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Tetraceno[2,1,12,11-opqra]tetracene-extended tetrathiafulvalene - redox-controlled generation of a large PAH core. / Broman, Søren Lindbæk; Andersen, Cecilie Lindholm; Jousselin-Oba, Tanguy; Mansø, Mads; Hammerich, Ole; Frigoli, Michel; Nielsen, Mogens Brøndsted.
I:
Organic & Biomolecular Chemistry, Bind 15, Nr. 4, 2017, s. 807-811.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Harvard
Broman, SL, Andersen, CL, Jousselin-Oba, T, Mansø, M
, Hammerich, O, Frigoli, M
& Nielsen, MB 2017, '
Tetraceno[2,1,12,11-opqra]tetracene-extended tetrathiafulvalene - redox-controlled generation of a large PAH core',
Organic & Biomolecular Chemistry, bind 15, nr. 4, s. 807-811.
https://doi.org/10.1039/c6ob02666dAPA
Broman, S. L., Andersen, C. L., Jousselin-Oba, T., Mansø, M.
, Hammerich, O., Frigoli, M.
, & Nielsen, M. B. (2017).
Tetraceno[2,1,12,11-opqra]tetracene-extended tetrathiafulvalene - redox-controlled generation of a large PAH core.
Organic & Biomolecular Chemistry,
15(4), 807-811.
https://doi.org/10.1039/c6ob02666dVancouver
Broman SL, Andersen CL, Jousselin-Oba T, Mansø M
, Hammerich O, Frigoli M o.a.
Tetraceno[2,1,12,11-opqra]tetracene-extended tetrathiafulvalene - redox-controlled generation of a large PAH core.
Organic & Biomolecular Chemistry. 2017;15(4):807-811.
https://doi.org/10.1039/c6ob02666dAuthor
Broman, Søren Lindbæk ; Andersen, Cecilie Lindholm ; Jousselin-Oba, Tanguy ; Mansø, Mads ; Hammerich, Ole ; Frigoli, Michel ; Nielsen, Mogens Brøndsted. / Tetraceno[2,1,12,11-opqra]tetracene-extended tetrathiafulvalene - redox-controlled generation of a large PAH core. I: Organic & Biomolecular Chemistry. 2017 ; Bind 15, Nr. 4. s. 807-811.
Bibtex
@article{dd0667d18ed94706a19e50ff9ed1dd51,
title = "Tetraceno[2,1,12,11-opqra]tetracene-extended tetrathiafulvalene - redox-controlled generation of a large PAH core",
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}",
year = "2017",
doi = "10.1039/c6ob02666d",
language = "English",
volume = "15",
pages = "807--811",
journal = "Organic & Biomolecular Chemistry",
issn = "1470-4358",
publisher = "Royal Society of Chemistry",
number = "4",
}
RIS
TY - JOUR
T1 - Tetraceno[2,1,12,11-opqra]tetracene-extended tetrathiafulvalene - redox-controlled generation of a large PAH core
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
C2 - 28054066
VL - 15
SP - 807
EP - 811
JO - Organic & Biomolecular Chemistry
JF - Organic & Biomolecular Chemistry
SN - 1470-4358
IS - 4
ER -
