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A Naked-Eye Colorimetric Receptor for Anions Based on Nitro Group Featuring with Benzimidazole Unit
Corresponding Author(s) : R. Rahmawati
Asian Journal of Chemistry,
Vol. 30 No. 9 (2018): Vol 30 Issue 9
Abstract
A novel receptor based on nitro group featuring with benzimidazole unit (S2) was successfully synthesized and applied to the anion (CN–, F– and H2PO4–) recognition. The S2 changed its colour for light yellow to dark yellow on addition of the anions in DMSO solvent. The LOD and Kass values determined by UV-visible titration was 2.8 × 10–6 M and 1.2 (± 0.25) × 106 M–1 for CN– ion; 1.14 × 10–6 M and 2.5 (± 0.25) × 106 M–1 for F– ion; and 1.23 × 10–5 M and 6.25 (± 0.177) × 106 M–1 for H2PO4– ion, respectively.
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- B. Hu, P. Lu and Y. Wang, Sens. Actuators B Chem., 195, 320 (2014); https://doi.org/10.1016/j.snb.2014.01.058.
- D. Udhayakumari, S. Velmathi, W.-C. Chen and S.-P. Wu, Sens. Actuators B Chem., 204, 375 (2014); https://doi.org/10.1016/j.snb.2014.07.109.
- X. Bao and Y. Zhou, Sens. Actuators B Chem., 147, 434 (2010); https://doi.org/10.1016/j.snb.2010.03.068.
- R. Jin, W. Sun and S. Tang, Int. J. Mol. Sci., 13, 10986 (2012); https://doi.org/10.3390/ijms130910986.
- K.S. Moon, N. Singh, G.W. Lee and D.O. Jang, Tetrahedron, 63, 9106 (2007); https://doi.org/10.1016/j.tet.2007.06.091.
- 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.
- A. Okudan, S. Erdemir and O. Kocyigit, J. Mol. Struct., 1048, 392 (2013); https://doi.org/10.1016/j.molstruc.2013.04.077.
- R. Rahmawati, B. Purwono and S. Matsjeh, Asian J. Chem., 29, 1959 (2017); https://doi.org/10.14233/ajchem.2017.20662.
- Z. Karimi-Jaberi and M. Amiri, E-J. Chem., 9, 167 (2012); https://doi.org/10.1155/2012/793978.
- U. Yadav, H. Mande and P. Ghalsasi, J. Chem. Educ., 89, 268 (2012); https://doi.org/10.1021/ed100957v.
- S. Ghosh, M.A. Alam, A. Ganguly and N. Guchhait, Spectrochim. Acta A, 149, 869 (2015); https://doi.org/10.1016/j.saa.2015.04.025.
- V. Suryanti, M. Bhadbhade, H.M. Chawla, E. Howe, P. Thordarson, D.S. Black and N. Kumar, Spectrochim. Acta A, 121, 662 (2014); https://doi.org/10.1016/j.saa.2013.11.108.
- N.A. Hamedan, S. Hasan, H.M. Zaki and N.Z. Alias, IOP Conf. Series: Mater. Sci. Eng., 172, 012038 (2017); https://doi.org/10.1088/1757-899X/172/1/012038.
References
B. Hu, P. Lu and Y. Wang, Sens. Actuators B Chem., 195, 320 (2014); https://doi.org/10.1016/j.snb.2014.01.058.
D. Udhayakumari, S. Velmathi, W.-C. Chen and S.-P. Wu, Sens. Actuators B Chem., 204, 375 (2014); https://doi.org/10.1016/j.snb.2014.07.109.
X. Bao and Y. Zhou, Sens. Actuators B Chem., 147, 434 (2010); https://doi.org/10.1016/j.snb.2010.03.068.
R. Jin, W. Sun and S. Tang, Int. J. Mol. Sci., 13, 10986 (2012); https://doi.org/10.3390/ijms130910986.
K.S. Moon, N. Singh, G.W. Lee and D.O. Jang, Tetrahedron, 63, 9106 (2007); https://doi.org/10.1016/j.tet.2007.06.091.
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.
A. Okudan, S. Erdemir and O. Kocyigit, J. Mol. Struct., 1048, 392 (2013); https://doi.org/10.1016/j.molstruc.2013.04.077.
R. Rahmawati, B. Purwono and S. Matsjeh, Asian J. Chem., 29, 1959 (2017); https://doi.org/10.14233/ajchem.2017.20662.
Z. Karimi-Jaberi and M. Amiri, E-J. Chem., 9, 167 (2012); https://doi.org/10.1155/2012/793978.
U. Yadav, H. Mande and P. Ghalsasi, J. Chem. Educ., 89, 268 (2012); https://doi.org/10.1021/ed100957v.
S. Ghosh, M.A. Alam, A. Ganguly and N. Guchhait, Spectrochim. Acta A, 149, 869 (2015); https://doi.org/10.1016/j.saa.2015.04.025.
V. Suryanti, M. Bhadbhade, H.M. Chawla, E. Howe, P. Thordarson, D.S. Black and N. Kumar, Spectrochim. Acta A, 121, 662 (2014); https://doi.org/10.1016/j.saa.2013.11.108.
N.A. Hamedan, S. Hasan, H.M. Zaki and N.Z. Alias, IOP Conf. Series: Mater. Sci. Eng., 172, 012038 (2017); https://doi.org/10.1088/1757-899X/172/1/012038.