Evidence map›Paper›PMID 37864613›Full record

ArticleJournal of fluorescence2024

Multicomponent Reaction Based Tolyl-substituted and Pyrene-Pyridine Conjugated Isomeric Ratiometric Fluorescent Probes: A Comparative Investigation of Photophysical and Hg(II)-Sensing Behaviors.

Raghvendra Niranjan, G Durga Prasad, Simi Achankunju, Mariyaraj Arockiaraj, Kotteswaran Velumani, Kiruthika Nachimuthu, Ashok K Sundramoorthy, Ishita Neogi, Jothi L Nallasivam, Venkatachalam Rajeshkumar and 1 more

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Article in Journal of fluorescence, 2024. 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
1.8field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 12 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors at 5 institutions in 1 country.

Raghvendra NiranjanDepartment of Chemistry, School of Sciences, National Institute of Technology Andhra Pradesh, Tadepalligudem, 534101, Andhra Pradesh, India.
G Durga PrasadDepartment of Chemistry, School of Sciences, National Institute of Technology Andhra Pradesh, Tadepalligudem, 534101, Andhra Pradesh, India.
Simi AchankunjuChemical Sciences and Technology Division, CSIR-NIIST, Thiruvananthapuram, 695019, Kerala, India.
Mariyaraj ArockiarajOrganic Synthesis & Catalysis Lab, Department of Chemistry, National Institute of Technology Warangal, Hanumakonda, 506004, Telangana, India.
Kotteswaran VelumaniCentre for Nano-Biosensors, Department of Prosthodontics, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Poonamallee High Road, Velappanchavadi, Chennai, 600077, Tamil Nadu, India.
Kiruthika NachimuthuDepartment of Chemistry, National Institute of Technology, Tiruchirappalli, 620015, Tamil Nadu, India.
Ashok K SundramoorthyCentre for Nano-Biosensors, Department of Prosthodontics, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Poonamallee High Road, Velappanchavadi, Chennai, 600077, Tamil Nadu, India.
Ishita NeogiChemical Sciences and Technology Division, CSIR-NIIST, Thiruvananthapuram, 695019, Kerala, India.
Jothi L NallasivamDepartment of Chemistry, National Institute of Technology, Tiruchirappalli, 620015, Tamil Nadu, India.
Venkatachalam RajeshkumarOrganic Synthesis & Catalysis Lab, Department of Chemistry, National Institute of Technology Warangal, Hanumakonda, 506004, Telangana, India.
Surendra H MahadevegowdaDepartment of Chemistry, School of Sciences, National Institute of Technology Andhra Pradesh, Tadepalligudem, 534101, Andhra Pradesh, India. surendra@nitandhra.ac.in.
National Institute of Technology Andhra Pradesh · INNational Institute for Interdisciplinary Science and Technology · INNational Institute of Technology Tiruchirappalli · INNational Institute of Technology Warangal · INSaveetha University · IN

Funding

National Institute of Technology Andhra Pradesh SEED grant No. NITAP/SD-G/19/2020
6 · The paper itself

Abstract

Herein, the synthesis of pyrene conjugated 2,6-di-ortho-tolylpyridine and 2,6-di-para-tolylpyridine structural isomers were achieved efficiently through multicomponent Chichibabin pyridine synthesis reaction. The DFT, TD-DFT and experimental investigations were carried out to investigate the photophysical behaviors of the synthesized novel pyrene-pyridine based isomeric probes. Our studies revealed that, due to the continuous conjugation of the pyrene, pyridine and tolyl moieties, the dihedral angles of the trisubstituents on the central pyridine moiety significantly influences the photophysical properties of the synthesized novel pyrene based fluorescent probes. Further, we have comparatively investigated the sensing behaviors of the synthesized tolyl-substituted isomeric ratiometric fluorescent probes with metal ions, our studies reveals that both the ortho and para tolyl ratiometric fluorescent probes have distinct photoemissive properties in selectively sensing of Hg

Indexed as

Hg2+ ionsIsomeric probesMulticomponent reactionNaked-eye detectionRatiometric fluorescent chemosensors

Identifiers

PMID37864613
OpenAlexW4387848079

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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.