Evidence map›Paper›PMID 38784753›Full record

ArticleChemical science2024

Influence of the substitution position on spin communication in photoexcited perylene-nitroxide dyads.

Philipp Thielert, Mélissa El Bitar Nehme, Maximilian Mayländer, Michael Franz, Simon L Zimmermann, Fabienne Fisch, Peter Gilch, Andreas Vargas Jentzsch, Michel Rickhaus, Sabine Richert

Abstract read
In one paragraph

Article in Chemical science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Philipp ThielertInstitute of Physical Chemistry, University of Freiburg Albertstraße 21 79104 Freiburg Germany sabine.richert@physchem.uni-freiburg.de.ORCID https://orcid.org/0009-0000-9364-7951
Mélissa El Bitar NehmeDepartment of Chemistry, University of Zurich Winterthurerstrasse 190 8057 Zurich Switzerland.
Maximilian MayländerInstitute of Physical Chemistry, University of Freiburg Albertstraße 21 79104 Freiburg Germany sabine.richert@physchem.uni-freiburg.de.ORCID https://orcid.org/0000-0002-2610-0195
Michael FranzInstitute of Physical Chemistry, University of Freiburg Albertstraße 21 79104 Freiburg Germany sabine.richert@physchem.uni-freiburg.de.ORCID https://orcid.org/0000-0002-9482-1920
Simon L ZimmermannInstitute of Physical Chemistry, Heinrich Heine University Düsseldorf Universitätsstraße 1 40225 Düsseldorf Germany.ORCID https://orcid.org/0009-0009-1404-7612
Fabienne FischDepartment of Chemistry, University of Zurich Winterthurerstrasse 190 8057 Zurich Switzerland.
Peter GilchInstitute of Physical Chemistry, Heinrich Heine University Düsseldorf Universitätsstraße 1 40225 Düsseldorf Germany.ORCID https://orcid.org/0000-0002-6602-9397
Andreas Vargas JentzschSAMS Research Group, Université de Strasbourg, CNRS, Institut Charles Sadron UPR 22 67000 Strasbourg France.ORCID https://orcid.org/0000-0003-1386-3174
Michel RickhausDepartment of Chemistry, University of Zurich Winterthurerstrasse 190 8057 Zurich Switzerland.ORCID https://orcid.org/0000-0002-6107-2310
Sabine RichertInstitute of Physical Chemistry, University of Freiburg Albertstraße 21 79104 Freiburg Germany sabine.richert@physchem.uni-freiburg.de.ORCID https://orcid.org/0000-0002-2990-974X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

By virtue of the modularity of their structures, their tunable optical and magnetic properties, and versatile applications, photogenerated triplet-radical systems provide an ideal platform for the study of the factors controlling spin communication in molecular frameworks. Typically, these compounds consist of an organic chromophore covalently attached to a stable radical. After formation of the chromophore triplet state by photoexcitation, two spin centres are present in the molecule that will interact. The nature of their interaction is governed by the magnitude of the exchange interaction between them and can be studied by making use of transient electron paramagnetic resonance (EPR) techniques. Here, we investigate three perylene-nitroxide dyads that only differ with respect to the position where the nitroxide radical is attached to the perylene core. The comparison of the results from transient UV-vis and EPR experiments reveals major differences in the excited state properties of the three dyads, notably their triplet state formation yield, excited state deactivation kinetics, and spin coherence times. Spectral simulations and quantum chemical calculations are used to rationalise these findings and demonstrate the importance of considering the structural flexibility and the contribution of rotational conformers for an accurate interpretation of the data.

Identifiers

PMID38784753
PMCPMC11110163

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.