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A Novel 4-(1H-Benzimidazol-2-yl)-2-methoxy-phenol Derived Fluorescent Sensor for Determination of CN– Ion
Corresponding Author(s) : R. Rahmawati
Asian Journal of Chemistry,
Vol. 29 No. 9 (2017): Vol 29 Issue 9
Abstract
A novel fluorescent sensor 4-(1H-benzimidazol-2-yl)-2-methoxy-phenol derivative was synthesized. Solution of 4-(1H-benzimidazol-2-yl)-2-methoxy-phenol (1 × 10–7 M) in DMSO displays highly sensitives and rapid respons to CN– ion [values of LOD = 1.8 × 10–6 M and Ka = 2.5 (± 0.26) × 106 M–1]. Sensor 4-(1H-benzimidazol-2-yl)-2-methoxy-phenol coordinated with CN– ion form with a 1:1 binding stoichiometry.
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- H. Khanmohammadi, K. Rezaeian and A. Abdollahi, Spectrochim. Acta A, 139, 405 (2015); https://doi.org/10.1016/j.saa.2014.12.088.
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References
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X. Shang, Y. Wang, X. Wei, Z. Fu, J. Zhang and X. Xu, Molecules, 18, 14840 (2013); https://doi.org/10.3390/molecules181214840.
N. Dikshit, M. Tiwari and A. Dewan, Natl. J. Med. Res., 4, 106 (2014).
G.J. Park, I.H. Hwang, E.J. Song, H. Kim and C. Kim, Tetrahedron, 70, 2822 (2014); https://doi.org/10.1016/j.tet.2014.02.055.
R.M.F. Batista, R.C.M. Ferreira, M.M.M. Raposo and S.P.G. Costa, Tetrahedron, 68, 7322 (2012); https://doi.org/10.1016/j.tet.2012.06.087.
Z. Karimi-Jaberi and M. Amiri, E-J. Chem., 9, 167 (2012); https://doi.org/10.1155/2012/793978.
X. Bao and Y. Zhou, Sens. Actuators B Chem., 147, 434 (2010); https://doi.org/10.1016/j.snb.2010.03.068.
G.J. Park, Y.W. Choi, D. Lee and C. Kim, Spectrochim. Acta A, 132, 771 (2014); https://doi.org/10.1016/j.saa.2014.06.001.
O. Çimen, H. Dinçalp and C. Varlikli, Sens. Actuators B Chem., 209, 853 (2015); https://doi.org/10.1016/j.snb.2014.12.056.
L. Chen, H. Nie, G. Zhang, F. Gong, Y. Yang, C. Gong, Q. Tang and K. Xiao, Tetrahedron Lett., 55, 3017 (2014); https://doi.org/10.1016/j.tetlet.2014.03.097.
S.-Y. Na and H.-J. Kim, Tetrahedron Lett., 56, 493 (2015); https://doi.org/10.1016/j.tetlet.2014.12.083.
J.-B. Li, J.-H. Hu, J.-J. Chen and J. Qi, Spectrochim. Acta A, 133, 773 (2014); https://doi.org/10.1016/j.saa.2014.06.060.
Y. Zhang, B. Zou, Z. Chen, Y. Pan, H. Wang, H. Liang and X. Yi, Bioorg. Med. Chem. Lett., 21, 6811 (2011); https://doi.org/10.1016/j.bmcl.2011.09.029.
N. Kaur, G. Dhaka and J. Singh, Tetrahedron Lett., 56, 1162 (2015); https://doi.org/10.1016/j.tetlet.2015.01.128.
A.S. Gupta, K. Paul and V. Luxami, Inorg. Chim. Acta, 443, 57 (2016); https://doi.org/10.1016/j.ica.2015.11.024.
W. Zheng, X. He, H. Chen, Y. Gao and H. Li, Spectrochim. Acta A, 124, 97 (2014); https://doi.org/10.1016/j.saa.2013.12.098.
Y.-C. Wang, L.-Z. Liu, Y.-M. Pan and H.-S. Wang, Molecules, 16, 100 (2010); https://doi.org/10.3390/molecules16010100.
L. Jun, L. Qi, Y.M. Zhang and T.B. Wei, Sci. China Chem., 57, 1257 (2014); https://doi.org/10.1007/s11426-014-5108-9.
T.B. Nguyen, J.L. Bescont, L. Ermolenko and A. Al-Mourabit, Org. Lett., 15, 6218 (2013); https://doi.org/10.1021/ol403064z.
Y. Kim, M.R. Kumar, N. Park, Y. Heo and S. Lee, J. Org. Chem., 76, 9577 (2011); https://doi.org/10.1021/jo2019416.
M. Rekha, A. Hamza, B.R. Venugopal and N. Nagaraju, Chin. J. Catal., 33, 439 (2012); https://doi.org/10.1016/S1872-2067(11)60338-0.
W. Cui, R.B. Kargbo, Z. Sajjadi-Hashemi, F. Ahmed and J.F. Gauuan, Synlett, 247 (2012); https://doi.org/10.1055/s-0031-1290129.
V. Reena, S. Suganya and S. Velmathi, J. Fluor. Chem., 153, 89 (2013); https://doi.org/10.1016/j.jfluchem.2013.05.010.
J. Shao, Dyes Pigments, 87, 272 (2010); https://doi.org/10.1016/j.dyepig.2010.04.007.
C.R. Nicoleti, V.G. Marini, L.M. Zimmermann and V.G. Machado, J. Braz. Chem. Soc., 23, 1488 (2012); https://doi.org/10.1590/S0103-50532012005000007.
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