A facile method of modifying graphite powder with aminophenyl groups in bulk quantities

Adam T. Masheter; Gregory G. Wildgoose; Alison Crossley; John H. Jones; Richard G. Compton

doi:10.1039/b704118g

A facile method of modifying graphite powder with aminophenyl groups in bulk quantities

Adam T. Masheter, Gregory G. Wildgoose, Alison Crossley, John H. Jones, Richard G. Compton

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46 Citations (Scopus)

Abstract

A facile and rapid method of covalently modifying the surface of graphite powders with aminophenyl groups is described. This chem. modification strategy gave bulk quantities of amino-modified C powder. 4-Nitrophenyl groups are covalently attached to graphite powder via the chem. redn. of the corresponding 4-nitrobenzenediazonium tetrafluoroborate salt using aq. hypophosphorous acid. The 4-nitrophenyl groups on the C surface are then reduced to the corresponding 4-aminophenyl groups using alk. Fe(II) ammonium sulfate solns. Electrochem. and x-ray photoelectron spectroscopic characterization is carried out at each stage of the synthesis. [on SciFinder(R)]

Original language	English
Pages (from-to)	3008-3014
Number of pages	7
Journal	Journal of Materials Chemistry
Volume	17
Issue number	29
Early online date	10 May 2007
DOIs	https://doi.org/10.1039/b704118g
Publication status	Published - 2007

Keywords

modification graphite powder aminophenyl group
cyclic voltammetry aminophenyl modified carbon
nitrobenzoyl chloride reaction product aminophenyl modified carbon cyclic voltammetry

Access to Document

10.1039/b704118g

Cite this

@article{1ee0f732aab14b409c6e8ed72b315fac,

title = "A facile method of modifying graphite powder with aminophenyl groups in bulk quantities",

abstract = "A facile and rapid method of covalently modifying the surface of graphite powders with aminophenyl groups is described. This chem. modification strategy gave bulk quantities of amino-modified C powder. 4-Nitrophenyl groups are covalently attached to graphite powder via the chem. redn. of the corresponding 4-nitrobenzenediazonium tetrafluoroborate salt using aq. hypophosphorous acid. The 4-nitrophenyl groups on the C surface are then reduced to the corresponding 4-aminophenyl groups using alk. Fe(II) ammonium sulfate solns. Electrochem. and x-ray photoelectron spectroscopic characterization is carried out at each stage of the synthesis. [on SciFinder(R)]",

keywords = "modification graphite powder aminophenyl group, cyclic voltammetry aminophenyl modified carbon, nitrobenzoyl chloride reaction product aminophenyl modified carbon cyclic voltammetry",

author = "Masheter, {Adam T.} and Wildgoose, {Gregory G.} and Alison Crossley and Jones, {John H.} and Compton, {Richard G.}",

year = "2007",

doi = "10.1039/b704118g",

language = "English",

volume = "17",

pages = "3008--3014",

journal = "Journal of Materials Chemistry",

issn = "0959-9428",

publisher = "Royal Society of Chemistry",

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T1 - A facile method of modifying graphite powder with aminophenyl groups in bulk quantities

AU - Masheter, Adam T.

AU - Wildgoose, Gregory G.

AU - Crossley, Alison

AU - Jones, John H.

AU - Compton, Richard G.

PY - 2007

Y1 - 2007

N2 - A facile and rapid method of covalently modifying the surface of graphite powders with aminophenyl groups is described. This chem. modification strategy gave bulk quantities of amino-modified C powder. 4-Nitrophenyl groups are covalently attached to graphite powder via the chem. redn. of the corresponding 4-nitrobenzenediazonium tetrafluoroborate salt using aq. hypophosphorous acid. The 4-nitrophenyl groups on the C surface are then reduced to the corresponding 4-aminophenyl groups using alk. Fe(II) ammonium sulfate solns. Electrochem. and x-ray photoelectron spectroscopic characterization is carried out at each stage of the synthesis. [on SciFinder(R)]

AB - A facile and rapid method of covalently modifying the surface of graphite powders with aminophenyl groups is described. This chem. modification strategy gave bulk quantities of amino-modified C powder. 4-Nitrophenyl groups are covalently attached to graphite powder via the chem. redn. of the corresponding 4-nitrobenzenediazonium tetrafluoroborate salt using aq. hypophosphorous acid. The 4-nitrophenyl groups on the C surface are then reduced to the corresponding 4-aminophenyl groups using alk. Fe(II) ammonium sulfate solns. Electrochem. and x-ray photoelectron spectroscopic characterization is carried out at each stage of the synthesis. [on SciFinder(R)]

KW - modification graphite powder aminophenyl group

KW - cyclic voltammetry aminophenyl modified carbon

KW - nitrobenzoyl chloride reaction product aminophenyl modified carbon cyclic voltammetry

U2 - 10.1039/b704118g

DO - 10.1039/b704118g

M3 - Article

VL - 17

SP - 3008

EP - 3014

JO - Journal of Materials Chemistry

JF - Journal of Materials Chemistry

SN - 0959-9428

IS - 29

ER -