Ahmet Battal , Nuray Altinolcek Gultekin , Mustafa Tavasli , Yavuz Onganer
{"title":"A highly selective carbazole-based D-π-D-A fluorescence turn-off sensor for Fe3+ detection in aqueous media","authors":"Ahmet Battal , Nuray Altinolcek Gultekin , Mustafa Tavasli , Yavuz Onganer","doi":"10.1016/j.jlumin.2025.121503","DOIUrl":null,"url":null,"abstract":"<div><div>In this study, N-hexyl-6-(4-methoxyphenyl)carbazole-3-carbaldehyde with donor-π-donor-acceptor (D-π-D-A) structure was designated as a probe <strong>N</strong> and its fluorescence sensor properties were investigated against 30 different analytes. Probe <strong>N</strong> in DMSO gave a structureless emission band with a maximum at 470 nm and a high photoluminescence quantum yield (80 %). In going from non-polar to polar solvents, the emission maximum of probe <strong>N</strong> red-shifted by 72 nm and Stokes shifts observed between absorption and emission spectra was 71 nm (3689 cm<sup>−1</sup>). It was found that the emission maximum of probe <strong>N</strong> at 470 nm was more significantly quenched by Fe<sup>3+</sup> than by Fe<sup>2+</sup> among the analytes studied. Probe <strong>N</strong> showed high selectivity and high sensitivity with a 0.8 nM limit of detection (LOD) against Fe<sup>3+</sup> in the presence of competing analytes. The LOD value is the lowest value reported so far for the detection of Fe<sup>3+</sup>. Job's plot indicated a 2:1 ratio between probe <strong>N</strong> and Fe<sup>3+</sup>. <sup>1</sup>H NMR and FT-IR provided further evidence that probe <strong>N</strong> complexed Fe<sup>3+</sup> via the non-bonding electrons on the oxygen atoms of the aldehyde and methoxy groups. In practical applications, probe <strong>N</strong> successfully detected Fe<sup>3+</sup>. These results revealed that probe <strong>N</strong> could be an effective turn-off fluorescence sensor in the determination of Fe<sup>3+</sup> in liquid environments.</div></div>","PeriodicalId":16159,"journal":{"name":"Journal of Luminescence","volume":"287 ","pages":"Article 121503"},"PeriodicalIF":3.6000,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Luminescence","FirstCategoryId":"101","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022231325004430","RegionNum":3,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OPTICS","Score":null,"Total":0}
引用次数: 0
Abstract
In this study, N-hexyl-6-(4-methoxyphenyl)carbazole-3-carbaldehyde with donor-π-donor-acceptor (D-π-D-A) structure was designated as a probe N and its fluorescence sensor properties were investigated against 30 different analytes. Probe N in DMSO gave a structureless emission band with a maximum at 470 nm and a high photoluminescence quantum yield (80 %). In going from non-polar to polar solvents, the emission maximum of probe N red-shifted by 72 nm and Stokes shifts observed between absorption and emission spectra was 71 nm (3689 cm−1). It was found that the emission maximum of probe N at 470 nm was more significantly quenched by Fe3+ than by Fe2+ among the analytes studied. Probe N showed high selectivity and high sensitivity with a 0.8 nM limit of detection (LOD) against Fe3+ in the presence of competing analytes. The LOD value is the lowest value reported so far for the detection of Fe3+. Job's plot indicated a 2:1 ratio between probe N and Fe3+. 1H NMR and FT-IR provided further evidence that probe N complexed Fe3+ via the non-bonding electrons on the oxygen atoms of the aldehyde and methoxy groups. In practical applications, probe N successfully detected Fe3+. These results revealed that probe N could be an effective turn-off fluorescence sensor in the determination of Fe3+ in liquid environments.
期刊介绍:
The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid.
We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.