Cargando…

Acridino-Diaza-20-Crown-6 Ethers: New Macrocyclic Hosts for Optochemical Metal Ion Sensing

Acridino-diaza-20-crown-6 ether derivatives as new turn-on type fluorescent chemosensors with an excellent functionality and photophysical properties have been designed and synthesized for metal ion-selective optochemical sensing applications. Spectroscopic studies revealed that in an acetonitrile-b...

Descripción completa

Detalles Bibliográficos
Autores principales: Golcs, Ádám, Kovács, Korinna, Vezse, Panna, Tóth, Tünde, Huszthy, Péter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8272042/
https://www.ncbi.nlm.nih.gov/pubmed/34279381
http://dx.doi.org/10.3390/molecules26134043
_version_ 1783721132983058432
author Golcs, Ádám
Kovács, Korinna
Vezse, Panna
Tóth, Tünde
Huszthy, Péter
author_facet Golcs, Ádám
Kovács, Korinna
Vezse, Panna
Tóth, Tünde
Huszthy, Péter
author_sort Golcs, Ádám
collection PubMed
description Acridino-diaza-20-crown-6 ether derivatives as new turn-on type fluorescent chemosensors with an excellent functionality and photophysical properties have been designed and synthesized for metal ion-selective optochemical sensing applications. Spectroscopic studies revealed that in an acetonitrile-based semi-aqueous medium, the sensor molecules exhibited a remarkable fluorescence enhancement with high sensitivity only toward Zn(2+), Al(3+) and Bi(3+), among 23 different metal ions. Studies on complexation showed a great coordinating ability of logK > 4.7 with a 1:1 complex stoichiometry in each case. The detection limits were found to be from 59 nM to micromoles. The new ionophores enabled an optical response without being affected either by the pH in the range of 5.5–7.5, or the presence of various anions or competing metal ions. Varying the N-substituents of the new host-backbone provides diverse opportunities in both immobilization and practical applications without influencing the molecular recognition abilities.
format Online
Article
Text
id pubmed-8272042
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-82720422021-07-11 Acridino-Diaza-20-Crown-6 Ethers: New Macrocyclic Hosts for Optochemical Metal Ion Sensing Golcs, Ádám Kovács, Korinna Vezse, Panna Tóth, Tünde Huszthy, Péter Molecules Article Acridino-diaza-20-crown-6 ether derivatives as new turn-on type fluorescent chemosensors with an excellent functionality and photophysical properties have been designed and synthesized for metal ion-selective optochemical sensing applications. Spectroscopic studies revealed that in an acetonitrile-based semi-aqueous medium, the sensor molecules exhibited a remarkable fluorescence enhancement with high sensitivity only toward Zn(2+), Al(3+) and Bi(3+), among 23 different metal ions. Studies on complexation showed a great coordinating ability of logK > 4.7 with a 1:1 complex stoichiometry in each case. The detection limits were found to be from 59 nM to micromoles. The new ionophores enabled an optical response without being affected either by the pH in the range of 5.5–7.5, or the presence of various anions or competing metal ions. Varying the N-substituents of the new host-backbone provides diverse opportunities in both immobilization and practical applications without influencing the molecular recognition abilities. MDPI 2021-07-01 /pmc/articles/PMC8272042/ /pubmed/34279381 http://dx.doi.org/10.3390/molecules26134043 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Golcs, Ádám
Kovács, Korinna
Vezse, Panna
Tóth, Tünde
Huszthy, Péter
Acridino-Diaza-20-Crown-6 Ethers: New Macrocyclic Hosts for Optochemical Metal Ion Sensing
title Acridino-Diaza-20-Crown-6 Ethers: New Macrocyclic Hosts for Optochemical Metal Ion Sensing
title_full Acridino-Diaza-20-Crown-6 Ethers: New Macrocyclic Hosts for Optochemical Metal Ion Sensing
title_fullStr Acridino-Diaza-20-Crown-6 Ethers: New Macrocyclic Hosts for Optochemical Metal Ion Sensing
title_full_unstemmed Acridino-Diaza-20-Crown-6 Ethers: New Macrocyclic Hosts for Optochemical Metal Ion Sensing
title_short Acridino-Diaza-20-Crown-6 Ethers: New Macrocyclic Hosts for Optochemical Metal Ion Sensing
title_sort acridino-diaza-20-crown-6 ethers: new macrocyclic hosts for optochemical metal ion sensing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8272042/
https://www.ncbi.nlm.nih.gov/pubmed/34279381
http://dx.doi.org/10.3390/molecules26134043
work_keys_str_mv AT golcsadam acridinodiaza20crown6ethersnewmacrocyclichostsforoptochemicalmetalionsensing
AT kovacskorinna acridinodiaza20crown6ethersnewmacrocyclichostsforoptochemicalmetalionsensing
AT vezsepanna acridinodiaza20crown6ethersnewmacrocyclichostsforoptochemicalmetalionsensing
AT tothtunde acridinodiaza20crown6ethersnewmacrocyclichostsforoptochemicalmetalionsensing
AT huszthypeter acridinodiaza20crown6ethersnewmacrocyclichostsforoptochemicalmetalionsensing