@article { ISI:000279836400026,
	title = {Synthesis and characterization of polyurethane-grafted single-walled carbon nanotubes via click chemistry},
	journal = {Journal of Nanoscience and Nanotechnology},
	volume = {10},
	number = {9},
	year = {2010},
	month = {SEP},
	pages = {5700-5707},
	publisher = {AMER SCIENTIFIC PUBLISHERS},
	address = {26650 THE OLD RD, STE 208, VALENCIA, CA 91381-0751 USA},
	abstract = {<p>Polyurethane (PU)-grafted carbon nanotubes were synthesized by the coupling of alkyne moiety decorated single walled carbon nanotube (SWCNT) with azide moiety containing PU using Cu(I) catalyzed Huisgen [3 + 2] cycloaddition click chemistry. The azide moiety containing poly(E-caprolactone)diol was synthesized by ring-opening polymerization and further used for PU synthesis. Alkyne-functionalizion of SWCNT was completed by the reaction of p-aminophenyl propargyl ether with SWCNT using a solvent free diazotization procedure. Nuclear magnetic resonance, Fourier transform infrared, and Raman spectroscopic measurements confirmed the functionalization of SWCNT. Scanning electron microscopy and transmission electron microscopy images showed an excellent dispersion of SWCNTs, and specially debundling of SWCNTs could be observed due to polymer assisted dispersion. A quantitative grafting was successfully achieved even at high content of functional groups.</p>},
	keywords = {Carbon nanotubes, Click chemistry, dispersion, polyurethane},
	issn = {1533-4880},
	doi = {10.1166/jnn.2010.2434},
	author = {Rana, Sravendra and Cho, Jae Whan and Kumar, Indresh}
}
@article { ISI:000276573700013,
	title = {Synthesis of hybrid 1,2,3-triazolo-delta-lactams/lactones using Huisgen [3+2] cycloaddition {\textquoteleft}click-chemistry{\textquoteright} in water},
	journal = {Tetrahedron-Asymmetry},
	volume = {21},
	number = {3},
	year = {2010},
	month = {MAR},
	pages = {352-355},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>The synthesis of a new class of hybrid 1,2,3-triazozlo-delta-lactams/lactones has been achieved using the Huisgen [3+2] dipolar cycloaddition {\textquoteleft}click-chemistry{\textquoteright} reaction of various organic azides with an activated alkyne in water, followed by cyclization. (C) 2010 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2010.02.002},
	author = {Kumar, Indresh and Rana, Sravendra and Cho, Jae Whan and Rode, Chandrashekhar V.}
}
