{"title":"New cationic fluorescent dyes for optical sensing of chloride","authors":"Karl L. Sterz, Torsten Mayr and Sergey M. Borisov","doi":"10.1039/D5TC02192H","DOIUrl":null,"url":null,"abstract":"<p >Lucigenin (10,10′-dimethyl-[9,9′-biacridine]-10,10′-diium nitrate) is a fluorescent compound known for more than a century for its chloride sensitivity, but further research since then has not yielded definitive improvements or extensive structure–property relations. Chloride indicators that absorb and emit at longer wavelengths are highly desirable to minimize interference through scattering, autofluorescence of optical components and samples, particularly when measuring in biological probes. Herein, the synthesis and spectral properties of new π-extended lucigenin analogs are reported. <em>N</em>-Methyl benzo[<em>b</em>]acridinium (<strong>1</strong>) and two-fold-charged dyes incorporating the benzo[<em>b</em>]acridinium backbone (<strong>2</strong>, <strong>3</strong>) are not emissive, and a fluorescent π-extended derivative incorporating a fluorene structure (<strong>4</strong>) does not show a sizeable response to chloride (<em>K</em><small><sub>SV NaCl</sub></small> = 0.8 M<small><sup>−1</sup></small>). A novel dicationic perylene analog, 3,9-dimethylbenzo[1,2,3-<em>de</em>:4,5,6-<em>d</em>′<em>e</em>′]diquinoline-3,9-diium (<strong>6</strong>), shows typical spectral characteristics of perylene and fluorescence quantum yield close to unity but also a strong fluorescence response to chloride (<em>K</em><small><sub>SV NaCl</sub></small> = 160 M<small><sup>−1</sup></small>). Compared to lucigenin (<em>ε</em> = 7.5 × 10<small><sup>3</sup></small> M<small><sup>−1</sup></small> cm<small><sup>−1</sup></small> at 433 nm, <em>Φ</em> = 52%), <strong>6</strong> shows much higher (∼5-fold) brightness in the visible spectral range (<em>ε</em> = 2.2 × 10<small><sup>4</sup></small> M<small><sup>−1</sup></small> cm<small><sup>−1</sup></small> at 455 nm, <em>Φ</em> = 97%). Finally, a hybrid of acridinium and quinolinium, 10-methyl-9-(1-methylquinolin-1-ium-5-yl)acridin-10-ium (<strong>5</strong>), is characterized by spectral properties, brightness (<em>ε</em> = 5.1 × 10<small><sup>3</sup></small> M<small><sup>−1</sup></small> cm<small><sup>−1</sup></small> at 426 nm, <em>Φ</em> = 83%) and chloride response (<em>K</em><small><sub>SV NaCl</sub></small> = 145 M<small><sup>−1</sup></small>) which are similar to lucigenin, but without detectable crosstalk to common anions such as nitrate and sulfate (<em>K</em><small><sub>SV NaNO<small><sub>3</sub></small></sub></small> ≈ 0, <em>K</em><small><sub>SV Na<small><sub>2</sub></small>SO<small><sub>4</sub></small></sub></small> ≈ 0). In addition, the indicator features extraordinarily long fluorescence lifetime (<em>τ</em> = 24.5 ns) that also decreases in presence of chloride, which suggests high potential of the new dye as a water-soluble probe for chloride mapping by fluorescence lifetime imaging methods. The dye can also be photoimmobilized into partly hydrolyzed poly(acrylonitrile) providing a sensor material with similar characteristics to lucigenin, but without crosstalk to nitrate and sulfate.</p>","PeriodicalId":84,"journal":{"name":"Journal of Materials Chemistry C","volume":" 39","pages":" 20259-20268"},"PeriodicalIF":5.1000,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/tc/d5tc02192h?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Chemistry C","FirstCategoryId":"1","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/tc/d5tc02192h","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Lucigenin (10,10′-dimethyl-[9,9′-biacridine]-10,10′-diium nitrate) is a fluorescent compound known for more than a century for its chloride sensitivity, but further research since then has not yielded definitive improvements or extensive structure–property relations. Chloride indicators that absorb and emit at longer wavelengths are highly desirable to minimize interference through scattering, autofluorescence of optical components and samples, particularly when measuring in biological probes. Herein, the synthesis and spectral properties of new π-extended lucigenin analogs are reported. N-Methyl benzo[b]acridinium (1) and two-fold-charged dyes incorporating the benzo[b]acridinium backbone (2, 3) are not emissive, and a fluorescent π-extended derivative incorporating a fluorene structure (4) does not show a sizeable response to chloride (KSV NaCl = 0.8 M−1). A novel dicationic perylene analog, 3,9-dimethylbenzo[1,2,3-de:4,5,6-d′e′]diquinoline-3,9-diium (6), shows typical spectral characteristics of perylene and fluorescence quantum yield close to unity but also a strong fluorescence response to chloride (KSV NaCl = 160 M−1). Compared to lucigenin (ε = 7.5 × 103 M−1 cm−1 at 433 nm, Φ = 52%), 6 shows much higher (∼5-fold) brightness in the visible spectral range (ε = 2.2 × 104 M−1 cm−1 at 455 nm, Φ = 97%). Finally, a hybrid of acridinium and quinolinium, 10-methyl-9-(1-methylquinolin-1-ium-5-yl)acridin-10-ium (5), is characterized by spectral properties, brightness (ε = 5.1 × 103 M−1 cm−1 at 426 nm, Φ = 83%) and chloride response (KSV NaCl = 145 M−1) which are similar to lucigenin, but without detectable crosstalk to common anions such as nitrate and sulfate (KSV NaNO3 ≈ 0, KSV Na2SO4 ≈ 0). In addition, the indicator features extraordinarily long fluorescence lifetime (τ = 24.5 ns) that also decreases in presence of chloride, which suggests high potential of the new dye as a water-soluble probe for chloride mapping by fluorescence lifetime imaging methods. The dye can also be photoimmobilized into partly hydrolyzed poly(acrylonitrile) providing a sensor material with similar characteristics to lucigenin, but without crosstalk to nitrate and sulfate.
期刊介绍:
The Journal of Materials Chemistry is divided into three distinct sections, A, B, and C, each catering to specific applications of the materials under study:
Journal of Materials Chemistry A focuses primarily on materials intended for applications in energy and sustainability.
Journal of Materials Chemistry B specializes in materials designed for applications in biology and medicine.
Journal of Materials Chemistry C is dedicated to materials suitable for applications in optical, magnetic, and electronic devices.
Example topic areas within the scope of Journal of Materials Chemistry C are listed below. This list is neither exhaustive nor exclusive.
Bioelectronics
Conductors
Detectors
Dielectrics
Displays
Ferroelectrics
Lasers
LEDs
Lighting
Liquid crystals
Memory
Metamaterials
Multiferroics
Photonics
Photovoltaics
Semiconductors
Sensors
Single molecule conductors
Spintronics
Superconductors
Thermoelectrics
Topological insulators
Transistors