Synthesis, characterization, theoretical calculations, DNA binding and colorimetric anion sensing applications of 1-[(E)-[(6-methoxy-1,3-benzothiazol-2-yl)imino]methyl]naphthalen-2-ol

•Title molecule was full characterized.•Molecular geometry was theoretically determined by using DFT method.•The binding ability of Schiff base to CT-DNA was characterized by spectroscopy.•The colorimetric response of the Schiff base receptors in DMSO was investigated. We report the synthesis of a S...

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Bibliographic Details
Published in:Sensors and actuators. B, Chemical Chemical, 2015-08, Vol.215, p.52-61
Main Authors: Barare, Belygona, Yıldız, Mustafa, Alpaslan, Gökhan, Dilek, Nefise, Ünver, Hüseyin, Tadesse, Solomon, Aslan, Kadir
Format: Article
Language:English
Subjects:
2-amino-6-methoxybenzothiazole
Anion sensors
Anions
Binding
Calf thymus-DNA
Color
Colorimetry
Density functional theory
Deoxyribonucleic acid
Mathematical analysis
Molecular structure
Schiff base
Synthesis (chemistry)
X-ray crystallography
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Summary:•Title molecule was full characterized.•Molecular geometry was theoretically determined by using DFT method.•The binding ability of Schiff base to CT-DNA was characterized by spectroscopy.•The colorimetric response of the Schiff base receptors in DMSO was investigated. We report the synthesis of a Schiff base 1-(E)-[(6-methoxy-1,3-benzothiazol-2-yl)imino]methyl]naphthalen-2-ol from the reaction of 2-hydroxy-1-naphtaldehyde with 2-amino-6-methoxybenzothiazole. The molecular structure of the title compound was experimentally determined using X-ray single-crystal data and was compared to the structure predicted by theoretical calculations using density functional theory (DFT). In addition, nonlinear optical (NLO) effects of the title compound was predicted using DFT. The colorimetric response of the title compound in DMSO to the addition of equivalent amount of anions (F−, CN−, H2PO4−, OH−, Br−, I−, SCN−, ClO4−, HSO4− N3− and AcO−) was investigated. In this regard, while the addition of F−, CN−, H2PO4−, OH−, and AcO− anions into the solution containing the title compound resulted in a significant color change, the addition of Br−, I−, SCN−, ClO4−, HSO4− and N3− anions resulted in no color change. The most discernable color change in the title compound was caused by CN−, which demonstrated that the title compound can be used to selectively detect CN−. The order of anion-binding power of the title compound was determined to be OH−>CN−>F−∼AcO−>H2PO4−. The interactions between the receptor and anions were investigated using 1H NMR titration method. Theoretical and UV–VIS spectroscopy studies of the interactions between the title compound and calf thymus DNA (CT-DNA) showed that the title compound interacts with CT-DNA via intercalative binding.
ISSN:0925-4005
1873-3077
DOI:10.1016/j.snb.2015.03.025