Literature DB >> 33488226

A novel selective fluorescent chemosensor for Fe 3+ ions based on phthalonitrile dimer: synthesis, analysis, and theoretical studies.

Shaya Al-Raqa1, İpek ÖmeroĞlu2, Doğan Erbahar3, Mahmut DurmuŞ2.   

Abstract

Phenyl-4,4-di(3,6-dibutoxyphthalonitrile) ( 3 ) was synthesized by the reaction of 1,4-phenylenebisboronic acid ( 1 ) and 4-bromo-3,6-dibutoxyphthalonitrile ( 2 ), using Suzuki cross-coupling reaction. The newly synthesized compound ( 3 ) was characterized by FT-IR, MALDI-MS, ESI-MS, 1 H-NMR, 13 C-NMR, and 13 C-DEPT-135-NMR. The fluorescence property of phenyl-4,4-di(3,6-dibutoxyphthalonitrile) ( 3 ) towards various metal ions was investigated by fluorescence spectroscopy, and it was observed thatthe compound ( 3 ) displayed a significantly 'turn-off' response to Fe 3+ , which was referred to 1:2 complex formation between ligand ( 3 ) and Fe 3+ . The compound was also studied via density functional theory calculations revealing the interaction mechanism of the molecule with Fe 3+ ions.
Copyright © 2020 The Author(s).

Entities:  

Keywords:  Fe 3+ ion ; Phthalonitrile; Suzuki cross-coupling; chemosensor; fluorescence

Year:  2020        PMID: 33488226      PMCID: PMC7751899          DOI: 10.3906/kim-2004-68

Source DB:  PubMed          Journal:  Turk J Chem        ISSN: 1300-0527            Impact factor:   1.239


  13 in total

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5.  Phthalocyaninodehydroannulenes.

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9.  Carbon Quantum Dots as Fluorescence Turn-Off-On Probe for Detecting Fe3+ and Ascorbic Acid.

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10.  Acridine-based fluorescence chemosensors for selective sensing of Fe3+ and Ni2+ ions.

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