Synthesis of redox-active donor/acceptor chromophores with a central indenofluorene or indacenodithiophene core

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Standard

Synthesis of redox-active donor/acceptor chromophores with a central indenofluorene or indacenodithiophene core. / Andersen, Dianna; Nygaard, David Bo; Kragh, Rasmus Refsgaard; Broløs, Line; Nielsen, Mogens Brøndsted.

I: Tetrahedron Letters, Bind 61, Nr. 23, 151939, 01.06.2020.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Andersen, D, Nygaard, DB, Kragh, RR, Broløs, L & Nielsen, MB 2020, 'Synthesis of redox-active donor/acceptor chromophores with a central indenofluorene or indacenodithiophene core', Tetrahedron Letters, bind 61, nr. 23, 151939. https://doi.org/10.1016/j.tetlet.2020.151939

APA

Andersen, D., Nygaard, D. B., Kragh, R. R., Broløs, L., & Nielsen, M. B. (2020). Synthesis of redox-active donor/acceptor chromophores with a central indenofluorene or indacenodithiophene core. Tetrahedron Letters, 61(23), [151939]. https://doi.org/10.1016/j.tetlet.2020.151939

Vancouver

Andersen D, Nygaard DB, Kragh RR, Broløs L, Nielsen MB. Synthesis of redox-active donor/acceptor chromophores with a central indenofluorene or indacenodithiophene core. Tetrahedron Letters. 2020 jun. 1;61(23). 151939. https://doi.org/10.1016/j.tetlet.2020.151939

Author

Andersen, Dianna ; Nygaard, David Bo ; Kragh, Rasmus Refsgaard ; Broløs, Line ; Nielsen, Mogens Brøndsted. / Synthesis of redox-active donor/acceptor chromophores with a central indenofluorene or indacenodithiophene core. I: Tetrahedron Letters. 2020 ; Bind 61, Nr. 23.

Bibtex

@article{5ad45cf531ee4da1ad7595a9bc6a4a98,
title = "Synthesis of redox-active donor/acceptor chromophores with a central indenofluorene or indacenodithiophene core",
abstract = "Tetrathiafulvalene (TTF) and tetracyanoquinodimethane (TCNQ) are classical redox-active molecules that can be oxidized and reduced, respectively, in two one-electron steps. Herein we present the synthesis of a selection of extended derivatives based on either an indenofluorene or indacenodithiophene core and containing either two dithiafulvene units (extended TTF), two dicyanomethylene units (extended TCNQ) or one of each of these units (donor–acceptor system). The optical and redox properties of the molecules are also presented.",
author = "Dianna Andersen and Nygaard, {David Bo} and Kragh, {Rasmus Refsgaard} and Line Brol{\o}s and Nielsen, {Mogens Br{\o}ndsted}",
year = "2020",
month = jun,
day = "1",
doi = "10.1016/j.tetlet.2020.151939",
language = "English",
volume = "61",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Pergamon Press",
number = "23",

}

RIS

TY - JOUR

T1 - Synthesis of redox-active donor/acceptor chromophores with a central indenofluorene or indacenodithiophene core

AU - Andersen, Dianna

AU - Nygaard, David Bo

AU - Kragh, Rasmus Refsgaard

AU - Broløs, Line

AU - Nielsen, Mogens Brøndsted

PY - 2020/6/1

Y1 - 2020/6/1

N2 - Tetrathiafulvalene (TTF) and tetracyanoquinodimethane (TCNQ) are classical redox-active molecules that can be oxidized and reduced, respectively, in two one-electron steps. Herein we present the synthesis of a selection of extended derivatives based on either an indenofluorene or indacenodithiophene core and containing either two dithiafulvene units (extended TTF), two dicyanomethylene units (extended TCNQ) or one of each of these units (donor–acceptor system). The optical and redox properties of the molecules are also presented.

AB - Tetrathiafulvalene (TTF) and tetracyanoquinodimethane (TCNQ) are classical redox-active molecules that can be oxidized and reduced, respectively, in two one-electron steps. Herein we present the synthesis of a selection of extended derivatives based on either an indenofluorene or indacenodithiophene core and containing either two dithiafulvene units (extended TTF), two dicyanomethylene units (extended TCNQ) or one of each of these units (donor–acceptor system). The optical and redox properties of the molecules are also presented.

U2 - 10.1016/j.tetlet.2020.151939

DO - 10.1016/j.tetlet.2020.151939

M3 - Journal article

VL - 61

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 23

M1 - 151939

ER -

ID: 242663118