Antenna effect on Zn(II) porphyrin–based molecular ensembles for the detection of 2,4-dinitrophenol through energy and electron transfer process

IF 5.3 2区 化学 Q1 CHEMISTRY, ANALYTICAL
Prasanth Palanisamy, Mageshwari Anandan, Gurusamy Raman, Venkatramaiah Nutalapati
{"title":"Antenna effect on Zn(II) porphyrin–based molecular ensembles for the detection of 2,4-dinitrophenol through energy and electron transfer process","authors":"Prasanth Palanisamy,&nbsp;Mageshwari Anandan,&nbsp;Gurusamy Raman,&nbsp;Venkatramaiah Nutalapati","doi":"10.1007/s00604-024-06795-2","DOIUrl":null,"url":null,"abstract":"<div><p>Two modular systems were synthesized composed of triphenylamine (ZnTPAP) and pyrene (ZnPyP) covalently linked at meso position of the Zn(II) porphyrins. Both compounds behaved as energy transfer antenna and orthogonal units to enhance the electron donating ability of Zn(II) porphyrins. Detailed photophysical and aggregation studies reveal that an appreciable electronic interaction exists between peripheral units to the porphyrin <i>π</i>-system so that they behave like strong donor materials. The electrochemical and computational studies demonstrate delocalization of the frontier highest occupied molecular orbital (−5.08 eV) over the triphenylamine entities (ZnTPAP) in addition to the porphyrin macrocycle. Fluorescence experiments with ZnTPAP and ZnPyP in the presence of different nitro analytes at various concentrations show <i>turn-off</i> fluorescence behaviour and exhibit superior selectivity towards 2,4-dinitrophenol (DNP) with limit of detection (LOD) of ~ 2.3 and 9.2 ppm for ZnTPAP and ZnPyP. Photoinduced electron transfer process is involved in the static and dynamic fluorescence quenching process. A Stern–Volmer quenching association constant (K<sub>sv</sub>) determination revealed that ZnTPAP is more sensitive than the ZnPyP. This is attributed to the strong donating behaviour of TPA units caused by intermolecular interaction through metal center and strong <i>π</i>–<i>π</i> interactions with nitro analytes. The present study provides new insights into the ability to tune the affinity and selectivity of porphyrin-based sensors utilising electronic factors associated with the central Zn(II) ion. Furthermore, a smartphone-interfaced portable fluorimetric method by recognising colour variations in RGB and the luminance (L) values facilitate sensitive and real-time sensing at low concentration levels will have a significant impact on development of a new class of chemosensors.</p><h3>Graphical Abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":705,"journal":{"name":"Microchimica Acta","volume":"192 1","pages":""},"PeriodicalIF":5.3000,"publicationDate":"2024-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microchimica Acta","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s00604-024-06795-2","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Two modular systems were synthesized composed of triphenylamine (ZnTPAP) and pyrene (ZnPyP) covalently linked at meso position of the Zn(II) porphyrins. Both compounds behaved as energy transfer antenna and orthogonal units to enhance the electron donating ability of Zn(II) porphyrins. Detailed photophysical and aggregation studies reveal that an appreciable electronic interaction exists between peripheral units to the porphyrin π-system so that they behave like strong donor materials. The electrochemical and computational studies demonstrate delocalization of the frontier highest occupied molecular orbital (−5.08 eV) over the triphenylamine entities (ZnTPAP) in addition to the porphyrin macrocycle. Fluorescence experiments with ZnTPAP and ZnPyP in the presence of different nitro analytes at various concentrations show turn-off fluorescence behaviour and exhibit superior selectivity towards 2,4-dinitrophenol (DNP) with limit of detection (LOD) of ~ 2.3 and 9.2 ppm for ZnTPAP and ZnPyP. Photoinduced electron transfer process is involved in the static and dynamic fluorescence quenching process. A Stern–Volmer quenching association constant (Ksv) determination revealed that ZnTPAP is more sensitive than the ZnPyP. This is attributed to the strong donating behaviour of TPA units caused by intermolecular interaction through metal center and strong ππ interactions with nitro analytes. The present study provides new insights into the ability to tune the affinity and selectivity of porphyrin-based sensors utilising electronic factors associated with the central Zn(II) ion. Furthermore, a smartphone-interfaced portable fluorimetric method by recognising colour variations in RGB and the luminance (L) values facilitate sensitive and real-time sensing at low concentration levels will have a significant impact on development of a new class of chemosensors.

Graphical Abstract

求助全文
约1分钟内获得全文 求助全文
来源期刊
Microchimica Acta
Microchimica Acta 化学-分析化学
CiteScore
9.80
自引率
5.30%
发文量
410
审稿时长
2.7 months
期刊介绍: As a peer-reviewed journal for analytical sciences and technologies on the micro- and nanoscale, Microchimica Acta has established itself as a premier forum for truly novel approaches in chemical and biochemical analysis. Coverage includes methods and devices that provide expedient solutions to the most contemporary demands in this area. Examples are point-of-care technologies, wearable (bio)sensors, in-vivo-monitoring, micro/nanomotors and materials based on synthetic biology as well as biomedical imaging and targeting.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信