Email this article 
Hide
Show all
OPEN ACCESS | 
PEER-REVIEWED |
RESEARCH ARTICLE
|
DOWNLOAD PDF
|
VIEW FULL-TEXT PDF
| TOTAL VIEWS
Synthesis and recognition properties of colorimetric anion chemosensor bearing 2,4-dinitrophenylhydrazone and indene-1,3-dione moieties
Fatma Aydın (1,*)
(1) Çanakkale Onsekiz Mart University, Department of Chemistry, 17100, Çanakkale, Turkey
(*) Corresponding Author
Received: 06 Feb 2014 | Accepted: 02 Mar 2014 | Published: 30 Jun 2014 | Issue Date: June 2014
Abstract
A new receptor named, 2-(2-(2,4-dinitrophenyl)hydrazono)2H-indene-1,3-dione, used as a colorimetric sensor based on 2,4-dinitrophenylhydrazone derivative of ninhydrin was synthesized by simple step with good yields and characterized by IR and 1H, 13C NMR and MS spectroscopic techniques. The anion recognition properties were studied by UV-Vis spectroscopic technique. The results showed that the receptor had a higher affinity to F-, CN-, H2PO4-, CH3COO- and OH-, but showed no evident binding with Cl-, Br- and I-. Binding of the reseptor to anions such as CN-, AcO-, F-, H2PO4- and OH-exhibited an obvious color change from greenish yellow to purplish blue, which was possible to observe by the naked eye.
Announcements
Our editors have decided to support scientists to publish their manuscripts in European Journal of Chemistry without any financial constraints.
1- The article processing fee will not be charged from the articles containing the single-crystal structure characterization between July 1, 2022 and August 15, 2022 (Voucher code: SINGLE2022).
2. Young writers will not be charged for the article processing fee between July 1, 2022 and August 15, 2022 (Voucher code: YOUNG2022).
3. The article processing fee will not be charged from the articles containing a part of the PhD thesis between July 1, 2022 and August 15, 2022 (Voucher code: PhD2022).
Editor-in-Chief
European Journal of Chemistry
Keywords
Full Text:
PDF
DOI: 10.5155/eurjchem.5.2.370-373.1032
Links for Article
| | | | | | |
| | | | | | |
| | | |
Related Articles
Article Metrics
This Abstract was viewed 858 times |
PDF Article downloaded 442 times
Funding information
Çanakkale Onsekiz Mart University Research Fund (Project No: BAP-2010-57), Çanakkale Onsekiz Mart University, Çanakkale, Turkey
Citations
[1]. Vetriarasu Venkatesan, S. K. Ashok Kumar, Suban K. Sahoo
Spectrophotometric and RGB performances of a new tetraphenylcyclopenta-derived Schiff base for the quantification of cyanide ions
Analytical Methods 11(8), 1137, 2019
DOI: 10.1039/C8AY02401D
[2]. P. Karuppusamy, S. Sarveswari
A 4-phenyl thiophene appended 2,4-dinitrophenylhydrazone as a colorimetric chemosensor for selective detection of cyanide ion and its application for real-life samples
Journal of Molecular Structure 1248, 131494, 2022
DOI: 10.1016/j.molstruc.2021.131494
References
[1]. Beer, P. D.; Gale, P. A. Angew. Chem. Int. Ed. 2001, 40, 486-516.
http://dx.doi.org/10.1002/1521-3773(20010202)40:3<486::AID-ANIE486>3.0.CO;2-P
[2]. Gale, P. A. Coord. Chem. Rev. 2001, 213, 79-128.
http://dx.doi.org/10.1016/S0010-8545(00)00364-7
[3]. Gale, P. A. Coord. Chem. Rev. 2003, 240, 191-221.
http://dx.doi.org/10.1016/S0010-8545(02)00258-8
[4]. Li, J.; Lin, H.; Lin, H. J. Coord. Chem. 2009, 62(12), 1921-1927.
http://dx.doi.org/10.1080/00958970802702239
[5]. Athikomrattanakul, U.; Promptmas, C.; Katterle, M. Tetrahedron Lett. 2009, 50, 359-362.
http://dx.doi.org/10.1016/j.tetlet.2008.11.015
[6]. Shao, J.; Lin, H.; Lin, H. Dyes and Pigments 2009, 80, 259-263.
http://dx.doi.org/10.1016/j.dyepig.2008.07.012
[7]. Inoue, Y.; Kanbara, T.; Yamamoto, T. Tetrahedron Lett. 2003,44, 5167-5169.
http://dx.doi.org/10.1016/S0040-4039(03)01271-1
[8]. Best, M. D.; Tobey, S. L.; Anslyn, E. V. Coord. Chem. Rev. 2003, 240, 3-15.
http://dx.doi.org/10.1016/S0010-8545(02)00256-4
[9]. Lu, Q. S.; Dong, L.; Zhang, J.; Li, J.; Jiang, L.; Huang, Y.; Qin, S.; Hu, C. W.; Yu, X. Q. Org. Lett. 2009, 11(3), 669-672.
http://dx.doi.org/10.1021/ol8027303
[10]. Shao, J.; Qiao, Y. H.; Lin, H.; Lin, H. J. Lumin. 2008, 128, 1985-1988.
http://dx.doi.org/10.1016/j.jlumin.2008.06.010
[11]. Esteban-Gomez, D.; Fabbrizzi, L.; Licchelli, M. J. Org. Chem. 2005, 70, 5717-5720.
http://dx.doi.org/10.1021/jo050528s
[12]. Bondy, C. R.; Loeb, S. Coord. Chem. Rev. 2003, 240, 77-99.
http://dx.doi.org/10.1016/S0010-8545(02)00304-1
[13]. Li, J.; Chen, H.; Lin, H.; Lin, H. J. Photochem. Photobiol. B 2009, 97, 18-21.
http://dx.doi.org/10.1016/j.jphotobiol.2009.07.006
[14]. Chen, Q. Y.; Chen, C. F. Tetrahedron Lett. 2004, 45, 6493-6496.
http://dx.doi.org/10.1016/j.tetlet.2004.06.135
[15]. Adminal, D. J.; Krishna, D. K.; Ganguly, B.; Das, A. Org. Lett. 2004, 6(20), 3445-3448.
http://dx.doi.org/10.1021/ol048829w
[16]. Aydin, F.; Tunoglu, N.; Aykac, D.; Arslan, N. B.; Kazak, C. Turk. J. Chem. 2012, 36(5), 764-777.
[17]. Lee, K. H.; Hong, J. I. Tetrahedron Lett. 2000, 41, 6083-6087.
http://dx.doi.org/10.1016/S0040-4039(00)00966-7
[18]. Beer, P. D.; Gale, P. A.; Hesek, D. Tetrahedron Lett. 1995, 36, 767-770.
http://dx.doi.org/10.1016/0040-4039(94)02363-G
[19]. Cafeo, G.; Kohnke, F. H.; White, A. J. P.; Garozzo, D.; Messina, A. Chem. Eur. J. 2007, 13, 649-656.
http://dx.doi.org/10.1002/chem.200600452
[20]. Dydio, P.; Zieliniski, T.; Jurczak, J. J. Org. Chem. 2009, 74, 1525-1530.
http://dx.doi.org/10.1021/jo802288u
[21]. Shao, J.; Wang, Y.; Lin, H.; Li, J.; Lin, H. Sens. Actuators B, Chem. 2008, 134, 849-853.
http://dx.doi.org/10.1016/j.snb.2008.06.052
[22]. Shao, J.; Lin, H.; Yu, M.; Cai, Z.; Lin, H. Talanta 2008, 75, 551-555.
http://dx.doi.org/10.1016/j.talanta.2007.11.048
[23]. Li, J.; Wang, Y.; Lin, H.; Lin, H. J. Incl. Phenom. Macrocycl. Chem. 2009, 63, 281-285.
http://dx.doi.org/10.1007/s10847-008-9518-1
[24]. Bourson, J.; Pouget, J.; Valeur, B. J. Phys. Chem. 1993, 97, 4552-4557.
http://dx.doi.org/10.1021/j100119a050
How to cite
The other citation formats (EndNote | Reference Manager | ProCite | BibTeX | RefWorks) for this article can be found online at: How to cite item
DOI Link: https://doi.org/10.5155/eurjchem.5.2.370-373.1032
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
Save to Zotero
Save to Mendeley
European Journal of Chemistry 2014, 5(2), 370-373 | doi: https://doi.org/10.5155/eurjchem.5.2.370-373.1032 | Get rights and content
Refbacks
- There are currently no refbacks.
Copyright (c)
© Copyright 2010 - 2022 • Atlanta Publishing House LLC • All Right Reserved.
The opinions expressed in all articles published in European Journal of Chemistry are those of the specific author(s), and do not necessarily reflect the views of Atlanta Publishing House LLC, or European Journal of Chemistry, or any of its employees.
Copyright 2010-2022 Atlanta Publishing House LLC. All rights reserved. This site is owned and operated by Atlanta Publishing House LLC whose registered office is 2850 Smith Ridge Trce Peachtree Cor GA 30071-2636, USA. Registered in USA.