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Thiol-functionalized anthraquinones: mass spectrometry and electrochemical studies
ABSTRACT: In this work, the synthesis of various thiol-functionalized anthraquinone compounds is presented. The studied compounds were characterized by mass spectrometry and the main fragmentation pathways are discussed. The compounds studied formed stable self-assembled monolayers (SAMs) in the gol...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4494848/ https://www.ncbi.nlm.nih.gov/pubmed/26166853 http://dx.doi.org/10.1007/s00706-011-0623-2 |
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author | Niedziałkowski, Paweł Ossowski, Tadeusz Majewski, Radosław Nowakowska, Zdzisława Schroeder, Grzegorz |
author_facet | Niedziałkowski, Paweł Ossowski, Tadeusz Majewski, Radosław Nowakowska, Zdzisława Schroeder, Grzegorz |
author_sort | Niedziałkowski, Paweł |
collection | PubMed |
description | ABSTRACT: In this work, the synthesis of various thiol-functionalized anthraquinone compounds is presented. The studied compounds were characterized by mass spectrometry and the main fragmentation pathways are discussed. The compounds studied formed stable self-assembled monolayers (SAMs) in the gold surface. The parameters for the reduction processes in the gold surface of the studied new anthraquinones were determined by cyclic voltamperometry tests. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-4494848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-44948482015-07-09 Thiol-functionalized anthraquinones: mass spectrometry and electrochemical studies Niedziałkowski, Paweł Ossowski, Tadeusz Majewski, Radosław Nowakowska, Zdzisława Schroeder, Grzegorz Monatsh Chem Original Paper ABSTRACT: In this work, the synthesis of various thiol-functionalized anthraquinone compounds is presented. The studied compounds were characterized by mass spectrometry and the main fragmentation pathways are discussed. The compounds studied formed stable self-assembled monolayers (SAMs) in the gold surface. The parameters for the reduction processes in the gold surface of the studied new anthraquinones were determined by cyclic voltamperometry tests. GRAPHICAL ABSTRACT: [Image: see text] Springer Vienna 2011-09-09 2011 /pmc/articles/PMC4494848/ /pubmed/26166853 http://dx.doi.org/10.1007/s00706-011-0623-2 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Paper Niedziałkowski, Paweł Ossowski, Tadeusz Majewski, Radosław Nowakowska, Zdzisława Schroeder, Grzegorz Thiol-functionalized anthraquinones: mass spectrometry and electrochemical studies |
title | Thiol-functionalized anthraquinones: mass spectrometry and electrochemical studies |
title_full | Thiol-functionalized anthraquinones: mass spectrometry and electrochemical studies |
title_fullStr | Thiol-functionalized anthraquinones: mass spectrometry and electrochemical studies |
title_full_unstemmed | Thiol-functionalized anthraquinones: mass spectrometry and electrochemical studies |
title_short | Thiol-functionalized anthraquinones: mass spectrometry and electrochemical studies |
title_sort | thiol-functionalized anthraquinones: mass spectrometry and electrochemical studies |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4494848/ https://www.ncbi.nlm.nih.gov/pubmed/26166853 http://dx.doi.org/10.1007/s00706-011-0623-2 |
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