Evidence map›Paper›PMID 29777157›Full record

ArticleNature communications2018

Transient metal-centered states mediate isomerization of a photochromic ruthenium-sulfoxide complex.

Amy A Cordones, Jae Hyuk Lee, Kiryong Hong, Hana Cho, Komal Garg, Martial Boggio-Pasqua, Jeffrey J Rack, Nils Huse, Robert W Schoenlein, Tae Kyu Kim

Abstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
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  7. Photocrystallography of [Ru(bpy)Chemical science · 2023
    Article
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  14. Chemical interactions and dynamics with femtosecond X-ray spectroscopy and the role of X-ray free-electron lasers.Philosophical transactions. Series A, Mathematical, physical, and engineering sciences · 2019
    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

10 authors.

Amy A CordonesPULSE Institute, SLAC National Accelerator Laboratory, Stanford University, Menlo Park, CA, 94025, USA.ORCID http://orcid.org/0000-0001-9897-5380
Jae Hyuk LeePohang Accelerator Laboratory, Pohang, 37673, Republic of Korea.
Kiryong HongCenter for Gas Analysis, Division of Chemical and Medical Metrology, Korea Research Institute of Standards and Science, Daejeon, 34113, Republic of Korea.ORCID http://orcid.org/0000-0002-3590-3635
Hana ChoCenter for Analytical Chemistry, Division of Chemical and Medical Metrology, Korea Research Institute of Standards and Science, Daejeon, 34113, Republic of Korea.
Komal GargNanoscale and Quantum Phenomena Institute, Department of Chemistry and Biochemistry, Ohio University, Athens, OH, 45701, USA.
Martial Boggio-PasquaLaboratoire de Chimie et Physique Quantiques, CNRS et Université de Toulouse, 118 route de Narbonne, UMR 5626, IRSAMC, Toulouse, 31062, France.ORCID http://orcid.org/0000-0001-6684-5223
Jeffrey J RackNanoscale and Quantum Phenomena Institute, Department of Chemistry and Biochemistry, Ohio University, Athens, OH, 45701, USA.
Nils HuseInstitute for Nanostructure and Solid State Physics, Department of Physics, University of Hamburg, Hamburg, 22761, Germany. nils.huse@uni-hamburg.de.ORCID http://orcid.org/0000-0002-3281-7600
Robert W SchoenleinPULSE Institute, SLAC National Accelerator Laboratory, Stanford University, Menlo Park, CA, 94025, USA. rwschoen@slac.stanford.edu.
Tae Kyu KimDepartment of Chemistry and Chemistry Institute of Functional Materials, Pusan National University, Busan, 46241, Republic of Korea. tkkim@pusan.ac.kr.ORCID http://orcid.org/0000-0002-9578-5722

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ultrafast isomerization reactions underpin many processes in (bio)chemical systems and molecular materials. Understanding the coupled evolution of atomic and molecular structure during isomerization is paramount for control and rational design in molecular science. Here we report transient X-ray absorption studies of the photo-induced linkage isomerization of a Ru-based photochromic molecule. X-ray spectra reveal the spin and valence charge of the Ru atom and provide experimental evidence that metal-centered excited states mediate isomerization. Complementary X-ray spectra of the functional ligand S atoms probe the nuclear structural rearrangements, highlighting the formation of two metal-centered states with different metal-ligand bonding. These results address an essential open question regarding the relative roles of transient charge-transfer and metal-centered states in mediating photoisomerization. Global temporal and spectral data analysis combined with time-dependent density functional theory reveals a complex mechanism for photoisomerization with atomic details of the transient molecular and electronic structure not accessible by other means.

Identifiers

PMID29777157
PMCPMC5959936

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Registered trials

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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.