Browse > Article
http://dx.doi.org/10.5012/jkcs.2012.56.6.716

Fe(HSO4)3 as an Efficient Catalyst for Diazotization and Diazo Coupling Reactions  

Rahimizadeh, Mohammad (Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad)
Eshghi, Hossein (Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad)
Shiri, Ali (Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad)
Ghadamyari, Zohreh (Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad)
Matin, Maryam M. (Department of Biology, Faculty of Science, Ferdowsi University of Mashhad)
Oroojalian, Fatemeh (Department of Life Science Engineering, Faculty of New Sciences and Technologies, University of Tehran)
Pordeli, Parvaneh (Department of Biology, Faculty of Science, Ferdowsi University of Mashhad)
Publication Information
Journal of the Korean Chemical Society / v.56, no.6, 2012 , pp. 716-719 More about this Journal
Abstract
Diazo coupling reactions of aromatic amines with 2-naphthol in a green, efficient and easy procedure is described. Ferric hydrogensulfate catalyses this reaction in water at room temperature and short reaction time with high yields. The antibacterial activities of the synthesized compounds against four pathogenic bacteria are also investigated.
Keywords
Diazotization; $Fe(HSO_4)_3$; 2-Naphthol;
Citations & Related Records
Times Cited By KSCI : 2  (Citation Analysis)
연도 인용수 순위
1 Koch, L.; Milligan, R.; Zuckerman, S. Ind. Eng. Chem. 1944, 16, 755.
2 Smyth, R. B.; McKeown, G. G. J. Chromatogr. 1961, 5, 395.   DOI
3 Zaugg, H. E. J. Am. Chem. Soc. 1945, 67, 1861.
4 Rowe, F. M. J. Soc. Dyes Colour 1924, 40, 218.
5 Clinical and Laboratory Standards Institute, Methods for the Antimicrobial Susceptibility Testing of Anaerobic Bacteria; Approved Standard-Eighth Edition Approved Standard M11-A8, 2012, Villanova, PA, USA.
6 Oroojalian, F.; Kasra-Kermanshahi, R.; Azizi, M.; Bassami, M. R. Food Chem. 2010, 120, 765.   DOI   ScienceOn
7 Zollinger, H. Azo and Diazo Chemistry, Aliphatic and Aromatic Compounds; Interscience Publishers: London, England, 1961.
8 Saunders, K. H.; R. Allen, L. M. Aromatic Diazo Compounds; 3rd Ed.; Edward Arnold Publishers: London, England, 1985.
9 Jin, J.; Wen, Z.; Wang, Y.; Matsuura, T.; Meng, J. Synth. Commun. 2000, 30, 829.   DOI
10 Dabbagh, H. A.; Teimouri, A.; Najafi, A. Appl. Catal., B 2007, 76, 24.   DOI
11 Zollinger, H. Color Chemistry, 3rd ed.; Verlag, Switzerland, 2003; p 165
12 Jarrahpour, A. A.; Motamedifar, M.; Pakshir, K.; Hadi, N.; Zarei, M. Molecules 2004, 9, 815.   DOI   ScienceOn
13 Clark, J. H. Chemistry of waste minimization; Chapman and Hall: London, England, 1995.
14 Bahulayan, D.; John, L.; Lalithambika, M. Synth. Commun. 2003, 33, 863.   DOI
15 Novak, P.; Lycka, A.; Cisarova, I.; Buchta, V.; Silva, L.; Kolarova, L.; Ruzicka, A.; Holecek, J. Appl. Organomet. Chem. 2005, 19, 500.   DOI
16 Kurtoglu, N. J. Serb. Chem. Soc. 2009, 74, 917.   DOI
17 Xu, H.; Zeng, X. Bioorg. Med. Chem. Lett. 2010, 20, 4193.   DOI
18 Okahara, T. Chem. Rev. 2002, 102, 3641.   DOI   ScienceOn
19 Eshghi, H.; Bakavoli, M.; Moradi, H. Chin. Chem. Lett. 2008, 19, 1423.
20 Bakavoli, M.; Rahimizadeh, M.; Eshghi, H.; Shiri, A.; Ebrahimpour, Z.; Takjoo, R. Bull. Korean Chem. Soc. 2010, 31, 949.   DOI
21 Rahimizadeh, M.; Bakhtiarpoor, Z.; Eshghi, H.; Pordel, M.; Rajabzadeh, G. Monat. Chem. 2009, 140, 1465.   DOI
22 Rahimizadeh, M.; Bakavoli, M.; Shiri, A.; Eshghi, H. Bull. Korean Chem. Soc. 2009, 30, 1699.   DOI
23 Rahimizadeh, M.; Bakavoli, M.; Shiri, A.; Eshghi, H.; Saberi, S. J. Chem. Res. 2008, 704.
24 Bakavoli, M.; Rahimizadeh, M.; Shiri, A.; Eshghi, H.; Vaziri- Mehr, S.; Pordeli, P.; Nikpour, M. Heterocycl. Commun. 2011, 17, 49.
25 Eshghi, H.; Rahimizadeh, M.; Saberi, S. Catal. Commun. 2008, 9, 2460.   DOI
26 Yamada, T.; Tanaka, N.; Morisawa, T.; Nishikuri, M.; Kaji, A. Bull. Chem. Soc. Jpn. 1970, 43, 908.   DOI