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dc.contributor.authorSubrahmanyam, K S-
dc.contributor.authorGhosh, Anupama-
dc.contributor.authorGomathi, A-
dc.contributor.authorGovindaraj, A-
dc.contributor.authorRao, C N R-
dc.date.accessioned2011-03-29T05:00:38Z-
dc.date.available2011-03-29T05:00:38Z-
dc.date.issued2009-03-
dc.identifier1941-4900en_US
dc.identifier.citationNanoscience and Nanotechnology Letters 1(1), 28-31 (2009)en_US
dc.identifier.urihttps://libjncir.jncasr.ac.in/xmlui/10572/81-
dc.descriptionRestricted access.en_US
dc.description.abstractWhile 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.urihttp://dx.doi.org/10.1166/nnl.2009.1014en_US
dc.language.isoenen_US
dc.publisherAmerican Scientific Publishersen_US
dc.rights© 2009 American Scientific Publishersen_US
dc.subjectGrapheneen_US
dc.subjectFunctionalizationen_US
dc.subjectSolubilizationen_US
dc.subjectRaman Spectroscopyen_US
dc.subjectTransmission Electron Microscopyen_US
dc.titleCovalent and Noncovalent Functionalization and Solubilization of Grapheneen_US
dc.typeArticleen_US
Appears in Collections:Research Papers (Prof. C.N.R. Rao)

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