A green light emitting polymer in a PMMA matrix: oligo(azomethine-ether) with benzothiazole moieties

This study aimed to synthesize an oligo(azomethine-ether) with benzothiazole moiety in organic medium by means of chemical oxidative polycondensation (OP). Optical properties were examined by photoluminescence (PL) and UV-Vis measurements both in solutions and solid film involved a poly (methyl methacrylate) (PMMA) matrix. Oligomer film in the PMMA matrix emitted a fine green light with a fluorescence quantum yield (QY) of 3.30%. Spectral and thermal observations showed a high rate of C--O--C coupling (cross-linking) for the oligomer. SEC results indicated low molecular weight (\sim3200--4650 g mol^{-1}) and the oligomer was soluble in organic solvents with high polarity. Electrochemical behavior was characterized by cyclic voltammetry (CV), morphological properties by scanning electron microscopy (SEM), and thermal characteristics by TG-DTA and DSC techniques.

A green light emitting polymer in a PMMA matrix: oligo(azomethine-ether) with benzothiazole moieties

This study aimed to synthesize an oligo(azomethine-ether) with benzothiazole moiety in organic medium by means of chemical oxidative polycondensation (OP). Optical properties were examined by photoluminescence (PL) and UV-Vis measurements both in solutions and solid film involved a poly (methyl methacrylate) (PMMA) matrix. Oligomer film in the PMMA matrix emitted a fine green light with a fluorescence quantum yield (QY) of 3.30%. Spectral and thermal observations showed a high rate of C--O--C coupling (cross-linking) for the oligomer. SEC results indicated low molecular weight (\sim3200--4650 g mol^{-1}) and the oligomer was soluble in organic solvents with high polarity. Electrochemical behavior was characterized by cyclic voltammetry (CV), morphological properties by scanning electron microscopy (SEM), and thermal characteristics by TG-DTA and DSC techniques.

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  • EHOM O: –(4.39 + Eox) ELU M O: –(4.39 + Ered) Eg: ELU M O–EHOM O, ′ where Eoxand Eredare oxidation and reduction peak potentials, respectively. Pron, A.; Rannou, P. Prog. Polym. Sci. 2002, 27, 135–190.
  • Waris, G.; Siddiqi, H. M.; Twyman, L. J.; Hussain, R.; Akhter, Z.; Butt, M. S. Turk. J. Chem. 2013, 37, 946–958.
  • Lee, B. R.; Kim, J. S.; Nam, Y. S.; Jeong, H. J.; Jeong, S. Y.; Lee, G. W.; Han, J. T.; Song, M. H. J. Mater. Chem. 2012, 22, 21481–21486.
  • Chuang, C. N.; Chuang, H. J.; Wang, Y. X.; Chen, S. H.; Huang, J. J.; Leung, M. K.; Hsieh, K. H. Polymer 2012, 53, 4983–4992.
  • Karasz, F. E.; Hu, B.; Yang, Z. Turk. J. Chem. 1997, 21, 1–5.
  • Deniz, T. K.; Apaydın, D. H.; ¨Ozel¸ca˘glayan, A. C.; Toppare, L. K.; C¸ ırpan, A. Turk. J. Chem. 2013, 37, 538–546.
  • Takagi, S.; Makuta, S.; Veamatahau, A.; Otsuka, Y.; Tachibana, Y. J. Mater. Chem. 2012, 22, 22181–22189.
  • Bozkurt, A. Turk. J. Chem. 2002, 26, 663–668.
  • Benzarti-Ghedira, M.; Hrichi, H.; Jaballah, N.; Ben Chaabane, R.; Majdoub, M.; Ben Ouada, H. Physica B 2012, 407, 1051–1054.
  • Goncalves, V. C.; Balogh, D. T. Sensor. Actuat. B-Chem. 2012, 162, 307–312.
  • Lu, Y.; Li, X.; Wang, G. K.; Tang, W. Biosens. Bioelectron. 2013, 39, 231–235.
  • More, A. S.; Sane, P. S.; Patil, A. S.; Wadgaonkar, P. P. Polym. Degrad. Stabil. 2010, 95, 1727–1735.
  • Demir, H. O. Polym. J. 2012, 44, 699–705.
  • Kaya, ˙I.; Yıldırım, M. J. Appl. Polym. Sci. 2007, 106, 2282–2289.
  • Kaya, ˙I.; Aydın, A. E-Polymers, 2008, 71, 1.
  • Bilici, A.; Kaya, ˙I.; Yıldırım, M.; Dogan, F. J. Mol. Catal. B-Enzym. 2010, 64, 89–95.
  • Kaya, ˙I.; Yıldırım, M.; Kamacı, M. Eur. Polym. J. 2009, 45, 1586–1598.
  • Bilici, A.; Dogan, F.; Yıldırım, M.; Kaya, ˙I. J. Phys. Chem. C 2012, 116, 19934–19940.
  • Kaya, ˙I.; Yıldırım, M.; Aydın, A.; S¸enol, D. React. Funct. Polym. 2010, 70, 815–826.
  • Yıldırım, M.; Kaya, ˙I. Synthetic Met. 2012, 162, 2443–2450.
  • Akgul, C.; Yıldırım, M. J. Serb. Chem. Soc. 2010, 75, 1203–1208.
  • Liu, C.; Wang, J. Y.; Lin, E. C.; Zong, L. S.; Jian, X. G. Polym. Degrad. Stabil. 2012, 97, 460–468.
  • Yang, J.; Yang, X. L.; Zou, Y. K.; Zhan, Y. Q.; Zhao, R.; Liu, X. B. J. Appl. Polym. Sci. 2012, 126, 1129–1135.
  • Kalamaras, I.; Daletou, M. K.; Neophytides, S. G.; Kallitsis, J. K. J. Membrane Sci. 2012, 415, 42–50.
  • Bilici, A.; Kaya, ˙I.; Yıldırım, M. Eur. Polym. J. 2011, 47, 1005–1017.
  • Topal, S. Z.; Yuksel, F.; Gurek, A. G.; Ertekin, K.; Yenigul, B.; Ahsen, V. J. Photoch. Photobio. A 2009, 202, 205–213.
  • Yigitsoy, B.; Varis, S.; Tanyeli, C.; Akhmedov, I. M.; Toppare, L. Thin Solid Films 2007, 515, 3898–3904.
  • Yıldırım, M.; Kaya, ˙I. Synthetic Met. 2012, 162, 834–842.
  • Peng, Y.; Liu, H. W.; Zhang, X. Y.; Li, Y. S.; Liu, S. Y. J. Polym. Sci. Pol. Chem. 2009, 47, 1627–1635.
  • Bilici, A.; Dogan, F.; Yıldırım, M.; Kaya, ˙I. Mater. Chem. Phys. 2013, 140, 66–74.
  • Cırpan, A.; Argun, A. A.; Grenier, C. R. G.; Reeves, B. D.; Reynolds, J. R. J. Mater. Chem. 2003, 13, 2422–2428.
  • Colladet, K.; Nicolas, M.; Goris, L.; Lutsen, L.; Vanderzande, D. Thin Solid Films 2004, 451, 7–11.
  • Williams, A. T. R.; Winfield, S. A.; Miller, J. N. Analyst 1983, 108, 1067–1071.
  • Cervini, R.; Li, X. C.; Spencer, G. W. C.; Holmes, A. B.; Moratti, S. C.; Friend, R. H. Synthetic Met. 1997, 84, 359–360.
Turkish Journal of Chemistry-Cover
  • ISSN: 1300-0527
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
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