Double-hydrophilic block copolymer nanoreactor for the synthesis of copper nanoparticles and for application in click chemistry

Journal of Nanoscience and Nanotechnology

Volumn 11, Issue 7, 2011, Pages 6162-6166

  Kim, Aram ^a   Sharma, Bhawana ^b   Kim, Byeong Su ^b   Park, Kang Hyun ^a  

^a Pusan National University   (South Korea)

^b Ulsan National Institute of Science and Technology   (South Korea)

Author keywords

Block Copolymer; Catalyst; Click Reaction; Copper (Cu); Heterogeneous; Nanoparticles (NPs)

Indexed keywords

CATALYTIC METALS; CLICK CHEMISTRY; CLICK REACTION; COPPER NANOPARTICLES; DOUBLE-HYDROPHILIC BLOCK COPOLYMERS; ENERGY TRANSFER PROCESS; ENVIRONMENT FRIENDLY; GOOD YIELD; HETEROGENEOUS; HIGH YIELD; NON-CONVENTIONAL ENERGY SOURCES; ORGANIC CHEMISTRY; ORGANIC TRANSFORMATIONS; REACTION CONDITIONS; REGIO-SELECTIVE; SHORT REACTION TIME; TERMINAL ALKYNE; WATER-SOLUBLE COPPER;

ACETYLENE; BLOCK COPOLYMERS; CATALYSTS; COPPER; ENERGY TRANSFER; HYDROPHILICITY; METAL NANOPARTICLES; NITROGEN COMPOUNDS; REGIOSELECTIVITY;

NANOREACTORS;

ALKYNE; AZIDE; COPPER; METAL NANOPARTICLE;

ARTICLE; CHEMICAL PHENOMENA; CHEMICAL STRUCTURE; CHEMISTRY; CLICK CHEMISTRY; INSTRUMENTATION; METHODOLOGY; NANOTECHNOLOGY; SYNTHESIS; TRANSMISSION ELECTRON MICROSCOPY; ULTRASOUND; ULTRAVIOLET SPECTROPHOTOMETRY; X RAY DIFFRACTION;

ALKYNES; AZIDES; CLICK CHEMISTRY; COPPER; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; METAL NANOPARTICLES; MICROSCOPY, ELECTRON, TRANSMISSION; MODELS, MOLECULAR; NANOTECHNOLOGY; SONICATION; SPECTROPHOTOMETRY, ULTRAVIOLET; X-RAY DIFFRACTION;

EID: 84855393378     PISSN: 15334880     EISSN: None     Source Type: Journal    
DOI: 10.1166/jnn.2011.4355     Document Type: Conference Paper

References (17)

1. B. Bridier and J. Perez-Ramirez, J. Am. Chem. Soc. 132, 4321 (2008).
2. B. L. Liu, Y. P. Fu, and M. L. Wang, J. Nanosci. Nanotechnol. 9, 1491 (2009).
3. P. Poizot, S. Laruelle, S. Grugeon, L. Dupont, and J.-M. Tarascon, Nature 407, 496 (2000).
4. M. Izaki, T. Shinagawa, K. Mizuno, Y. Ida, M. Inaba, and A. Tasaka, J. Phys. D. 40, 3326 (2007).
5. I. W. Hamley, Angew. Chem. Int. Ed. 42, 1692 (2003).
6. G. Basina, G. Mountrichas, E. Devlin, N. Boukos, D. Niarchos, D. Petridis, S. Pispas, and V. Tzitzios, J. Nanosci. Nanotechnol. 9, 4753 (2009).
7. T. Higuchi, H. Yabu, and M. Shimomura, J. Nanosci. Nanotechnol. 7, 856 (2007).
8. H. C. Kolb, M. G. Finn, and K. B. Sharpless, Angew. Chem. Int. Ed. 40, 2004 (2001).
9. H. Kang, H. S. Jung, J. Y. Kim, J. C. Park, M. Kim, H. Song, and K. H. Park, J. Nanosci. Nanotechnol. 10, 6504 (2010).
10. C. W. Tornoe, C. Christensen, and M. Meldal, J. Org. Chem. 67, 3057 (2002).
11. J. E. Moses and A. D. Moorhouse, Chem. Soc. Rev. 36, 1249 (2007).
12. Z. Zhnag, Z. Zha, C. Gan, C. Pan, Y. Zhou, Z. Wang, and M. Zhou, J. Org. Chem. 71, 4339 (2006).
13. P. Cintas, A. Barge, S. Tagliapietra, L. Boffa, and G. Cravotto, Nature Protocols 5, 607 (2010).
14. Z. X. Wang and H. L. Qin, Chem. Commun. 2450 (2003).
15. H. Colfen, Macromol. Rapid Commun. 22, 219 (2001).
16. D. B. Pedersen and S. Wang, J. Phys. Chem. C. 111, 17493 (2007).
17. C. K. Wu, M. Yin, S. O'Brien, and J. T. Koberstein, Chem. Mater. 18, 6054 (2006).