10.57647/ijc.2026.1601.06

Functionalizing Fullerene Soot Nanoparticles with Energetic Groups Using Copper-Catalyzed Oxidative Deboration of Nitrophenylboronic Acid

  1. 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

How to Cite

Hosseini, F. S., & Zamani, M. (2026). Functionalizing Fullerene Soot Nanoparticles with Energetic Groups Using Copper-Catalyzed Oxidative Deboration of Nitrophenylboronic Acid. Iranian Journal of Catalysis, 16(1 (March 2026). https://doi.org/10.57647/ijc.2026.1601.06

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

  1. Q.L. Yan, M. Gozin, F.Q. Zhao, A. Cohen, S.P. Pang, Nanoscale 8 (2016) 4799-4851. doi: 10.1039/C5NR07855E
  2. B. Duan, J. Li, H. Mo, X. Lu, M. Xu, B. Wang, N. Liu, Molecules 26 (2021) 5650. doi: 10.3390/molecules26185650
  3. S. Sriramrao, P. Raman, A. Dhas, S. Banerjee, Energ. Mater. Front. 5 (2024) 47-51. doi: 10.1016/j.enmf.2024.02.001
  4. Z. Yang, H. Qi, J. Bo, P. Rufang, Chin. J. Explos. Propellants 45 (2022) 770. doi: 10.14077/j.issn.1007-7812.202208009
  5. J. Anderson, D. Fitzgerald, In: 32nd Joint Propulsion Conference and Exhibit, 1996, 3211. doi: 10.2514/6.1996-3211
  6. 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
  7. G. Fan, L. Shufen, J. Energ. Mater. 21 (2003) 33-41. doi: 10.1080/07370650305586
  8. S. Li, D. He, W. Shan, F. Zhao, S. Li, J. Propul. Technol. 18 (1997) 79-83.
  9. F. Zhao, S. Li, W. Shan, S. Li, J. Propul. Technol. 21 (2000) 72-76.
  10. 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
  11. 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
  12. B.E. Greiner, R.A. Frederick Jr, M.D. Moser, J. Propul. Power 19 (2003) 713-715. doi: 10.2514/2.6161
  13. 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
  14. 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
  15. V.V. Chaban, E.E. Fileti, O.V. Prezhdo, J. Phys. Chem. Lett. 6 (2015) 913-917. doi: 10.1021/acs.jpclett.5b00120
  16. 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
  17. M. Manafi Moghadam, M. Zamani, S.A. Pourmousavi, J. Phys. Chem. Solids 154 (2021) 110101. doi: 10.1016/j.jpcs.2021.110101
  18. M. Manafi Moghadam, M. Zamani, Int. J. Quantum Chem. 121 (2021) e26504. doi: 10.1002/qua.26504
  19. J.T. Abrahamson, C. Song, J.H. Hu, J.M. Forman, et al., Chem. Mater. 23 (2011) 4557-4562. doi: 10.1021/cm201947y
  20. S. Sarvarian, M. Zamani, Struct. Chem. 32 (2021) 1205-1217. doi: 10.1007/s11224-020-01703-9
  21. Z. Shareh, M. Zamani, Fullerenes, Nanotubes Carbon Nanostruct. 31 (2023) 523-537. doi: 10.1080/1536383X.2023.2187786
  22. F.S. Hosseini, M. Zamani, Fullerenes, Nanotubes Carbon Nanostruct. 33 (2025) 142-163. doi: 10.1080/1536383X.2024.2398799
  23. M. Manafi Moghadam, M. Zamani, Comput. Theor. Chem. 1198 (2021) 113185. doi: 10.1016/j.comptc.2021.113185
  24. S. Sarvarian, M. Zamani, S.A. Pourmousavi, J. Nanostruct. 11 (2021) 252-268. doi: 10.22052/JNS.2021.02.006
  25. M. Korivand, M. Zamani, J. Solid State Chem. 294 (2021) 121851. doi: 10.1016/j.jssc.2020.121851
  26. Z. Shareh, M. Zamani, Compos. Interfaces 30 (2023) 1173-1200. doi: 10.1080/09276440.2023.2200600
  27. Z. Shareh, M. Zamani, Fullerenes, Nanotubes Carbon Nanostruct. 32 (2024) 192-206. doi: 10.1080/1536383X.2023.2270090
  28. D. G. Hall, Chem. Soc. Rev. 48 (2019) 3475-3496. doi: 10.1039/C9CS00191C
  29. M. Sheng, D. Frurip, D. Gorman, J. Loss Prev. Process Ind. 38 (2015) 114-118. doi: 10.1016/j.jlp.2015.09.004
  30. N. Oger, E. Le Grognec, F.X. Felpin, Org. Chem. Front. 2 (2015) 590-614. doi: 10.1039/C5QO00037H
  31. C. Cougnon, F. Gohier, D. Bélanger, J. Mauzeroll, Angew. Chem. 121 (2009) 4066-4068. doi: 10.1002/ange.200900498
  32. 4-Nitrophenylboronic acid, Sigma-Aldrich Chemie GmbH. 2022. www.sigmaaldrich.com/DE/en/sds/aldrich/673854 (Accessed: 09.06.2024).
  33. C.N. McEwen, R.G. McKay, B.S. Larsen, J. Am. Chem. Soc. 114 (1992) 4412-4414. doi: 10.1021/ja00037a064
  34. B.C. Yadav, R. Kumar, Int. J. Nanotechnol. Appl. 2 (2008) 15-24.
  35. X. Yang, A. Ebrahimi, J. Li, Q. Cui, Int. J. Nanomed. 9 (2014) 77-92. doi: 10.2147/IJN.S52829
  36. E.B. Zeynalov, N.S. Allen, N.I. Salmanova, Polym. Degrad. Stab. 94 (2009) 1183-1189. doi: 10.1016/j.polymdegradstab.2009.04.027
  37. K. Kokubo, S. Yamakura, Y. Nakamura, et al. Fullerenes, Nanotubes Carbon Nanostruct. 22 (2014) 250-261. doi: 10.1080/1536383X.2013.812637
  38. Z. Markovic, V. Trajkovic, Biomaterials 29 (2008) 3561-3573. doi: 10.1016/j.biomaterials.2008.05.005
  39. M.D. Tzirakis, M. Orfanopoulos, Chem. Rev. 113 (2013) 5262-5321. doi: 10.1021/cr300475r
  40. P. Bhakta, B. Barthunia, J. Indian Acad. Oral Med. Radiol. 32 (2020) 159-163. doi: 10.4103/jiaomr.jiaomr_191_19
  41. E. Carella, M. Ghiazza, M. Alfè, E. Gazzano, D. Ghigo, et al. BioNanoScience 3 (2013) 112-122. doi: 10.1007/s12668-013-0077-6
  42. 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
  43. R. Czochara, J. Kusio, M. Symonowicz, G. Litwinienko, Ind. Eng. Chem. Res. 55 (2016) 9887-9894. doi: 10.1021/acs.iecr.6b02564
  44. W. Zhu, D.E. Miser, W.G. Chan, M.R. Hajaligol, Carbon 42 (2004) 1463-1471. doi: 10.1016/j.carbon.2004.01.076
  45. 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
  46. D.I. Bugaenko, A.A. Volkov, A.V. Karchava, M.A. Yurovskaya, Russ. Chem. Rev. 90 (2021) 116. doi: 10.1070/RCR4959
  47. N. Kvasovs, V. Gevorgyan, Chem. Soc. Rev. 50 (2021) 2244-2259. doi: 10.1039/D0CS00589D
  48. G. Yan, M. Yang, X. Wu, Org. Biomol. Chem. 11 (2013) 7999-8008. doi: 10.1039/C3OB41851K
  49. 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
  50. N. Miyaura, Advances in Metal-Organic Chemistry, Vol. 6, Elsevier, 1998, pp. 187-243. doi: 10.1016/S1045-0688(98)80007-5
  51. X. Guan, H. Zhu, T.G. Driver, ACS Catal. 11 (2021) 12417-12422. doi: 10.1021/acscatal.1c03113
  52. F. Behmagham, S.B. Azimi, M. Ubaid, et al. RSC Adv. 13 (2023) 33390-33402. doi: 10.1039/D3RA05100E
  53. T. Sakaguchi, K. Fukuoka, T. Matsuki, M. Kawase, A. Tazawa, et al. Synlett. 36 (2025) 161-165. doi: 10.1055/a-2315-8369
  54. M. Patel, D. Bhavyesh, N. Kumar, Asian J. Org. Chem. 13 (2024). e202400064. doi: 10.1002/ajoc.202400064
  55. J.S. Tang, Y.X. Xie, Z.Q. Wang, J.H. Li, Synthesis 2011 (2011) 2789-2795. doi: 10.1055/s-0030-1260126
  56. J. Zhang, J. Chen, J. Ding, M. Liu, H. Wu, Tetrahedron 67 (2011) 9347-9351. doi: 10.1016/j.tet.2011.09.135
  57. R.L. McLaren, C.J. Laycock, D.J. Morgan, G.R. Owen, New J. Chem. 44 (2020) 19144-19154. doi: 10.1039/D0NJ04187D
  58. Ü. Çalışır, B. Çiçek, M. Doğan, Fullerenes, Nanotubes Carbon Nanostruct. 29 (2021) 899-906. doi: 10.1080/1536383X.2021.1913727
  59. K.A. Kurnia, W. Setyaningsih, N. Darmawan, B. Yuliarto, J. Mol. Liq. 326 (2021) 115321. doi: 10.1016/j.molliq.2021.115321
  60. 4-Nitrophenylboronic acid application, Sigma-Aldrich Chemie, www.sigmaaldrich.com/DE/en/product/aldrich/673854 (Accessed: 09.06.2024).
  61. J. Huang, F. Ding, P. Rojsitthisak, F.S. He, J. Wu, Org. Chem. Front. 7 (2020) 2873-2898. doi: 10.1039/D0QO00563K
  62. L. Hao, G. Ding, D.A. Deming, Q. Zhang, Eur. J. Org. Chem. 2019 (2019) 7307-7321. doi: 10.1002/ejoc.201901303
  63. K. Inamoto, K. Nozawa, M. Yonemoto, Y. Kondo, Chem. Commun. 47 (2011) 11775-11777. doi: 10.1039/C1CC14974A
  64. W. Yin, X. Pan, W. Leng, J. Chen, H. He, Green Chem. 21 (2019) 4614-4618. doi: 10.1039/C9GC01965K
  65. R.N. Dhital, H. Sakurai, Asian J. Org. Chem. 3 (2014) 668-684. doi: 10.1002/ajoc.201300283
  66. 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
  67. 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
  68. 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
  69. D.N. Mai, R.D. Baxter, Top. Catal. 60 (2017) 580-588. doi: 10.1007/s11244-017-0734-z
  70. Chemistry of Boronic Esters, https://www.aablocks.com/node/31 (Accessed: October 2023)
  71. S. Pillitteri, P. Ranjan, E.V. Van der Eycken, U.K. Sharma, Adv. Synth. Catal. 364 (2022) 1643-1665. doi: 10.1002/adsc.202200204
  72. Q. Wang, Y. Mei, R. Zhou, S. Komarneni, J. Ma, Colloids Surf., A 648 (2022) 129315. doi: 10.1016/j.colsurfa.2022.129315
  73. C.A. Contreras-Celedón, L. Chacón-García, N.J. Lira-Corral, J. Chem. 2014 (2014) 569572. doi: 10.1155/2014/569572
  74. 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
  75. C. McCarthy, N. Losada‐Garcia, J.M. Palomo, ChemistrySelect 5 (2020) 7492-7496. doi: 10.1002/slct.202002110
  76. V. Sadhasivam, M. Harikrishnan, G. Elamathi, et al. New J. Chem. 44 (2020) 6222-6231. doi: 10.1039/C9NJ05759E
  77. I. Kumar, R. Sharma, R. Kumar, R. Kumar, U. Sharma, Adv. Synth. Catal. 360 (2018) 2013-2019. doi: 10.1002/adsc.201701573
  78. E. Tsui, H. Wang, R.R. Knowles, Chem. Sci. 11 (2020) 11124-11141. doi: 10.1039/D0SC04542J
  79. 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
  80. 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
  81. G. Ghigo, A. Maranzana, G. Tonachini, C.M. Zicovich-Wilson, M. Causà, J. Phys. Chem. B 108 (2004) 3215-3223. doi: 10.1021/jp037011+
  82. 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
  83. E. Destandau, T. Michel, C. Elfakir, in: M.A. Rostagno, J.M. Prado (Eds.), RSC, 2013, pp. 113-156. doi: 10.1039/9781849737579-00113
  84. A. Kumar, Y. Kuang, Z. Liang, X. Sun, Mater. Today Nano 11 (2020) 100076. doi: 10.1016/j.mtnano.2020.100076
  85. F.A. Bassyouni, S.M. Abu-Bakr, M.A. Rehim, Res. Chem. Intermed. 38 (2012) 283-322. doi: 10.1007/s11164-011-0348-1
  86. 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
  87. 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
  88. Y. Shimoyama, Y. Nakajima, ChemSusChem 16 (2023) e202300684. doi: 10.1002/cssc.202300684
  89. M. Dmitrenko, A. Chepeleva, V. Liamin, A. Mazur, K. Semenov, N. Solovyev, A. Penkova, Polymers 14 (2022) 691. doi: 10.3390/polym14040691
  90. 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
  91. N.T. Rebeck, Y. Li, D.M. Knauss, J. Polym. Sci., Part B: Polym. Phys. 51 (2013) 1770-1778. doi: 10.1002/polb.23245
  92. H. Cong,et al., Manufacturing of Nanocomposites with Eng. Plastics, Woodhead, 2015, 99-224. doi: 10.1016/B978-1-78242-308-9.00009-4
  93. 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
  94. H. Behniafar, S. Khosravi-borna, Polym. Int. 58 (2009) 1299-1307. doi: 10.1002/pi.2663
  95. C.L. Chung, T.W. Tzu, S.H. Hsiao, J. Polym. Res. 13 (2006) 495-506. doi: 10.1007/s10965-006-9072-8
  96. B. Rai, A. Kumar Patel, J.M. Keller, R. Bajpai, Int. J. Sci. Res. Dev. 4 (2016) 1197-1200.
  97. S. Kaur, P. Kumar, R. Thangaraj, Polym. Bull. 70 (2013) 2269-2276. doi: 10.1007/s00289-013-0948-6
  98. M.A. Semsarzadeh, A. Sh Dadkhah, A. Sabzevari, Polym. Polym. Compos. 30 (2022) 09673911221104678. doi: 10.1177/09673911221104678
  99. U.R. Nair, S.N. Asthana, A.S. Rao, B.R. Gandhe, Def. Sci. J. 60 (2010) 137. doi: 10.14429/dsj.60.327
  100. G. Ćirić-Marjanović, I. Pašti, S. Mentus, Prog. Mater. Sci. 69 (2015) 61-182. doi: 10.1016/j.pmatsci.2014.08.002
  101. K.N. Wood, R. O'Hayre, S. Pylypenko, Energy Environ. Sci. 7 (2014) 1212-1249. doi: 10.1039/C3EE44078H
  102. O.Y. Podyacheva, Z.R. Ismagilov, Catal. Today 249 (2015) 12-22. doi: 10.1016/j.cattod.2014.10.033
  103. Z.H. Yang, H.Q. Wu, Mater. Lett. 50 (2001) 108-114. doi: 10.1016/S0167-577X(00)00425-0
  104. M. Galizia, C. Daniel, G. Fasano, G. Guerra, G. Mensitieri, Macromol. 45 (2012) 3604-3615. doi: 10.1021/ma3000626
  105. 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
  106. H.A. Dabbagh, M. Zamani, Appl. Catal., A 404 (2011) 141-148. doi: 10.1016/j.apcata.2011.07.024
  107. J. Li, D. Liu, B. Li, J. Wang, S. Han, L. Liu, H. Wei, CrystEngComm 17 (2015) 520-525. doi: 10.1039/C4CE01632G
  108. P. Manjunathan, M. Kumar, S.R. Churipard, et al., RSC Adv. 6 (2016) 82654-82660. doi: 10.1039/C6RA18609B
  109. C. Badeen, R. Turcotte, E. Hobenshield, S. Berretta, J. Hazard. Mater. 188 (2011) 52-57. doi: 10.1016/j.jhazmat.2011.01.063
  110. R.G. Ferrillo, A. Wilson, Thermochim. Acta 4 (1972) 273-281. doi: 10.1016/0040-6031(72)87011-4
  111. 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
  112. Ł. Gutowski, S. Cudziło, Def. Technol. 17 (2021) 775-784. doi: 10.1016/j.dt.2020.05.008
  113. X. Zhang, H. Xiong, H. Yang, G. Cheng, Propellants, Explos., Pyrotech. 42 (2017) 942-946. doi: 10.1002/prep.201700030