Piperazine appended napthalimide scaffold as turn on fluorescent probe for hydrogen sulfide

被引:9
|
作者
Sureshkumar, Kempahanumakkagari [1 ]
Ramakrishnappa, Thippeswamy [1 ]
Samrat, Devarmane [2 ]
机构
[1] BMS Inst Technol & Management, Doddaballapura Main Rd, Bengaluru 560064, Karnataka, India
[2] RV Inst Technol & Management, Chaithanya Layout,8th Phase, Bengaluru 560076, Karnataka, India
关键词
FRET; Sulfide; Naked eye detection; Water samples; Napthalimide; LIVING CELLS; H2S; THIOLYSIS; GAS; ION;
D O I
10.1016/j.microc.2020.105019
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The H2S specific fluorescent sensor based on FRET (Forster resonance energy transfer) was designed and synthesized. The probe was synthesized by appending 7-nitro-1, 2,3-benzoxadiazole (NBD) amine to the piperazine coupled napthalimide scaffold. The sulfide induces red color to the probe which was colorless when it is alone. Similarly when illuminate under light the aqueous solution of probe in the presence of sulfide its exhibits strong green fluorescence. The naked eye detectable color as well as fluorescent changes of the probe is highly specific to sulfide no other anions normally present in natural water like fluoride, sulfite and sulfate and biologically relevant species like cysteine, homocysteine and glutathione. The probe exhibits excellent sensitivity towards H2S i.e. linear range of about 1.0-100 mu M and LOD of about 0.016 mu M. The present sensor system was applied for monitoring H2S in various water samples.
引用
收藏
页数:6
相关论文
共 50 条
  • [1] A turn-on fluorescent probe for selective and sensitive detection of hydrogen sulfide
    Ma, Fang
    Sun, Mingtai
    Zhang, Kui
    Yu, Huan
    Wang, Zhenyang
    Wang, Suhua
    ANALYTICA CHIMICA ACTA, 2015, 879 : 104 - 110
  • [2] A turn-on fluorescent probe for the detection of hydrogen sulfide and thiophenol in water and beer samples
    Xu, Jia-Rui
    Zheng, Yi
    Liu, Tian-Zhen
    Zhao, Bao-Xiang
    Wang, Kai-Ming
    JOURNAL OF FOOD COMPOSITION AND ANALYSIS, 2024, 128
  • [3] A novel colorimetric NIR fluorescent probe for turn-on detection and imaging of hydrogen sulfide
    Lu, Guifen
    Duan, Luyao
    Hu, Qikang
    Meng, Suci
    Cai, Peiyang
    Chen, Yuting
    Wang, Xiaochun
    Dong, Ting
    JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2024, 448
  • [4] A turn-on fluorescent probe for detection of hydrogen sulfide in aqueous solution and living cells
    Zhu, Dongjian
    Xue, Lin
    Li, Guoping
    Che, Yanke
    Jiang, Hua
    ORGANIC CHEMISTRY FRONTIERS, 2014, 1 (05): : 501 - 505
  • [5] Synthesis and characterizations of a highly sensitive and selective fluorescent probe for hydrogen sulfide
    Huang, Yan
    Zhang, Changyu
    Xi, Zhen
    Yi, Long
    TETRAHEDRON LETTERS, 2016, 57 (10) : 1187 - 1191
  • [6] A near-infrared turn-on fluorescent probe for the detection of hydrogen sulfide in water samples and food spoilage
    Cai, Wenjuan
    Xin, Tian
    Tu, Yayi
    Sun, Leilei
    Liao, Guanming
    Liu, Gang
    Fan, Congbin
    ANALYTICA CHIMICA ACTA, 2024, 1320
  • [7] Piperazine-tuned NBD-based colorimetric and fluorescent turn-off probes for hydrogen sulfide
    Xu, Zhong-yong
    Wu, Zi-ying
    Tan, Hui-ya
    Yan, Jin-wu
    Liu, Xiao-lin
    Li, Jia-ying
    Xu, Zi-yan
    Dong, Chang-zhi
    Zhang, Lei
    ANALYTICAL METHODS, 2018, 10 (27) : 3375 - 3379
  • [8] Fluorescent Turn-on Probe Based on Napthalimide Fused Triphenylamine Unit for Quickly Detecting Thiophenol in Aqueous Solution
    Sun Jiaojiao
    Cao Jian
    Cheng Hailong
    Wang Jincheng
    Wang Shuxin
    CHEMICAL RESEARCH IN CHINESE UNIVERSITIES, 2019, 35 (06) : 990 - 996
  • [9] A BODIPY-based turn-on fluorescent probe for the selective detection of hydrogen sulfide in solution and in cells
    Wang, Jiamin
    Yu, Hui
    Li, Qian
    Shao, Shijun
    TALANTA, 2015, 144 : 763 - 768
  • [10] Synthesis of a Turn-On Fluorescent Probe for Hydrogen Sulfide and Its Application in Red Wine and Living Cells
    Yang Yaxin
    Chen Lin
    Hu Xiaoling
    Zhong Keli
    Li Shidi
    Yan Xiaomei
    Zhang Jinglin
    Tang Lijun
    CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2023, 43 (01) : 308 - 312