A Novel Benzimidazole-Based Chemosensor for Fluorometric Determination of Zinc Ions DOI
Ersin Orhan, Ece Ergun, Koray Şarkaya

et al.

Journal of Fluorescence, Journal Year: 2021, Volume and Issue: 31(6), P. 1833 - 1842

Published: Sept. 14, 2021

Language: Английский

A Review on Thiazole Based Colorimetric and Fluorimetric Chemosensors for the Detection of Heavy Metal Ions DOI

Mohsen A. M. Alhamami,

Jari S. Algethami, Sikandar Khan

et al.

Critical Reviews in Analytical Chemistry, Journal Year: 2023, Volume and Issue: 54(8), P. 2689 - 2713

Published: April 8, 2023

Thiazole and its derivatives play an important role in biological non-biological fields due to several structural electronic behaviors associated with it. act as chemosensors because they formed metal complexes upon interacting various heavy ions like Cd2+, Co2+, Cr3+, Fe3+, Ag+, Al3+, Cu2+, Pd2+, Hg2+, Ni2+, Ga3+, In3+, Sn4+, Pb2+, Zn2+ well other cations. These are of prime importance from the environmental point view high. This review article focuses on thiazole-based colorimetric fluorometric sensor for recognition different cations specimens agricultural, biological, environmental. It also summarizes binding stoichiometry, detection limit, pH, structure, practical application reported chemosensors. Further, sensing performances, have been discussed compared some organic sensors.

Language: Английский

Citations

40

Organic heterocyclic-based colorimetric and fluorimetric chemosensors for the detection of different analytes: a review (from 2015 to 2022) DOI
Nawaf Bin Darwish,

A. Kurdi,

S. Alshihri

et al.

Materials Today Chemistry, Journal Year: 2023, Volume and Issue: 27, P. 101347 - 101347

Published: Jan. 1, 2023

Language: Английский

Citations

25

Cutting-edge advances in colorimetric and fluorescent chemosensors for detecting lethal cyanide ion: A comprehensive review DOI
C. Immanuel David, Hyung‐il Lee

Microchemical Journal, Journal Year: 2024, Volume and Issue: 200, P. 110359 - 110359

Published: March 19, 2024

Language: Английский

Citations

15

Microwave assisted palladium catalyzed carbon-carbon bond formation on novel benzimidazole derivatives: photophysical properties, molecular docking and DFT study. DOI Creative Commons

Vijayabharathi Sundharaj,

S. Sarveswari

Heliyon, Journal Year: 2025, Volume and Issue: 11(3), P. e42105 - e42105

Published: Jan. 22, 2025

In the present study, novel benzimidazole compounds are synthesized, utilizing Suzuki coupling and acid-amine reaction. The formation of all synthesized derivatives was confirmed through various spectroscopic techniques, including 1H, 13C, Carbon DEPT-135, H-H COSY, HSQC, HRMS. UV-Vis fluorescence spectra were recorded. Particularly, among compounds, compound 9o (304.06 nm) exhibited higher λmax in spectroscopy, while 9j (396.16 highest emmision intensity spectroscopy. Furthermore, density functional theory (DFT) calculations performed at B3LYP/6-31G'(d,p) foundational level set. These aimed to predict chemical reactivity newly by assessing parameters such as HOMO-LUMO energy gap value, ionization potential, electrostaic electron affinity, electronegativity, global hardness, softness values. Subsequently, a molecular docking analysis on protein associated with Bcl-2 conjunction venetoclax, 9g (-10.77 kcal/mol) indicating most significant binding affinity investigated.

Language: Английский

Citations

1

Construction of a simple dual-channel fluorescence chemosensor for Cu2+ ion and GSSG detection and its mitochondria-targeting bioimaging applications DOI
Palanisamy Ravichandiran,

D. S. Prabakaran,

Nikhil Maroli

et al.

Analytica Chimica Acta, Journal Year: 2021, Volume and Issue: 1181, P. 338896 - 338896

Published: July 29, 2021

Language: Английский

Citations

51

Chemosensors based on N-heterocyclic dyes: advances in sensing highly toxic ions such as CN and Hg2+ DOI Creative Commons

María-Camila Ríos,

Néstor-Fabián Bravo,

Christian-Camilo Sánchez

et al.

RSC Advances, Journal Year: 2021, Volume and Issue: 11(54), P. 34206 - 34234

Published: Jan. 1, 2021

This review considers the most recent advances in sensing highly toxic ions such as CN − and Hg 2+ . Specifically, probes bearing N-heterocyclic compounds for their proven versatility applications development of chemosensors are analyzed.

Language: Английский

Citations

51

a Versatile Schiff Base Chemosensor for the Determination of Trace Co2+, Ni2+, Cu2+, and Zn2+ in the Water and Its Bioimaging Applications DOI Creative Commons
Hongmei Liu,

Shangli Ding,

Quan Lu

et al.

ACS Omega, Journal Year: 2022, Volume and Issue: 7(9), P. 7585 - 7594

Published: Feb. 28, 2022

In this work, a simple and versatile Schiff base chemosensor (L) was developed for the detection of four adjacent row 4 metal ions (Co2+, Ni2+, Cu2+, Zn2+) through colorimetric or fluorescent analyses. L could recognize target in solutions containing wide range other cations anions. The recognition mechanisms were verified with Job's plot, HR-MS assays, 1H NMR titration experiments. Then, employed to develop test strips TLC plates Co2+. Meanwhile, capable quantitatively measuring amount tap water river samples. Notably, used imaging Zn2+ HepG2 cells, zebrafish, tumor-bearing mice, which demonstrated its potential biological applications. Therefore, can probably serve as tool environmental

Language: Английский

Citations

36

A benzimidazole-derived fluorescent chemosensor for Cu(ii)-selective turn-off and Zn(ii)-selective ratiometric turn-on detection in aqueous solutions DOI Creative Commons

Wan-Yu Zhu,

Kai Liu, Xuan Zhang

et al.

Sensors & Diagnostics, Journal Year: 2023, Volume and Issue: 2(3), P. 665 - 675

Published: Jan. 1, 2023

A benzimidazole-derived fluorescent chemosensor for Cu( ii )-selective turn-off and Zn( ratiometric turn-on detection is developed in an aqueous solution.

Language: Английский

Citations

23

Computational, spectroscopic, sensor and biological studies of Cu(II) complex of Fluoro substituted Schiff base DOI Creative Commons

Chinnaraj Kanagavalli,

M. Kalanithi,

Shunmugasundaram Gurusamy

et al.

Chemical Physics Impact, Journal Year: 2024, Volume and Issue: 8, P. 100582 - 100582

Published: March 23, 2024

Schiff base ligand (FHPB - 2-[N-(fluorophenyl)-4-hydroxy-4-phenyl] 3-butene), and its copper complex Cu[FHPB]2 were prepared the structural framework of compounds characterized by analytical, spectroscopic DFT calculation techniques. The result suggests that, Cu[FPB]2 possesses square planar geometry. Electrochemical studies reveal that is quasi reversible in nature. Sensing ability with various cations analyzed absorption emission spectral techniques infer FHPB highly sensitive selective sensor for Cu2+ ion as compared to other selected metal ions. Antimicrobial activities against bacterial fungal strains checked Disc Diffusion method. DNA interaction spectrophotometric spectrofluorometric analysis illustrates synthesized interact calf thymus way an intercalation mode. Moreover, binding demonstrated molecular docking it evidences strong CT-DNA double helix.

Language: Английский

Citations

8

A Simple and Rapid Quinoline Schiff Base as a Fluorescent Probe for Zn2+ and Its Application in Test Strips DOI
Yuwei Dong, Yang Wang, Yang Song

et al.

ChemistrySelect, Journal Year: 2024, Volume and Issue: 9(9)

Published: March 1, 2024

Abstract A simple fluorescent probe, ( E )‐ N ‐(3‐methoxy‐4‐methylphenyl)‐1‐(quinolin‐2‐yl)methanimine L ), was synthesized via Schiff base condensation reaction between quinoline‐2‐carboxaldehyde and 3‐methoxy‐4‐methylaniline. can be used as a ′turn‐on′ probe for the selective sensitive detection of Zn 2+ ions in CH 3 OH/HEPES medium. The limit 1.04×10 −7 M. Job plot analysis shows that binding stoichiometry is 1 : 1, further verified by single crystal structure. fluorescence‐enhanced response towards may related to chelation‐enhanced fluorescence (CHEF) supported theoretical calculations. By adding EDTA, reversibility demonstrated, enabling construction functional molecular logic circuit. In addition, successfully incorporated into test strips quantitative .

Language: Английский

Citations

7