Evidence map›Paper›PMID 27530631›Full record

ArticleJournal of fluorescence2016

Indole-Based NLOphoric Donor-π-Acceptor Styryl Dyes: Synthesis, Spectral Properties and Computational Studies.

Santosh Chemate, Nagaiyan Sekar

Abstract read
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In one paragraph

Article in Journal of fluorescence, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

2 authors.

Santosh ChemateDepartment of Dyestuff Technology, Institute of Chemical Technology, Mumbai, 400 019, India.
Nagaiyan SekarDepartment of Dyestuff Technology, Institute of Chemical Technology, Mumbai, 400 019, India. n.sekar@ictmumbai.edu.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Donor-π- acceptor styryl chromophores based on indole core were synthesized by Knoevenagel condensation of N-ethyl indole-3-carbaldehyde and different active methylene compounds. The absorption and emission properties of these dyes in different solvents were studied. The dyes displayed a broad absorption maximum in the UV and visible region between 397 and 469 nm with FWHM, 50 to 75 nm. Due to the extended π - conjugated systems this styryl chromophores shows strong intramolecular charge transfer characteristics. The dyes showed solid state emission and emission in solid state was red shifted as compared to their emission in less polar solvents. Density Functional Theory [B3LYP/6-311 + G(d)] computations were used to correlate the structural, molecular, electronic and photo physical parameters of styryl dye with experimental study. Synthesized dyes were confirmed by using FT-IR,

Indexed as

DFTIndole-3-carbaldehydeSolid state fluorescenceStyryl

Identifiers

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Registered trials

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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.