A new turn-on fluorescent chemosensor based on sensitive Schiff base for Mn2+ ion

被引:29
作者
Roy, Nayan [1 ]
Dutta, Abhijit [1 ]
Mondal, Paritosh [1 ]
Paul, Pradip C. [1 ]
Singh, T. Sanjoy [1 ]
机构
[1] Assam Univ, Dept Chem, Silchar 788011, Assam, India
关键词
Schiff base; Fluorescence; Mn2+ ion; Selectivity; Binding constant; Density functional theory; SELECTIVE RECOGNITION; MANGANESE UPTAKE; COMPLEXES; ZN2+; SENSOR; ZN(II); PROBE; ZINC; CADMIUM; NICKEL;
D O I
10.1016/j.jlumin.2015.04.040
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
A Schiff-base fluorescent probe - N,N'-bis((6-(thiophen-3-yl)pyridine-2-yl) methylene) benzene-1,2-diamine (L) - was synthesized and evaluated as a chemoselective Mn2+ sensor. Upon treatment with Mn2+, the complexation of L with Mn2+ resulted in a red-shift with a pronounced enhancement in the fluorescence emission intensity in ethanol solution. Moreover, other common alkali, alkaline earth and transition metal ions failed to induce response or minimal spectral changes. Fluorescence studies on L and L-Mn2+ complex reveal that the quantum yield strongly increases upon coordination. The complex solution of L with Mn2+ ion exhibited reversibility with EDTA and regenerated free ligand for further Mn2+ sensing. The stoichiometric ratio and association constant were evaluated using Benesi-Hildebrand relation giving 1:1 stoichiometry. This further corroborated 1:1 complex formation based on Job's plot analyses. This chemosensor exhibits a very good fluorescence sensing ability to Mn2+ over a wide acidic range. This chemosensor can be used as an important application for detection of Mn2+ in real water samples. Both L and L-Mn2+ complex were optimized using density functional theory and vibrational frequency calculations confirmed that both are at local minima on the potential energy surfaces. The corresponding energy differences between HOMO and LUMO of L and L-Mn2+ complex are 2.210 eV and 0.550 eV, respectively which implies a low kinetic stability and high chemical reactivity. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:167 / 173
页数:7
相关论文
共 54 条
[1]  
[Anonymous], 2001, Nature's building blocks
[2]   DENSITY-FUNCTIONAL EXCHANGE-ENERGY APPROXIMATION WITH CORRECT ASYMPTOTIC-BEHAVIOR [J].
BECKE, AD .
PHYSICAL REVIEW A, 1988, 38 (06) :3098-3100
[3]   A SPECTROPHOTOMETRIC INVESTIGATION OF THE INTERACTION OF IODINE WITH AROMATIC HYDROCARBONS [J].
BENESI, HA ;
HILDEBRAND, JH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1949, 71 (08) :2703-2707
[4]  
BIRD ED, 1984, NEUROTOXICOLOGY, V5, P59
[5]   Solvent-controlled assembly of manganese(II) tetrachloroterephthalates with 1D chain, 2D layer, and 3D coordination Architectures [J].
Chen, Sheng-Chun ;
Zhang, Zhi-Hui ;
Huang, Kun-Lin ;
Chen, Qun ;
He, Ming-Yang ;
Cui, Ai-Jun ;
Li, Chao ;
Liu, Qi ;
Du, Miao .
CRYSTAL GROWTH & DESIGN, 2008, 8 (09) :3437-3445
[6]  
Czarnik A.W., 1992, Fluorescent Chemosensors for Ion and Molecule Recognition
[7]   Double-strand DNA cleavage induced by oxindole-Schiff base copper(II) complexes with potential antitumor activity [J].
da Silveira, Vivian Chagas ;
Luz, Juliana Silva ;
Oliveira, Carla Columbano ;
Graziani, Ilaria ;
Ciriolo, Maria Rosa ;
da Costa Ferreira, Ana Maria .
JOURNAL OF INORGANIC BIOCHEMISTRY, 2008, 102 (5-6) :1090-1103
[8]   Signaling recognition events with fluorescent sensors and switches [J].
de Silva, AP ;
Gunaratne, HQN ;
Gunnlaugsson, T ;
Huxley, AJM ;
McCoy, CP ;
Rademacher, JT ;
Rice, TE .
CHEMICAL REVIEWS, 1997, 97 (05) :1515-1566
[9]   AN ALL-ELECTRON NUMERICAL-METHOD FOR SOLVING THE LOCAL DENSITY FUNCTIONAL FOR POLYATOMIC-MOLECULES [J].
DELLEY, B .
JOURNAL OF CHEMICAL PHYSICS, 1990, 92 (01) :508-517
[10]   EFFICIENT AND ACCURATE EXPANSION METHODS FOR MOLECULES IN LOCAL DENSITY MODELS [J].
DELLEY, B ;
ELLIS, DE .
JOURNAL OF CHEMICAL PHYSICS, 1982, 76 (04) :1949-1960