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Syntheses and properties of thienyl-substituted dithienophenazines

A series of dithienophenazines with different lengths of the oligomeric thiophene units (quaterthiophenes and sexithiophenes) was synthesized. The thiophene and phenazine units act as electron donors and acceptors, respectively, resulting in characteristic absorption spectra. The optical spectra wer...

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Detalles Bibliográficos
Autores principales: Meyer, Annemarie, Sigmund, Eva, Luppertz, Friedhelm, Schnakenburg, Gregor, Gadaczek, Immanuel, Bredow, Thomas, Jester, Stefan-S, Höger, Sigurd
Formato: Texto
Lenguaje:English
Publicado: Beilstein-Institut 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001992/
https://www.ncbi.nlm.nih.gov/pubmed/21160561
http://dx.doi.org/10.3762/bjoc.6.135
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author Meyer, Annemarie
Sigmund, Eva
Luppertz, Friedhelm
Schnakenburg, Gregor
Gadaczek, Immanuel
Bredow, Thomas
Jester, Stefan-S
Höger, Sigurd
author_facet Meyer, Annemarie
Sigmund, Eva
Luppertz, Friedhelm
Schnakenburg, Gregor
Gadaczek, Immanuel
Bredow, Thomas
Jester, Stefan-S
Höger, Sigurd
author_sort Meyer, Annemarie
collection PubMed
description A series of dithienophenazines with different lengths of the oligomeric thiophene units (quaterthiophenes and sexithiophenes) was synthesized. The thiophene and phenazine units act as electron donors and acceptors, respectively, resulting in characteristic absorption spectra. The optical spectra were calculated using time-dependent density functional theory at the B3LYP/TZVP level and verify the experimental data. Adsorption of the dithienophenazines on highly ordered pyrolytic graphite (HOPG) was investigated by scanning tunneling microscopy, showing that one of the compounds forms highly organized self-assembled monolayers.
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spelling pubmed-30019922010-12-15 Syntheses and properties of thienyl-substituted dithienophenazines Meyer, Annemarie Sigmund, Eva Luppertz, Friedhelm Schnakenburg, Gregor Gadaczek, Immanuel Bredow, Thomas Jester, Stefan-S Höger, Sigurd Beilstein J Org Chem Full Research Paper A series of dithienophenazines with different lengths of the oligomeric thiophene units (quaterthiophenes and sexithiophenes) was synthesized. The thiophene and phenazine units act as electron donors and acceptors, respectively, resulting in characteristic absorption spectra. The optical spectra were calculated using time-dependent density functional theory at the B3LYP/TZVP level and verify the experimental data. Adsorption of the dithienophenazines on highly ordered pyrolytic graphite (HOPG) was investigated by scanning tunneling microscopy, showing that one of the compounds forms highly organized self-assembled monolayers. Beilstein-Institut 2010-12-13 /pmc/articles/PMC3001992/ /pubmed/21160561 http://dx.doi.org/10.3762/bjoc.6.135 Text en Copyright © 2010, Meyer et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Meyer, Annemarie
Sigmund, Eva
Luppertz, Friedhelm
Schnakenburg, Gregor
Gadaczek, Immanuel
Bredow, Thomas
Jester, Stefan-S
Höger, Sigurd
Syntheses and properties of thienyl-substituted dithienophenazines
title Syntheses and properties of thienyl-substituted dithienophenazines
title_full Syntheses and properties of thienyl-substituted dithienophenazines
title_fullStr Syntheses and properties of thienyl-substituted dithienophenazines
title_full_unstemmed Syntheses and properties of thienyl-substituted dithienophenazines
title_short Syntheses and properties of thienyl-substituted dithienophenazines
title_sort syntheses and properties of thienyl-substituted dithienophenazines
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001992/
https://www.ncbi.nlm.nih.gov/pubmed/21160561
http://dx.doi.org/10.3762/bjoc.6.135
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