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

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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


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