Dergiler / Turkish Journal of Chemistry / 2018 / Cilt: 42 - Sayı: 1

Synthesis and some optical results of long chain substituted phthalocyanines

Sayfa
21–28
Yayın Tarihi
2022-11-05
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Transmittance spectra of the phthalocyanines synthesized using different metal ions showed a variation of about 8% and 15% in transmittance spectra of the Q band region was obtained by mixing the two metal phthalocyanine (indium and zinc) solutions.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Four metallo (zinc, copper, vanadyl, and indium) phthalocyanine derivatives bearing four aliphatic (hexylthio) groups were prepared from corresponding phthalonitrile compounds.
📊
Temel Bulgular & Veri:The metallophthalocyanines were characterized with ultraviolet{visible spectroscopy (UV-Vis), proton nuclear magnetic resonance ( 1 H NMR), Fourier transform-infrared spectroscopy (FT-IR), and mass and elemental analyses techniques.
💡
Sonuç & Katkı:Transmittance spectra of the phthalocyanines synthesized using different metal ions showed a variation of about 8% and 15% in transmittance spectra of the Q band region was obtained by mixing the two metal phthalocyanine (indium and zinc) solutions.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

Four metallo (zinc, copper, vanadyl, and indium) phthalocyanine derivatives bearing four aliphatic (hexylthio) groups were prepared from corresponding phthalonitrile compounds. The metallophthalocyanines were characterized with ultraviolet{visible spectroscopy (UV-Vis), proton nuclear magnetic resonance ( 1 H NMR), Fourier transform-infrared spectroscopy (FT-IR), and mass and elemental analyses techniques. Aggregation properties of metallophthalocyanines in solution were studied in varied concentration ranges. Thin lms of metallophthalocyanines were obtained by spin coating technique. Optical measurements showed that transmittance values of metallophthalocyanine thin lms obviously changed with respect to the metal ion in the phthalocyanines. Transmittance spectra of the phthalocyanines synthesized using different metal ions showed a variation of about 8% and 15% in transmittance spectra of the Q band region was obtained by mixing the two metal phthalocyanine (indium and zinc) solutions.

🔖

Bu Makaleye Atıf Yap

SORAR, İ., ÖZÇEŞMECİ, İ. (2022). Synthesis and some optical results of long chain substituted phthalocyanines. Turkish Journal of Chemistry, Cilt: 42 - Sayı: 1, 21–28. https://ajindex.com/articles/601760

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (19)

  1. McKeown, N. B. Phthalocyanine Materials: Materials: Synthesis, Structure, and Function; Cambridge University Press: Cambridge, UK, 1998
  2. Leznoff, C. C.; Lever, A. B. P. Phthalocyanines: Properties and Applications; VCH Publishers: New York, NY, USA, 1989. 3.  Ozcesmeci, _ I.; Sorar, _ I.; Gul, A. Inorg. Chem. Commun. 2011, 14, 1254-1257
  3. Li, L.; Tang, Q.; Li, H.; Hu, W.; Yang, X.; Shuai, Z.; Liu, Y.; Zhu, D. Pure Appl. Chem. 2008, 80, 2231-2240
  4. Sorar, _ I.; Sener, M. K.; Tepehan, F.; Gul, A. Thin Solid Films 2008, 516, 2894-2898
  5. Komino, T.; Matsuda, M.; Tajima, H. Thin Solid Films 2009, 518, 688-691. 7.  Ozcesmeci, _ I.; Sorar, _ I.; Gul, A. Philos. Mag. 2016, 96, 2986-2999
  6. Banimuslem, H.; Hassan, A.; Basova, T.; Gulmez, A. D.; Tuncel, S.; Durmus, M.; Gurek, A. G.; Ahsen, V. Sensor Actuat B-Chem. 2014, 190, 990-998
  7. Basova, T. V.; Parkhomenko, R. G.; Polyakov, M., Gurek, A. G.; Atilla, D.; Yuksel, F.; Ryabchikova, E. I.; Kadem, B. Y.; Hassan, A. K. Dyes Pigm. 2016, 125, 266-273
  8. Matsuda, H.; Okada, S.; Masaki, A.; Nakanishi, H.; Suda, Y.; Shigehara, K.; Yamada, A. Proc. SPIE. 1990, 1337, 105- 113
  9. Gurol, _ I.; Ahsen, V.; Bekaroglu,  O. J. Chem. Soc. Dalton. Trans. 1994, 497-500
  10. Gurek, A. G.; Ahsen, V.; Heinemann, F.; Zugenmaier, P. Mol. Cryst. Liq. Cryst. 2000, 338, 75-97
  11. Gursel, Y. H.; Senkal, B. F.; Kandaz, M.; Yakuphanoglu, F. Polyhedron 2009, 28, 1490-1496
  12. Suda, Y.; Shigehara, K.; Yamada, A.; Matsuda, H.; Okada, S.; Masaki, A.; Nakanishi, H. Proc. SPIE. 1991, 1560, 75-83
  13. Bayr, Z. A. Dyes Pigm. 2005, 65, 235-242. 16.  Ozcesmeci, _ I; Guner, S.; Okur, A. _ I.; Gul, A. J. Porphyrins Phthalocyanines 2007, 11, 531-536
  14. Selcukoglu, M.; Hamuryudan, E. Dyes Pigm. 2007, 74, 17-20. 18.  Ozcesmeci, M. J. Organomet. Chem. 2014, 767, 16-21
  15. Evren, D.; Burat, A. K.;  Ozcesmeci, _ I.; Sesalan, B. S. Dyes Pigm. 2013, 96, 475-482. 20.  Ozcesmeci, _ I. Synth. Met. 2013, 176, 128-133. 21.  Ozcesmeci, M.;  Ozkan, E.; Hamuryudan, E. J. Porphyrins Phthalocyanines 2013, 17, 1-8
  16. Jiang, Z.; Ou, Z.; Chen, N.; Wang, J.; Huang, J.; Shao, J.; Kadish, K. M. J. Porphyr. Phthalocyanines 2005, 9, 352-360
  17. Adebayo, A. I.; Nyokong, T. Polyhedron 2009, 28, 2831-2838
  18. Erdogmus, A.; Durmus, M.; Ugur, A. L.; Avciata, O.; Avciata, U.; Nyokong, T. Synth. Met. 2010, 160, 1868-1876
  19. Kurt,  O.;  Ozcesmeci, _ I.; Gul, A.; Ko