Synthesis and investigation of bis(phenyl)fluorene and carbazole appended dipodal Schiff base for fluorescence sensing towards Sn(II) ion and its regioselective polymerization


KOLCU F., Çulhaoğlu S., KAYA İ.

Journal of Photochemistry and Photobiology A: Chemistry, cilt.441, 2023 (SCI-Expanded) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 441
  • Basım Tarihi: 2023
  • Doi Numarası: 10.1016/j.jphotochem.2023.114665
  • Dergi Adı: Journal of Photochemistry and Photobiology A: Chemistry
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, BIOSIS, Chemical Abstracts Core, Chimica, INSPEC
  • Anahtar Kelimeler: Benesi-Hildebrand, CHEF, Fluorescent chemosensor, Oxidative polycondensation, Schiff base, Sn2+
  • Çanakkale Onsekiz Mart Üniversitesi Adresli: Evet

Özet

One-pot condensation reaction between 9,9-Bis(4-aminophenyl)fluorene and 9-Ethyl-9H-carbazole-3-carbaldehyde afforded a chemosensor ((N,N′)-4,4′-(9H-fluorene-9,9-diyl)bis(N-((9-ethyl-9H-carbazol-2-yl)methylene)aniline, SB) having Schiff base skeleton. The further step was the synthesis of the polymer (P-SB) via oxidative polycondesation reaction of SB. FT-IR, 1H NMR and 13C NMR instruments were used to characterize the functional groups on the monomer and polymer. Thermal stability and electrochemical features of SB and P-SB were characterized by thermogravimetric analysis-differential thermal analyses (TG-DTA) and cyclic voltammetry (CV), respectively. The glass transition and surface image of P-SB were determined from DSC and SEM measurements, respectively. UV–vis and photoluminescence spectroscopy (PL) allowed to determine the optical properties of SB and P-SB. The obtained polymer, which had the weight average molecular weight of 8400 Da identified by gel permeation chromatography (GPC), exhibited fluorescence property. The synthesized turn-on fluorogenic chemosensor SB showed high selectivity and sensitivity towards Sn2+ among the cations of Ag+, K+, Hg2+, Mn2+, Cd2+, Sn2+, Ca2+, Pb2+, Zn2+, Co2+, Ni2+, Cu2+, Fe3+, Al3+, Cr3+ and Cr6+. The fluorescence turn-on recognition process for the detection of Sn2+ was related to the restriction of C[dbnd]N isomerization, followed by inhibiting intramolecular charge transfer (ICT), with consequent chelation-enhanced fluorescence (CHEF) mechanism. The stoichiometry ratio of the analyte-sensor adduct in the solution was found to be 1:1 by Job's plot method concomitant with a dramatic increase in fluorescent signal at 471 nm and a marked color change from colorless to turquoise blue upon addition of Sn2+ ions. Limit of detection value for the formation of SB-Sn2+ chelation was calculated as 3.37 nM. No change in PL intensity of SB-Sn2+ chelation was observed in the company of other metal ions. Reversibility of the chemosensor in its binding towards Sn2+ was demonstrated in the presence of chelating agent EDTA. The synthesized SB could effectively detect Sn2+ ion as a fluorescent sensor.