Naphthalimide‐Hydroxyquinoline Conjugates for Discriminative Detection of Nitro Aromatic Compounds in Aqueous Medium and Soil Sample. Issue 16 (22nd April 2022)
- Record Type:
- Journal Article
- Title:
- Naphthalimide‐Hydroxyquinoline Conjugates for Discriminative Detection of Nitro Aromatic Compounds in Aqueous Medium and Soil Sample. Issue 16 (22nd April 2022)
- Main Title:
- Naphthalimide‐Hydroxyquinoline Conjugates for Discriminative Detection of Nitro Aromatic Compounds in Aqueous Medium and Soil Sample
- Authors:
- Singh, Prabhpreet
Sharma, Ananay
Kumar, Sanjeev - Abstract:
- Abstract: Naphthalimide‐hydroxyquinoline based conjugates (NQ1 and NQ2 ) were synthesized for the detection of nitroaromatics in HEPES buffer/DMSO (9/1, v/v, pH=7.4) and Fe 3+ /Pd 2+ in CH3 CN solvent. The NQ1 and NQ2 were characterized using NMR ( 1 H, 13 C, COSY) and IR spectroscopies. Theoretical studies revealed that 8‐HQ moiety in NQ1 and NQ2 placed at orthogonal position with respect to naphthalimide core to minimize steric crowding. The energy gap between HOMO and LUMO for NQ1 and NQ2 were found to be −3.1 eV. The emission spectrum of NQ1 and NQ2 showed decrease in the emission intensity at 450 nm upon addition of picric acid (PA) and trinitrotoluene (TNT) whereas addition of 2‐nitroaniline caused quenching with concomitant red‐shift of the emission band in 90 % HEPES buffer‐DMSO. The detection limit of NQ1 for PA, TNT and 2‐NA detection was calculated as 8.7×10 −6 M, 2.2×10 −5 M and 1.8×10 −5 M. The complexation of NQ1 with PA, TNT and 2‐NA was further supported by Job's plot, dynamic light scattering studies and NMR titrations. We successfully utilized NQ1 and NQ2 for the detection of PA, TNT and 2‐NA in real soil samples with excellent recovery. NQ1 also showed quenching of the emission intensity at 450 nm upon addition of Fe 3+ and Pd 2+ ions in CH3 CN. Thus, NQ1 showed solvent‐dependent dual chemosensor type behavior. The functioning of NOR gate has been achieved using Fe 3+ /NACs with NQ1 . Abstract : 1, 8‐Naphthalimide appended with hydroxyquinoline showedAbstract: Naphthalimide‐hydroxyquinoline based conjugates (NQ1 and NQ2 ) were synthesized for the detection of nitroaromatics in HEPES buffer/DMSO (9/1, v/v, pH=7.4) and Fe 3+ /Pd 2+ in CH3 CN solvent. The NQ1 and NQ2 were characterized using NMR ( 1 H, 13 C, COSY) and IR spectroscopies. Theoretical studies revealed that 8‐HQ moiety in NQ1 and NQ2 placed at orthogonal position with respect to naphthalimide core to minimize steric crowding. The energy gap between HOMO and LUMO for NQ1 and NQ2 were found to be −3.1 eV. The emission spectrum of NQ1 and NQ2 showed decrease in the emission intensity at 450 nm upon addition of picric acid (PA) and trinitrotoluene (TNT) whereas addition of 2‐nitroaniline caused quenching with concomitant red‐shift of the emission band in 90 % HEPES buffer‐DMSO. The detection limit of NQ1 for PA, TNT and 2‐NA detection was calculated as 8.7×10 −6 M, 2.2×10 −5 M and 1.8×10 −5 M. The complexation of NQ1 with PA, TNT and 2‐NA was further supported by Job's plot, dynamic light scattering studies and NMR titrations. We successfully utilized NQ1 and NQ2 for the detection of PA, TNT and 2‐NA in real soil samples with excellent recovery. NQ1 also showed quenching of the emission intensity at 450 nm upon addition of Fe 3+ and Pd 2+ ions in CH3 CN. Thus, NQ1 showed solvent‐dependent dual chemosensor type behavior. The functioning of NOR gate has been achieved using Fe 3+ /NACs with NQ1 . Abstract : 1, 8‐Naphthalimide appended with hydroxyquinoline showed discriminative detection of NACs with quenching of fluorescence at 450 nm with PA, TNT and quenching along with concomitant red‐shift with 2‐NA in 90 % buffer. NQ1 can be used for the detection of NACs in real soil samples with excellent recovery. NQ1 showed solvent‐dependent dual chemosensor type behavior with quenching of fluorescence with Pd 2+ and Fe 3+ ions in CH3 CN. … (more)
- Is Part Of:
- ChemistrySelect. Volume 7:Issue 16(2022)
- Journal:
- ChemistrySelect
- Issue:
- Volume 7:Issue 16(2022)
- Issue Display:
- Volume 7, Issue 16 (2022)
- Year:
- 2022
- Volume:
- 7
- Issue:
- 16
- Issue Sort Value:
- 2022-0007-0016-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-04-22
- Subjects:
- Fluorescence -- Naphthalimide -- Picric acid -- Sensors -- Supramolecular chemistry
Chemistry -- Periodicals
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2365-6549 ↗ - DOI:
- 10.1002/slct.202200126 ↗
- Languages:
- English
- ISSNs:
- 2365-6549
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.241000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21324.xml