[1] Zollinger, H., "Color Chemistry, Synthesis, Propertiesand Application of Organic Dyes and Pigments", Wiley-VCH: Weinheim, (2003).
[2] Gregory, P., "High-Technology Applications of Organic Colorants", Plenum Press: New York, (1991).
[3] Viscardi, G., Quagliotto, P., Barolo, C., Caputo, G., Digilio, G., Degani, I., Barni, E., "
Highly bright and photostable cyanine dye-doped silica nanoparticles for optical imaging", Dyes and Pigments, 57,pp. 87-91, (2003).
[4] Tanaka, K.,“Solvent-free Organic Synthesis”. Wiley-VCH GmbH & Co. KgaA: Weinheim, Germany. (2003).
[5] Noroozi-Pesyan, N., Khalafy, J., Malekpoor, Z., "
Diazotization of aniline derivatives and diazo Couplings in the Presence of p-Toluenesulfonic Acid by Grinding Color",
Color,
Colorants and Coatings
Journal, 2, pp. 61-65, (2009).
[6] Roglans, A., Pla-Quintana, A., Moreno-Manas, M., "Diazonium salts as substrates in palladium-catalyzed cross-coupling reaction", Chemical Review, 106,pp. 4622–4643, (2006).
[7] Mandic, Z., Nigovic, Z., Simunic, B., "The mechanism and kinetics of the electrochemical cleavage of azo bond of 2-hydroxy-5-sulfophenyl-azo-benzoic acids", Electrochimica Acta, 49,pp. 607–615, (2004).
[8] Kub, Y., Maeda, S., Tokita, S., Kubo, M., "Colorimetric chiral recognition by a molecular sensor", Nature, 382, pp. 522-524, (1996).
[9] Steinstrasser, R., Pohl, L., "Chemistry and applications of liquid crystals", Angewandte Chemie International Edition, 12, pp. 617–630, (1973).
[10] He, Y., Gu, X., Guo, M., Wang, X., "Dendritic azo compounds as a new type amorphous molecular material with quick photoinduced surface-relief-grating formation ability", Optical Materials, 31,pp. 18-27, (2008).
[11] Pieraccini, S., Masiero, S., Spada, G. P., Gottarelli, P., "A new axially-chiral photochemical switch", Chemical. Communications, 9, pp. 598–599, (2003).
[12] Węglarz-Tomczak, E., Górecki, L., "Azodyes–biological activity and synthetic strategy", Chemik, 66, pp. 298–307, (2012).
[13]
Shokoofehpoor, F.,
Mousavi, S. H.,
Mohammadi, A.,
Zanjanchi, M. A., "γ-CD-Functionalized TiO
2 Nanoparticles For the Photocatalytic Degradation of Organic", The
Progress in
Color,
Colorants and Coatings Journal (pccc), 13, pp. 23-39, (2020).
[14] Hay, A. E., Aumond, M. C., Mallet, S., Dumontet, V., Litaudon, M., Rondeau, D., Richomme, P., "Antioxidant xanthones from Garcinia vieillardii", Journal of Natural Products, 67, pp. 707–709, (2004).
[15] Zelefack, F., Guilet, D., Fabre, N., Bayet, C., Chevalley, S. V., Ngouela, S. R., Lenta, B. N., Valentin, A., Tsamo, E., Dijoux-Franca, M. G. V. "Cytotoxic and antiplasmodial xanthones from Pentadesma butyracea", Journal of Natural Products, 72, pp. 954–957, (2009).
[16] Khurana, J. M., Magoo, D., Aggarwal, K., Aggarwal, N., Kumar, R., Srivastava, C.,”Synthesis of novel 12-aryl-8, 9, 10, 12-tetrahydrobenzo[a]xanthene-11-thiones and evaluation of their biocidal effects", European Journal of Medicinal Chemistry, 58, pp. 470-477, (2012).
[17] Niu, S. L., Li, Z. L., Ji, F., Liu, G. Y. Zhao, N., Liu, X. O., Jing, Y. K., Hua, H. M., "Xanthones from the stem bark of Garcinia bracteata with growth inhibitory effects against HL-60 cells", Phytochemistry, 77, pp. 280–286, (2012).
[18] Laphookhieo, S., Syers, J. K., Kiattansakul, R., Chantrapromma, K., "Cytotoxic and antimalarial prenylated xanthones from Cratoxylum cochinchinense", Chemical and Pharmaceutical Bulletin (Tokyo), 54, pp. 745–747, (2006).
[19] Liama, E. F., del Campo, C., Capo, M., Anadon, M., "Synthesis and antinociceptive activity of 9-phenyl-oxy or 9-acyl-oxy derivatives of xanthene, thioxanthene and acridine", European Journal of Medicinal Chemistry, 24, pp. 391–396, (1989).
[20] Omolo, J. J., Johnson, M. M., Van Vuuren, S. F., De Koning, C.B. "The synthesis of xanthones, xanthenediones, and spirobenzofurans: their antibacterial and antifungal activity", Bioorganic Medical Chemical Letters. 21, pp. 7085–7088, (2011).
[21] Jamison, J. M., Krabill, K., Hatwalkar, A., Jamison, E., Tsai, C. C., "Potentiation of the antiviral activity of poly r(A–U) by xanthenes dyes", Cell Biology International Reports, 14, pp. 1075–1084, (1990).
[22] Hafez, H. N., Hegab, M. I., Ahmed-Farag, I. S., El-Gazzar, A. B. A., "A facile regioselective synthesis of novel spiro-thioxanthene and spiroxanthene-9’,2-[1,3,4]thiadiazole derivatives as potential analgesic and anti-inflammatory agents", Bioorganic & Medicinal Chemistry Letters, 18, pp. 4538-4543, (2008).
[23] Merino, E., "Synthesis of azobenzenes: the coloured pieces of molecular materials", Chemical Society Review, 40, pp. 3835–3853, (2011).
[24] Giri, R., Goodell, J. R., Xing, C., Benoit, A., Kaur, H., Hiasa, H., Ferguson, D.M.”Synthesis and cancer cell cytotoxicity of substituted xanthenes", Bioorganic & Medicinal Chemistry, 18, pp. 1456–1463, (2010).
[25] Chen, X., Pradhan, T., Wang, F., Kim, J. S., Yoon, J., "Flourescent chemosensors based on spiroring-opening of xanthenes and related derivatives", Chemical. Reviw, 112: pp.1910- 1956, (2011).
[26] Zhen, W., Han, H., Anguiano, M., Lemere, C., Cho, C. G., Lansbury, P. T. "Synthesis and amyloid binding properties of rhenium complexes: preliminary progress toward a reagent for SPECT imaging of Alzheimer's disease brain", Journal of Medical Chemistry, 42, pp. 2805–2815, (1999).
[27] Mirjalili, B. F., Bamoniri, A., Akbari, A., "BF3.SiO2: an efficient catalyst for the synthesis of azo dyes at room temperature", Current Chemistry Letters, 1, pp. 109–114, (2012).
[28] Bokare, A. D., Chikate, R. C., Rode, C. V., Paknikar, K. M., "Iron-nickel bimetallic nanoparticles for reductive degradation of azo dye Orange G in aqueous solution", Applied Catalysis. B, 79, pp. 270-278, (2008).
[29] Qian, H., Jiang, D. E., Li, G., Gayathri, C., Das, A., Gil, R. R., Jin, R.
Monoplatinum doping of gold nanoclusters and catalytic application. Journal of American Chemical Society, 134, pp. 16159-62, (2012).
[30] Li, M., Li, J., Liu, B., Zhou, Y., Li, X., Xue, X., Hou, Z., Luo, X., "
Crystal Structures, and Anti-Drug-Resistant Staphylococcus Aureus Activities of Novel 4-hydroxycoumarin Derivatives", European Journal of Pharmacol, 721, pp. 151-157 (2013).
[31] Reilly, R. O., Ohms, J., Motley, C., "Synthesis of furo[3,2-c] benzopyran-4-one through acid catalysed 1,2- elimination", Journal of Biology Chemical, 244, pp. 1303-1305, (1969).
[32] Zhao, H., Neamati, N., Hong, H., Mazumder, A., Wang, S., Sunder, S., Milne, G.W.A., Pommier, Y., Burke Jr, T. R., "
Coumarin-based inhibitors of HIV integrase", Journal of Medical Chemistry, 40, pp. 242-249, (1997).
[34] Sen, K., Bagchi, P., "Studies on the Ultraviolet Absorption Spectra of Coumarins and Chromones", Journal of Organic Chemistry, 24, pp. 316-319, (1959).
[35] Bamoniri, A., Mirjalili, B. B. F., Moshtael-Arani, N., "Environmentally green approach to synthesize azo dyes based on 1-naphthol using nano BF3·SiO2 under solvent-free conditions", Green Chemistry Letters Reviews, 7, pp. 393–403, (2014).
[36] Bamoniri, A., Moshtael-Arani, N., "Nano-Fe3O4 encapsulated-silica supported boron trifluoride as a novel heterogeneous solid acid for solvent-free synthesis of arylazo-1-naphthol derivatives", RSC Adv, 5, pp. 16911-16920, (2015).
[37] Bamoniri, A., Pourali, A. R., Nazifi, S. M. R., "Facile synthesis of 1-naphthol azo dyes with nano SiO2/HClO4 under solvent-free condition", Bulletin Chemical Society Ethiopia, 27, pp. 439-445, (2013).
[38]
Benkhaya, S.,
M'rabet, S., "Classifications, properties, recent synthesis and applications of azo dyes", Heliyon,
6, p. e03271, (2020).
[39] Kwasi Adu, H., Amengor, C. D. K., Mohammed, N. J., "Synthesis and In Vitro Antimicrobial and Anthelminthic Evaluation of Naphtholic and Phenolic Azo Dyes", Tropical Medicine, 2, pp. 1-8, (2020).
[40]
Davasaz Rabbani, M. A.,
Khalili, B.,
Saeidian, H., "Novel edaravone-based azo dyes: efficient synthesis, characterization, antibacterial activity, DFT calculations and comprehensive investigation of the solvent effect on the absorption spectra",
RSC Advanced, 10, pp. 35729-35739, (2020).
[41] Gur, M., "Synthesis, Characterization, and Antimicrobial Properties of New 1,3,4‐Thiadiazoles Derived from Azo Dyes", Journal of Heterocyclic chemistry,
56, pp. 980-987, (2019).
[42] Noroozi Pesyana, N., Gholsanamlooa, V., Moradi Parb, M., "
Synthesis, characterization and spectroscopic properties of new azo dyes derived from aniline derivatives based on acetylacetone and azo-metal (II) complexes and singular value decomposition (SVD) investigation", Iranian Chemical Communications, 7, pp. 1-9, (2019).
[43] Bamoniri, A., Mirjalili, F., Fouladgar, S., Moshtael-Arani, N., "Nano Silica Phosphoric Acid: A Highly Efficient and Heterogeneous Catalyst for Synthesis of Azo Dyes Based on 1- and 2-Naphthol at Room Temperature", National Academy Science Letters, 39, pp. 1-4, (2015).
[44] Bamoniri, A., Moshtael-Arani, N., "Nano-Fe3O4 encapsulated-silica supported boron trifluoride as a novel heterogeneous solid acid for solvent-free synthesis of arylazo-1-naphthol derivatives", RSC Adv, 5, pp. 16911–16920, (2015).
[45] Bamonori, A., Mirjalili, B. B., "Nano Silica Phosphoric Acid: A Highly Efficient and Heterogeneous Catalyst for Synthesis of Azo Dyes Based on 1- and 2-Naphthol at Room Temperature", National Academy Science Letters, 39, pp. 25-28, (2016).
[46] Rahimizadeh, M., Eshghi, H., Shiri, A., Ghadamyari, Z., Matin, M. M., Oroojalian, F., Pordeli, P., "Fe(HSO4)3 as an Efficient Catalyst for Diazotization and Diazo Coupling Reactions", Journal of Korean Chemical Society. 56, pp. 716-719, (2012).
[47] Ghaffari, N., Abd Hamid, Sh., Hazarkhanic, H., "TiO
2 nanotubes and sonication: Synthesis of azo-linked xanthenes",
Inorganic Nano Metal Chemistry, 47, pp. 1-26 (2017).
[48] Kolvari, E., Koukabi, N., Hosseini, M. M., Vahidian, M., Ghobadi, E., "Nano-ZrO2 sulfuric acid: a heterogeneous solid acid nano catalyst for Biginelli reaction under solvent free conditions", RSC Advances, 6, pp. 7419-7425, (2016).
[49] Zare Fekri, L., Nikpasand, M., "Synthesis of bis(coumarinyl) methanes-aza linked using ionic liquid[DBU]OAc", Journal of Color Science and Technology, Vol. 2, pp. 137-143, In Persian, (2017).
[50] Zarei, A., Hajipour, A. R., Khazdooz, L., Mirjalili, B.F., "Najafi
A Rapid and efficient diazotization and diazo coupling reactions on silica sulfuric acid under solvent-free conditions", Dye & Pigments, 81, pp. 240-244, (2009).
[51] Bamoniri, A., Mirjalili, B. F., Ghorbani-Choghamarani, A., Akbari, M. E., Yazdanshenas, A., Shayanfar. A., "
Nano silica chromic acid/Wet SiO2 and NaNO2 as an efficient reagent for one-pot synthesis of azo dyes based on 2-naphthol at room temperature under solvent-free conditions", Iranian Journal of Organic Chemistry, 3, pp. 603-606, (2011).
[52] Ginni, S., Karnawat, R., Sharma, I. K., Verma, P. S., "
Synthesıs, Characterısatıon and Antımıcrobıal Screenıng of Some Azo Compounds", International Journal A. Biology Pharmaceutical Technology, 2, pp. 332-338, (2011).
[53] Bamoniri, A., Pourali, A. R., Nazifi, S. M. R., "
Solvent-free synthesis and characterization of antibacterial azo dyes in the presence of Bronsted-acid ionic liquid as a green catalyst", Iranian Journal of Catalysis, 4, pp. 185-189, (2012).
[54] Bamoniri, A., Mirjalili, B. B. F., Ghorbani-Choghamarani, A., Yazdanshenas, M.E., Shayanfar, A., Akbari, A., "
Nanosilica chromic acid/wet SiO2and NaNO2 as an efficient reagent system for synthesis of azo dyes based on 1-naphthol atroom temperature and solvent-free conditions", Iranian Journal of Catalyst, 1, pp. 51-54, (2011).
[55] Bamoniri, A., Mirjalili, B. B. F., Fouladgari, S., Moshtael-Arani, N., "
Nano Silica Phosphoric Acid: A Highly Efficient and Heterogeneous Catalyst for Synthesis of Azo Dyes Based on 1- and 2-Naphthol at Room Temperature", National Academy Science Letters, 39, pp. 25-28, (2016).
[56] Ghaffari Khaligh, N., Abd Hamid, Sh. B., Mihankhah, T., "
TiO2 nanotubes catalyzed the synthesis of azo-linked xanthenes under ultrasonic conditions", Inorganic Nano Metal Chemistry, 47,pp. 1057-1063, (2017).
[58] Khatab, T. T., El-Mekabaty, A. M., Gamala, Z., Kandil E. M., "
An Efficient Catalytic Synthesis of 1,8-Dioxo-octahydroxanthene Derivatives with Anti-oxidant Scanning", Egypt Journal of Chemistry, 61, pp. 661-66, (2018).