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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
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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). |
format | Online Article Text |
id | pubmed-6264341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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