Evidence map›Paper›PMID 33219724›Full record

ArticleChemphyschem : a European journal of chemical physics and physical chemistry2021

Deciphering the Electronic Transitions of Thiophene-Based Donor-Acceptor-Donor Pentameric Ligands Utilized for Multimodal Fluorescence Microscopy of Protein Aggregates.

Camilla Gustafsson, Hamid Shirani, Petter Leira, Dirk R Rehn, Mathieu Linares, K Peter R Nilsson, Patrick Norman, Mikael Lindgren

Open access · hybridAbstract read
In one paragraph

Article in Chemphyschem : a European journal of chemical physics and physical chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
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  5. Article
  6. Review
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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

8 authors at 3 institutions in 2 countries.

Camilla GustafssonDepartment of Theoretical Chemistry and Biology, School of Engineering Sciences in Chemistry, Biotechnology and Health KTH Royal Institute of Technology, 106 91, Stockholm, Sweden.
Hamid ShiraniDivision of Chemistry, Department of Physics, Chemistry and Biology Linköping University, 581 83, Linköping, Sweden.
Petter LeiraDepartment of Physics-Faculty of Natural Sciences, Norwegian University of Science and Technology (NTNU), 7491, Trondheim, Norway.
Dirk R RehnDepartment of Theoretical Chemistry and Biology, School of Engineering Sciences in Chemistry, Biotechnology and Health KTH Royal Institute of Technology, 106 91, Stockholm, Sweden.
Mathieu LinaresDepartment of Theoretical Chemistry and Biology, School of Engineering Sciences in Chemistry, Biotechnology and Health KTH Royal Institute of Technology, 106 91, Stockholm, Sweden.
K Peter R NilssonDivision of Chemistry, Department of Physics, Chemistry and Biology Linköping University, 581 83, Linköping, Sweden.
Patrick NormanDepartment of Theoretical Chemistry and Biology, School of Engineering Sciences in Chemistry, Biotechnology and Health KTH Royal Institute of Technology, 106 91, Stockholm, Sweden.
Mikael LindgrenDepartment of Physics-Faculty of Natural Sciences, Norwegian University of Science and Technology (NTNU), 7491, Trondheim, Norway.ORCID 0000-0001-6649-7871
KTH Royal Institute of Technology · SELinköping University · SENorwegian University of Science and Technology · NO

Funding

Swedish National Infrastructure (SNIC)Swedish Research Council 2016-00748 (KPRN)Swedish Research Council 2018-4343 (PN)
6 · The paper itself

Abstract

Anionic pentameric thiophene acetates can be used for fluorescence detection and diagnosis of protein amyloid aggregates. Replacing the central thiophene unit by benzothiadiazole (BTD) or quinoxaline (QX) leads to large emission shifts and basic spectral features have been reported [Chem. Eur. J. 2015, 21, 15133-13137]. Here we present new detailed experimental results of solvent effects, time-resolved fluorescence and examples employing multi-photon microscopy and lifetime imaging. Quantum chemical response calculations elucidate how the introduction of the BTD/QX groups changes the electronic states and emissions. The dramatic red-shift follows an increased conjugation and quinoid character of the π-electrons of the thiophene backbone. An efficient charge transfer in the excited states S

Indexed as

ElectronsLigandsMicroscopy, FluorescenceProteinsThiophenesLigandsProteinsThiophenesamyloid detectionfluorescent biomarkersluminescent conjugated oligothiophenessolvent effectsspectroscopy calculations

Identifiers

PMID33219724
PMCPMC7898931
OpenAlexW3005480313

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.