Synthesis and characterization of iminothiazole bearing polyphenol with adjustable white-yellow photoluminescence color


Yildirim M., KAYA İ.

SYNTHETIC METALS, cilt.162, sa.24, ss.2443-2450, 2012 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 162 Sayı: 24
  • Basım Tarihi: 2012
  • Doi Numarası: 10.1016/j.synthmet.2012.11.019
  • Dergi Adı: SYNTHETIC METALS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.2443-2450
  • Anahtar Kelimeler: Photoluminescence, Conjugated polymers, Thiazole polymers, Polyazomethine
  • Çanakkale Onsekiz Mart Üniversitesi Adresli: Evet

Özet

A new kind of thiazole based Schiff base, 2-[(benzothiazol-2-ylimino)methyl]phenol (2HBABT), was synthesized and then converted to its oligomer structure (O-2HBABT). Structural characterizations were made by Fourier transform infrared (FT-IR), nuclear magnetic resonance (NMR), size exclusion chromatography (SEC), and scanning electron microscopy (SEM) techniques. Optical properties were investigated by UV-vis and fluorescence analyses. Optical band gaps (E-g) were determined by absorption edges. Photoluminescence (PL) properties were determined in solution forms. Changes in PL characteristics in different solvents and applied excitation wavelengths were examined. O-2HBABT showed white and yellow emission colors in DMF by changing of applied excitation wavelength. Solid state electrical conductivities were measured by four-point probe technique. Cyclic voltammetry (CV) measurements were carried out and HOMO-LUMO energy levels and electrochemical band gaps (E ' g) were calculated. Thermal data were obtained by TG-DTA and DSC techniques. (c) 2012 Elsevier B.V. All rights reserved.
A new kind of thiazole based Schiff base, 2-[(benzothiazol-2-ylimino)methyl]phenol (2HBABT), was synthesized and then converted to its oligomer structure (O-2HBABT). Structural characterizations were made by Fourier transform infrared (FT-IR), nuclear magnetic resonance (NMR), size exclusion chromatography (SEC), and scanning electron microscopy (SEM) techniques. Optical properties were investigated by UV–vis and fluorescence analyses. Optical band gaps (Eg) were determined by absorption edges. Photoluminescence (PL) properties were determined in solution forms. Changes in PL characteristics in different solvents and applied excitation wavelengths were examined. O-2HBABT showed white and yellow emission colors in DMF by changing of applied excitation wavelength. Solid state electrical conductivities were measured by four-point probe technique. Cyclic voltammetry (CV) measurements were carried out and HOMO–LUMO energy levels and electrochemical band gaps (E'g) were calculated. Thermal data were obtained by TG-DTA and DSC techniques.