Evidence map›Paper›PMID 28553466›Full record

ArticleChemical science2015

Ultrafast delocalization of excitation in synthetic light-harvesting nanorings.

Chaw-Keong Yong, Patrick Parkinson, Dmitry V Kondratuk, Wei-Hsin Chen, Andrew Stannard, Alex Summerfield, Johannes K Sprafke, Melanie C O'Sullivan, Peter H Beton, Harry L Anderson and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Chemical science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
11.2field-weighted citation impact, top 1% of its field
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

29 citing papers in PubMed, 109 citations in OpenAlex.

  1. Article
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  7. A porphyrin pentamer as a bright emitter for NIR OLEDs.Journal of materials chemistry. C · 2022
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  15. Tuning the Circumference of Six-Porphyrin Nanorings.Journal of the American Chemical Society · 2019
    Article
  16. Article
  17. Single-Acetylene Linked Porphyrin Nanorings.Journal of the American Chemical Society · 2017
    Article
  18. Article
  19. Article
  20. Synthesis of Five-Porphyrin Nanorings by Using Ferrocene and Corannulene Templates.Angewandte Chemie (International ed. in English) · 2016
    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

11 authors at 4 institutions in 2 countries.

Chaw-Keong YongUniversity of Oxford , Department of Physics , Clarendon Laboratory , Parks Road , Oxford , OX1 3PU , UK . Email: l.herz@physics.ox.ac.uk.
Patrick ParkinsonUniversity of Oxford , Department of Physics , Clarendon Laboratory , Parks Road , Oxford , OX1 3PU , UK . Email: l.herz@physics.ox.ac.uk.
Dmitry V KondratukUniversity of Oxford , Department of Chemistry , Chemistry Research Laboratory , Oxford , OX1 3TA , UK . Email: harry.anderson@chem.ox.ac.uk.
Wei-Hsin ChenUniversity of Oxford , Department of Physics , Clarendon Laboratory , Parks Road , Oxford , OX1 3PU , UK . Email: l.herz@physics.ox.ac.uk.
Andrew StannardSchool of Physics & Astronomy , University of Nottingham , Nottingham , NG7 2RD , UK.
Alex SummerfieldSchool of Physics & Astronomy , University of Nottingham , Nottingham , NG7 2RD , UK.
Johannes K SprafkeUniversity of Oxford , Department of Chemistry , Chemistry Research Laboratory , Oxford , OX1 3TA , UK . Email: harry.anderson@chem.ox.ac.uk.
Melanie C O'SullivanUniversity of Oxford , Department of Chemistry , Chemistry Research Laboratory , Oxford , OX1 3TA , UK . Email: harry.anderson@chem.ox.ac.uk.
Peter H BetonSchool of Physics & Astronomy , University of Nottingham , Nottingham , NG7 2RD , UK.
Harry L AndersonUniversity of Oxford , Department of Chemistry , Chemistry Research Laboratory , Oxford , OX1 3TA , UK . Email: harry.anderson@chem.ox.ac.uk.
Laura M HerzUniversity of Oxford , Department of Physics , Clarendon Laboratory , Parks Road , Oxford , OX1 3PU , UK . Email: l.herz@physics.ox.ac.uk.
University of Oxford · GBUniversity of Nottingham · GBScience Oxford · GBClarendon College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rings of chlorophyll molecules harvest sunlight remarkably efficiently during photosynthesis in purple bacteria. The key to their efficiency lies in their highly delocalized excited states that allow for ultrafast energy migration. Here we show that a family of synthetic nanorings mimic the ultrafast energy transfer and delocalization observed in nature. π-Conjugated nanorings with diameters of up to 10 nm, consisting of up to 24 porphyrin units, are found to exhibit excitation delocalization within the first 200 fs of light absorption. Transitions from the first singlet excited state of the circular nanorings are dipole-forbidden as a result of symmetry constraints, but these selection rules can be lifted through static and dynamic distortions of the rings. The increase in the radiative emission rate in the larger nanorings correlates with an increase in static disorder expected from Monte Carlo simulations. For highly symmetric rings, the radiative rate is found to increase with increasing temperature. Although this type of thermally activated superradiance has been theoretically predicted in circular chromophore arrays, it has not previously been observed in any natural or synthetic systems. As expected, the activation energy for emission increases when a nanoring is fixed in a circular conformation by coordination to a radial template. These nanorings offer extended chromophores with high excitation delocalization that is remarkably stable against thermally induced disorder. Such findings open new opportunities for exploring coherence effects in nanometer molecular rings and for implementing these biomimetic light-harvesters in man-made devices.

Identifiers

PMID28553466
PMCPMC5424671
OpenAlexW2121987600

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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.