Bis(vinylenedithio)tetrathiafulvalene analogues of BEDT-TTF

This review aims to give an overview of the current status of our research on the synthesis of π-electron donor bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF, ET) analogues prepared from 1,8-diketones via a ring forming reaction. The new synthesized π-electron donors have vinyl moieties producing...

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Detalles Bibliográficos
Autores principales: Ertas, Erdal, Demirtas, İlknur, Ozturk, Turan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419507/
https://www.ncbi.nlm.nih.gov/pubmed/25977714
http://dx.doi.org/10.3762/bjoc.11.46
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author Ertas, Erdal
Demirtas, İlknur
Ozturk, Turan
author_facet Ertas, Erdal
Demirtas, İlknur
Ozturk, Turan
author_sort Ertas, Erdal
collection PubMed
description This review aims to give an overview of the current status of our research on the synthesis of π-electron donor bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF, ET) analogues prepared from 1,8-diketones via a ring forming reaction. The new synthesized π-electron donors have vinyl moieties producing extended π-electron delocalization over the substituent phenyl rings at the peripheries.
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spelling pubmed-44195072015-05-14 Bis(vinylenedithio)tetrathiafulvalene analogues of BEDT-TTF Ertas, Erdal Demirtas, İlknur Ozturk, Turan Beilstein J Org Chem Review This review aims to give an overview of the current status of our research on the synthesis of π-electron donor bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF, ET) analogues prepared from 1,8-diketones via a ring forming reaction. The new synthesized π-electron donors have vinyl moieties producing extended π-electron delocalization over the substituent phenyl rings at the peripheries. Beilstein-Institut 2015-03-27 /pmc/articles/PMC4419507/ /pubmed/25977714 http://dx.doi.org/10.3762/bjoc.11.46 Text en Copyright © 2015, Ertas 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 Review
Ertas, Erdal
Demirtas, İlknur
Ozturk, Turan
Bis(vinylenedithio)tetrathiafulvalene analogues of BEDT-TTF
title Bis(vinylenedithio)tetrathiafulvalene analogues of BEDT-TTF
title_full Bis(vinylenedithio)tetrathiafulvalene analogues of BEDT-TTF
title_fullStr Bis(vinylenedithio)tetrathiafulvalene analogues of BEDT-TTF
title_full_unstemmed Bis(vinylenedithio)tetrathiafulvalene analogues of BEDT-TTF
title_short Bis(vinylenedithio)tetrathiafulvalene analogues of BEDT-TTF
title_sort bis(vinylenedithio)tetrathiafulvalene analogues of bedt-ttf
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419507/
https://www.ncbi.nlm.nih.gov/pubmed/25977714
http://dx.doi.org/10.3762/bjoc.11.46
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