Dergiler / Bor Dergisi / 2019 / Cilt: 4 - Sayı: 1

Synthesis of a new boron complex with imine ligand: Synthesis, characterization and fluorescent properties

Sayfa
46–52
Yayın Tarihi
2022-10-11
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)

Moreover, the measurements of the fluorescence quantum yields (up to 48%)were performed.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:In this study, it is aimed to obtain of N,N’-Bis(3-tert-Butyl-5-methylsalicylidene)-1,2-diaminoethane-boron complex (3) in three-step reaction.
📊
Temel Bulgular & Veri:The condensation reaction was carried out to give theimine derivative as a Schiff base ligand (2).
💡
Sonuç & Katkı:Moreover, the measurements of the fluorescence quantum yields (up to 48%)were performed.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

In this study, it is aimed to obtain of N,N’-Bis(3-tert-Butyl-5-methylsalicylidene)-1,2-diaminoethane-boron complex (3) in three-step reaction. In the first step, an aromaticaldehyde derivative was synthesized by the o-formylation reaction with commerciallyavailable an aromatic phenol. The condensation reaction was carried out to give theimine derivative as a Schiff base ligand (2). The fluorine chelated boron complexwas synthesized through the reaction of BF3.OEt2 with ligand (2). This Schiff baseboron complex was reported for the first time and was fully characterized by commonspectroscopic techniques such as 1H-NMR, 13C-NMR, FT-IR, UV–Vis, MS and elementalanalysis. The spectroscopic properties of the target boron-complex were examined withthe absorption and fluorescence spectroscopy. It was determined that the obtained boroncomplex is highly emissive molecule in different solvents with large Stokes shifts reaching100 nm. Moreover, the measurements of the fluorescence quantum yields (up to 48%)were performed.

🔖

Bu Makaleye Atıf Yap

Şen, P. (2022). Synthesis of a new boron complex with imine ligand: Synthesis, characterization and fluorescent properties. Bor Dergisi, Cilt: 4 - Sayı: 1, 46–52. https://ajindex.com/articles/467428

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (15)

  1. Treibs A., Kreuzer F.H., Difluorboryl komplexe von di und tripyrrylmethenen, Justus Liebigs Ann. Chem., 718, 208-223, 1968
  2. Burghart A., Kim H., Welch M.B., Thoresen L. H., Reibenspies J., Burgess K., 3, 5-Diaryl-4, 4-difluoro4-bora-3a, 4a-diaza-s-indacene (BODIPY) dyes: synthesis, spectroscopic, electrochemical, and structural properties, J. Org. Chem., 64, 7813-7819, 1999
  3. Liu Y., Guo J., Zhang H., Wang Y., Highly efficient white organic electroluminescence from a double-layer device based on a boron hydroxyphenylpyridine complex, angew. Chem. Int. Ed. 41, 182-184, 2002
  4. Maar R.R., Barbon S.M., Sharma N., Groom H., Luyt L.G., Gilroy J.B., Evaluation of anisole-substituted boron difluoride formazanate complexes for fluorescence cell imaging, Chem. Eur. J. 21, 15589-15599, 2015
  5. Kowada T., Maeda H., Kikuchi K., BODIPY-based probes for the fluorescence imaging of biomolecules in living cells, Chem. Soc. Rev., 44, 4953-4972, 2015
  6. Kamkaew A., Lim S.H., Lee H.B., Kiew L.V., Chung L.Y., Burgess K., BODIPY dyes in photodynamic therapy, Chem. Soc. Rev., 7, 42 (1), 77-88, 2013
  7. Moon S.Y., Cha N.R., Kim Y.H., Chang S., New Hg2+ -selective chromo- and fluoroionophore based upon 8-hydroxyquinoline. J. Org. Chem., 69, 181–183, 2004
  8. Hawthorne M.F., The role of chemistry in the development of boron neutron capture therapy of cancer, Angw. Chem. Iht. Ed. Engl., 32, 950-984, 1993
  9. Qiao F., Liu A., Zhou Y., Xiao Y., Yang P.O., Bulk heterojunction organic solar cell based on a novel fluorescent fluorine–boron complex, J. Mater. Sci., 44, 1283- 1286, 2009
  10. Tamgho I., Hasheminasa A., Engle J.T., Nemykin V.N., Ziegler C.J., A new highly fluorescent and symmetric pyrrole-BF2 chromophore: BOPHY, J. Am. Chem. Soc., 136, 5623−5626, 2014
  11. Yu C., Zhang L.J.P., Feng Z., Cheng C., Wei Y., Mu X., Hao E., Highly fluorescent BF2 complexes of hydrazine–schiff base linked bispyrrole, Org. Lett., 16, 3048- 3051, 2014
  12. Zhang H., Huo C., Zhang J., Zhang P., Tian W., Wang Y., Efficient single-layer electroluminescent device based on a bipolar emitting boron-containing material, Chem. Commun., 3, 281-283, 2006
  13. Guieu S., Cardona F., Rochab J., Silva A.M.S., Luminescent bi-metallic fluoroborates derivatives of bulky Salen ligands, New. J. Chem., 38, 5411-5414, 2014
  14. Perrin D.D., Armarego W.L.F., Perrin D.R. Purification of laboratory chemicals, New York: Pergamon Press, 2013
  15. Larrow J.F., Jacobsen E.N., A practical method for th