Araştırma Makalesi
BibTex RIS Kaynak Göster
Yıl 2018, Cilt: 14 Sayı: 2, 209 - 216, 30.06.2018
https://doi.org/10.18466/cbayarfbe.399162

Öz

Kaynakça

  • 1. Allcock, H.R, Recent advances in phosphazene (phosphonitrilic) chemistry, Chemical Reviews, 1972, 72, 315-356.
  • 2. Chandrasekhar, V, Krishnan, V, Advances in the chemistry of chloro-cyclophosphazenes, Advances in Inorganic Chemistry, 2002, 53, 159-211.
  • 3. Yıldırım, T, Bilgin, K, Yenilmez Çiftçi, G, Tanrıverdi Eçik, E, Şenkuytu, E, Uludağ, Y, Tomak, L, Kılıç, A, Synthesis, cytotoxicity and apoptosis of cyclotriphosphazene compounds as anti-cancer agents, European Journal of Medicinal Chemistry, 2012, 52, 213-220.
  • 4. Bolink, H.J, Barea, E, Costa, R.D., Coronado, E, Sudhakar, S, Zhen, C, Sellinger, A Efficient blue emitting organic light emitting diodes based on fluorescent solution processable cyclic phosphazenes, Organ-ic Electronics, 2008, 9, 155–163.
  • 5. Moriya, K, Masuda, T, Suzuki, T, Yano, S, Kajiwara, M, Liquid Crystalline Phase Transition in Hexakis (4-(N-(41-alkoxyphenyl) iminomethyl) phenoxy) cyclotriphosphazene. Molecular Crystals and Liquid Crystals Science and Technology Section A. Molecular Crys-tals and Liquid Crystals, 1998, 318(1), 267-278.
  • 6. Davarcı, D, Zorlu, Y, Group 12 metal coordination polymers built on a flexible hexakis(3-pyridyloxy)cyclotriphosphazene ligand: Effect of the central metal ions on the construction of coordination polymers, Polyhedron, 2017, 127, 1–8.
  • 7. Şenkuytu, E, Tanrıverdi Eçik, E, Durmuş, M, Yenilmez Çiftçi, G, Monofunctional amines substituted fluorenylidene bridged cyclotri-phosphazenes: ‘Turn-off’ fluorescence chemosensors for Cu2+ and Fe3+ ions, Polyhedron, 2015, 101, 223–229.
  • 8. Yenilmez Çiftçi, G, Şenkuytu, E, Bulut, M, Durmuş, M, Novel Coumarin Substituted Water Soluble Cyclophosphazenes as “Turn-Off” Type Fluorescence Chemosensors for Detection of Fe3+ ions in Aqueous Media, Journal of Fluorescence, 2015, 25, 1819–1830.
  • 9. Kundu, A, Hariharan, P.S, Prabakaran, K, Anthony, S.P, Synthesis of new colori/ A fluorimetric chemosensor for selective sensing of bi-ologically important Fe3+, Cu2+ and Zn2+ metal ions, Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2015, 151, 426–431.
  • 10. Li, C.Y, Zou, C.X, Li, Y.F, Tang, J.L, Weng, C, A new rhodamine-based fluorescent chemosensor for Fe3+ and its application in living cell imaging, Dyes and Pigments, 2014, 104, 110-115.
  • 11. Wanga, D, Zheng, J.Q, Zhenga, X.J, Fanga, D.C, Yuanc, D.Q, Jin, L.P, A fluorescent chemosensor for the sequential detection of cop-per(II) and histidine and its biological applications, Sensors and Actu-ators B, 2016, 228, 387–394.
  • 12. Evstatiev, R, Gasche, C, Iron sensing and signalling, Gut, 2012, 61, 933–952.
  • 13. Que, E.L, Domaille, D.W, Chang, C.J, Metals in Neurobiology: Probing Their Chemistry and Biology with Molecular Imaging, Chemical Reviews, 2008, 108, 1517–1549.
  • 14. Andrews, N, Disorders of Iron Metabolism, The New England Jour-nal of Medicine, 1999, 341, 1986–1995.
  • 15. Squittia, R, Ghidoni, R, Simonelli, I, Ivanova, I.D, Colabufo, N.A, Zuin, M, Benussi, L, Binetti, G, Cassetta, E, Rongioletti, M, Siotto, M, Copper dyshomeostasis in Wilson disease and Alzheimer's disease as shown by serum and urine copper indicators, Journal of Trace El-ements in Medicine and Biology, 2018, 45, 181–188.
  • 16. Wang, C, Liu, Y, Cheng, J , Song, J, Zhao, Y, Ye, Y, Efficient FRET-based fuorescen tratiometric chemosensors for Fe3+ and it sap-plication in living cells, Journal of Luminescence, 2015, 157, 143–148.
  • 17. Park, G.J, You, G.R, Choi, Y.W, Kim, C, A naked-eye chemosensor for simultaneous detection of iron and copper ions and its copper complex for colorimetric/fluorescentsensing of cyanide, Sensors and Actuators B, 2016, 229, 257–271.
  • 18. Cheng, P.F, Xu, K.X, Yao, W, Xie, E, Liu, J, Novel fluorescent chemosensors based on carbazole for Cu2+ and Fe3+ in aqueous media, Journal of Luminescence, 2013, 143, 583–586.
  • 19. Carriedo, G.A, Catuxo, L.F, Alonso, F.J.G, Elipe, P.G, Gonzalez, P.A, Preparation of a New Type of Phosphazene High Polymers Con-taining 2,2’-Dioxybiphenyl Groups, Macromolecules, 1996, 29, 5320-5325.
  • 20. Parker, C.A, Rees, W, Correction of Fluorescence Spectra and Meas-urement of Fluorescence Quantum Efficiency, Analyst, 1960, 85(1013), 587-600.

Novel Aminopyrene Substituted Monospiro/Dispiro Cyclotriphosphazenes: Synthesis, Characterization and Chemosensor Properties

Yıl 2018, Cilt: 14 Sayı: 2, 209 - 216, 30.06.2018
https://doi.org/10.18466/cbayarfbe.399162

Öz

In the present work, the novel aminopyrene
substituted monospiro/dispiro
cyclotriphosphazenes (6 and 7) have been synthesized. This
compounds were characterized general spectroscopic techniques such as mass, 1H
and 31P NMR spectrometry. The photophysical and chemosensor
properties toward various metals (Fe3+, Cr3+, Co2+,
Al3+, Hg+, Mn2+, Ni2+, Cu2+,
Cd2+, Zn2+, Mg2+, Ca2+, Ba2+,
Li+, Na+, K+, Cs+) in THF solutions
of aminopyrene substituted compounds were investigated by fluorescence
spectroscopy. The metal sensing results showed that compounds 6 and 7 can be candidate fluorescent chemosensors for Cu2+ and
Fe3+ ions due to their displaying high selectivity and low limit of
detection.

Kaynakça

  • 1. Allcock, H.R, Recent advances in phosphazene (phosphonitrilic) chemistry, Chemical Reviews, 1972, 72, 315-356.
  • 2. Chandrasekhar, V, Krishnan, V, Advances in the chemistry of chloro-cyclophosphazenes, Advances in Inorganic Chemistry, 2002, 53, 159-211.
  • 3. Yıldırım, T, Bilgin, K, Yenilmez Çiftçi, G, Tanrıverdi Eçik, E, Şenkuytu, E, Uludağ, Y, Tomak, L, Kılıç, A, Synthesis, cytotoxicity and apoptosis of cyclotriphosphazene compounds as anti-cancer agents, European Journal of Medicinal Chemistry, 2012, 52, 213-220.
  • 4. Bolink, H.J, Barea, E, Costa, R.D., Coronado, E, Sudhakar, S, Zhen, C, Sellinger, A Efficient blue emitting organic light emitting diodes based on fluorescent solution processable cyclic phosphazenes, Organ-ic Electronics, 2008, 9, 155–163.
  • 5. Moriya, K, Masuda, T, Suzuki, T, Yano, S, Kajiwara, M, Liquid Crystalline Phase Transition in Hexakis (4-(N-(41-alkoxyphenyl) iminomethyl) phenoxy) cyclotriphosphazene. Molecular Crystals and Liquid Crystals Science and Technology Section A. Molecular Crys-tals and Liquid Crystals, 1998, 318(1), 267-278.
  • 6. Davarcı, D, Zorlu, Y, Group 12 metal coordination polymers built on a flexible hexakis(3-pyridyloxy)cyclotriphosphazene ligand: Effect of the central metal ions on the construction of coordination polymers, Polyhedron, 2017, 127, 1–8.
  • 7. Şenkuytu, E, Tanrıverdi Eçik, E, Durmuş, M, Yenilmez Çiftçi, G, Monofunctional amines substituted fluorenylidene bridged cyclotri-phosphazenes: ‘Turn-off’ fluorescence chemosensors for Cu2+ and Fe3+ ions, Polyhedron, 2015, 101, 223–229.
  • 8. Yenilmez Çiftçi, G, Şenkuytu, E, Bulut, M, Durmuş, M, Novel Coumarin Substituted Water Soluble Cyclophosphazenes as “Turn-Off” Type Fluorescence Chemosensors for Detection of Fe3+ ions in Aqueous Media, Journal of Fluorescence, 2015, 25, 1819–1830.
  • 9. Kundu, A, Hariharan, P.S, Prabakaran, K, Anthony, S.P, Synthesis of new colori/ A fluorimetric chemosensor for selective sensing of bi-ologically important Fe3+, Cu2+ and Zn2+ metal ions, Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2015, 151, 426–431.
  • 10. Li, C.Y, Zou, C.X, Li, Y.F, Tang, J.L, Weng, C, A new rhodamine-based fluorescent chemosensor for Fe3+ and its application in living cell imaging, Dyes and Pigments, 2014, 104, 110-115.
  • 11. Wanga, D, Zheng, J.Q, Zhenga, X.J, Fanga, D.C, Yuanc, D.Q, Jin, L.P, A fluorescent chemosensor for the sequential detection of cop-per(II) and histidine and its biological applications, Sensors and Actu-ators B, 2016, 228, 387–394.
  • 12. Evstatiev, R, Gasche, C, Iron sensing and signalling, Gut, 2012, 61, 933–952.
  • 13. Que, E.L, Domaille, D.W, Chang, C.J, Metals in Neurobiology: Probing Their Chemistry and Biology with Molecular Imaging, Chemical Reviews, 2008, 108, 1517–1549.
  • 14. Andrews, N, Disorders of Iron Metabolism, The New England Jour-nal of Medicine, 1999, 341, 1986–1995.
  • 15. Squittia, R, Ghidoni, R, Simonelli, I, Ivanova, I.D, Colabufo, N.A, Zuin, M, Benussi, L, Binetti, G, Cassetta, E, Rongioletti, M, Siotto, M, Copper dyshomeostasis in Wilson disease and Alzheimer's disease as shown by serum and urine copper indicators, Journal of Trace El-ements in Medicine and Biology, 2018, 45, 181–188.
  • 16. Wang, C, Liu, Y, Cheng, J , Song, J, Zhao, Y, Ye, Y, Efficient FRET-based fuorescen tratiometric chemosensors for Fe3+ and it sap-plication in living cells, Journal of Luminescence, 2015, 157, 143–148.
  • 17. Park, G.J, You, G.R, Choi, Y.W, Kim, C, A naked-eye chemosensor for simultaneous detection of iron and copper ions and its copper complex for colorimetric/fluorescentsensing of cyanide, Sensors and Actuators B, 2016, 229, 257–271.
  • 18. Cheng, P.F, Xu, K.X, Yao, W, Xie, E, Liu, J, Novel fluorescent chemosensors based on carbazole for Cu2+ and Fe3+ in aqueous media, Journal of Luminescence, 2013, 143, 583–586.
  • 19. Carriedo, G.A, Catuxo, L.F, Alonso, F.J.G, Elipe, P.G, Gonzalez, P.A, Preparation of a New Type of Phosphazene High Polymers Con-taining 2,2’-Dioxybiphenyl Groups, Macromolecules, 1996, 29, 5320-5325.
  • 20. Parker, C.A, Rees, W, Correction of Fluorescence Spectra and Meas-urement of Fluorescence Quantum Efficiency, Analyst, 1960, 85(1013), 587-600.
Toplam 20 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Mühendislik
Bölüm Makaleler
Yazarlar

Elif Şenkuytu

Yayımlanma Tarihi 30 Haziran 2018
Yayımlandığı Sayı Yıl 2018 Cilt: 14 Sayı: 2

Kaynak Göster

APA Şenkuytu, E. (2018). Novel Aminopyrene Substituted Monospiro/Dispiro Cyclotriphosphazenes: Synthesis, Characterization and Chemosensor Properties. Celal Bayar University Journal of Science, 14(2), 209-216. https://doi.org/10.18466/cbayarfbe.399162
AMA Şenkuytu E. Novel Aminopyrene Substituted Monospiro/Dispiro Cyclotriphosphazenes: Synthesis, Characterization and Chemosensor Properties. CBUJOS. Haziran 2018;14(2):209-216. doi:10.18466/cbayarfbe.399162
Chicago Şenkuytu, Elif. “Novel Aminopyrene Substituted Monospiro/Dispiro Cyclotriphosphazenes: Synthesis, Characterization and Chemosensor Properties”. Celal Bayar University Journal of Science 14, sy. 2 (Haziran 2018): 209-16. https://doi.org/10.18466/cbayarfbe.399162.
EndNote Şenkuytu E (01 Haziran 2018) Novel Aminopyrene Substituted Monospiro/Dispiro Cyclotriphosphazenes: Synthesis, Characterization and Chemosensor Properties. Celal Bayar University Journal of Science 14 2 209–216.
IEEE E. Şenkuytu, “Novel Aminopyrene Substituted Monospiro/Dispiro Cyclotriphosphazenes: Synthesis, Characterization and Chemosensor Properties”, CBUJOS, c. 14, sy. 2, ss. 209–216, 2018, doi: 10.18466/cbayarfbe.399162.
ISNAD Şenkuytu, Elif. “Novel Aminopyrene Substituted Monospiro/Dispiro Cyclotriphosphazenes: Synthesis, Characterization and Chemosensor Properties”. Celal Bayar University Journal of Science 14/2 (Haziran 2018), 209-216. https://doi.org/10.18466/cbayarfbe.399162.
JAMA Şenkuytu E. Novel Aminopyrene Substituted Monospiro/Dispiro Cyclotriphosphazenes: Synthesis, Characterization and Chemosensor Properties. CBUJOS. 2018;14:209–216.
MLA Şenkuytu, Elif. “Novel Aminopyrene Substituted Monospiro/Dispiro Cyclotriphosphazenes: Synthesis, Characterization and Chemosensor Properties”. Celal Bayar University Journal of Science, c. 14, sy. 2, 2018, ss. 209-16, doi:10.18466/cbayarfbe.399162.
Vancouver Şenkuytu E. Novel Aminopyrene Substituted Monospiro/Dispiro Cyclotriphosphazenes: Synthesis, Characterization and Chemosensor Properties. CBUJOS. 2018;14(2):209-16.