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Triazolobithiophene Light Absorbing Self-Assembled Monolayers: Synthesis and Mass Spectrometry Applications

The synthesis of five light absorbing triazolobithiophenic thiols, which were utilized for producing self-assembled monolayers (SAMs) on gold surfaces, is presented. The monolayer formation was monitored by cyclic voltammetry, indicating excellent surface coverage. The new triazolobithiophenic compo...

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Autores principales: Kenfack, Ghislain Tsague, Schinkovitz, Andreas, Babu, Suresh, Elouarzaki, Kamal, Dias, Marylène, Derbré, Séverine, Helesbeux, Jean-Jacques, Levillain, Eric, Richomme, Pascal, Séraphin, Denis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264341/
http://dx.doi.org/10.3390/molecules16108758
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author Kenfack, Ghislain Tsague
Schinkovitz, Andreas
Babu, Suresh
Elouarzaki, Kamal
Dias, Marylène
Derbré, Séverine
Helesbeux, Jean-Jacques
Levillain, Eric
Richomme, Pascal
Séraphin, Denis
author_facet Kenfack, Ghislain Tsague
Schinkovitz, Andreas
Babu, Suresh
Elouarzaki, Kamal
Dias, Marylène
Derbré, Séverine
Helesbeux, Jean-Jacques
Levillain, Eric
Richomme, Pascal
Séraphin, Denis
author_sort Kenfack, Ghislain Tsague
collection PubMed
description The synthesis of five light absorbing triazolobithiophenic thiols, which were utilized for producing self-assembled monolayers (SAMs) on gold surfaces, is presented. The monolayer formation was monitored by cyclic voltammetry, indicating excellent surface coverage. The new triazolobithiophenic compounds exhibited an absorption maximum around 340 nm, which is close to the emission wavelength of a standard nitrogen laser. Consequently these compounds could be used to aid ionization in laser desorption mass spectrometry (MS).
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spelling pubmed-62643412018-12-10 Triazolobithiophene Light Absorbing Self-Assembled Monolayers: Synthesis and Mass Spectrometry Applications Kenfack, Ghislain Tsague Schinkovitz, Andreas Babu, Suresh Elouarzaki, Kamal Dias, Marylène Derbré, Séverine Helesbeux, Jean-Jacques Levillain, Eric Richomme, Pascal Séraphin, Denis Molecules Article The synthesis of five light absorbing triazolobithiophenic thiols, which were utilized for producing self-assembled monolayers (SAMs) on gold surfaces, is presented. The monolayer formation was monitored by cyclic voltammetry, indicating excellent surface coverage. The new triazolobithiophenic compounds exhibited an absorption maximum around 340 nm, which is close to the emission wavelength of a standard nitrogen laser. Consequently these compounds could be used to aid ionization in laser desorption mass spectrometry (MS). MDPI 2011-10-19 /pmc/articles/PMC6264341/ http://dx.doi.org/10.3390/molecules16108758 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Kenfack, Ghislain Tsague
Schinkovitz, Andreas
Babu, Suresh
Elouarzaki, Kamal
Dias, Marylène
Derbré, Séverine
Helesbeux, Jean-Jacques
Levillain, Eric
Richomme, Pascal
Séraphin, Denis
Triazolobithiophene Light Absorbing Self-Assembled Monolayers: Synthesis and Mass Spectrometry Applications
title Triazolobithiophene Light Absorbing Self-Assembled Monolayers: Synthesis and Mass Spectrometry Applications
title_full Triazolobithiophene Light Absorbing Self-Assembled Monolayers: Synthesis and Mass Spectrometry Applications
title_fullStr Triazolobithiophene Light Absorbing Self-Assembled Monolayers: Synthesis and Mass Spectrometry Applications
title_full_unstemmed Triazolobithiophene Light Absorbing Self-Assembled Monolayers: Synthesis and Mass Spectrometry Applications
title_short Triazolobithiophene Light Absorbing Self-Assembled Monolayers: Synthesis and Mass Spectrometry Applications
title_sort triazolobithiophene light absorbing self-assembled monolayers: synthesis and mass spectrometry applications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264341/
http://dx.doi.org/10.3390/molecules16108758
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