[1] R. Botros, "Azomethine dyes derived from an o-hydroxyaromatic aldehydes and a 2-aminopyridine", US Patent, 4.051,119 (1977).
[2] A. Jarrahpour, M. Motamedifar, K. Pakshir, N. Hadi, M. Zarei, "Synthesis of Novel azo Schiff bases and their antibacterial and antifungal activities", Molecules, 9(10), 815 (2004).
[3] N. C. Oforka, and V. N. Mkpenie, "A new method of synthesis of azo Schiff base ligands with azo and azomrthine donors: Synthesis of N-4-methoxybenzylidene-2-(3-hydroxyphenylazo)-5-hydroxyaniline and its nickel (II) complex", Chinese Journal of Chemistry,25, 869 (2007).
[4] H. Khanmohammadi, and M. Darvishpour, "New azo ligands containing azomethine groups in the pyridazine-based chain: Synthesis and characterization", Dyes and Pigments, 81, 167 (2009).
[5] H. Dinçalp, F. Toker, , Durucasu, N. Avcıbaşı, S. Icli,"New thiophene-based azo ligands containing azo methane group in the main chain for the determination of copper (II) ions", Dyes and Pigments, 75, 11 (2007).
[6] M. H. Fekri, M. Darvishpour, H. Khanmohammadi, and M. Rashidipour, "Synthesis and biological activity of a new Schiff base ligand pyridazine based", Journal of Chemical Health Risks, 3(4), 63 (2013).
[7] E. İspir, "the synthesis, characterization, electrochemical character, catalytic and antimicrobial activity of novel, azo-contining Schiff bases and their metal complexes". Dyes and Pigments,82(1), 13 (2009).
[8] R. T. Mahdi, A. M. Ali, and H. A. Noaman, "Preparation and characterization of some metal complexes with new heterocyclic Schiff-azo ligand". Journal of Al-Nahrain University, 17, 51 (2014).
[9] A. A. S. Al-Hamdani, A. Balkhi, A. Falah, and S. A. Shaker, "New azo-Schiff base derived with Ni(II), Pd(II) and Pt(II) complexes: Preparation, spectroscopic investigation, structural studies and biological activity", Journal of Chilean Chemical Society, 60, 2774 (2015).
[10] S. M. Mahdi, and A. M. Ali, "Preparation and identification of new azo-Schiff ligands with its complexes", Iraqi National Journal of Chemistry, 15(2), 214 (2015).
[11] W. Al Zoubi, A. A. S. Al-Hamdani, S. D. Ahmed, Y. G. Ko, "A new azo-Schiff base: Synthesis, characterization, biological activity and theoretical studies of its complexes", Applied Organometallic Chemistry, e 3895. 1 (2017).
[12] F. Purtas, K. Sayin, G. Ceyhan, M. Kose, M. Kurtoglu, "New fluorescent azo-Schiff base Cu (II) and Zn (II) metal chelates; spectral, structural, electrochemical, photoluminescence and computational studies", Journal of Molecular Structure, 1137, 461 (2017).
[13] S. M. Mahdi, A. K. Ismail, "Preparation and identification of new azo-Schiff base ligand (NASAR) and its divalent transition metal complexes", Journal of Pharmaceutical Sciences and Research, 10(9), 2175 (2018).
[14] F. Kunitake, J-Y Kim, S. Yagi, S. Yamzaki, T. Haraguchi and T. Akitsu, "Chiral Recognition of azo-Schiff base ligands, their Cu(II) complexes, and their docking to laccase as mediators", Symmetry, 2019, 11,666, 1 (2019).
[15] M. S. Kasare, P. P. Dhavan, B. L. Jadhav, S. D. Pawar, "Synthesis of Azo Schiff base ligands and their Ni(II), Cu(II) and Zn (II) metal complexes as highly active antibacterial agents". Chemistry Select, 4(36), 10792 (2019).
[16] H. H. Eissa, "Synthesis and characterization of azo-Schiff bases and study of biological activity", Journal of Current Research in Science, 1, 444 (2013).
[17] S. A. Shreekanta, T. V. Venkatesh, P. N. Paramesshwara and K. S. Shoba, "Electrosynthesis, electrochemical behaviour, antibacterial and antifungal activity of novel azo-Schiff`s bases", Indian Journal of Applied Research, 4, 91 (2014).
[18] H. N. Azeez, A. A. Al-Kadhmi, N. O. Tapabashi, Synthesis, "characterization and biological evaluation of some azo and azo-Schiff compounds", Kirkuk Journal of Scientific Researches, 14(1), 97 (2019).
[19] Ö. Özdemir, "Synthesis of novel azo linkage-based Schiff bases including anthranilic acid and hexanoic acid moieties: investigation of azo-hydrazone and phenol-keto tautomerism, solvatochromism, and ionchromism", Turkish Journal of Chemistry, 43, 266 (2019).
[20] S. Slassi, A. Fix-Tailler, G. Larcher, A. Amine, A. El-Ghayoury, "Imidazole and Azo-Based Schiff bases ligands as highly active antifungal and antioxidant components", Heteroatom chemistry, 2019, Article ID 6862170, 1 (2019).
[21] N. O. Tapabashi, K. M. Al-Janabi, S. A. Mohammed, Thermal performance, photostability and Uv-visible spectroscopic studies of some synthesized azo-Schiff and bis-azo-Schiff bases, International Journal of Engineering and Advanced Research Technology, 3, 19 (2017).
[22] T. H. Hilal, H. J. Mohammed, H. F. Mohsin, "Synthesis with spectral investigation of new azomethine-azo ligands derived from 4-amino antipyrine with its some complexes", International Journal of Pharmaceutical Research, 10(3), 385 (2018).
[23] H. S. Al-Atbi, B. K. Al-Salami, I. J. Al-Assadi, "New azo-azomethine derivative of sulfanilamide: Synthesis, characterization, spectroscopic, antimicrobial and antioxidant activity Study", Journal of Physics: Conference series (2nd International Science Conference), 1294 052033 (2019).
[24] N. I. Taha, N. O. Tapabashi, M. M. El-Subeyhi, "Green synthesis of new tetra Schiff bases and bis-azo bis-Schiff bases derived from 2,6-diaminopyridine as promising photosensitizers", International Journal of Organic Chemistry, 8, 309 (2018).
[25] S. A. Hashimi, S. Suematsu, K. Naoi, "All solid-state redox supercapacitors based on supramolacular 1,5-diaminoanthraquinone oligomeric electrode and polymeric electrolytes", Journal of Power Sources,137 (1), 145 (2004).
[26] K. Naoi, S. Suematsu, M. Hanada, H. Takenouchi, "Enhanced Cyclability of π-π stacked supramolecular (1, 5-diaminoanthraquinone) oligomer as an electrochemical capacitor material"., Journal of The Electrochemical Society, 149 (4), 472 (2002).
[27] G. Suganthi, C. Meenakshi, V. Ramakrishnan, "Preferential solvation study of 1,5-diaminoanthraquinone in binary liquid mixtures", Journal of Fluorescence, 20, 95 (2010).
[28] K. Naoi, S. Suematsu, A. Manago, "Electrochemistry of poly (1,5 diaminoanthraquinone) and its application in electrochemical capacitor materials". Journal of The Electrochemical Society, 144 (2), 420 (2000).
[29] H. Liu, G. Zhang, Y. Zhou, M. Gao, F. Yang, "One-step potentiodynamic synthesis of poly (1,5-diaminoanthraquinone)/reduced grapheme oxide nanohybride with improved electrcatalytic activity", Journal of Material Chemistry, 1, 13902 (2013).
[30] M. Sun, O. Tang, T. Zhang, G. Wang, "Rational synthesis of novel π- conjugated poly (1, 5 diaminoanthraquinone) for high- performance supercapacitors", The Journal of Royal society of Chemistry advances, 4, 7774 (2014).
[31] A. J. Abdul-Ghani, and N. O. Tapabashi, "Light induced hydrogen production from ethanolic aqueous solution sensitized by 2,4-dimethoxy benzylidine-2-hydroxy aniline and some of its metal complexes", Ibn Al-Haitham Journal for Pure and Applied Sciences., 20(1), 128 (2007).
[32] J. B. Lambert, H. F. Shurvell, D. A. Lighter, R. G. Cooks, "Organic Structural Spectroscopy", Prentice Hall, New Jersy (2007).
[33] Z. A. Shawkat, N. O. Tapabashi, N. I. Taha, "Schiff bases and its related cyclic compounds derived from4-aminoantipyrine as new type of push-pull compounds", Al-utroha, 4, 39 (2020).
)
