A Schiff base fluorescent chemsensor for the double detection of Al3+ and PPi through aggregation induced emission in environmental physiology

被引:38
作者
Wang, Qi [1 ]
Wen, Xiaoye [1 ]
Fan, Zhefeng [1 ]
机构
[1] Shanxi Normal Univ, Dept Chem, Linfen 041004, Peoples R China
关键词
Schiff base; Aggregation induced emission; Al3+; PPi; Fluorescent probe; RECEPTOR CHEMISTRY HIGHLIGHTS; AIE ACTIVE PROBE; TURN-ON; LIVING CELLS; SELECTIVE RECOGNITION; COLORIMETRIC SENSOR; ALZHEIMERS-DISEASE; CHEMOSENSOR; ALUMINUM; IONS;
D O I
10.1016/j.jphotochem.2018.03.004
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this paper, a simple Schiff base fluorescent probe was synthesized by aggregation-induced emission. The probe detected Al3+ with an "off-on" behavior, because the molecular rotation was restricted, the molecular rigidity was increased. The stoichiometry ratio of the probe to Al3+ was 1:2. The detection limit of Al3+ was 0.39 mu M, which was exceedingly below the WHO standard (7.41 mu M) and the acceptable Al3+ levels of (1.85 mu M) in drinking water. In view of the strong binding ability between pyrophosphate (PPi) and Al3+, the probe-Al3+. detected PPi with an "on-off" behavior over other physiological relevant metal ions, anion and biomolecules investigated in this study. The detection limit of PPi was 0.75 mu M. Therefore, the proposed probe is a promising fluorescent sensor that can be used to detect Al3+ and PPi. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:92 / 99
页数:8
相关论文
共 59 条
  • [1] Selective optical sensing of copper(II) ions based on a novel cyclobutane-substituted Schiff base ligand embedded in polymer films
    Aksuner, Nur
    Henden, Emur
    Yilmaz, Ibrahim
    Cukurovali, Alaadin
    [J]. SENSORS AND ACTUATORS B-CHEMICAL, 2008, 134 (02) : 510 - 515
  • [2] Aminobenzohydrazide based colorimetric and 'turn-on' fluorescence chemosensor for selective recognition of fluoride
    Anand, Thangaraj
    Sivaramana, Gandhi
    Iniya, Murugan
    Siva, Ayyanar
    Chellappa, Duraisamy
    [J]. ANALYTICA CHIMICA ACTA, 2015, 876 : 1 - 8
  • [3] Aminoquinoline based highly sensitive fluorescent sensor for lead(II) and aluminum(III) and its application in live cell imaging
    Anand, Thangaraj
    Sivaraman, Gandhi
    Mahesh, Ayyavu
    Chellappa, Duraisamy
    [J]. ANALYTICA CHIMICA ACTA, 2015, 853 : 596 - 601
  • [4] Quinazoline copper(II) ensemble as turn-on fluorescence sensor for cysteine and chemodosimeter for NO
    Anand, Thangaraj
    Sivaraman, Gandhi
    Chellappa, Duraisamy
    [J]. JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2014, 281 : 47 - 52
  • [5] A novel aluminum-sensitive fluorescent nano-chemosensor based on naphthalene macrocyclic derivative
    Azadbakht, Reza
    Khanabadi, Javade
    [J]. TETRAHEDRON, 2013, 69 (15) : 3206 - 3211
  • [6] A novel highly sensitive and selective optical sensor based on a symmetric tetradentate Schiff-base embedded in PVC polymeric film for determination of Zn2+ ion in real samples
    Aziz, Ayman A. Abdel
    [J]. JOURNAL OF LUMINESCENCE, 2013, 143 : 663 - 669
  • [7] A turn-on and reversible Schiff base fluorescence sensor for Al3+ ion
    Chen, Chang-Hung
    Liao, De-Jhong
    Wan, Chin-Feng
    Wu, An-Tai
    [J]. ANALYST, 2013, 138 (09) : 2527 - 2530
  • [8] An AIE-active hemicyanine fluorogen with stimuli-responsive red/blue emission: extending the pH sensing range by "switch+knob" effect
    Chen, Sijie
    Liu, Jianzhao
    Liu, Yang
    Su, Huimin
    Hong, Yuning
    Jim, Cathy K. W.
    Kwok, Ryan T. K.
    Zhao, Na
    Qin, Wei
    Lam, Jacky W. Y.
    Wong, Kam Sing
    Tang, Ben Zhong
    [J]. CHEMICAL SCIENCE, 2012, 3 (06) : 1804 - 1809
  • [9] Rhodamine-based molecular clips for highly selective recognition of Al3+ ions: synthesis, crystal structure and spectroscopic properties
    Dhara, Anamika
    Jana, Atanu
    Guchhait, Nikhil
    Ghosh, Prasanta
    Kar, Susanta K.
    [J]. NEW JOURNAL OF CHEMISTRY, 2014, 38 (04) : 1627 - 1634
  • [10] The coordination chemistry of aluminium in neurodegenerative disease
    Exley, Christopher
    [J]. COORDINATION CHEMISTRY REVIEWS, 2012, 256 (19-20) : 2142 - 2146