Functionalizing Fullerene Soot Nanoparticles with Energetic Groups Using Copper-Catalyzed Oxidative Deboration of Nitrophenylboronic Acid
- School of Chemistry, Damghan University, Damghan, Iran
Received: 2025-06-17
Revised: 2025-10-22
Accepted: 2025-11-10
Published in Issue 2026-03-31
Published Online: 2025-11-25

This work is licensed under a Creative Commons Attribution 4.0 International License.
How to Cite
PDF views: 105
Abstract
In this study, 4-nitrophenylboronic acid is used as a radical precursor for functionalizing fullerene soot nanoparticles with 4-nitrophenyl and 4-nitrophenoxy groups. The oxidative deboration of 4-nitrophenylboronic acid for the formation of 4-nitrophenyl radical is carried out by employing potassium persulfate as oxidant and copper (II) sulfate as catalyst dissolved in water/dichloromethane under autoclave, oil-bath, or microwave heating conditions. The 4-nitrophenoxy radical is formed from the corresponding phenolic byproduct in the presence of persulfate/copper (II). The potentially energetic solid containing 4-nitrophenoxy groups involved in ether linkages is produced in the absence of fullerene soot. The 4-nitrophenyl and 4-nitrophenoxy radicals are efficiently trapped in the presence of fullerene soot to eventually afford samples with high nitrogen contents. The reaction conditions are optimized against temperature, time, and the amounts of starting materials. The characterization of products is performed by EDX and elemental maps, FT-IR, XRD, FESEM, and TGA-DSC. Results show that the oxidative deboration reaction can occur even in the absence of a catalyst. However, copper (II) catalyst can be used to obtain samples with more nitrogen content (up to 19.60 wt.% by EDX line scan) and better energetic performance. DSC thermograms of these samples exhibit a significant exothermic peak assigned to the decomposition of energetic groups.
Highlights
· 4-Nitrophenylboronic acid is used as radical precursor for functionalizing fullerene soot.
· The oxidative deboration of 4-nitrophenylboronic acid is carried out by employing potassium persulfate as oxidant and copper(II) sulfate as catalyst.
· Cupper(II) catalyst can be used to obtain samples with more nitrogen content (up to 19.60 wt.%) and better energetic performance.
· The samples prepared in the longer reaction times and the higher temperatures have more energetic properties.
· The sample prepared in the presence of catalyst in oil-bath has higher nitrogen content and better energetic performance among others.
· The equiv. ratio of 1:3:0.2 for reactant, oxidant and catalyst is preferred.
· These findings may be helpful for the development of novel energetic compositions from carbon nanomaterials.
Keywords
- Arylboronic acid, Aryl and aryloxy radicals, Energetic groups, Fullerene soot nanoparticles, Oxidative deboration, Persulfate/copper(II),
References
- Q.L. Yan, M. Gozin, F.Q. Zhao, A. Cohen, S.P. Pang, Nanoscale 8 (2016) 4799-4851. doi: 10.1039/C5NR07855E
- B. Duan, J. Li, H. Mo, X. Lu, M. Xu, B. Wang, N. Liu, Molecules 26 (2021) 5650. doi: 10.3390/molecules26185650
- S. Sriramrao, P. Raman, A. Dhas, S. Banerjee, Energ. Mater. Front. 5 (2024) 47-51. doi: 10.1016/j.enmf.2024.02.001
- Z. Yang, H. Qi, J. Bo, P. Rufang, Chin. J. Explos. Propellants 45 (2022) 770. doi: 10.14077/j.issn.1007-7812.202208009
- J. Anderson, D. Fitzgerald, In: 32nd Joint Propulsion Conference and Exhibit, 1996, 3211. doi: 10.2514/6.1996-3211
- X. Han, T.F. Wang, Z.K. Lin, D.L. Han, S.F. Li, F.Q. Zhao, L.Y. Zhang, Def. Sci. J. 59 (2009) 284-293. doi: 10.14429/dsj.59.1522
- G. Fan, L. Shufen, J. Energ. Mater. 21 (2003) 33-41. doi: 10.1080/07370650305586
- S. Li, D. He, W. Shan, F. Zhao, S. Li, J. Propul. Technol. 18 (1997) 79-83.
- F. Zhao, S. Li, W. Shan, S. Li, J. Propul. Technol. 21 (2000) 72-76.
- X. Han, Y.L. Sun, T.F. Wang, Z.K. Lin, S.F. Li, F.Q. Zhao, et al. J. Therm. Anal. Calorim. 91 (2008) 551-557. doi: 10.1007/s10973-007-8290-6
- S. Li, X. Han, Y. Sun, et al. In: 41st AIAA/ASME/SAE/ASEE Joint Propulsion Conference & Exhibit, 2005, 4473. doi: 10.2514/6.2005-4473
- B.E. Greiner, R.A. Frederick Jr, M.D. Moser, J. Propul. Power 19 (2003) 713-715. doi: 10.2514/2.6161
- H.J. Guan, R.F. Peng, B. Jin, H. Liang, et al. Bull. Korean Chem. Soc. 35 (2014) 2257-2262. doi: 10.5012/bkcs.2014.35.8.2257
- H.J. Guan, B., Jin, R.F., Peng, F.Q., Zhao, et al. Acta Armamentarii 35 (2014) 1756. doi: 10.3969/j.issn.1000-1093.2014.11.005
- V.V. Chaban, E.E. Fileti, O.V. Prezhdo, J. Phys. Chem. Lett. 6 (2015) 913-917. doi: 10.1021/acs.jpclett.5b00120
- Y. Zhao, Z. Chai, S. Ye, Y. Xiao, Q. Zhang, B. Jin, R. Peng, Thermochim. Acta 663 (2018) 110-117. doi: 10.1016/j.tca.2018.03.016
- M. Manafi Moghadam, M. Zamani, S.A. Pourmousavi, J. Phys. Chem. Solids 154 (2021) 110101. doi: 10.1016/j.jpcs.2021.110101
- M. Manafi Moghadam, M. Zamani, Int. J. Quantum Chem. 121 (2021) e26504. doi: 10.1002/qua.26504
- J.T. Abrahamson, C. Song, J.H. Hu, J.M. Forman, et al., Chem. Mater. 23 (2011) 4557-4562. doi: 10.1021/cm201947y
- S. Sarvarian, M. Zamani, Struct. Chem. 32 (2021) 1205-1217. doi: 10.1007/s11224-020-01703-9
- Z. Shareh, M. Zamani, Fullerenes, Nanotubes Carbon Nanostruct. 31 (2023) 523-537. doi: 10.1080/1536383X.2023.2187786
- F.S. Hosseini, M. Zamani, Fullerenes, Nanotubes Carbon Nanostruct. 33 (2025) 142-163. doi: 10.1080/1536383X.2024.2398799
- M. Manafi Moghadam, M. Zamani, Comput. Theor. Chem. 1198 (2021) 113185. doi: 10.1016/j.comptc.2021.113185
- S. Sarvarian, M. Zamani, S.A. Pourmousavi, J. Nanostruct. 11 (2021) 252-268. doi: 10.22052/JNS.2021.02.006
- M. Korivand, M. Zamani, J. Solid State Chem. 294 (2021) 121851. doi: 10.1016/j.jssc.2020.121851
- Z. Shareh, M. Zamani, Compos. Interfaces 30 (2023) 1173-1200. doi: 10.1080/09276440.2023.2200600
- Z. Shareh, M. Zamani, Fullerenes, Nanotubes Carbon Nanostruct. 32 (2024) 192-206. doi: 10.1080/1536383X.2023.2270090
- D. G. Hall, Chem. Soc. Rev. 48 (2019) 3475-3496. doi: 10.1039/C9CS00191C
- M. Sheng, D. Frurip, D. Gorman, J. Loss Prev. Process Ind. 38 (2015) 114-118. doi: 10.1016/j.jlp.2015.09.004
- N. Oger, E. Le Grognec, F.X. Felpin, Org. Chem. Front. 2 (2015) 590-614. doi: 10.1039/C5QO00037H
- C. Cougnon, F. Gohier, D. Bélanger, J. Mauzeroll, Angew. Chem. 121 (2009) 4066-4068. doi: 10.1002/ange.200900498
- 4-Nitrophenylboronic acid, Sigma-Aldrich Chemie GmbH. 2022. www.sigmaaldrich.com/DE/en/sds/aldrich/673854 (Accessed: 09.06.2024).
- C.N. McEwen, R.G. McKay, B.S. Larsen, J. Am. Chem. Soc. 114 (1992) 4412-4414. doi: 10.1021/ja00037a064
- B.C. Yadav, R. Kumar, Int. J. Nanotechnol. Appl. 2 (2008) 15-24.
- X. Yang, A. Ebrahimi, J. Li, Q. Cui, Int. J. Nanomed. 9 (2014) 77-92. doi: 10.2147/IJN.S52829
- E.B. Zeynalov, N.S. Allen, N.I. Salmanova, Polym. Degrad. Stab. 94 (2009) 1183-1189. doi: 10.1016/j.polymdegradstab.2009.04.027
- K. Kokubo, S. Yamakura, Y. Nakamura, et al. Fullerenes, Nanotubes Carbon Nanostruct. 22 (2014) 250-261. doi: 10.1080/1536383X.2013.812637
- Z. Markovic, V. Trajkovic, Biomaterials 29 (2008) 3561-3573. doi: 10.1016/j.biomaterials.2008.05.005
- M.D. Tzirakis, M. Orfanopoulos, Chem. Rev. 113 (2013) 5262-5321. doi: 10.1021/cr300475r
- P. Bhakta, B. Barthunia, J. Indian Acad. Oral Med. Radiol. 32 (2020) 159-163. doi: 10.4103/jiaomr.jiaomr_191_19
- E. Carella, M. Ghiazza, M. Alfè, E. Gazzano, D. Ghigo, et al. BioNanoScience 3 (2013) 112-122. doi: 10.1007/s12668-013-0077-6
- I.V. Mikheev, M.M. Sozarukova, D.Y. Izmailov, I.E. Kareev, et al. Int. J. Mol. Sci. 22 (2021) 5838. doi: 10.3390/ijms22115838
- R. Czochara, J. Kusio, M. Symonowicz, G. Litwinienko, Ind. Eng. Chem. Res. 55 (2016) 9887-9894. doi: 10.1021/acs.iecr.6b02564
- W. Zhu, D.E. Miser, W.G. Chan, M.R. Hajaligol, Carbon 42 (2004) 1463-1471. doi: 10.1016/j.carbon.2004.01.076
- L.J. Dunne, A.K. Sarkar, H.W. Kroto, J. Munn, et al. J. Phys. Condens. Matter 8 (1996) 2127. doi: 10.1088/0953-8984/8/13/005
- D.I. Bugaenko, A.A. Volkov, A.V. Karchava, M.A. Yurovskaya, Russ. Chem. Rev. 90 (2021) 116. doi: 10.1070/RCR4959
- N. Kvasovs, V. Gevorgyan, Chem. Soc. Rev. 50 (2021) 2244-2259. doi: 10.1039/D0CS00589D
- G. Yan, M. Yang, X. Wu, Org. Biomol. Chem. 11 (2013) 7999-8008. doi: 10.1039/C3OB41851K
- S.D. Yang, C.L. Sun, Z. Fang, B.J. Li, Y.Z. Li, Z.J. Shi, Angew. Chem., Int. Ed. 47 (2008) 1473-1476. doi: 10.1002/anie.200704619
- N. Miyaura, Advances in Metal-Organic Chemistry, Vol. 6, Elsevier, 1998, pp. 187-243. doi: 10.1016/S1045-0688(98)80007-5
- X. Guan, H. Zhu, T.G. Driver, ACS Catal. 11 (2021) 12417-12422. doi: 10.1021/acscatal.1c03113
- F. Behmagham, S.B. Azimi, M. Ubaid, et al. RSC Adv. 13 (2023) 33390-33402. doi: 10.1039/D3RA05100E
- T. Sakaguchi, K. Fukuoka, T. Matsuki, M. Kawase, A. Tazawa, et al. Synlett. 36 (2025) 161-165. doi: 10.1055/a-2315-8369
- M. Patel, D. Bhavyesh, N. Kumar, Asian J. Org. Chem. 13 (2024). e202400064. doi: 10.1002/ajoc.202400064
- J.S. Tang, Y.X. Xie, Z.Q. Wang, J.H. Li, Synthesis 2011 (2011) 2789-2795. doi: 10.1055/s-0030-1260126
- J. Zhang, J. Chen, J. Ding, M. Liu, H. Wu, Tetrahedron 67 (2011) 9347-9351. doi: 10.1016/j.tet.2011.09.135
- R.L. McLaren, C.J. Laycock, D.J. Morgan, G.R. Owen, New J. Chem. 44 (2020) 19144-19154. doi: 10.1039/D0NJ04187D
- Ü. Çalışır, B. Çiçek, M. Doğan, Fullerenes, Nanotubes Carbon Nanostruct. 29 (2021) 899-906. doi: 10.1080/1536383X.2021.1913727
- K.A. Kurnia, W. Setyaningsih, N. Darmawan, B. Yuliarto, J. Mol. Liq. 326 (2021) 115321. doi: 10.1016/j.molliq.2021.115321
- 4-Nitrophenylboronic acid application, Sigma-Aldrich Chemie, www.sigmaaldrich.com/DE/en/product/aldrich/673854 (Accessed: 09.06.2024).
- J. Huang, F. Ding, P. Rojsitthisak, F.S. He, J. Wu, Org. Chem. Front. 7 (2020) 2873-2898. doi: 10.1039/D0QO00563K
- L. Hao, G. Ding, D.A. Deming, Q. Zhang, Eur. J. Org. Chem. 2019 (2019) 7307-7321. doi: 10.1002/ejoc.201901303
- K. Inamoto, K. Nozawa, M. Yonemoto, Y. Kondo, Chem. Commun. 47 (2011) 11775-11777. doi: 10.1039/C1CC14974A
- W. Yin, X. Pan, W. Leng, J. Chen, H. He, Green Chem. 21 (2019) 4614-4618. doi: 10.1039/C9GC01965K
- R.N. Dhital, H. Sakurai, Asian J. Org. Chem. 3 (2014) 668-684. doi: 10.1002/ajoc.201300283
- Y. Ding, L. Fu, X. Peng, M. Lei, C. Wang, J. Jiang, Chem. Eng. J. 427 (2022) 131776. doi: 10.1016/j.cej.2021.131776
- C.J. Liang, C.J. Bruell, M.C. Marley, K.L. Sperry, Soil Sediment Contam.: Int. J. 12 (2003) 207-228. doi: 10.1080/713610970
- D.D. Sun, X.X. Yan, W.P. Xue, Adv. Mater. Res. 610 (2012) 1209-1212. doi: 10.4028/www.scientific.net/AMR.610-613.1209
- D.N. Mai, R.D. Baxter, Top. Catal. 60 (2017) 580-588. doi: 10.1007/s11244-017-0734-z
- Chemistry of Boronic Esters, https://www.aablocks.com/node/31 (Accessed: October 2023)
- S. Pillitteri, P. Ranjan, E.V. Van der Eycken, U.K. Sharma, Adv. Synth. Catal. 364 (2022) 1643-1665. doi: 10.1002/adsc.202200204
- Q. Wang, Y. Mei, R. Zhou, S. Komarneni, J. Ma, Colloids Surf., A 648 (2022) 129315. doi: 10.1016/j.colsurfa.2022.129315
- C.A. Contreras-Celedón, L. Chacón-García, N.J. Lira-Corral, J. Chem. 2014 (2014) 569572. doi: 10.1155/2014/569572
- M. Gohain, M. du Plessis, J.H. van Tonder, B.C. Bezuidenhoudt, Tetrahedron Lett. 55 (2014) 2082-2084. doi: 10.1016/j.tetlet.2014.02.048
- C. McCarthy, N. Losada‐Garcia, J.M. Palomo, ChemistrySelect 5 (2020) 7492-7496. doi: 10.1002/slct.202002110
- V. Sadhasivam, M. Harikrishnan, G. Elamathi, et al. New J. Chem. 44 (2020) 6222-6231. doi: 10.1039/C9NJ05759E
- I. Kumar, R. Sharma, R. Kumar, R. Kumar, U. Sharma, Adv. Synth. Catal. 360 (2018) 2013-2019. doi: 10.1002/adsc.201701573
- E. Tsui, H. Wang, R.R. Knowles, Chem. Sci. 11 (2020) 11124-11141. doi: 10.1039/D0SC04542J
- Q. Mei, H. Cao, D. Han, M. Li, S. Yao, J. Xie, J. Zhan, et al., J. Hazard. Mater. 389 (2020) 121901. doi: 10.1016/j.jhazmat.2019.121901
- Y. Ji, Y. Shi, Y. Yang, P. Yang, L. Wang, J. Lu, J. Li, L. Zhou, et al., J. Hazard. Mater. 361 (2019) 152-161. doi: 10.1016/j.jhazmat.2018.08.083
- G. Ghigo, A. Maranzana, G. Tonachini, C.M. Zicovich-Wilson, M. Causà, J. Phys. Chem. B 108 (2004) 3215-3223. doi: 10.1021/jp037011+
- S. Antusch, M. Dienwiebel, E. Nold, P. Albers, U. Spicher, M. Scherge, Wear 269 (2010) 1-12. doi: 10.1016/j.wear.2010.02.028
- E. Destandau, T. Michel, C. Elfakir, in: M.A. Rostagno, J.M. Prado (Eds.), RSC, 2013, pp. 113-156. doi: 10.1039/9781849737579-00113
- A. Kumar, Y. Kuang, Z. Liang, X. Sun, Mater. Today Nano 11 (2020) 100076. doi: 10.1016/j.mtnano.2020.100076
- F.A. Bassyouni, S.M. Abu-Bakr, M.A. Rehim, Res. Chem. Intermed. 38 (2012) 283-322. doi: 10.1007/s11164-011-0348-1
- S. Kobayashi, in: S. Kobayashi, et al., Encyclopedia of Polymeric Nanomaterials, Springer, 2014, pp. 1-7. doi: 10.1007/978-3-642-36199-9_416-1
- G. Wypych, in: G. Wypych (Ed.), Handbook of Polymers, ChemTec Publishing, 2016, pp. 522-525. doi: 10.1016/B978-1-895198-92-8.50162-2
- Y. Shimoyama, Y. Nakajima, ChemSusChem 16 (2023) e202300684. doi: 10.1002/cssc.202300684
- M. Dmitrenko, A. Chepeleva, V. Liamin, A. Mazur, K. Semenov, N. Solovyev, A. Penkova, Polymers 14 (2022) 691. doi: 10.3390/polym14040691
- S.Y. Lee, S.H. Mun, J.H. Jin, Y.K. Hong, Elastomers Compos. 46 (2011) 257-261. doi: 10.7473/EC.2011.46.3.257
- N.T. Rebeck, Y. Li, D.M. Knauss, J. Polym. Sci., Part B: Polym. Phys. 51 (2013) 1770-1778. doi: 10.1002/polb.23245
- H. Cong,et al., Manufacturing of Nanocomposites with Eng. Plastics, Woodhead, 2015, 99-224. doi: 10.1016/B978-1-78242-308-9.00009-4
- Y. Hu, G. Yu, C. Xing, S. Liu, C. Wei, H. Liu, J. Jiang, X. Li, ChemCatChem 13 (2021) 4591-4601. doi: 10.1002/cctc.202101016
- H. Behniafar, S. Khosravi-borna, Polym. Int. 58 (2009) 1299-1307. doi: 10.1002/pi.2663
- C.L. Chung, T.W. Tzu, S.H. Hsiao, J. Polym. Res. 13 (2006) 495-506. doi: 10.1007/s10965-006-9072-8
- B. Rai, A. Kumar Patel, J.M. Keller, R. Bajpai, Int. J. Sci. Res. Dev. 4 (2016) 1197-1200.
- S. Kaur, P. Kumar, R. Thangaraj, Polym. Bull. 70 (2013) 2269-2276. doi: 10.1007/s00289-013-0948-6
- M.A. Semsarzadeh, A. Sh Dadkhah, A. Sabzevari, Polym. Polym. Compos. 30 (2022) 09673911221104678. doi: 10.1177/09673911221104678
- U.R. Nair, S.N. Asthana, A.S. Rao, B.R. Gandhe, Def. Sci. J. 60 (2010) 137. doi: 10.14429/dsj.60.327
- G. Ćirić-Marjanović, I. Pašti, S. Mentus, Prog. Mater. Sci. 69 (2015) 61-182. doi: 10.1016/j.pmatsci.2014.08.002
- K.N. Wood, R. O'Hayre, S. Pylypenko, Energy Environ. Sci. 7 (2014) 1212-1249. doi: 10.1039/C3EE44078H
- O.Y. Podyacheva, Z.R. Ismagilov, Catal. Today 249 (2015) 12-22. doi: 10.1016/j.cattod.2014.10.033
- Z.H. Yang, H.Q. Wu, Mater. Lett. 50 (2001) 108-114. doi: 10.1016/S0167-577X(00)00425-0
- M. Galizia, C. Daniel, G. Fasano, G. Guerra, G. Mensitieri, Macromol. 45 (2012) 3604-3615. doi: 10.1021/ma3000626
- M. Khayet, J.P.G. Villaluenga, M.P. Godino, et al., J. Colloid Interface Sci. 278 (2004) 410-422. doi: 10.1016/j.jcis.2004.06.021
- H.A. Dabbagh, M. Zamani, Appl. Catal., A 404 (2011) 141-148. doi: 10.1016/j.apcata.2011.07.024
- J. Li, D. Liu, B. Li, J. Wang, S. Han, L. Liu, H. Wei, CrystEngComm 17 (2015) 520-525. doi: 10.1039/C4CE01632G
- P. Manjunathan, M. Kumar, S.R. Churipard, et al., RSC Adv. 6 (2016) 82654-82660. doi: 10.1039/C6RA18609B
- C. Badeen, R. Turcotte, E. Hobenshield, S. Berretta, J. Hazard. Mater. 188 (2011) 52-57. doi: 10.1016/j.jhazmat.2011.01.063
- R.G. Ferrillo, A. Wilson, Thermochim. Acta 4 (1972) 273-281. doi: 10.1016/0040-6031(72)87011-4
- S. Weng, W. Feng, W. Wu, Z. Guo, L. Chen, W. Chen, Org. Process Res. Dev. 27 (2023) 1027-1035. doi: 10.1021/acs.oprd.2c00403
- Ł. Gutowski, S. Cudziło, Def. Technol. 17 (2021) 775-784. doi: 10.1016/j.dt.2020.05.008
- X. Zhang, H. Xiong, H. Yang, G. Cheng, Propellants, Explos., Pyrotech. 42 (2017) 942-946. doi: 10.1002/prep.201700030
10.57647/ijc.2026.1601.06
