Functionalization of Single-Walled Carbon Nanotubes with Azides Derived from Amino Acids Using Click Chemistry

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DC Field	Value	Language
dc.contributor.author	Kumar, Indresh	-
dc.date.accessioned	2021-10-27T04:13:51Z	-
dc.date.available	2021-10-27T04:13:51Z	-
dc.date.issued	2008-07	-
dc.identifier.uri	https://www.ingentaconnect.com/content/asp/jnn/2008/00000008/00000007/art00007	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2993	-
dc.description.abstract	Single-walled carbon nanotubes (SWCNTs) were chemically functionalized with amino acid-based moieties. The covalent functionalization of alkyne-derived SWCNTs with well defined azides derived from amino acids was accomplished through Cu(I)-catalyzed Huisgen [3 + 2] dipolar cycloaddition click chemistry. Transmission electron microscopy, Raman spectroscopy, and infrared spectroscopic measurements confirmed the functionalization of SWCNTs by organic molecules derived from amino acids, and the resulting material showed some good solubility in the organic solvents such as tetrahydrofuran, CH2Cl2, and CHCl3.	en_US
dc.language.iso	en	en_US
dc.publisher	Ingenta	en_US
dc.subject	Chemistry	en_US
dc.subject	Amino acids	en_US
dc.subject	Carbon nanotubes	en_US
dc.subject	Click chemistry	en_US
dc.title	Functionalization of Single-Walled Carbon Nanotubes with Azides Derived from Amino Acids Using Click Chemistry	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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