European Journal of Chemistry

Benzo[g]quinoline heterocyclic derivative as a typical precursor in the synthesis of new class of cyanine-like dyes



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Maha Mobaruk Gomaa
Naglaa Salah El-Deen
Nadia Ali El-Kanzi

Abstract

New unsymmetrical cyanine-like dyes have been synthesized including monomethine, dimethine, and tetramethine, containing heterocyclic quinone of benzo[g]quinoline derivative. The new synthesized compounds were identified by elemental analysis, IR and 1H NMR. The UV visible absorption spectra of dyes are also reported.

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Gomaa, M. M.; El-Deen, N. S.; El-Kanzi, N. A. Benzo[g]quinoline Heterocyclic Derivative As a Typical Precursor in the Synthesis of New Class of Cyanine-Like Dyes. Eur. J. Chem. 2012, 3, 461-467.

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References

[1]. Harinath, B. B.; Subba, R. N. V. Proc. Indian Acad. Sci. 1968, 67A, 31-36.

[2]. El-Kanzi, N. A. IOSR J. Appl. Chem. 2012, 1(1), 18-30.

[3]. Shellhammer, C. W. Petersen S. Ann. 1959, 624, 108-119.

[4]. Liao, T. K.; Nyberg, W. H.; Cheng, C. C. Angew. Chem. (Int. Edn.). 1967, 6, 82-82.

[5]. Silva, A. J. M.; Netto, C. D.; Pacienza-Lima, W.; Torres-Santos, E. C.; Rossi-Bergmann, B.; Maurel, S.; Valentin, A.; Costa, P. R. R. J. Braz. Chem. Soc. 2009, 20, 176-182.
http://dx.doi.org/10.1590/S0103-50532009000100026

[6]. Gonzalez-Ibarra, M.; Farfan, N.; Trejo, C.; Uribe, S.; Lotina-Hennsen, B. J. Agric. Food Chem. 2005, 53, 3415-3420.
http://dx.doi.org/10.1021/jf047883o
PMid:15853381

[7]. Khalafallah, A. K.; Koraiem, A. I. M.; Elmaghraby, M. A.; Shindy, H. A. Egypt Chem. 1993, 36(3), 159-166.

[8]. Abd El-Aal, R. M.; Koraiem, A. I. M.; El-Deen N. S. Dyes Pigments 2004, 63, 301-314.
http://dx.doi.org/10.1016/j.dyepig.2004.03.008

[9]. Sturnmer, D. M.; Heseltine, D. W.; James, T. H. Sensitizing and desensitizing dyes-the theory of photographic processes, 4th edn, New York, Macmillan, 1977; Chapter 8.

[10]. Matsuoka, M. Infrared absorbing dyes, New York, Plenum Press, 1990.

[11]. Okawara, M.; Kitao, T.; Hirashima, T.; Matsuoka, M. Organic colorants-a handbook of data of selected dyes for electro-optical applications. Amsterdam, Elsevier Science Publishers, B. V., 1988.
PMCid:282473

[12]. Fabian, J.; Nakazumi, H.; Matsuoka, M. Chem. Rev. 1992, 92(6), 1197-1226.
http://dx.doi.org/10.1021/cr00014a003

[13]. Haugland, R. F. Handbook of fluorescent probes and research chemicals, 7th edn. Molecular Probes, Inc., 1999.

[14]. Broker, L. G. S.; Keyes, G. H. J. Am. Chem. Soc. 1935, 57, 2488-2492.
http://dx.doi.org/10.1021/ja01315a050

[15]. Shindy, H. A.; Koraiem, A. I. M. Proc. Indian Acad. Sci. (Chem. Sci.) 2002, 114(2), 125-136.

[16]. Elkanzi N. A. A. Phosphorus Sulfur 2008, 183(8), 2040-2057.
http://dx.doi.org/10.1080/10426500701841821

[17]. Presiado, I.; Karton-Lifshin, N.; Erez, Y.; Gepshtein, R.; Shabat, D.; Huppert, D. J. Phys. Chem. A 2012, 116(27), 7353-7363.
http://dx.doi.org/10.1021/jp304123y
PMid:22672017

[18]. Koraiem, A. I. M.; Abu El-Hamd, R. M.; Khalafallah, A. K.; Hammam, A. S.; El-Maghraby, M. A.; Gomaa, M. M. Dyes Pigments 1996, 30(2), 89-98.
http://dx.doi.org/10.1016/0143-7208(95)00047-X

[19]. Koraiem, A. I. M.; Abd El-Aal, R. M.; El-Deen N. S. Dyes Pigments 2006, 68, 235-242.
http://dx.doi.org/10.1016/j.dyepig.2005.01.007

[20]. Koraiem, A. I. M.; Girgis, M. M.; Khalil, Z. H.; EL-Hamd, R. M. A. Dyes Pigments 1991, 15(2), 89-105.
http://dx.doi.org/10.1016/0143-7208(91)87010-K

[21]. Ramos, S. S.; Santos, P. F.; Reis, L. V.; Almeida, P. Dyes Pigments 2002, 53, 143-152.
http://dx.doi.org/10.1016/S0143-7208(02)00003-7

[22]. Abd El-Aal, R. M.; Younis, M. Bioorganic Chem. 2004, 32(4), 193-210.
http://dx.doi.org/10.1016/j.bioorg.2004.04.001
PMid:15210335

[23]. Abd El-Aal, R. M.; Koraiem, A. I. M. Dyes Pigments 2002, 54, 121-129.
http://dx.doi.org/10.1016/S0143-7208(02)00034-7

[24]. Abd El-Aal, R. M.; Koraiem, A. I. M.; Khalil, Z. H.; El-Kodey, A. M. M. Dyes Pigments 2005, 66, 201-209.
http://dx.doi.org/10.1016/j.dyepig.2004.09.015

[25]. Ohira, S.; Hales, J. M.; Thorley, K. J.; Anderson, H. L.; Perry, J. W.; Breedas, J. J. Am. Chem. Soc. 2009, 131 (17), 6099-6101.
http://dx.doi.org/10.1021/ja9007003
PMid:19354289

[26]. Mykola, P. S.; Viktor, P. Y; Andriy, O. G; Olexiy, D. K; Yevgen, M. P; Yuriy, P. K. Eur. J. Org. Chem. 2012, 9, 1825-1834.

[27]. Khalafallah, A. K.; Abd El-Aal, R. M.; El Kanzi, N. A. A. J. Chin. Chem. Soc. 2002, 49, 387-396.

[28]. Katritzky, A. R.; Meth-Cohn, O.; Pattenden G. Comprehensive organic functional group transformations: Synthesis of carbon with one heteroatom attached by multiple bond, Pattenden G. Editor, Elsevier Pub., 1995, vol. 3.

[29]. Mshalker, U. C.; Audi, A. A. Indian J. Chem. B 2006, 45, 967-971.

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Department of Chemistry, Aswan-Faculty of Science, Aswan University, Egypt
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