Evidence map›Paper›PMID 38307994›Full record

ArticleNature chemistry2024

Ultrafast electronic relaxation pathways of the molecular photoswitch quadricyclane.

Kurtis D Borne, Joseph C Cooper, Michael N R Ashfold, Julien Bachmann, Surjendu Bhattacharyya, Rebecca Boll, Matteo Bonanomi, Michael Bosch, Carlo Callegari, Martin Centurion and 31 more

Abstract read
In one paragraph

Article in Nature chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. DONKEY: A Flexible and Accurate Algorithm for Clustering.Journal of chemical theory and computation · 2025
    Article
  13. Article
  14. Article
  15. Article
  16. Article
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

41 authors.

Kurtis D Borne *J.R. Macdonald Laboratory, Department of Physics, Kansas State University, Manhattan, KS, USA.
Joseph C Cooper *Physical and Theoretical Chemistry Laboratory, Department of Chemistry, University of Oxford, Oxford, UK.
Michael N R AshfoldSchool of Chemistry, Cantocks Close, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0001-5762-7048
Julien BachmannChemistry of Thin Film Materials, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.ORCID http://orcid.org/0000-0001-6480-6212
Surjendu BhattacharyyaJ.R. Macdonald Laboratory, Department of Physics, Kansas State University, Manhattan, KS, USA.
Rebecca BollEuropean XFEL, Schenefeld, Germany.ORCID http://orcid.org/0000-0001-6286-4064
Matteo BonanomiIstituto di Fotonica e Nanotecnologie (CNR-IFN), CNR, Milano, Italy.
Michael BoschChemistry of Thin Film Materials, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.ORCID http://orcid.org/0000-0003-0837-8780
Carlo CallegariElettra - Sincrotrone Trieste S.C.p.A., Trieste, Italy.ORCID http://orcid.org/0000-0001-5491-7752
Martin CenturionDepartment of Physics and Astronomy, University of Nebraska-Lincoln, Lincoln, NE, USA.ORCID http://orcid.org/0000-0002-5662-2293
Marcello CorenoElettra - Sincrotrone Trieste S.C.p.A., Trieste, Italy.
Basile F E CurchodSchool of Chemistry, Cantocks Close, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0002-1705-473X
Miltcho B DanailovElettra - Sincrotrone Trieste S.C.p.A., Trieste, Italy.
Alexander DemidovichElettra - Sincrotrone Trieste S.C.p.A., Trieste, Italy.ORCID http://orcid.org/0000-0003-2355-2257
Michele Di FraiaElettra - Sincrotrone Trieste S.C.p.A., Trieste, Italy.ORCID http://orcid.org/0000-0001-8102-0799
Benjamin ErkDeutsches Elektronen-Synchrotron DESY, Hamburg, Germany.ORCID http://orcid.org/0000-0001-8413-3588
Davide FaccialàIstituto di Fotonica e Nanotecnologie (CNR-IFN), CNR, Milano, Italy.ORCID http://orcid.org/0000-0002-5072-0394
Raimund FeifelDepartment of Physics, University of Gothenburg, Gothenburg, Sweden.ORCID http://orcid.org/0000-0001-5234-3935
Ruaridh J G ForbesLinac Coherent Light Source, SLAC National Accelerator Laboratory, Menlo Park, CA, USA.ORCID http://orcid.org/0000-0003-2097-5991
Christopher S HansenSchool of Chemistry, University of New South Wales, Sydney, New South Wales, Australia.ORCID http://orcid.org/0000-0002-8954-0825
David M P HollandDaresbury Laboratory, Warrington, UK.ORCID http://orcid.org/0000-0003-1351-605X
Rebecca A IngleDepartment of Chemistry, University College London, London, UK.ORCID http://orcid.org/0000-0002-0566-3407
Roland LindhDepartment of Chemistry - BMC, Uppsala University, Uppsala, Sweden.ORCID http://orcid.org/0000-0001-7567-8295
Lingyu MaDepartment of Chemistry, Brown University, Providence, RI, USA.
Henry G McGheeDepartment of Chemistry, University College London, London, UK.
Sri Bhavya MuvvaDepartment of Physics and Astronomy, University of Nebraska-Lincoln, Lincoln, NE, USA.ORCID http://orcid.org/0000-0002-1051-019X
Joao Pedro Figueira NunesDepartment of Physics and Astronomy, University of Nebraska-Lincoln, Lincoln, NE, USA.ORCID http://orcid.org/0000-0003-0670-6023
Asami OdateDepartment of Chemistry, Brown University, Providence, RI, USA.
Shashank PathakJ.R. Macdonald Laboratory, Department of Physics, Kansas State University, Manhattan, KS, USA.ORCID http://orcid.org/0000-0002-7916-0191
Oksana PlekanElettra - Sincrotrone Trieste S.C.p.A., Trieste, Italy.
Kevin C PrinceElettra - Sincrotrone Trieste S.C.p.A., Trieste, Italy.ORCID http://orcid.org/0000-0002-5416-7354
Primoz RebernikElettra - Sincrotrone Trieste S.C.p.A., Trieste, Italy.
Arnaud RouzéeMax-Born-Institut, Berlin, Germany.
Artem RudenkoJ.R. Macdonald Laboratory, Department of Physics, Kansas State University, Manhattan, KS, USA.ORCID http://orcid.org/0000-0002-9154-8463
Alberto SimoncigElettra - Sincrotrone Trieste S.C.p.A., Trieste, Italy.
Richard J SquibbDepartment of Physics, University of Gothenburg, Gothenburg, Sweden.
Anbu Selvam VenkatachalamJ.R. Macdonald Laboratory, Department of Physics, Kansas State University, Manhattan, KS, USA.
Caterina VozziIstituto di Fotonica e Nanotecnologie (CNR-IFN), CNR, Milano, Italy.ORCID http://orcid.org/0000-0002-0212-0191
Peter M WeberDepartment of Chemistry, Brown University, Providence, RI, USA.ORCID http://orcid.org/0000-0003-3017-336X
Adam KirranderPhysical and Theoretical Chemistry Laboratory, Department of Chemistry, University of Oxford, Oxford, UK. adam.kirrander@chem.ox.ac.uk.ORCID http://orcid.org/0000-0002-3347-8137
Daniel RollesJ.R. Macdonald Laboratory, Department of Physics, Kansas State University, Manhattan, KS, USA. rolles@phys.ksu.edu.ORCID http://orcid.org/0000-0002-3965-3477

Funding

Department of Education and Training | Australian Research Council (ARC) DE200100549Deutsche Forschungsgemeinschaft (German Research Foundation) 392607742DOE | SC | Basic Energy Sciences (BES) DE-AC02-76SF00515DOE | SC | Chemical Sciences, Geosciences, and Biosciences Division (Chemical Sciences, Geosciences, and Energy Biosciences) DE-FG02-86ER13491DOE | SC | Chemical Sciences, Geosciences, and Biosciences Division (Chemical Sciences, Geosciences, and Energy Biosciences) DE-SC0020276EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 803718Leverhulme Trust RPG-2020-208National Science Foundation (NSF) PHYS-1753324RCUK | Engineering and Physical Sciences Research Council (EPSRC) EP/V006819RCUK | Engineering and Physical Sciences Research Council (EPSRC) EP/V049240Royal Society RGS/R2/202009Vetenskapsrådet (Swedish Research Council) 2020-03182
6 · The paper itself

Abstract

The light-induced ultrafast switching between molecular isomers norbornadiene and quadricyclane can reversibly store and release a substantial amount of chemical energy. Prior work observed signatures of ultrafast molecular dynamics in both isomers upon ultraviolet excitation but could not follow the electronic relaxation all the way back to the ground state experimentally. Here we study the electronic relaxation of quadricyclane after exciting in the ultraviolet (201 nanometres) using time-resolved gas-phase extreme ultraviolet photoelectron spectroscopy combined with non-adiabatic molecular dynamics simulations. We identify two competing pathways by which electronically excited quadricyclane molecules relax to the electronic ground state. The fast pathway (<100 femtoseconds) is distinguished by effective coupling to valence electronic states, while the slow pathway involves initial motions across Rydberg states and takes several hundred femtoseconds. Both pathways facilitate interconversion between the two isomers, albeit on different timescales, and we predict that the branching ratio of norbornadiene/quadricyclane products immediately after returning to the electronic ground state is approximately 3:2.

Identifiers

PMID38307994
PMCPMC10997510

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.