Solvent-free derivatization of oxidized single-walled carbon nanotubes and nanodiamond with aminobenzo-crown ethers

References

• Karousis, N., Tagmatarchis, N., and Tasis, D. (2010) Current progress on the chemical modification of carbon nanotubes. Chem. Rev., 110: 5366–5397.
   PubMed Web of Science ®Google Scholar
• Hamon, M. A., Chen, J., Hu, H., Chen, Y., Itkis, M. E., Rao, A. M., Eklund, P. C., and Haddon, R. C. (1999) Dissolution of single-walled carbon nanotubes. Adv. Mater., 11: 834–840.
   Web of Science ®Google Scholar
• Hamon, M. A., Hu, H., Bhowmik, P., Niyogi, S., Zhao, B., Itkis, M. E., and Haddon, R. C. (2001) End-group and defect analysis of soluble single-walled carbon nanotubes. Chem. Phys. Lett., 347: 8–12.
   Web of Science ®Google Scholar
• Pompeo, F., and Resasco, D. E. (2002) Water solubilization of single-walled carbon nanotubes by functionalization with glucosamine. Nano Lett., 2: 369–373.
   Web of Science ®Google Scholar
• Liu, L., Zhang, S., Hu, T., Guo, Z. X., Ye, C., Dai, L., and Zhu, D. (2002) Solubilized multi-walled carbon nanotubes with broadband optical limiting effect. Chem. Phys. Lett., 359: 191–195.
   Web of Science ®Google Scholar
• Chen, W. Y., Chen, C. Y., Hsu, K. Y., Wang, C. C., and Ling, Y. C. (2004) Reaction monitoring of polyaniline film formation on carbon nanotubes with TOF-SIMS. Appl. Surf. Sci., 231: 845–849.
   Web of Science ®Google Scholar
• D'Este, M., Nardi, M., and de Menna, E. (2006) A co-functionalization approach to soluble and functional single-walled carbon nanotubes. Eur. J. Org. Chem., 11: 2517–2522.
   Web of Science ®Google Scholar
• Kirikova, M. N., Ivanov, A. S., Savilov, S. V., and Lunin, V. V. (2008) Modification of multi-walled carbon nanotubes by carboxy groups and determination of the degree of functionalization. Russ. Chem. Bull. Int. Ed., 57: 298–303.
   Web of Science ®Google Scholar
• Damian, C. M., Pandele, A. M., Andronescu, C., Ghebaur, A., Garea, S. A., and Iovu, H. (2011) Epoxy-based nanocomposites reinforced with new amino functionalized multi-walled carbon nanotubes. Fullerenes Nanotubes Carbon Nanostruct. 19: 197–209.
   Web of Science ®Google Scholar
• Takassi, M. A., and Zadehnazari, A. (2016) Nanocomposites of triazole functionalized multi-walled carbon nanotube with chemically grafted polyimide: Preparation, characterization, and properties. Fullerenes Nanotubes Carbon Nanostruct. 24: 128–138.
   Web of Science ®Google Scholar
• Dolmatov, V. Yu. (2001) Detonation synthesis ultradispersed diamonds: Properties and applications. Russ. Chem. Rev., 70: 607–626.
   Google Scholar
• Mochalin, V. N., Shenderova, O., Ho, D., and Gogotsi, Y. (2011) The properties and applications of nanodiamonds. Nature Nanotechnol., 7: 11–23.
   PubMed Web of Science ®Google Scholar
• Shenderova, O. A., and Gruen, D. M. Eds. (2012) In: Ultrananocrystalline Diamond: Synthesis, Properties and Applications, 2nd Ed.; Elsevier: Oxford, UK.
   Google Scholar
• Jiang, T., and Xu, K. (1995) FTIR study of ultradispersed diamond powder synthesized by explosive detonation. Carbon, 33: 1663–1671.
   Web of Science ®Google Scholar
• Shakun, A., Vuorinen, J., Hoikkanen, M., Poikelispää, M., and Das, A. (2014) Hard nanodiamonds in soft rubbers: Past, present and future – A review. Composites: Part A, 64: 49–69.
   Web of Science ®Google Scholar
• Yakovlev, R. Yu., Solomatin, A. S., Leonidov, N. B., Kulakova, I. I., and Lisichkin, G. V. (2014) Detonation diamond—A perspective carrier for drug delivery systems. Russ. J. General Chem., 84: 379–390.
   Web of Science ®Google Scholar
• Moosa, B., Fhayli, K., Li, S., Julfakyan, K., Ezzeddine, A., and Khashab, N. M. (2014) Applications of nanodiamonds in drug delivery and catalysis. J. Nanosci. Nanotechnol., 14: 332–343.
   PubMed Web of Science ®Google Scholar
• Basiuk, E.V., Basiuk, V. A., Bañuelos, J.-G., Saniger-Blesa, J. M., Pokrovskiy, V. A., Gromovoy, T. Yu., Mischanchuk, A. V., and Mischanchuk, B. G. (2002) Interaction of oxidized single-walled carbon nanotubes with vaporous aliphatic amines. J. Phys. Chem. B, 106: 1588–1597.
   Web of Science ®Google Scholar
• Basiuk, V. A., Salvador-Morales, C., Basiuk, E. V., Jacobs, R. M. J., Ward, M., Chu, B. T., Sim, R. B., and Green, M. L. H. (2006) “Green” derivatization of carbon nanotubes with Nylon 6 and l-alanine. J. Mater. Chem., 16: 4420–4426.
   Web of Science ®Google Scholar
• Basiuk, E. V., Ramírez-Calera, I. J., Meza-Laguna, V., Abarca-Morales, E., Pérez-Rey, L. A., Re, M., Prete, P., Lovergine, N., Álvarez-Zauco, E., and Basiuk, V. A. (2015) Solvent-free functionalization of carbon nanotube buckypaper with amines. Appl. Surf. Sci., 357: 1355–1368.
   Web of Science ®Google Scholar
• Basiuk, E. V., and Basiuk, V. A. (2014) Green chemistry of carbon nanomaterials. J. Nanosci. Nanotechnol., 14: 644–672.
   PubMed Web of Science ®Google Scholar
• Basiuk, E. V., Basiuk, V. A., Meza-Laguna, V., Contreras-Torres, F. F., Martinez, M., Rojas-Aguilar, A., Salerno, M., Zavala, G., Falqui, A., and Brescia, R. (2012) Solvent-free covalent functionalization of multi-walled carbon nanotubes and nanodiamond with diamines: Looking for cross-linking effects. Appl. Surf. Sci., 259: 465–476.
   Web of Science ®Google Scholar
• Basiuk, E. V., Santamaría-Bonfil, A., Meza-Laguna, V., Gromovoy, T. Yu., Alvares-Zauco, E., Contreras-Torres, F. F., Rizo, J., Zavala, G., and Basiuk, V. A. (2013) Solvent-free covalent functionalization of nanodiamond with amines. Appl. Surf. Sci., 275: 324–334.
   Web of Science ®Google Scholar
• Bottari, G., Trukhina, O., Ince, M., and Torres, T. (2012) Towards artificial photosynthesis: Supramolecular, donor–acceptor, porphyrin- and phthalocyanine/carbon nanostructure ensembles. Coord. Chem. Rev., 256: 2453–2477.
   Web of Science ®Google Scholar
• Huang, K.-C., Chang, Y.-H., Chen, C.-Y., Liu, C.-Y., Lin, L.-Y., Vittal, R., Wu, C.-G., Lin, K.-F., and Ho, K.-C. (2011) Improved exchange reaction in an ionic liquid electrolyte of a quasi-solid-state dye-sensitized solar cell by using 15-crown-5-functionalized MWCNT. J. Mater. Chem., 21: 18467–18474.
   Web of Science ®Google Scholar
• Khazaei, A., Borazjani, M. K., and Moradian, K. M. (2012) Functionalization of oxidized single-walled carbon nanotubes with 4-benzo-9-crown-3 ether. J. Chem. Sci., 124: 1127–1135.
   Web of Science ®Google Scholar
• Khazaei, A., Rad, M. N. S., Borazjani, M. K., Saednia, S., Borazjani, M. K., and Soudbar, D. (2011) Functionalization of single-walled carbon nanotubes with 4-benzo-9-crown-3 ether. Synlett, 15: 2145–2150.
   Web of Science ®Google Scholar
• Torrejos, R. E. C., Nisola, G. M., Park, M. J., Shon, H. K., Seo, J. G., Koo, S., and Chung, W.-J. (2015) Synthesis and characterization of multi-walled carbon nanotubes-supported dibenzo-14-crown-4 ether with proton ionizable carboxyl sidearm as Li+ adsorbents. Chem. Eng. J., 264: 89–98.
   Web of Science ®Google Scholar
• Camarena, J. P., Espinoza-Gómez, H., Somanathan, R., Tiznado, H., Vélez-López, E., Romero-Rivera, R., Martínez-López, M. A., Avalos-Borja, M., Bek, A., Alonso-Nuñez, G., and Rogel-Hernández, E. (2011) Molecular assembly of multi-wall carbon nanotubes with amino crown ether: Synthesis and characterization. J. Nanosci. Nanotechnol., 11: 5539–5545.
   PubMed Web of Science ®Google Scholar
• Sundararajan, M. (2013) Designing novel nanomaterials through functionalization of carbon nanotubes with supramolecules for application in nuclear waste management. Separation Sci. Technol., 48: 2391–2396.
   Web of Science ®Google Scholar
• Mochalin, V., Osswald, S., and Gogotsi, Y. (2009) Contribution of functional groups to the Raman spectrum of nanodiamond powders. Chem. Mater., 21: 273–279.
   Web of Science ®Google Scholar