Philipp
Dierks
a,
Ayla
Kruse
b,
Olga S.
Bokareva
bc,
Mohammed J.
Al-Marri
bd,
Jens
Kalmbach
e,
Marc
Baltrun
a,
Adam
Neuba
a,
Roland
Schoch
a,
Stephan
Hohloch
f,
Katja
Heinze
g,
Michael
Seitz
e,
Oliver
Kühn
b,
Stefan
Lochbrunner
b and
Matthias
Bauer
*a
aFaculty of Science, Chemistry Department and Centre for Sustainable Systems Design, Paderborn University, 33098 Paderborn, Germany. E-mail: matthias.bauer@upb.de
bInstitute of Physics and Department of Life, Light and Matter, University of Rostock, 18051 Rostock, Germany
cDepartment of Physical Chemistry, Kazan Federal University, 420008 Kazan, Russia
dCollege of Engineering, Qatar University, P.O. Box 2713, Doha, Qatar
eInstitute of Inorganic Chemistry, University of Tübingen, Auf der Morgenstelle 18, 72076 Tübingen, Germany
fUniversity of Innsbruck, Faculty of Chemistry and Pharmacy, Institute for General, Inorganic and Theoretical Chemistry, Innrain 80-82, Innsbruck 6020, Austria
gDepartment of Chemistry, Johannes Gutenberg, University of Mainz, 55128 Mainz, Germany
First published on 23rd February 2023
Correction for ‘Distinct photodynamics of κ-N and κ-C pseudoisomeric iron(II) complexes’ by Philipp Dierks et al., Chem. Commun., 2021, 57, 6640–6643, https://doi.org/10.1039/D1CC01716K.
It was originally reported that the complex Fe1 sensitizes the formation of 1O2 with high energy excitation, however it has subsequently been found out by careful optical experiments (emission, excitation) that this reaction is not caused by the complex itself, but a minor fraction of another (luminescent) species, possibly derived from dissociated ligand. This does not affect the overall conclusions of the original article.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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