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Diazonium-functionalized thin films from the spontaneous reaction of p-phenylenebis(diazonium) salts

Salts of the diazonium coupling agent p-phenylenebis(diazonium) form diazonium-terminated conjugated thin films on a variety of conductive and nonconductive surfaces by spontaneous reaction of the coupling agent with the surface. The resulting diazonium-bearing surface can be reacted with various or...

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Autores principales: Marshall, Nicholas, Rodriguez, Andres, Crittenden, Scott
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078370/
https://www.ncbi.nlm.nih.gov/pubmed/35540433
http://dx.doi.org/10.1039/c8ra00792f
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author Marshall, Nicholas
Rodriguez, Andres
Crittenden, Scott
author_facet Marshall, Nicholas
Rodriguez, Andres
Crittenden, Scott
author_sort Marshall, Nicholas
collection PubMed
description Salts of the diazonium coupling agent p-phenylenebis(diazonium) form diazonium-terminated conjugated thin films on a variety of conductive and nonconductive surfaces by spontaneous reaction of the coupling agent with the surface. The resulting diazonium-bearing surface can be reacted with various organic and inorganic nucleophiles to form a functionalized surface. These surfaces have been characterized with voltammetry, XPS, infrared and Raman spectroscopy, and atomic force microscopy. Substrates that can be conveniently and quickly modified with this process include ordinary glass, gold, and an intact, fully assembled commercial screen-printed carbon electrode. The scope and convenience of this process make it promising for practical surface modification.
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spelling pubmed-90783702022-05-09 Diazonium-functionalized thin films from the spontaneous reaction of p-phenylenebis(diazonium) salts Marshall, Nicholas Rodriguez, Andres Crittenden, Scott RSC Adv Chemistry Salts of the diazonium coupling agent p-phenylenebis(diazonium) form diazonium-terminated conjugated thin films on a variety of conductive and nonconductive surfaces by spontaneous reaction of the coupling agent with the surface. The resulting diazonium-bearing surface can be reacted with various organic and inorganic nucleophiles to form a functionalized surface. These surfaces have been characterized with voltammetry, XPS, infrared and Raman spectroscopy, and atomic force microscopy. Substrates that can be conveniently and quickly modified with this process include ordinary glass, gold, and an intact, fully assembled commercial screen-printed carbon electrode. The scope and convenience of this process make it promising for practical surface modification. The Royal Society of Chemistry 2018-02-09 /pmc/articles/PMC9078370/ /pubmed/35540433 http://dx.doi.org/10.1039/c8ra00792f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Marshall, Nicholas
Rodriguez, Andres
Crittenden, Scott
Diazonium-functionalized thin films from the spontaneous reaction of p-phenylenebis(diazonium) salts
title Diazonium-functionalized thin films from the spontaneous reaction of p-phenylenebis(diazonium) salts
title_full Diazonium-functionalized thin films from the spontaneous reaction of p-phenylenebis(diazonium) salts
title_fullStr Diazonium-functionalized thin films from the spontaneous reaction of p-phenylenebis(diazonium) salts
title_full_unstemmed Diazonium-functionalized thin films from the spontaneous reaction of p-phenylenebis(diazonium) salts
title_short Diazonium-functionalized thin films from the spontaneous reaction of p-phenylenebis(diazonium) salts
title_sort diazonium-functionalized thin films from the spontaneous reaction of p-phenylenebis(diazonium) salts
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078370/
https://www.ncbi.nlm.nih.gov/pubmed/35540433
http://dx.doi.org/10.1039/c8ra00792f
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