Tetraceno[2,1,12,11-opqra]tetracene-extended tetrathiafulvalene - redox-controlled generation of a large PAH core

Søren Lindbæk Broman; Cecilie Lindholm Andersen; Tanguy Jousselin-Oba; Mads Mansø; Ole Hammerich; Michel Frigoli; Mogens Brøndsted Nielsen

doi:10.1039/c6ob02666d

Tetraceno[2,1,12,11-opqra]tetracene-extended tetrathiafulvalene - redox-controlled generation of a large PAH core

Søren Lindbæk Broman, Cecilie Lindholm Andersen, Tanguy Jousselin-Oba, Mads Mansø, Ole Hammerich, Michel Frigoli, Mogens Brøndsted Nielsen

Department of Chemistry

16 Citations (Scopus)

113 Downloads (Pure)

Abstract

Two tetraceno[2,1,12,11-opqra]tetracene-extended tetrathia-fulvalenes were prepared and found to undergo reversible conversion into their planar polycyclic aromatic hydrocarbons (PAHs) upon electrochemical oxidation – at potentials probing the best valence bond representations

Original language	English
Journal	Organic & Biomolecular Chemistry
Volume	15
Issue number	4
Pages (from-to)	807-811
Number of pages	5
ISSN	1477-0520
DOIs	https://doi.org/10.1039/c6ob02666d
Publication status	Published - 2017

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Tetraceno[2,1,12,11-opqra]tetracene-extended tetrathiafulvalene – redox-controlled generation of a large PAH coreFinal published version, 1.15 MBLicence: CC BY

Cite this

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abstract = "Two tetraceno[2,1,12,11-opqra]tetracene-extended tetrathia-fulvalenes were prepared and found to undergo reversible conversion into their planar polycyclic aromatic hydrocarbons (PAHs) upon electrochemical oxidation – at potentials probing the best valence bond representations",

author = "Broman, {S{\o}ren Lindb{\ae}k} and Andersen, {Cecilie Lindholm} and Tanguy Jousselin-Oba and Mads Mans{\o} and Ole Hammerich and Michel Frigoli and Nielsen, {Mogens Br{\o}ndsted}",

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AU - Broman, Søren Lindbæk

AU - Andersen, Cecilie Lindholm

AU - Jousselin-Oba, Tanguy

AU - Mansø, Mads

AU - Hammerich, Ole

AU - Frigoli, Michel

AU - Nielsen, Mogens Brøndsted

PY - 2017

Y1 - 2017

N2 - Two tetraceno[2,1,12,11-opqra]tetracene-extended tetrathia-fulvalenes were prepared and found to undergo reversible conversion into their planar polycyclic aromatic hydrocarbons (PAHs) upon electrochemical oxidation – at potentials probing the best valence bond representations

AB - Two tetraceno[2,1,12,11-opqra]tetracene-extended tetrathia-fulvalenes were prepared and found to undergo reversible conversion into their planar polycyclic aromatic hydrocarbons (PAHs) upon electrochemical oxidation – at potentials probing the best valence bond representations

U2 - 10.1039/c6ob02666d

DO - 10.1039/c6ob02666d

M3 - Journal article

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SN - 1470-4358

VL - 15

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EP - 811

JO - Journal of the Chemical Society, Perkin Transactions 1

JF - Journal of the Chemical Society, Perkin Transactions 1

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