Copyright (c) 2019 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
A 4-(1H-Benzo[d]oxazole-2-yl)-2-methoxyphenol as Dual Selective Sensor for Cyanide Ion Detection
Corresponding Author(s) : R. Rahmawati
Asian Journal of Chemistry,
Vol. 31 No. 3 (2019): Vol 31 Issue 3
Abstract
A dual sensor based on benzoxazole containing moiety S3 was successfully synthesized and applied for detection of CN− ion. The S3 molecule changed its colour for dark brown to dark green on addition of the CN− ion only in DMSO solvent. The limit of detection (LOD) and association constant (Kass) values was 0.4 × 10−6 M and 1.0 × 107 M−1; and 0.46 × 10−4 M and 1.0 × 105 M−1 determined by UV-visible spectroscopic titration and fluorescence titration, respectively.
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- S.O. Obare, C. De, W. Guo, T.L. Haywood, T.A. Samuels, C.P. Adams, N.O. Masika, D.H. Murray, G.A. Anderson, K. Campbell and K. Fletcher, Sensors, 10, 7018 (2010); https://doi.org/10.3390/s100707018.
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- P. Golamzadeh, G.H. Ziarani, N. Lashgari, A. Badiei, A. Shayesteh and M. Jafari, J. Fluoresc., 26, 1857 (2016); https://doi.org/10.1007/s10895-016-1879-z.
- 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.
- L. Lan, T. Li, T. Wei, H. Pang, T. Sun, E. Wang, H. Liu and Q. Niu, Spectrochim. Acta A Mol. Biomol. Spectrosc., 193, 289 (2018); https://doi.org/10.1016/j.saa.2017.12.039.
- R. Rahmawati, B. Purwono and S. Matsjeh, Asian J. Chem., 29, 1959 (2017); https://doi.org/10.1016/j.saa.2017.12.039.
- H. Reyes, H.I. Beltran and E. Rivera-Becerril, Tetrahedron Lett., 52, 308 (2011); https://doi.org/10.1016/j.tetlet.2010.11.038.
- J.-C. Qin, T.-R. Li, B.-D. Wang, Z.-Y. Yang and L. Fan, Synth. Metals, 195, 141 (2014); https://doi.org/10.1016/j.synthmet.2014.06.002.
- J.-C. Qin and Z.-Y.Yang, Synth. Metals, 209, 570-576 (2015); https://doi.org/10.1016/j.synthmet.2015.09.021.
- J. Shao, H. Lin, M. Yu, Z. Cai and H. Lin, Talanta, 75, 551 (2008); https://doi.org/10.1016/j.talanta.2007.11.048.
- L. Zou, B. Yan, D. Pan, Z. Tan and X. Bao, Spectrochim. Acta A Mol. Biomol. Spectrosc., 148, 78 (2015); https://doi.org/10.1016/j.saa.2015.03.109.
- L.Q. Yan, M.F. Cui, Y. Zhou, Y. Ma and Z.J. Qi, Anal. Sci., 31, 1055 (2015); https://doi.org/10.2116/analsci.31.1055.
- A. Okudan, S. Erdemir and O. Kocygit, J. Mol. Struct., 1048, 392 (2013); https://doi.org/10.1016/j.molstruc.2013.04.077.
- V. Reena, S. Suganya and S. Velmathi, J. Fluorine Chem., 153, 89 (2013); https://doi.org/10.1016/j.jfluchem.2013.05.010.
References
S.O. Obare, C. De, W. Guo, T.L. Haywood, T.A. Samuels, C.P. Adams, N.O. Masika, D.H. Murray, G.A. Anderson, K. Campbell and K. Fletcher, Sensors, 10, 7018 (2010); https://doi.org/10.3390/s100707018.
R. Wang, Y. Ma, J. Zhao, A. Zhang, S. Yang, H. Shen, G. Li and Z. Shi Sens. Actuators B, 260, 719 (2010); https://doi.org/10.1016/j.snb.2017.12.171.
P. Golamzadeh, G.H. Ziarani, N. Lashgari, A. Badiei, A. Shayesteh and M. Jafari, J. Fluoresc., 26, 1857 (2016); https://doi.org/10.1007/s10895-016-1879-z.
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.
L. Lan, T. Li, T. Wei, H. Pang, T. Sun, E. Wang, H. Liu and Q. Niu, Spectrochim. Acta A Mol. Biomol. Spectrosc., 193, 289 (2018); https://doi.org/10.1016/j.saa.2017.12.039.
R. Rahmawati, B. Purwono and S. Matsjeh, Asian J. Chem., 29, 1959 (2017); https://doi.org/10.1016/j.saa.2017.12.039.
H. Reyes, H.I. Beltran and E. Rivera-Becerril, Tetrahedron Lett., 52, 308 (2011); https://doi.org/10.1016/j.tetlet.2010.11.038.
J.-C. Qin, T.-R. Li, B.-D. Wang, Z.-Y. Yang and L. Fan, Synth. Metals, 195, 141 (2014); https://doi.org/10.1016/j.synthmet.2014.06.002.
J.-C. Qin and Z.-Y.Yang, Synth. Metals, 209, 570-576 (2015); https://doi.org/10.1016/j.synthmet.2015.09.021.
J. Shao, H. Lin, M. Yu, Z. Cai and H. Lin, Talanta, 75, 551 (2008); https://doi.org/10.1016/j.talanta.2007.11.048.
L. Zou, B. Yan, D. Pan, Z. Tan and X. Bao, Spectrochim. Acta A Mol. Biomol. Spectrosc., 148, 78 (2015); https://doi.org/10.1016/j.saa.2015.03.109.
L.Q. Yan, M.F. Cui, Y. Zhou, Y. Ma and Z.J. Qi, Anal. Sci., 31, 1055 (2015); https://doi.org/10.2116/analsci.31.1055.
A. Okudan, S. Erdemir and O. Kocygit, J. Mol. Struct., 1048, 392 (2013); https://doi.org/10.1016/j.molstruc.2013.04.077.
V. Reena, S. Suganya and S. Velmathi, J. Fluorine Chem., 153, 89 (2013); https://doi.org/10.1016/j.jfluchem.2013.05.010.