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Development of Rhodamine 6G-Based Fluorescent Chemosensors for Al(3+)-Ion Detection: Effect of Ring Strain and Substituent in Enhancing Its Sensing Performance

[Image: see text] Four rhodamine 6G-based chemosensors (H(3)L1–H(3)L4) are designed for selective detection of Al(3+) ion. They are characterized using various spectroscopic techniques and X-ray crystallography. All absorption and emission spectral studies have been performed in 10 mM N-(2-hydroxyet...

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Autores principales: Mandal, Jayanta, Ghorai, Pravat, Pal, Kunal, Bhaumik, Tanurima, Karmakar, Parimal, Saha, Amrita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963915/
https://www.ncbi.nlm.nih.gov/pubmed/31956761
http://dx.doi.org/10.1021/acsomega.9b02181
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author Mandal, Jayanta
Ghorai, Pravat
Pal, Kunal
Bhaumik, Tanurima
Karmakar, Parimal
Saha, Amrita
author_facet Mandal, Jayanta
Ghorai, Pravat
Pal, Kunal
Bhaumik, Tanurima
Karmakar, Parimal
Saha, Amrita
author_sort Mandal, Jayanta
collection PubMed
description [Image: see text] Four rhodamine 6G-based chemosensors (H(3)L1–H(3)L4) are designed for selective detection of Al(3+) ion. They are characterized using various spectroscopic techniques and X-ray crystallography. All absorption and emission spectral studies have been performed in 10 mM N-(2-hydroxyethyl)piperazine-N′-ethanesulfonic acid (HEPES) buffer solution at pH 7.4 in H(2)O/MeOH (9:1, v/v) at 25 °C. In absorption spectra, chemosensors exhibit an intense band around 530 nm in the presence of Al(3+) ion. Chemosensors (H(3)L1–H(3)L4) are nonfluorescent when excited around 490 nm. The presence of Al(3+) ion enhances the emission intensity (555 nm) many times. The formation of complexes 1–4 is established with the aid of different spectroscopic techniques. The limit of detection value obtained in the nanomolar range confirms the high sensitivity of the probes toward Al(3+) ion. It has been observed that the presence of aliphatic spacers in the diamine part and different halogen substituents in the salicylaldehyde part strongly influences the selectivity of the chemosensors toward Al(3+) ion. The propensity of the chemosensors to identify intracellular Al(3+) ions in triple-negative human breast cancer cell line MDA-MB-468 by fluorescence imaging is also examined in this study.
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spelling pubmed-69639152020-01-17 Development of Rhodamine 6G-Based Fluorescent Chemosensors for Al(3+)-Ion Detection: Effect of Ring Strain and Substituent in Enhancing Its Sensing Performance Mandal, Jayanta Ghorai, Pravat Pal, Kunal Bhaumik, Tanurima Karmakar, Parimal Saha, Amrita ACS Omega [Image: see text] Four rhodamine 6G-based chemosensors (H(3)L1–H(3)L4) are designed for selective detection of Al(3+) ion. They are characterized using various spectroscopic techniques and X-ray crystallography. All absorption and emission spectral studies have been performed in 10 mM N-(2-hydroxyethyl)piperazine-N′-ethanesulfonic acid (HEPES) buffer solution at pH 7.4 in H(2)O/MeOH (9:1, v/v) at 25 °C. In absorption spectra, chemosensors exhibit an intense band around 530 nm in the presence of Al(3+) ion. Chemosensors (H(3)L1–H(3)L4) are nonfluorescent when excited around 490 nm. The presence of Al(3+) ion enhances the emission intensity (555 nm) many times. The formation of complexes 1–4 is established with the aid of different spectroscopic techniques. The limit of detection value obtained in the nanomolar range confirms the high sensitivity of the probes toward Al(3+) ion. It has been observed that the presence of aliphatic spacers in the diamine part and different halogen substituents in the salicylaldehyde part strongly influences the selectivity of the chemosensors toward Al(3+) ion. The propensity of the chemosensors to identify intracellular Al(3+) ions in triple-negative human breast cancer cell line MDA-MB-468 by fluorescence imaging is also examined in this study. American Chemical Society 2019-12-27 /pmc/articles/PMC6963915/ /pubmed/31956761 http://dx.doi.org/10.1021/acsomega.9b02181 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Mandal, Jayanta
Ghorai, Pravat
Pal, Kunal
Bhaumik, Tanurima
Karmakar, Parimal
Saha, Amrita
Development of Rhodamine 6G-Based Fluorescent Chemosensors for Al(3+)-Ion Detection: Effect of Ring Strain and Substituent in Enhancing Its Sensing Performance
title Development of Rhodamine 6G-Based Fluorescent Chemosensors for Al(3+)-Ion Detection: Effect of Ring Strain and Substituent in Enhancing Its Sensing Performance
title_full Development of Rhodamine 6G-Based Fluorescent Chemosensors for Al(3+)-Ion Detection: Effect of Ring Strain and Substituent in Enhancing Its Sensing Performance
title_fullStr Development of Rhodamine 6G-Based Fluorescent Chemosensors for Al(3+)-Ion Detection: Effect of Ring Strain and Substituent in Enhancing Its Sensing Performance
title_full_unstemmed Development of Rhodamine 6G-Based Fluorescent Chemosensors for Al(3+)-Ion Detection: Effect of Ring Strain and Substituent in Enhancing Its Sensing Performance
title_short Development of Rhodamine 6G-Based Fluorescent Chemosensors for Al(3+)-Ion Detection: Effect of Ring Strain and Substituent in Enhancing Its Sensing Performance
title_sort development of rhodamine 6g-based fluorescent chemosensors for al(3+)-ion detection: effect of ring strain and substituent in enhancing its sensing performance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963915/
https://www.ncbi.nlm.nih.gov/pubmed/31956761
http://dx.doi.org/10.1021/acsomega.9b02181
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