Citation: QIN A-Hui,  GONG Shuai,  ZHANG Yan,  GAO Yu,  WANG Zhong-Long,  WANG Shi-Fa. A Novel Isolongifolanylindazole Derivatives Colorimetric Probe for Naked-eye Detection of H2S in Water Environment[J]. Chinese Journal of Analytical Chemistry, ;2021, 49(11): 1845-1854. doi: 10.19756/j.issn.0253-3820.210449 shu

A Novel Isolongifolanylindazole Derivatives Colorimetric Probe for Naked-eye Detection of H2S in Water Environment

  • Corresponding author: WANG Shi-Fa, wangshifa65@163.com
  • Received Date: 19 April 2021
    Revised Date: 14 July 2021

    Fund Project: Supported by the National Natural Science Foundation of China (No.32071707).

  • Hydrogen sulfide (H2S) plays crucial roles in various physiological process and daily life. However, excess H2S is very harmful to health. Therefore, it is necessary to design a sensitive method for H2S detection.In this work, a novel colorimetric probe 5,5,9,9-tetramethyl-3-(4-nitrophenyl)-2,4,5,6,7,8,9,9a-octahydro-5a,8-methanobenzo[g]indazole (BN) for naked-eye detection of H2S was developed with longifolene derivative isolongifolenone as the starting material. This probe had great merits including rapid response time (0.4 min), high sensitivity (detection limit of 0.31 μmol/L), and high selectivity for H2S detection. The sensing mechanism was confirmed by 1H NMR and HRMS. The experiment results showed that the -NO2 group was reduced into -NH2 group by H2S, and the hydrogen atom on the indazole ring disappeared as soon as probe BN contacted with H2S. The photophysical properties of probe BN toward H2S were examined by density functional theory calculation. Additionally, the probe BN could be loaded on filter paper and was successfully applied to detection of H2S in environmental water samples.
  • 加载中
    1. [1]

      LANTTO V, MIZSEI J. Sens. Actuators, B, 1991, 5(1-4):21-25.

    2. [2]

      XU T L, SCAFA N, XU L P, ZHOU S F, ABDULLAHK A, MAHBOOB S, FUGETSU B, ZHANG X J. Analyst, 2016, 141(4):1185-1195.

    3. [3]

      WALLACE J L, WANG R. Nat. Rev. Drug Discov., 2015, 14(5):329-345.

    4. [4]

      ANDRUSK B, MCCAFFERTY D M, IGNACY T, MILLEN B, MCDOUGALLJ J. Am. J. Physiol. Regul. Integr. Comp. Physiol., 2008, 295(3):814-820.

    5. [5]

      CHEN Y H, WANG P P, WANG X M, HE Y J, YAO W Z, QI Y F, TANG C S. Cytokine, 2011, 53(3):334-341.

    6. [6]

      WANG R, FAN Q, ZHANG J, KANG Y, WANG Z. Transl. Oncol., 2018, 11(4):900-910.

    7. [7]

      HELLMICH M R, SZABO C. Handb. Exp. Pharmacol., 2015, 230:233-241.

    8. [8]

      LEE Z W, ZHOU J, CHEN C S, ZHAO Y, TAN C H, LI L, MOORE P K, DENG L W. PloS One, 2011, 6(6):21077.

    9. [9]

      WANG M, ZHU J, PAN Y, DONG J, ZHANG L, ZHANG X, ZHANG L. J. Neurosci. Res., 2015, 93(3):487-494.

    10. [10]

      FERNANDES V S, XIN W, PETKOV G V. Am. J. Physiol. Cell Physiol., 2015, 309(2):107-116.

    11. [11]

      KULKARNI K H, MONJOK E M, ZEYSSIG R, BONGMBA O N, OPERE C A, NJIE Y F, OHIA S E. Neurochem. Res., 2009, 34(3):400-406.

    12. [12]

      XUE R, HAO D D, SUN J P, LI W W, ZHAO M M, LI X H, CHEN Y, ZHU J H, DING Y J, LIU J, ZHU Y C. Antioxid. Redox. Signal., 2013, 19(1):5-23.

    13. [13]

      HU N, DONG M, REN J. Am. J. Physiol. Regul. Integr. Comp. Physiol., 2014, 306(10):761-771.

    14. [14]

      DU Z, SONG B, ZHANG W, DUAN C, WANG Y L, LIU C, ZHANG R, YUAN J. Angew. Chem., Int. Ed., 2018, 57(15):3999-4004.

    15. [15]

      WU M Y, LI K, HOU J T, HUANG Z, YU X Q. Org. Biomol. Chem., 2012, 10(41):8342-8347.

    16. [16]

      UBUKA T. J. Chromatogr. B, 2002, 781(1):227-249.

    17. [17]

      FURNE J, SAEED A, LEVITT M D. Am. J. Physiol. Regul. Integr. Comp. Physiol., 2008, 295(5):1479-1485.

    18. [18]

      TAYLOR H E, GIBSON J H, SKOGERBOE R K. Annu. Rev. Anal. Chem. (Palo Alto Calif)., 1970, 42(13):1569-1575.

    19. [19]

      MONNOT M, NOGUEIRAR P, ROCHE V, BERTHOME G, CHAUVEAU E, ESTEVEZ R, MANTEL M. Appl. Surf. Sci., 2017, 394(1):132-141.

    20. [20]

      KNAERY J R, CUTTER G A. Anal. Chem., 1993, 65(8):976-982.

    21. [21]

      CUTTER G A, OATTS T J. Anal. Chem., 1987, 59(5):717-721.

    22. [22]

      PANDEY S K, KIM K Y. Environ. Sci. Technol., 2009, 43(9):3020-3029.

    23. [23]

      PANDEY S K, KIM K H, TANG K T. TrAC-Trends Anal. Chem., 2012, 32:87-99.

    24. [24]

    25. [25]

      LAWRENCE N S, DEO R P, WANG J. Anal. Chim. Acta, 2004, 517(1):131-137.

    26. [26]

      LAWRENCE N S, DAVIS J, JIANG L, JONES T G J, DAVIES S N, COMPTON R G. Electroanalysis, 2000, 12(18):1453-1460.

    27. [27]

      LIN V S, LIPPERT A R, CHANG C J. Proc. Natl. Acad. Sci. U. S. A., 2013, 110(18):7131-7135.

    28. [28]

      RAJASWATHI K, JAYANTHI M, RAJMOHAN R, ANBAZHAGAN V, VAIRAKASH P. Spectrochim. Acta, Part A, 2019, 212:308-314.

    29. [29]

      WEI C, ZHU Q, LIU W, CHEN W, XI Z, YI L. Org. Biomol. Chem., 2014, 12(3):479-485.

    30. [30]

      ZHAO Y, ZHU X, KAN H, WANG W, ZHU B, DU B, ZHANG X. Analyst, 2012, 137(23):5576-5580.

    31. [31]

      ZHANG D, JIN W. Spectrochim. Acta, Part A, 2012, 90:35-39.

    32. [32]

      XIANG K, LIU Y, LI C, TIAN B, TONG T, ZHANG J. Dyes Pigm., 2015, 123:78-84.

    33. [33]

      LOU T, CHEN Z, WANG Y, CHEN L. J. Am. Chem. Soc., 2011, 3(5):1568-1573.

    34. [34]

      KAUR P, SAREEN D, SINGH K. Talanta, 2011, 83(5):1695-1700.

    35. [35]

      HE L W, YANG X L, LIU Y, LIN W Y. Anal. Methods, 2016, 8:8022-8027.

    36. [36]

      YANG Y, LIU Y U, YANG L, LIU J, LI K, LUO S. J. Chem. Sci., 2015, 127(3):359-363.

    37. [37]

      LIU Y, FENG G. Org. Biomol. Chem., 2013, 12(3):438-445.

    38. [38]

      KAUSHIK R, GHOSH A, SINGH A, JOSE D A. Anal. Chim. Acta, 2018, 1040:177-186.

    39. [39]

      WANG Z, YANG J, YANG Y, FANG H, XU X, RUI J, SU F, XU H, WANG S. RSC Adv., 2017, 7(53):33263-33272.

    40. [40]

    41. [41]

      ABHISHEK K J, ANKUR V, VEERESAMY R, KASHAW S K, AGRAWAL R K. Bioorg. Med. Chem., 2012, 20(11):3378-3395.

    42. [42]

      SALMAN A K, MOHAMMED Y. Eur. J. Med. Chem., 2008, 44(6):2597-2600.

    43. [43]

      AMIT V, SHAILENDRA K S. Eur. J. Med. Chem., 2008, 43(5):897-905.

    44. [44]

      WANG Z, ZHANG Y, LI M, YANG Y, XU X, XU H, LIU J, FANG H, WANG S. Tetrahedron, 2018, 74(24):3030-3037.

    45. [45]

      WANG Z, ZHANG Y, SONG J, LI M, YANG Y, XU X, XU H, WANG S. Sens. Actuators, B, 2020, 304:127083.

    46. [46]

      WANG Z, YANG J, LIU P, YANG Y, FANG H, XU X, RUI J, XU H, WANG S. Tetrahedron, 2017, 73(40):5912-5919.

    47. [47]

      WANG Z, ZHANG Y, SONG J, YANG Y, XU X, LI M, XU H, WANG S. Anal. Chim. Acta, 2019, 1051:169-178.

    48. [48]

      KUMAR N, BHALLA V, KUMAR M. Coord. Chem. Rev., 2013, 257(15):2335-2347.

    49. [49]

      LI J F, YIN C X, HUO F J. RSC Adv., 2015, 5(3):2191-2206.

    50. [50]

      LEE C, YANG W, PARR R G. Phys. Rev. B, 1988, 37:785-789.

    51. [51]

      WANG Y, CHENG X L, YANG X D, YANG X. J. Solution Chem., 2006, 35:869-878.

  • 加载中
    1. [1]

      Linfang ZHANGWenzhu YINGui YIN . A 2-dicyanomethylene-3-cyano-4,5,5-trimethyl-2,5-dihydrofuran-based near-infrared fluorescence probe for the detection of hydrogen sulfide and imaging of living cells. Chinese Journal of Inorganic Chemistry, 2025, 41(3): 540-548. doi: 10.11862/CJIC.20240405

    2. [2]

      Yikai Wang Xiaolin Jiang Haoming Song Nan Wei Yifan Wang Xinjun Xu Cuihong Li Hao Lu Yahui Liu Zhishan Bo . 氰基修饰的苝二酰亚胺衍生物作为膜厚不敏感型阴极界面材料用于高效有机太阳能电池. Acta Physico-Chimica Sinica, 2025, 41(3): 2406007-. doi: 10.3866/PKU.WHXB202406007

    3. [3]

      Jianfeng Yan Yating Xiao Xin Zuo Caixia Lin Yaofeng Yuan . Comprehensive Chemistry Experimental Design of Ferrocenylphenyl Derivatives. University Chemistry, 2024, 39(4): 329-337. doi: 10.3866/PKU.DXHX202310005

    4. [4]

      Yurong Tang Yunren Shi Yi Xu Bo Qin Yanqin Xu Yunfei Cai . Innovative Experiment and Course Transformation Practice of Visible-Light-Mediated Photocatalytic Synthesis of Isoquinolinone. University Chemistry, 2024, 39(5): 296-306. doi: 10.3866/PKU.DXHX202311087

    5. [5]

      Zhongyan Cao Shengnan Jin Yuxia Wang Yiyi Chen Xianqiang Kong Yuanqing Xu . Advances in Highly Selective Reactions Involving Phenol Derivatives as Aryl Radical Precursors. University Chemistry, 2025, 40(4): 245-252. doi: 10.12461/PKU.DXHX202405186

    6. [6]

      Yonghui ZHOURujun HUANGDongchao YAOAiwei ZHANGYuhang SUNZhujun CHENBaisong ZHUYouxuan ZHENG . Synthesis and photoelectric properties of fluorescence materials with electron donor-acceptor structures based on quinoxaline and pyridinopyrazine, carbazole, and diphenylamine derivatives. Chinese Journal of Inorganic Chemistry, 2024, 40(4): 701-712. doi: 10.11862/CJIC.20230373

    7. [7]

      Zhicheng JUWenxuan FUBaoyan WANGAo LUOJiangmin JIANGYueli SHIYongli CUI . MOF-derived nickel-cobalt bimetallic sulfide microspheres coated by carbon: Preparation and long cycling performance for sodium storage. Chinese Journal of Inorganic Chemistry, 2025, 41(4): 661-674. doi: 10.11862/CJIC.20240363

    8. [8]

      Jinghan ZHANGGuanying CHEN . Progress in the application of rare-earth-doped upconversion nanoprobes in biological detection. Chinese Journal of Inorganic Chemistry, 2024, 40(12): 2335-2355. doi: 10.11862/CJIC.20240249

    9. [9]

      Ke Li Chuang Liu Jingping Li Guohong Wang Kai Wang . 钛酸铋/氮化碳无机有机复合S型异质结纯水光催化产过氧化氢. Acta Physico-Chimica Sinica, 2024, 40(11): 2403009-. doi: 10.3866/PKU.WHXB202403009

    10. [10]

      Jinlong YANWeina WUYuan WANG . A simple Schiff base probe for the fluorescent turn-on detection of hypochlorite and its biological imaging application. Chinese Journal of Inorganic Chemistry, 2024, 40(9): 1653-1660. doi: 10.11862/CJIC.20240154

    11. [11]

      Yujia LITianyu WANGFuxue WANGChongchen WANG . Direct Z-scheme MIL-100(Fe)/BiOBr heterojunctions: Construction and photo-Fenton degradation for sulfamethoxazole. Chinese Journal of Inorganic Chemistry, 2024, 40(3): 481-495. doi: 10.11862/CJIC.20230314

    12. [12]

      Hong LIXiaoying DINGCihang LIUJinghan ZHANGYanying RAO . Detection of iron and copper ions based on gold nanorod etching colorimetry. Chinese Journal of Inorganic Chemistry, 2024, 40(5): 953-962. doi: 10.11862/CJIC.20230370

    13. [13]

      Peng GENGGuangcan XIANGWen ZHANGHaichuang LANShuzhang XIAO . Hollow copper sulfide loaded protoporphyrin for photothermal-sonodynamic therapy of cancer cells. Chinese Journal of Inorganic Chemistry, 2024, 40(10): 1903-1910. doi: 10.11862/CJIC.20240155

    14. [14]

      Yang Wang Yunpeng Fu Xiaoji Liu Guotao Zhang Guobin Li Wanqiang Liu Jinglun Wang . Structural Analysis of Nitrile Solutions Based on Infrared Spectroscopy Probes. University Chemistry, 2025, 40(4): 367-374. doi: 10.12461/PKU.DXHX202406113

    15. [15]

      Liwei Wang Guangran Ma Li Wang Fugang Xu . A Comprehensive Analytical Chemistry Experiment: Colorimetric Detection of Vitamin C Using Nanozyme and Smartphone. University Chemistry, 2024, 39(8): 255-262. doi: 10.3866/PKU.DXHX202312094

    16. [16]

      Jiakun BAITing XULu ZHANGJiang PENGYuqiang LIJunhui JIA . A red-emitting fluorescent probe with a large Stokes shift for selective detection of hypochlorous acid. Chinese Journal of Inorganic Chemistry, 2024, 40(6): 1095-1104. doi: 10.11862/CJIC.20240002

    17. [17]

      Qiangqiang SUNPengcheng ZHAORuoyu WUBaoyue CAO . Multistage microporous bifunctional catalyst constructed by P-doped nickel-based sulfide ultra-thin nanosheets for energy-efficient hydrogen production from water electrolysis. Chinese Journal of Inorganic Chemistry, 2024, 40(6): 1151-1161. doi: 10.11862/CJIC.20230454

    18. [18]

      Xiaofeng Zhu Bingbing Xiao Jiaxin Su Shuai Wang Qingran Zhang Jun Wang . Transition Metal Oxides/Chalcogenides for Electrochemical Oxygen Reduction into Hydrogen Peroxides. Acta Physico-Chimica Sinica, 2024, 40(12): 2407005-. doi: 10.3866/PKU.WHXB202407005

    19. [19]

      Jiaxi Xu Yuan Ma . Influence of Hyperconjugation on the Stability and Stable Conformation of Ethane, Hydrazine, and Hydrogen Peroxide. University Chemistry, 2024, 39(11): 374-377. doi: 10.3866/PKU.DXHX202402049

    20. [20]

      Mingyang Men Jinghua Wu Gaozhan Liu Jing Zhang Nini Zhang Xiayin Yao . 液相法制备硫化物固体电解质及其在全固态锂电池中的应用. Acta Physico-Chimica Sinica, 2025, 41(1): 2309019-. doi: 10.3866/PKU.WHXB202309019

Metrics
  • PDF Downloads(7)
  • Abstract views(582)
  • HTML views(69)

通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索
Address:Zhongguancun North First Street 2,100190 Beijing, PR China Tel: +86-010-82449177-888
Powered By info@rhhz.net

/

DownLoad:  Full-Size Img  PowerPoint
Return