Evidence map›Paper›PMID 33231590›Full record

ArticleChemical communications (Cambridge, England)2020

Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores.

Dominik Göbel, Pascal Rusch, Daniel Duvinage, Nadja C Bigall, Boris J Nachtsheim

Abstract read
In one paragraph

Article in Chemical communications (Cambridge, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

5 authors.

Dominik GöbelInstitute for Organic and Analytical Chemistry, University of Bremen, Leobener Straße NW2, D-28359 Bremen, Germany. nachtsheim@uni-bremen.de.
Pascal RuschLeibniz University Hannover, Institute of Physical Chemistry and Electrochemistry, Callinstraße 3a, D-30167 Hannover, Germany. nadja.bigall@pci.uni-hannover.de.
Daniel DuvinageInstitute for Inorganic and Crystallographic Chemistry, University of Bremen, Leobener Straße NW2, D-28359 Bremen, Germany.ORCID http://orcid.org/0000-0002-9387-7172
Nadja C BigallLeibniz University Hannover, Institute of Physical Chemistry and Electrochemistry, Callinstraße 3a, D-30167 Hannover, Germany. nadja.bigall@pci.uni-hannover.de.ORCID http://orcid.org/0000-0003-0171-1106
Boris J NachtsheimInstitute for Organic and Analytical Chemistry, University of Bremen, Leobener Straße NW2, D-28359 Bremen, Germany. nachtsheim@uni-bremen.de.ORCID http://orcid.org/0000-0002-3759-2770

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxazolinyl- and arylchalcogenazolyl-substituted hydroxyfluorenes exhibiting excited-state intramolecular proton transfer (ESIPT) are described as potent and highly modular luminophores. Emission color tuning was achieved by varying the π-expansion and the insertion of different chalcogen atoms.

Identifiers

PMID33231590
PMCPMC8517962

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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.