Evidence map›Paper›PMID 37486560›Full record

ArticleJournal of fluorescence2024

Experimental and Theoretical Studies of Fluorescent "Turn Off" Sensor Functionalized With Carboxylic Acid and Naphthalene Group for Selective Detection of 2,4,6-Trinitrophenol.

Manpreet Kaur

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of fluorescence, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

Manpreet KaurDepartment of Chemistry, Punjabi University, Patiala, 147002, Punjab, India. kmanpreet1557@gmail.com.

Funding

UGC, NEW Delhi, India Nov-2017_106796
6 · The paper itself

Abstract

A fluorescent sensor, 5-((2-hydroxynaphthalen-1-yl)methyleneamino)benzene-1,3-dicarboxylic acid (coded as SB), containing both π-π interacting sites (such as π-electron-rich moieties) and hydrogen bonding (H-bonding) interacting sites (such as highly acidic protons) has been developed via high yield reflux method. It was characterized by the various analytical techniques such as Fourier transform-infrared spectroscopy (FT-IR), proton nuclear magnetic resonance (

Indexed as

2,4,6-trinitrophenolDFTFluorescent Schiff base sensorHydrogen bondingNitro explosives detectionPhoto-induced electron transferSpectral overlap

Identifiers

What OpenQuestion holds

Textmetadata
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.