Evidence map›Paper›PMID 31172327›Full record

ArticleJournal of fluorescence2019

Chlorine (Cl) - Substituted Carbazole Based A-π-D-π-a Push-Pull Chromophores as Aggregation Enhanced Emission (AEE) Active Viscosity Sensors: Synthesis, DFT and NLO Approach.

Prerana K M Lokhande, Dinesh S Patil, Mayuri Kadam, Nagaiyan Sekar

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Article in Journal of fluorescence, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Prerana K M LokhandeDepartment of Dyestuff Technology, Institute of Chemical Technology, Matunga, Mumbai, 400 019, India.
Dinesh S PatilDepartment of Dyestuff Technology, Institute of Chemical Technology, Matunga, Mumbai, 400 019, India.
Mayuri KadamDepartment of Dyestuff Technology, Institute of Chemical Technology, Matunga, Mumbai, 400 019, India.
Nagaiyan SekarDepartment of Dyestuff Technology, Institute of Chemical Technology, Matunga, Mumbai, 400 019, India. n.sekar@ictmumbai.edu.in.ORCID http://orcid.org/0000-0001-7568-5129

Funding

University Grants Commission UGC CAS SAP
6 · The paper itself

Abstract

Three new carbazole functionalized A-π-D-π-A extended chromophores 4a, 4b and 4c comprising of different chemical functional groups on C=C bond with the assistance of chlorovinylene group in π-conjugation are synthesized and investigated spectroscopically. We have investigated the effect of different electron acceptors - carboxycyanomethylene, dicyanomethylene and 2-(benzothiazol-2-yl) cyanomethylene, the effect of the insertion of chlorine in π-conjugation on photophysical properties and the effect of double acceptors. The chromophores 4a, 4b and 4c exhibited positive solvatochromism with large Stokes shifts and bright orange to red solid-state fluorescence. Amongst all the three compounds 4c exhibited maximum emission wavelength at 615 nm in DMSO. They presented characteristic twisted intramolecular charge transfer (TICT) emission. Observations exhibited that 4c containing long hexyl group in donor unit and 2-(benzothiazol-2-yl) cyanomethylene as an acceptor group formed an aggregate in the mixture of solvents and exhibited better aggregation enhanced emission (AEE) compared to the other two derivatives. Amongst the three styryls, 4c showed the highest emission intensity 299 a.u. at 90% water:DMF fraction (f

Indexed as

AEEDFTExtended styrylFMRNLOSolvatochromism

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