3-Amino-5-Hidroksi-1H-Pirazol Bazlı Bazı Yeni Disazo Boyarmaddelerinin Sentezi ve Spektroskopik Özellikleri

Bu çalışmada, yeni bir dizi 3-amino-5-hidroksi-1H-pirazol türevi boyarmadde sentezlendi ve karakterize edildi. Bu maksatla, m- ve o- sübstitüe anilin türevleri öncelikle diazolandı, elde edilen bileşikler 3-amino krotononitril ile kenetlendi. Elde edilen ürün (1a-h) hidrazin monohidrat ile etkileştirilerek 5-amino-4-arilazo-3-metil-1H-pirazoller (2a-h) sentezlendi. Sonrasında 5-amino-4-arilazo-3-metil-1H-pirazoller diazolandı ve 3-amino-5-hidroksi-1H-pirazol ile kenetlenerek 8 adet yeni disazo boyarmaddesi (3a-h) sentezlenmiş oldu. Elde edilen sekiz boyarmaddenin yapısı Fourier dönüşümlü infrared spektroskopisi (FT-IR), Nükleer manyetik rezonans spektroskopisi (1H-NMR), Ultraviyole görünür bölge absorpsiyon spektroskopisi (UV-Vis) ve element analizi gibi çeşitli spektrofotometrik yöntemlerle belirlendi. Altı farklı çözücüde boyarmaddelerin maksimum absorpsiyon dalga boyları belirlendi ve absorpsiyon spektrumları üzerine asit-baz etkisi incelendi. Bu çalışma sonunda tekstil ve azo boyarmadde literatürüne 8 adet yeni aminopirazol türevi disazo boyarmaddeleri kazandırıldı.

Synthesis and Spectroscopic Properties of Some New Disazo Dyes Based on 3-Amino-5-Hydroxy-1H-Pyrazole

In this study, a new series of 3-amino-5-hydroxy-1H-pyrazole derivative dyes were synthesized and characterized. For this purpose, firstly the m- and o- substituted aniline derivatives were diazotised, the resulting compounds were coupled with 3-amino crotononitrile. 5-amino-4-arylazo-3-methyl-1H-pyrazoles (2a-h) were synthesized by reacting the obtained product (1a-h) with hydrazine monohydrate. Subsequently, the 5-amino-4-arylazo-3-methyl-1H-pyrazoles were diazotised and coupled with 3-amino-5-hydroxy-1H-pyrazole to synthesize 8 new disazo dyes (3a-h). The structure of the eight dyes obtained were determined by various spectrophotometric methods such as Fourier transform infrared spectroscopy (FT-IR), Nuclear magnetic resonance spectroscopy (1H-NMR), Ultraviolet visible region absorption spectroscopy (UV-Vis) and elemental analysis. The maximum absorption wavelengths of the dyes in six different solvents were determined and the acid-base effects on the absorption spectra were investigated. At the end of this study, 8 new aminopyrazole derivative disazo dyes were introduced to the textile and azo dyestuff literature.

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  • [1] J. F. Dawson, ‘‘Developments in disperse dyes,’’ Color. Technol., 9, 25–35, 1978.
  • [2] H. Zollinger, ‘‘Color Chemistry: Synthesis, Properties and Application of Organic Dyes and Pigments,’’ third ed. Wiley-VCH, Weinheim, 161-167, 2003.
  • [3] H. Yousefi, A. Yahyazadeh, E. O. Moradi Rufchahi, M. Rassa, ‘‘Synthesis, spectral properties, biological activity and application of new 4-(benzyloxy)phenol derived azo dyes for polyester fiber dyeing,’’ J. Mol. Liq., 180, 51-58, 2013.
  • [4] H. F. Rizk, S. A. Ibrahim, M. A. El-Borani, ‘‘Synthesis, fastness properties, color assessment and antimicrobial activity of some azo reactive dyes having pyrazole moiety,’’ Dyes and Pigments, 112, 86-92, 2015.
  • [5] L. He, L. Lu, S. Zhang, H. S. Freeman, ‘‘Synthesis and application of yellow azoanthraquinone disperse dyes for polylactide fibres,’’ Color. Technol., 126(2), 92-96, 2010.
  • [6] M. A. Metwally, E. Abdel-latif, F. A. Amer, G. Kaupp, ‘‘Synthesis of new 5-thiazolyl azo-disperse dyes for dyeing polyester fabrics,’’ Dyes and Pigments, 60(3), 249-264, 2004.
  • [7] N. M. Parekh, S. K. Sahoo, K. C. Maheria, ‘‘Quantum chemical studies and dyeing performance of some novel benzoquinoline based heterocyclic monoazo dyes on polyester fiber,’’ Dyes and Pigments, 95(1), 142-148, 2012.
  • [8] H. Z. Shams, M. H. Helal, F. Mohamed, S. A. Abd-Elhafiz, ‘‘A novel synthesis of 1-oxo-thieno [3ʹ, 2ʹ-3, 4] pyrazolo [1, 2-a] pyrazole azo dye systems for dyeing of synthetic and modified cellulose fibers,’’ Pigment Resin Technol., 30(3), 158-167, 2001.
  • [9] F. Karcı, A. Demirçalı, F. Karcı, I. Kara, F. Ucun, ‘‘The synthesis, spectroscopic properties and theoretical calculation of some novel disperse disazo dyes derived from 3-amino-5-hydroxy-1-phenylpyrazole,’’ J. Mol. Struct., 935, 19-26, 2009.
  • [10] J. H. Choi, J. Y. Choi, Y. Lee, A. D. Towns, C. Yoon, ‘‘Novel azo dyes derived from phthalimide. Part 2: dyeing properties and colour fastness on polyester fibres,’’ Color. Technol., 124(6), 364-369, 2008.
  • [11] A. Z. Sayed, M. S. Aboul-Fetouh, H. S. Nassar, ‘‘Synthesis, biological activity and dyeing performance of some novel azo disperse dyes incorporating pyrazolo [1, 5-a] pyrimidines for dyeing of polyester fabrics,’’ J. Mol. Struct., 1010, 146–151, 2012.
  • [12] G. H. Elgemeie, M. H. Helal, H. M. El-Sayed, ‘‘Recent trends in synthesis and application of nitrogen heterocyclic azo dyes,’’ Pigment Resin Technol., 30(4), 210-228, 2001.
  • [13] J. Mikroyannidis, D. Tsagkournos, P. Balraju, G. Sharma, ‘‘Low band gap dyes based on 2-styryl-5-phenylazo-pyrrole: synthesis and application for efficient dyesensitized solar cells,’’ J. Power Sources, 196, 4152–4161, 2011.
  • [14] F. Ruyffelaere, V. Nardello, R. Schmidt, J. M. Aubry, ‘‘Photosensitizing properties and reactivity of aryl azo naphtol dyes towards singlet oxygen,’’ J Photochem Photobiol A: Chem., 183, 98–105, 2006.
  • [15] O. A. Adegoke, T. E. Adesuji, O. E. Thomas, ‘‘Novel colorimetric sensors for cyanide based on azo-hydrazone tautomeric skeletons,’’ Spectrochim Acta A Mol Biomol Spectrosc., 128, 147–152, 2014.
  • [16] P. J. Coelho, L. M. Carvalho, A. M. C. Fonseca, M. M. M. Raposo, ‘‘Photochromic properties of thienylpyrrole azo dyes in solution,’’ Tetrahedron Lett., 47, 3711–3714, 2006.
  • [17] E. Pevzner, B. Ehrenberg, ‘‘Principal component analysis of the absorption and resonance Raman spectra of the metallochromic indicator antipyrylazo III,’’ Spectrochim Acta A Mol Biomol Spectrosc., 56, 637–651, 2000.
  • [18] A. Y. Al-Ahmad, Q. M. A. Hassan, H. A. Badran, K. A. Hussain, ‘‘Investigating some linear and nonlinear optical properties of the azo dye (1-amino-2-hydroxy naphthalin sulfonic acid-[3-(4-azo)]-4-amino diphenyl sulfone),’’ Opt Laser Technol., 44(5), 1450–1455, 2012.
  • [19] M. Erfantalab, H. Khanmohammadi, ‘‘New 1, 2, 4-triazole-based azo–azomethine dye. Part III: synthesis, characterization, thermal property, spectrophotometric and computational studies,’’ Spectrochim Acta A. Mol Biomol Spectrosc., 125, 345–352, 2014.
  • [20] F. Yıldırım, A. Demirçalı, F. Karcı, A. Bayrakdar, P. T. Taşlı, H. H. Kart, ‘‘New coumarin-based disperse disazo dyes: Synthesis, spectroscopic properties and theoretical calculations,’’ J. Mol Struc., 223, 557-565, 2016.
  • [21] M. Yazdanbakhsh, H. Yousefi, M. Mamaghani, E. Moradi, M. Rassa, H. Pouramir, ‘‘Synthesis, spectral characterization and antimicrobial activity of some new azo dyes derived from 4, 6-dihydroxypyrimidine,’’ J. Mol. Liq., 169, 21–26, 2012.
  • [22] F. Karcı, N. Şener, M. Yamaç, İ. Şener, A. Demirçalı, ‘‘The synthesis, antimicrobial activity and absorption characteristics of some novel heterocyclic disazo dyes,’’ Dyes and Pigments, 80, 47–52, 2009. [23] H. Xu, X. Zeng, ‘‘Synthesis of diaryl-azo derivatives as potential antifungal agents,’’ Bioorg Med Chem Lett., 20(14), 4193–4195, 2010.
  • [24] T. I. El-Emary, S. A. A. El-Mohsen, ‘‘Multi-component one-pot synthesis and antimicrobial activities of 3-Methyl-1,4-diphenyl-7-thioxo-4, 6, 8, 9-tetrahydro-pyrazolo[5, 4-b] pyrimidino [5, 4-e] pyridine-5-one and related derivatives,’’ Molecules, 17, 14464–14483, 2012
  • [25] A. P. Acharya, R. D. Kamble, S. V. Hese, S. N. Kadam, R. N. Gacche, B. S. Dawane, ‘‘Eco-friendly synthesis of novel indeno-pyrazole derivatives and their in-vitro antimicrobial screening,’’ Org. Commun, 7(2), 68-76, 2014.
  • [26] S. G. Alegaon, K. R. Alagawadi, M. Garg, K. Dushyant, D. Vinod, ‘‘1, 3, 4-Trisubstituted pyrazole analogues as promising anti-inflammatory agents,’’ Bioorg Chem., 54, 51–59, 2014.
  • [27] P. D. Gokulan, B. Jayakar, V. Alagarsamy, V. R. Solomon, ‘‘Synthesis and Pharmacological Investigation of 5-Substituted-3-Methylsulfanyl-1H-Pyrazole-4-Carboxylic Acid Ethyl Esters as New Analgesic and anti-Inflammatory Agents,’’ Arzneimittelforschung, 62, 457–462, 2012.
  • [28] H. M. Faidallah, M. M. Al-Mohammadi, K. A. Alamry, K. A. Khan, ‘‘Synthesis and Biological Evaluation of Fluoropyrazolesulfonylurea and Thiourea Derivatives as Possible AntidiabeticAgents,’’J. Enzyme Inhib. Med. Chem., 31, 157–163, 2016.
  • [29] A.R. Ali, E.R. El-Bendary, M. A. Ghaly, I. A. Shehata, ‘‘Synthesis, in vitro anticancer evaluation and in silico studies of novel imidazo [2, 1-b] thiazole derivatives bearing pyrazole moieties,’’ Eur J Med Chem., 75, 492–500, 2014.
  • [30] M. Abdel-Aziz, GE-DA Abuo-Rahma, AA Hassan, ‘‘Synthesis of novel pyrazole derivatives and evaluation of their antidepressant and anticonvulsant activities,’’ Eur J Med Chem., 44, 3480–3487, 2009
  • [31] V. Pathak, H. K. Maurya, S. Sharma, K. K. Srivastava, A. Gupta, ‘‘Synthesis and biological evaluation of substituted 4, 6-diarylpyrimidines and 3, 5-diphenyl-4, 5-dihydro-1H-pyrazoles as anti-tubercular agents,’’ Bioorg Med Chem Lett., 24, 2892–2896, 2014
  • [32] F. Yıldırım, A. Demirçalı, P. T. Taşlı, F. Karcı, ‘‘New disazo dyes derived from aminopyrazoles: synthesis, spectroscopic properties, computational study and structural properties’’ Coloration Technology, baskıda, 2021.
  • [33] M. H. Elnagdi, M. M. M. Sallam, H. M. Fahmy, S. A. M. Ibrahim, M. A. M. Elias, ‘‘Reactions with the Arylhydrazones of α-Cyanoketones: The Structure of 2-Arylhydrazono-3-ketimino-nitriles,’’ Helv Chim.Acta., 59(2), 551-557, 1976.
  • [34] M. H. Elnagdi, G. E. H. Elgemeie, F. A. E. Abd-Ellal, ‘‘Recent Developments in the Synthesis of Pyrazole Derivative,’’ Heterocycles, 23(12), 3121- 3153, 1985.
  • [35] F. Karcı, ‘‘Synthesis of disazo dyes derived from heterocyclic components,’’ Color Technol., 121, 275-280, 2005.
  • [36] F. Karcı, A. Demirçalı, ‘‘Synthesis of disazo pyrazolo[1,5-a]pyrimidines,’’ Dyes and Pigments, 74, 288-297, 2007.
Süleyman Demirel Üniversitesi Fen Edebiyat Fakültesi Fen Dergisi-Cover
  • Yayın Aralığı: Yılda 3 Sayı
  • Başlangıç: 2006
  • Yayıncı: Süleyman Demirel Üniversitesi Fen-Edebiyat Fakültesi