Evidence map›Paper›PMID 35519334›Full record

ArticleRSC advances2019

The enhancement of the D-A effect of an asymmetric Schiff base by introducing acetyl groups into diaminomaleonitrile: synthesis, red fluorescence and crystal structure.

Ke Wang, Hao Su, Pengfei Wang, Wenjie Wang, Hui Li

Abstract read
In one paragraph

Article in RSC advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Ke WangKey Laboratory of Cluster Science of Ministry of Education, School of Chemistry and Chemical Engineering, Beijing Institute of Technology Beijing 100081 P. R. China lihui@bit.edu.cn.
Hao SuKey Laboratory of Cluster Science of Ministry of Education, School of Chemistry and Chemical Engineering, Beijing Institute of Technology Beijing 100081 P. R. China lihui@bit.edu.cn.
Pengfei WangKey Laboratory of Cluster Science of Ministry of Education, School of Chemistry and Chemical Engineering, Beijing Institute of Technology Beijing 100081 P. R. China lihui@bit.edu.cn.
Wenjie WangKey Laboratory of Cluster Science of Ministry of Education, School of Chemistry and Chemical Engineering, Beijing Institute of Technology Beijing 100081 P. R. China lihui@bit.edu.cn.
Hui LiKey Laboratory of Cluster Science of Ministry of Education, School of Chemistry and Chemical Engineering, Beijing Institute of Technology Beijing 100081 P. R. China lihui@bit.edu.cn.ORCID https://orcid.org/0000-0001-7459-6618

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An asymmetrical salen-type organic ligand was designed and synthesized by a new strategy developed using a precursor Ac-DMN, which is a diaminomaleonitrile (DMN) incorporated with an acetyl group. In this study, two types of asymmetrical ligands, namely Ac-DMN-salicylaldehyde (L

Identifiers

PMID35519334
PMCPMC9063999

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.