Dergiler / Journal of the Turkish Chemical Society Section A: Chemistry / 2019 / Cilt: 6 - Sayı: 3

Synthesis and photophysical properties of usymmetrically substituted phthalocyanine-pyrene conjugate

Sayfa
319–328
Yayın Tarihi
2019-10-20
DOI
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The fluorescence quenching examinations were performed by adding the different concentration of benzoquinone in DMF and the Ksv and kq values of unsymmetrical zinc phthalocyanine (5) were determined.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Unsymmetrical zinc phthalocyanine (Pc) bearing one pyrene (Py) and six tert-butylphenoxy units was synthesized in 3 steps.
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Temel Bulgular & Veri:It was determined that the absorption of the pyrene structure around 350 nm was overlapping with the B-band of phthalocyanine after conjugation.
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Sonuç & Katkı:The fluorescence quenching examinations were performed by adding the different concentration of benzoquinone in DMF and the Ksv and kq values of unsymmetrical zinc phthalocyanine (5) were determined.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Zinc · pyrene · phthalocyanine

Abstract

Unsymmetrical zinc phthalocyanine (Pc) bearing one pyrene (Py) and six tert-butylphenoxy units was synthesized in 3 steps. The unsymmetric zinc phthalocyanine carrying the protecting group was synthesized in the first step. In the second stage, the protecting group was removed and in the final stage pyrene structure was introduced under the condition of the Sonagashira coupling reaction. The new compound was characterized by using spectroscopic techniques. The photophysical measurements of the conjugated structure were performed to determine the effect of the pyrene group on the fluorescence of Pc. It was determined that the absorption of the pyrene structure around 350 nm was overlapping with the B-band of phthalocyanine after conjugation. Fluorescence quantum yield and lifetime were calculated. The fluorescence quenching examinations were performed by adding the different concentration of benzoquinone in DMF and the Ksv and kq values of unsymmetrical zinc phthalocyanine (5) were determined.

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Bu Makaleye Atıf Yap

KARAOĞLU, H. P., BURAT, A. K. (2019). Synthesis and photophysical properties of usymmetrically substituted phthalocyanine-pyrene conjugate. Journal of the Turkish Chemical Society Section A: Chemistry, Cilt: 6 - Sayı: 3, 319–328. https://ajindex.com/articles/781269

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Kaynakça (13)

  1. Schmid G, Sommerauer M, Geyer M, Hanack M, Leznoff CC. A.B.P. Lever (Eds.), Phthalocyanines: Properties and Applications, vol. 4, VCH Publishers, New York, 1996, pp. 1–18
  2. Basova TV., Parkhomenko RG, Polyakov M, Gürek AG, Atilla D, Yuksel F, et al. Effect of dispersion of gold nanoparticles on the properties and alignment of liquid crystalline copper phthalocyanine films. Dye Pigment. 2016; 125: 266–73
  3. Çimen Y, Ermiş E, Dumludağ F, Özkaya AR, Salih B, Bekaroğlu Ö. Synthesis, characterization, electrochemistry and VOC sensing properties of novel ball-type dinuclear metallophthalocyanines. Sensors Actuators, B Chem. 2014; 202: 1137–47
  4. Nagel S, Lener M, Keil C, Gerdes R,Lapok L, Gorun SM, Schlettwein D. Electrochromic Switching of Evaporated Thin Films of Bulky, Electronic Deficient Metallo-Phthalocyanines. J Phys Chem C. 2011; 115: 8759-8767
  5. Maya EM, Garcia-Frutos EM, Vazquez P, Torres T, Martin G, Rojo G, Agullo-Lopez F, Gonzalez-Jonte RH, Ferro VR, Vega JMG, Ledoux I, Zyss J. Novel Push−Pull Phthalocyanines as Targets for Second-Order Nonlinear Applications. J Phys Chem A. 2003; 107: 2110-2117
  6. Walter MG, Rudine AB, Wamser CC. Porphyrins and phthalocyanines in solar photovoltaic cells. J Porphyrins Phthalocyanines. 2010; 14: 759–792
  7. Liu MO, Tai CH, Teh Hu A. The fluorescent and photoelectric conversion properties of phthalocyanineeperylene tetracarboxylic complexes. J Photochem Photobiol A. 2004; 165: 193-200
  8. Nyokong T, Antunes E. in The Handbook of Porphyrin Science, ed. Kadish KM, Smith KM and Guilard R. World Scientific. Singapore, 2010, ch. 34, vol 7
  9. Frahn MS, Abellon RD, Jager WF, Luthjens LH, Warman JM. Synthesis and characterization of a new fluorogenic probe molecule N-(1-pyrene)methacrylamide for monitoring radiation-induced polymerization. Nucl Instrum Methods Phys Res. Sect B. 2001; 185: 241-47
  10. Lerner MG, Resczenski JM, Amin A, Johnson RR, Goldsmith JI, Johnson ATC. Toward quantifying the electrostatic transduction mechanism in carbon nanotube molecular sensors. J Am Chem Soc. 2012; 134: 14318
  11. Valeur B. Molecular fluorescence principles and applications. Germany, Weinheim: Wiley-VCH; 2002
  12. Karabacak M, Cinar M, Kurt M, Sundaraganesan N. Experimental and theoretical FTIR and FT-Raman spectroscopic analysis of 1-pyrenecarboxylic acid. Spectrochim Acta Part A: Mol Biomol Spectrosc. 2013; 114: 509-519
  13. Roth A, Ragoussi ME, Wibmer L, Katsukis G, Torre G, Torres T, Guldi DM. Electron-accepting phthalo