Poly N-Aminorodaninin Elektrokimyasal Sentezi Ve Karakterizasyonu
Öz
Anahtar Kelimeler
Kaynakça
- [1] Shirakawa H. The discovery of polyacetylene film: The dawning of an era of conducting. Polymers Chem. Int. Ed. 2001; 40:2575-2580. [2] Hsiao S, Liou G, Kung Y, Lee Y. Synthesis and characterization of electrochromic poly(amide–imide)s based on the diimide-diacid from 4,4′-diamino-4″-methoxytriphenylamine and trimellitic anhydride. Eur. Polym J. 2010; 46:1355–1366. [3] Somboonsub B, Srisuwan S, Invernale MA, Praserthdam SP, Scola DA, Sotzing GA.Comparison of the thermally stable conducting polymers PEDOT, PANi, and PPy using sulfonated poly(imide) templates. Polymer 2010;51:4472-4476. [4] David V, Vinas C, Teixidor F. Poly(3,4-ethylenedioxythiophene) doped with a non-extrudable metallacarborane anion electroactive during synthesis. Polymer 2006;47:4694–4702. [5] Arslan A, Türkaslan Ö, Tanyel C, Akhmedov IM, Toppare L.Electrochromic properties of a soluble conducting polymer: Poly(1-(4-fluorophenyl)-2,5-di(thiophen-2-yl)-1H-pyrrole. Mater. Chem. Phys. 2007;104:410-416. [6] Alvarez-Romero GA, Garfias-Garcia E, Ramirez-Silva MT, Galan-Vidal C, Romero-Romo M, Palomar-Pardave M. Electrochemical and AFM characterization of the electropolimerization of pyrrole over a graphite–epoxy resin solid composite electrode, in the presence of different anions. Appl. Surf. Sci. 2006; 252:5783–5792. [7] Jiang Y, Xu J, Yu J. Conducting polymeric nanoparticles synthesized in reverse micelles and their gas sensitivity based on quartz crystal microbalance. Polymer 2007;48:4459–4465. [8] Solmaz R. Electrochemical synthesis of poly-2-aminothiazole on mild steel and its corrosion inhibition performance. Prog. Org. Coat. 2011;70:122–126. [9] Diaz AF. Electrochemical preparation and characterization of conducting polymers. Chem. Scr., 1981;17:145-148. [10] Tourillon G, Garnier F. New Electrochemically generated organic conducting polymers. J. Electroanal. Chem.,1982;135:173-178. [11] Pringlea JM, Efthimiadisb J, Howletta PC, MacFarlanea DR, Chaplinc AB, Hallc SB, Officerc L, Wallaced GG, Forsyth M.Electrochemical synthesis of polypyrrole in ionic liquids. Polymer 2004;45:1447–1453. [12] Tüken T, Özyılmaz AT, Yazıcı B, Erbil M. Electrochemical synthesis of polyaniline on mild steel in acetonitrile–LiClO4 and corrosion performance. Appl. Surf. Sci. 2004;236:292–305. [13] Lakard B, Herlem G, Fahys B. Electrochemical polymerization of 1,2-ethanedithiol as a new way to synthesize polyethylenedisulfide. Polymer 2008;49:1743-1747. [14] Inzelt G.Conducting Polymers: A New Erain Electrochemistry, Springer, Berlin, 1987 (Chapter4). [15] Malinauskas A.Electrocatalysis at conducting polymers. Synth. Met 1999;107:75-83. [16] Inzelt G, Pineri M, Schultze JW, Vorotyntsev MA. Electron and proton conducting polymers: recent developments and prospects. Electrochim. Acta 2000;45:2403-2421. [17] Solmaz R, Kardaş G. Electrochemical synthesis and characterization of poly-2-aminothiazole. Prog. Org. Coat. 2009;64:81–88. [18] Kardaş G, Solmaz R.Electrochemical synthesis and characterization of a new conducting polymer: Polyrhodanine. Appl. Surf. Sci. 2007;253:3402–3407. [19] Cutshall NS, Oday C, Prezhdo M. Rhodanine derivatives as inhibitors of JSP-1 Bioorg. Med. Chem. Lett. 2005;15:3374-3379. [20] Mishra S, Srivastava SK, Srivastava SD. Synthesis of 5-arylidene-2-aryl-3-(phenothiazino/benzotriazoloacetamidyl)-1,3-thiazolidine-4-ones as antiinflammatory, anticonvulsant, analgesic and antimicrobial agents. Indian J. Chem. Sect. B 1997;36:826-830. [21] Foye WO, Tovivich P. N-Glucopyranosyl-5-aralkylidenerhodanines: Synthesis and antibacterial and antiviral activities. J. Pharm. Sci. 1977;66:1607-1611. [22] Momose Y, Meguro K, Ikeda H, Hatanaka C, Oi S, Sohda T. Studies On Antidiabetic Agents .10. Synthesis And Biological-Activities Of Pioglitazone And Related-Compounds. Chem. Pharm. Bull. 1991; 39:1440-1445. [23] Sudo K, Matsumoto Y, Matsushima M, Fujiwara M, Konno K, Shimotohno K, Shigeta S, Yokota T. Novel Hepatitis C Virus Protease Inhibitors: Thiazolidine Derivatives. Biochem. Biophys. Res. Commun. 1997;238:643-647. [24] Habib NS, Rida SM, Badawey EAM, Fahmy HTY, Ghozlan HA. Synthesis and antimicrobial activity of rhodanine derivatives. Eur. J. Med. Chem. 1997;32:759-762. [25] Chandrakant GB, Gaikwad NJ. Synthesis and preliminary evaluation of some pyrazine containing thiazolines and thiazolidinones as antimicrobial agents. Bioorgan. Med. Chem. 2004;12:2151-2161. [26] Vittoria DM, Mazzoni O, Piscopo E, Caligmano A, Bolognese A.Synthesis and antihistaminic activity of some thiazolidin-4-ones. J.Med. Chem. 1992;35:2910-2912. [27] Sing W, Lee T, Yeo SL, Lim S, Sim P. Arylalkylidene rhodanine with bulky and hydrophobic functional group as selective HCV NS3 protease inhibitor. Bioorgan. Med. Chem. Lett. 2001;11:91-93. [28] Cutshall NS, O’Day C.Prezhdo Rhodanine derivatives as inhibitors of JSP-1. M. Bioorgan Med. Chem. Lett. 2005;15:3374–3379. [29] Altunbas E¸ Solmaz R, Kardas G. Corrosion behaviour of polyrhodanine coated copper electrode in 0.1 M H2SO4 solution. Mater. Chem. Phys. 2010;121:354–358. [30] Jabeen S, Rex A, Palmer BS, Potter M, Trevor JD, Babur ZC. Low Temperature Crystal Structures of Two Rhodanine Derivatives, 3-Amino Rhodanine and 3-Methyl Rhodanine: Geometry of the Rhodanine Ring. J Chem Crystallogr 2009;39:151–156. [31] Wessling B, Skotheim TA, Elsenbaumer RL, Reynolds JR. Editors, Handbook of conducting polymers, 2nd ed. New York: Marcel Dekker, 1998;p. 467. [32] Menon R, Yoon CO, Moses D, Heeger AJ. In: Skotheim TA, Elsenbaumer RL, Reynolds JR, editors. Handbook of conducting polymers,2nd ed.. New York: Marcel Dekker,. 1998;p. 27. [33] Yuehong P, He X, Xiaoyu L, Hongliu D, Yuxiao C, Guoyue S. Electrochemical synthesis, characterization, and electrochromic properties of poly(3-chlorothiophene) and its copolymer with 3-methylthiophene in a room temperature ionic liquid. Electrochem. Commun. 2006;8:1757–1763. [34] Casas J, Castellano E, Macias A, Playa N, Sanchez A, Sordo J, Varela J, Lopez E. Methyl- and phenylmercury(II) complexes of 5-(4′-dimethylaminobenzylidene)rhodanine (HDABRd) and 5-(2′-thiophenomethylene)rhodanine (HTRd). The crystal and molecular structure of [HgPh(DABRd)] and [HgMe(TRd)]. Polyhedron 2001;20:1845-1850
Ayrıntılar
Birincil Dil
Türkçe
Konular
-
Bölüm
Araştırma Makalesi
Yazarlar
Gülfeza Kardaş
Bu kişi benim
0000-0002-7871-6303
Yayımlanma Tarihi
15 Mart 2019
Gönderilme Tarihi
11 Temmuz 2018
Kabul Tarihi
28 Şubat 2019
Yayımlandığı Sayı
Yıl 2019 Cilt: 31 Sayı: 1