Evidence map›Paper›PMID 36557805›Full record

ArticleMolecules (Basel, Switzerland)2022

Donor-Acceptor Dyads and Triads Employing Core-Substituted Naphthalene Diimides: A Synthetic and Spectro (Electrochemical) Study.

Samuel Quinn, E Stephen Davies, Nicholas Pearce, Callum Rosenberg, Constance R Pfeiffer, Georgia R F Orton, Neil R Champness

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Samuel QuinnSchool of Chemistry, University of Nottingham, University Park, Nottingham NG7 2RD, UK.
E Stephen DaviesSchool of Chemistry, University of Nottingham, University Park, Nottingham NG7 2RD, UK.
Nicholas PearceSchool of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.ORCID 0000-0002-5463-9577
Callum RosenbergSchool of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.ORCID 0000-0002-8632-2371
Constance R PfeifferSchool of Chemistry, University of Nottingham, University Park, Nottingham NG7 2RD, UK.
Georgia R F OrtonSchool of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.
Neil R ChampnessSchool of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.ORCID 0000-0003-2970-1487

Funding

Engineering and Physical Sciences Research Council EP/S002995/2
6 · The paper itself

Abstract

Donor-acceptor dyads and triads comprising core-substituted naphthalene diimide (NDI) chromophores and either phenothiazine or phenoxazine donors are described. Synthesis combined with electrochemical and spectroelectrochemical investigations facilitates characterisation of the various redox states of these molecules, confirming the ability to combine arrays of electron donating and accepting moieties into single species that retain the redox properties of these individual moieties.

Indexed as

electrochemistrynaphthalene diimidephenothiazinephenoxazinespectroelectrochemistry

Identifiers

PMID36557805
PMCPMC9783862

What OpenQuestion holds

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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.