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• [1] P.M. Anbarasan, P.S. Kumar, K. Vasudevan, S.M. Babu, V. Aroulmoji, DFT and TD-DFT Calculations of Some Metal Free Phthalonitrile Derivatives for Enhancement of the Dye Sensitized Solar Cells, Acta Phys. Pol. A., 119, 2011, 395.
• [2] M. Koenig, G. Bottari, G. Brancato, V. Barone, D.M. Guldi, T. Torres, Unraveling the peculiar modus operandi of a new class of solvatochromic fluorescent molecular rotors by spectroscopic and quantum mechanical methods, Chem. Sci., 6, 2013, 2502.
• [3] M. Okutan, F. Yakuphanoglu, O. Köysal, M. Durmus¸ V. Ahsen, Dielectric spectroscopy analysis in employing liquid crystal phthalonitrile derivative in nematic liquid crystals, Spectrochim. Acta A., 67, 2007, 531-535.
• [4] S.B. Sastri, J.P. Armistead, T.M. Keller, Phthalonitrile-carbon fiber composites, Polym Compos., 17, 1996, 816-822.
• [5] T.M. Keller, C.M. Roland. High temperature adhesive, US Patent, 5, 1993, 242-755.
• [6] T.M. Keller, High-performance, electrically conductive polymersl, Chemtech., 18, 1988, 635.
• [7] L.K. Mittal, Polyimides and Other High Temperature Polymers: Synthesis, Characterization and Applications, CRC Press, Boston, 5, 2009, 71-92.
• [8] X.Y. Yu, K. Naito, C. Kang, X.W. Qu, Q.X. Zhang, Synthesis and Properties of a High-Temperature Naphthyl-Based Phthalonitrile Polymer, Macromol. Chem. Phys., 214, 2013, 361-369.
• [9] A. Aktas Kamiloglu, D. Akyüz, A. Koca, I. Acar, Synthesis and investigation of spectroelectrochemical properties of peripherally tetra-substituted phthalocyanine bearing 3-(4-{[3-(trifluoromethyl)benzyl]oxy}phenyl)propan-1-ol and its metallo compounds, Journal of Inclusion Phenomena and Macrocyclic Chemistry, 92, 2018, 223-235.
• [10] H. Kantekin, G. Sarkı, A. Koca, A. Aktas, R.Z. Uslu Kobak, M.B. Sağlam, Synthesis, structural characterizations, and electrochemical and spectroelectrochemical properties of novel peripherally octa-substituted metallophthalocyanines, Journal of Organometallic Chemistry, 789, 2015, 53-62.
• [11] R.D. George, A.W. Snow, Synthesis of 3-nitrophthalonitrile and tetra-α-substituted phthalocyanines, J. Heterocycl. Chem., 32, 1995, 495.
• [12] D.S. Terekhov, K.J.M. Nolan, C.R. McArthur, C.C. Leznoff, Synthesis of 2,3,9,10,16,17,23,24-Octaalkynylphthalocyanines and the Effects of Concentration and Temperature on Their 1H NMR Spectra, J. Org. Chem., 61, 1996, 3034-3040.
• [13] C.C. Leznoff, D.S. Terekhov, C.R. McArthur, S. Vigh, J. Li, Multisubstituted phthalonitriles, naphthalenedicarbonitriles, and phenanthrenetetracarbonitriles as precursors for phthalocyanine syntheses, Can.J. Chem., 73, 1995, 435-443.
• [14] Y. Zorlu, I. Ün, C. Hirel, F. Dumoulin, V. Ahsen, Phthalonitriles Functionalized for Click Chemistry. Design, Synthesis and Structural Characterization, J. Chem. Cryst., 43, 2013, 636.
• [15] F. Yuksel, A.G. Gürek, C. Lebrun, V. Ahsen, Synthesis and solvent effects on the spectroscopic properties of octatosylamido phthalocyanines, New. J. Chem., 29, 2005, 726-732.
• [16] V.L.C. Bagdassarian, K.S. Bagdassarian, M.S. Atanassova, Phenolic profile, antioxidant and antimicrobial activities from the apiaceae family (dry seeds), Mintage J Pharm Med Sci., 2(4), 2013, 26-31.
• [17] M.L. Go, X. Wu, X.L. Liu, Chalcones: an update on cytotoxic and chemoprotective properties, Curr Med Chem., 12(4), 2005, 481-99.
• [18] B.A. Bhat, K.L. Dhar, S.C. Puri, A.K. Saxena, M .Shanmugavel, G.N. Qazi, Synthesis and biological evaluation of chalcones and their derived pyrazoles as potential cytotoxic agents, Bioorg Med Chem Lett., 15, 2005, 3177-3180.
• [19] A. Jurasek, V. Knoppava, M. Dandarova, J. Kovac, L. Reinprecht, Furan derivatives III: Synthesis and properties of β-Ketosulfides and sülfür derivatives of chalcones of 5-Nitrofuran series, Tetrahedron, 34, 1978, 1833-1836.
• [20] J.C. Trivedi, J.B. Bariwal, K.D. Upadhyay, Y.T. Naliapara, S.K. Joshi, C.C. Pannecouque, E.D. Clercq, A.K. Shah, Improved and rapid synthesis of new coumarinyl chalcone derivatives and their antiviral activity, Tetrahedron Lett., 48, 2007, 8472-8474.
• [21] R. Li, G.L. Kenyon, F.E. Cohen, X. Chen, B. Gong, J.N. Dominguez, E. Davidson, G. Kurzban, R.E. Miller, E.O. Nuzum, P.J. Rosenthal, J.H. McKerrow, In vitro antimalarial activity of chalcones and their derivatives, J Med Chem., 38(26) 1995, 5031-5037.
• [22] N. Yayli, O. Üçüncü, E. Aydìn, Y. Gök, A. Yasar, C.N. Baltacì Yìldìrìm, M. Küçük, Stereoselective photochemistry of heteroaryl chalcones in solution and the antioxidant activities, J.Photochem Photobiol A: Chem., 169, 2005, 229-234.
• [23] S. Khatib, O. Narya, R. Musa, M. Shmuel, S. Tamir, J. Vaya, Chalcones as potent tyrosinase inhibitors: the importance of a 2,4-substituted resorcinol moiety, Bioorg. Med. Chem., 13, 2005, 433-441.
• [24] J.N. Domínguez, C. León, J. Rodrigues, N.G. de Domínguez, J. Gut, J. Philip, P.J. Rosenthal, Synthesis and antimalarial activity of sulfonamide chalcone derivatives, Farmaco., 60, 2005, 307-311.
• [25] L.F. Motta, A.C. Gaudio, Y. Takahata, Quantitati ve Structure–Activity Relationships of a Series of Chalcone Derivatives (1,3–Diphenyl–2–propen–1–one) as Anti Plasmodium falciparum Agents (Anti Malaria Agents), Internet Electronic J Mol Des., 5, 2006, 555-569.
• [26] S.K. Awasthi, N. Mishra, B. Kumar, M. Sharma, A. Bhattacharya, L.C. Mishra, V.K. Bhasin, Potent Antimalarial Activity of Newly Synthesized Substituted Chalcone Analogs in Vitro, Med Chem Res., 18, 2009, 407-420.
• [27] S. Çolak, S. Kahraman, S.Z. Yıldız, Synthesis, characterization, solution and antioxidant properties of novel tetrakis{4-[N-((3-dimethylamino)propyl)amide]phenoxy}nickel (II) phthalocyanine and its water soluble derivatives, Journal of Organometallic Chemistry, 823, 2016, 83-89.
• [28] B.C. Behera, N. Verma, A. Sonone, U. Makhija, Determination of antioxidative potential of lichen Usnea ghattensis in vitro, LWT Food Sci. Technol., 39, 2006, 80-85.
• [29] R.S. Kumar, B. Rajkapoor, P. Perumal, Antioxidant activities of Indigofera cassioides Rottl. Ex. DC. using various in vitro assay models, Asian Pac. J. Trop. Biomed., 2 (4), 2012, 256-261.
• [30] N. Erkan, H. Cetin, E. Ayranci, Antioxidant activities of Sideritis congesta Davis et Huber-Morath and Sideritis arguta Boiss et Heldr: Identification of free flavonoids and cinnamic acid derivatives, Food Res. Int., 44, 2011, 297-303.
• [31] B.M. Mistry, R.V. Patel, Y. Keum, D.H. Kim, Chrysin-benzothiazole conjugates as antioxidant and anticancer agents, Bioorg. Med. Chem. Lett., 25, 2015, 5561-5565.
• [32] A. Aktas Kamiloglu, H. Karaca, G. Celik, I. Acar, H. Kantekin, New chalcone-substituted metallophthalocyanines: Synthesis, characterization, and investigation of their properties, Journal of Chemical Research, 44(7-8), 2020, 367-375.
• [33] S. Syam, S.I. Abdelwahab, M.A. Al-Mamary, S. Mohan, Synthesis of Chalcones with Anticancer Activities, Molecules, 17, 2012, 6179-6195.