dc.contributor.author |
Subrahmanyam, K S
|
|
dc.contributor.author |
Ghosh, Anupama
|
|
dc.contributor.author |
Gomathi, A
|
|
dc.contributor.author |
Govindaraj, A
|
|
dc.contributor.author |
Rao, C N R
|
|
dc.date.accessioned |
2011-03-29T05:00:38Z |
|
dc.date.available |
2011-03-29T05:00:38Z |
|
dc.date.issued |
2009-03 |
|
dc.identifier |
1941-4900 |
en_US |
dc.identifier.citation |
Nanoscience and Nanotechnology Letters 1(1), 28-31 (2009) |
en_US |
dc.identifier.uri |
https://libjncir.jncasr.ac.in/xmlui/10572/81 |
|
dc.description |
Restricted access. |
en_US |
dc.description.abstract |
While solubilization of graphene in nonpolar solvents can be accomplished through covalent functionalization, by involving the preparation of a long-chain alkylamide derivative, it is more easily accomplished by interaction with an organosilane or an organotin reagent such as hexadecyltrimethoxysilane and dibutyldimethoxytin. Noncovalent functionalization of graphene through π-π interaction by using 1-pyrenebutanoic acid succinimidyl ester gives stable dispersions in dimethylformamide. Interaction of graphene with surfactants produces stable aqueous dispersions, Igepal being effective even at low concentrations. |
en_US |
dc.description.uri |
http://dx.doi.org/10.1166/nnl.2009.1014 |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
American Scientific Publishers |
en_US |
dc.rights |
© 2009 American Scientific Publishers |
en_US |
dc.subject |
Graphene |
en_US |
dc.subject |
Functionalization |
en_US |
dc.subject |
Solubilization |
en_US |
dc.subject |
Raman Spectroscopy |
en_US |
dc.subject |
Transmission Electron Microscopy |
en_US |
dc.title |
Covalent and Noncovalent Functionalization and Solubilization of Graphene |
en_US |
dc.type |
Article |
en_US |