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Grafting of 4-(2,4,6-Trimethylphenoxy)benzoyl onto Single-Walled Carbon Nanotubes in Poly(phosphoric acid) via Amide Function

Single-walled carbon nanotubes (SWCNTs), which were commercial grade containing 60–70 wt% impurity, were treated in a mild poly(phosphoric acid) (PPA). The purity of PPA treated SWCNTs was greatly improved with or without little damage to SWCNTs framework and stable crystalline carbon particles. An...

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Detalles Bibliográficos
Autores principales: Han, Sang-Wook, Oh, Se-Jin, Tan, Loon-Seng, Baek, Jong-Beom
Formato: Texto
Lenguaje:English
Publicado: Springer 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2893784/
https://www.ncbi.nlm.nih.gov/pubmed/20596516
http://dx.doi.org/10.1007/s11671-009-9308-8
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author Han, Sang-Wook
Oh, Se-Jin
Tan, Loon-Seng
Baek, Jong-Beom
author_facet Han, Sang-Wook
Oh, Se-Jin
Tan, Loon-Seng
Baek, Jong-Beom
author_sort Han, Sang-Wook
collection PubMed
description Single-walled carbon nanotubes (SWCNTs), which were commercial grade containing 60–70 wt% impurity, were treated in a mild poly(phosphoric acid) (PPA). The purity of PPA treated SWCNTs was greatly improved with or without little damage to SWCNTs framework and stable crystalline carbon particles. An amide model compound, 4-(2,4,6-trimethylphenoxy)benzamide (TMPBA), was reacted with SWCNTs in PPA with additional phosphorous pentoxide as “direct” Friedel–Crafts acylation reaction to afford TMPBA functionalized SWCNTs. All evidences obtained from Fourier-transform infrared spectroscopy, Raman spectroscopy, thermogravimetric analysis, scanning electron microcopy, and transmission electron microscopy strongly supported that the functionalization of SWCNTs with benzamide was indeed feasible.
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spelling pubmed-28937842010-06-30 Grafting of 4-(2,4,6-Trimethylphenoxy)benzoyl onto Single-Walled Carbon Nanotubes in Poly(phosphoric acid) via Amide Function Han, Sang-Wook Oh, Se-Jin Tan, Loon-Seng Baek, Jong-Beom Nanoscale Res Lett Nano Express Single-walled carbon nanotubes (SWCNTs), which were commercial grade containing 60–70 wt% impurity, were treated in a mild poly(phosphoric acid) (PPA). The purity of PPA treated SWCNTs was greatly improved with or without little damage to SWCNTs framework and stable crystalline carbon particles. An amide model compound, 4-(2,4,6-trimethylphenoxy)benzamide (TMPBA), was reacted with SWCNTs in PPA with additional phosphorous pentoxide as “direct” Friedel–Crafts acylation reaction to afford TMPBA functionalized SWCNTs. All evidences obtained from Fourier-transform infrared spectroscopy, Raman spectroscopy, thermogravimetric analysis, scanning electron microcopy, and transmission electron microscopy strongly supported that the functionalization of SWCNTs with benzamide was indeed feasible. Springer 2009-05-05 /pmc/articles/PMC2893784/ /pubmed/20596516 http://dx.doi.org/10.1007/s11671-009-9308-8 Text en Copyright © 2009 to the authors
spellingShingle Nano Express
Han, Sang-Wook
Oh, Se-Jin
Tan, Loon-Seng
Baek, Jong-Beom
Grafting of 4-(2,4,6-Trimethylphenoxy)benzoyl onto Single-Walled Carbon Nanotubes in Poly(phosphoric acid) via Amide Function
title Grafting of 4-(2,4,6-Trimethylphenoxy)benzoyl onto Single-Walled Carbon Nanotubes in Poly(phosphoric acid) via Amide Function
title_full Grafting of 4-(2,4,6-Trimethylphenoxy)benzoyl onto Single-Walled Carbon Nanotubes in Poly(phosphoric acid) via Amide Function
title_fullStr Grafting of 4-(2,4,6-Trimethylphenoxy)benzoyl onto Single-Walled Carbon Nanotubes in Poly(phosphoric acid) via Amide Function
title_full_unstemmed Grafting of 4-(2,4,6-Trimethylphenoxy)benzoyl onto Single-Walled Carbon Nanotubes in Poly(phosphoric acid) via Amide Function
title_short Grafting of 4-(2,4,6-Trimethylphenoxy)benzoyl onto Single-Walled Carbon Nanotubes in Poly(phosphoric acid) via Amide Function
title_sort grafting of 4-(2,4,6-trimethylphenoxy)benzoyl onto single-walled carbon nanotubes in poly(phosphoric acid) via amide function
topic Nano Express
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2893784/
https://www.ncbi.nlm.nih.gov/pubmed/20596516
http://dx.doi.org/10.1007/s11671-009-9308-8
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