Synthesis, characterization, optical and electrical properties of thermally stable polyazomethines derived from 4,4′-oxydianiline

References

• Adams R, Bullock JE, Wilson WC. Contribution to the structure of benzidine. J. Am. Chem. Soc. 1923;45:1–17.10.1021/ja01655a032
   Google Scholar
• Grigoras M, Catanescu C. Imine oligomers and polymers. J. Macromol. Sci. 2004;44:131–173.
   Web of Science ®Google Scholar
• Yang CJ, Jenekhe SA. Effects of structure on refractive index of conjugated polyimines. Chem. Mater. 1994;6:196–203.10.1021/cm00038a016
   Web of Science ®Google Scholar
• Wang C, Shieh S, LeGoff E, et al. Synthesis and characterization of a new conjugated aromatic poly(azomethine) derivative based on the 3,4-dibutyl-α-terthiophene building block. Macromolecules. 1996;29:3147–3156.10.1021/ma9514131
   Web of Science ®Google Scholar
• Marin L, Cozan V, Bruma M, et al. Synthesis and thermal behaviour of new poly(azomethine-ether). Eur. Polym. J. 2006;42:1173–1182.10.1016/j.eurpolymj.2005.11.010
   Web of Science ®Google Scholar
• Tanaka H, Shibahara Y, Sato T, et al. Preparation and thermal behavior of spin polymers and their precursors based on azomethine mesogens. Eur. Polym. J. 1993;29:1525–1530.10.1016/0014-3057(93)90241-7
   Web of Science ®Google Scholar
• Sun SJ, Chang TC, Li CH. Studies on thermotropic liquid crystalline polycarbonates-I. Synthesis and properties of thermotropic liquid crystalline poly(azomethine-carbonate)s. Eur. Polym. J. 1993;29:951–955.10.1016/0014-3057(93)90291-M
   Web of Science ®Google Scholar
• Li CH, Chang TC. Thermotropic liquid crystalline polymer. III. Synthesis and properties of poly(amide-azomethine-ester). J. Polym. Sci. Chem. 1991;29:361–367.
   Web of Science ®Google Scholar
• Marin L, Cozan V, Bruma M. Comparative study of new thermotropic polyazomethines. Polym. Adv. Technol. 2006;17:664–672.10.1002/(ISSN)1099-1581
   Web of Science ®Google Scholar
• Hong W, Sun B, Aziz H, et al. Conjugated polyazine containing diketopyrrolopyrrole for ambipolar organic thin film transistors. Chem. Commun. 2012;48:8413–8415.10.1039/c2cc33998f
   PubMed Web of Science ®Google Scholar
• Kaya İ, Gül M. Synthesis, characterization and thermal degradation of oligo-2-[(4-fluorophenyl) imino methylene] phenol and some of its oligomer-metal complexes. Eur. Polym. J. 2004;40:2025–2032.10.1016/j.eurpolymj.2004.05.023
   Web of Science ®Google Scholar
• Kaya I, Bilici A, Saçak M. Synthesis, characterization, and antimicrobial properties of oligo-4-[(pyridine-3-yl-methylene)amino]phenol. J. Appl. Polym. Sci. 2006;102:3327–3333.10.1002/(ISSN)1097-4628
   Web of Science ®Google Scholar
• Bilici A, Dogan F, Yidrim M, et al. Tunable multicolor emission in oligo(4-hydroxyquinoline). J. Phys. Chem. C. 2012;116:19934–19940.10.1021/jp304432k
   Web of Science ®Google Scholar
• Gąsiorowski J, Głowacki ED, Hajduk B, et al. Doping-induced immobile charge carriers in polyazomethine: a spectroscopic study. J. Phys. Chem. C. 2013;117:2584–2589.10.1021/jp306108f
   Web of Science ®Google Scholar
• Shaheen SE, Vangeneugden D, Kiebooms R, et al. Low band-gap polymeric photovoltaic devices. Synth. Met. 2001;121:1583–1584.10.1016/S0379-6779(00)01501-0
   Web of Science ®Google Scholar
• Lakowicz JR. Principles of fluorescence spectroscopy. 2nd ed. New York, (NY): Plenum Press; 1999.10.1007/978-1-4757-3061-6
   Google Scholar
• Bhalgat MK, Haugland RP, Pollack JS, et al. Green- and red-fluorescent nanospheres for the detection of cell surface receptors by flow cytometry. J. Immunol. Methods. 1998;219:57–68.10.1016/S0022-1759(98)00121-5
   PubMed Web of Science ®Google Scholar
• Niu HJ, Huang YD, Bai XD, et al. Novel poly-Schiff bases containing 4,4-diamino-triphenylamine as hole transport material for organic electronic device. Mater. Lett. 2004;58:2979–2983.10.1016/j.matlet.2004.05.007
   Web of Science ®Google Scholar
• Kaya I, Bilici A, Gul M. Schiffbase substituted polyphenol and its metal complexes derived from O-vanillin with 2,3-diaminopyridine: synthesis, characterization, thermal and conductivity properties. Polym. Adv. Technol. 2008;19:1154–1163.10.1002/pat.v19:9
   Web of Science ®Google Scholar
• Kaya I, Bilici A, Saçak M. New conjugated azomethine oligomers obtained from bis-(hydroxyphenyl)methylenediamine via oxidative polycondensation and their complexes with metals. Synth. Met. 2009;159:1414–1421.10.1016/j.synthmet.2009.03.014
   Web of Science ®Google Scholar
• Demetgül C, Karakaplan M, Serin S. Synthesis, characterization and thermal properties of oligo-N, N-bis (2,4-dihydroxybenzylidene) ethylenediamine and its cobalt (II) and manganese (II) complexes. Des. Monomers Polym. 2008;11:565–579.10.1163/156855508X363852
   Web of Science ®Google Scholar
• Premachandran RS, Banerjee S, Wu XK, et al. Enzymatic synthesis of fluorescent naphthol-based polymers. Macromolecules. 1996;29:6452–6460.10.1021/ma960468f
   Web of Science ®Google Scholar
• Colladet K, Nicolas M, Goris L, et al. Low-band gap polymers for photovoltaic applications. Thin Solid Films. 2004; 451–452:7–11.10.1016/j.tsf.2003.10.085
   Web of Science ®Google Scholar
• Movasaghi Z, Rehman S, Rehman I. Fourier transform infrared (FT-IR) spectroscopy of biological tissues. Appl. Spectrosc. Rev. 2008;43:134–179.10.1080/05704920701829043
   Web of Science ®Google Scholar
• Kaya I, Bilici A. Synthesis, characterization, and thermal degradation of oligo-2-(morpholinoiminomethyl)phenol and its Pb(II) complex compound. J. Appl. Polym. Sci. 2006;102:3795–3804.10.1002/(ISSN)1097-4628
   Web of Science ®Google Scholar
• Wang BC, Ren LH, Chih YH, et al. Theoretical investigation of stokes shift of 3,4-diaryl-substituted maleimide fluorophores. J. Lumin. 2005;113:321–328.10.1016/j.jlumin.2004.11.008
   Web of Science ®Google Scholar
• Hasegawa M, Horie K. Photophysics, photochemistry, and optical properties of polyimides. Prog. Polym. Sci. 2001;26:259–335.10.1016/S0079-6700(00)00042-3
   Web of Science ®Google Scholar
• Thomas SW, Swager TM. Synthesis and optical properties of simple amine-containing conjugated polymers. Macromolecules. 2005;38:2716–2721.10.1021/ma0478815
   Web of Science ®Google Scholar
• Oter O, Ertekin KR, Kılıncarslan M, et al. Photocharacterization of a novel fluorescent Schiff base and investigation of its utility as an optical Fe3+ sensor in PVC matrix. Dyes Pigm. 2007;74:730–735.10.1016/j.dyepig.2006.05.006
   Web of Science ®Google Scholar
• Dilek D, Doğan F, Bilici A, et al. Oxidative synthesis of a novel polyphenol having pendant Schiff base group: synthesis, characterization, non-isothermal decomposition kinetics. Thermochim. Acta. 2011;518:72–81.10.1016/j.tca.2011.02.009
   Web of Science ®Google Scholar
• Yildirim M, Kaya I. Synthesis and characterization of a novel kind soluble, conjugated, and fluorescent chelate polymer containing fluorene ring in the backbone: optical, electrical, and electrochemical properties. Synth. Met. 2011;161:13–32.10.1016/j.synthmet.2010.10.028
   Web of Science ®Google Scholar
• Diaz FR, Moreno J, Tagle LH, et al. Synthesis, characterization and electrical properties of polyimines derived from selenophene. Synth. Met. 1999;100:187–193.10.1016/S0379-6779(98)01484-2
   Web of Science ®Google Scholar
• McCullough RD. The chemistry of conducting polythiophenes. Adv. Mater. 1998;10:93–116.10.1002/(ISSN)1521-4095
   Web of Science ®Google Scholar
• Demetgul C, Delikanli A, Saribiyik OY, et al. Schiff base polymers obtained by oxidative polycondensation and their Co(II), Mn(II) and Ru(III) complexes: synthesis, characterization and catalytic activity in epoxidation of styrene. Des. Monomers Polym. 2012;15:75–91.
   Web of Science ®Google Scholar
• van Krevelen DW. Some basic aspects of flame resistance of polymeric materials. Polymer. 1975;16:615–620.10.1016/0032-3861(75)90157-3
   Web of Science ®Google Scholar
• Van Krevelen DW. Properties of polymers. New York, (NY): Elsevier; 1972.
   Google Scholar