app.22680 ↗
24. Suzuki · Polym. J. · 2019 · 51 · 103710.1038/s41428-019-0218-z ↗
25. Holmes · J. Mater. Sci. · 2006 · 41 · 410510.1007/s10853-005-5597-1 ↗
26. Walsh · J. Appl. Polym. Sci. · 2006 · 102 · 351710.1002/app.24788 ↗
27. Madasu · ACS Sustain. Chem. & Eng. · 2018 · 6 · 1107110.1021/acssuschemeng.8b02537 ↗
28. Shen · J. Am. Chem. Soc. · 2018 · 140 · 1646010.1021/jacs.8b11303 ↗
29. Kalidindi · Phys. Chem. Chem. Phys. · 2008 · 10 · 587010.1039/b805726e ↗
30. Lyu · Angew. Chem., Int. Ed. · 2021 · 60 · 190910.1002/anie.202011956 ↗
31. Jung · J. Am. Chem. Soc. · 2019 · 141 · 462410.1021/jacs.8b11237 ↗
32. Dai · Small Methods · 2020 · 4 · 200052110.1002/smtd.202000521 ↗
33. Hung · Adv. Mater. · 2010 · 22 · 191010.1002/adma.200903947 ↗
34. Yu · Chem. Mater. · 2017 · 29 · 141310.1021/acs.chemmater.6b05364 ↗
35. Chen · J. Am. Chem. Soc. · 2014 · 136 · 1673610.1021/ja509778y ↗
36. Carothers · Trans. Faraday Soc. · 1936 · 32 · 3910.1039/tf9363200039 ↗
37. G.Odian , Principles of Polymerization , 2004 , pp. 39–19710.1002/047147875X.ch2 ↗
38. Bhosale · ChemistrySelect · 2016 · 1 · 629710.1002/slct.201601484 ↗
39. Shi · Green Chem. · 2012 · 14 · 137210.1039/c2gc00006g ↗
40. Wei · J. Am. Chem. Soc. · 2018 · 140 · 462310.1021/jacs.8b00571 ↗
41. Seo · J. Am. Chem. Soc. · 2019 · 141 · 1178610.1021/jacs.9b05244 ↗
42. Chin · Polym. Degrad. Stab. · 2007 · 92 · 123410.1016/j.polymdegradstab.2007.03.030 ↗
43. Kanbargi · Polym. Degrad. Stab. · 2017 · 136 · 13110.1016/j.polymdegradstab.2016.12.015 ↗