A highly selective and sensitive chemosensor derived coumarin-thiazole for colorimetric and fluorimetric detection of CN- ion in DMSO and aqueous solution: synthesis, sensing ability, Pd(II)/Pt(II) complexes and theoretical studies
Yükleniyor...
Dosyalar
Tarih
2016
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Pergamon-Elsevier
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
A colorimetric and fluorescence turn-on cyanide probe, including coumarin-thiazole and imine (azomethine) group, has been designed and synthesized. It showed an immediate visible color change from yellow to deep red only in DMSO, and an appearance of strong yellow and green fluorescence when CN- was added to DMSO, and a mixture of DMSO:H2O (9:1), respectively. Thus, the sensor can be used to detect CN- in aqueous solution. The sensing mechanism of chemosensor 4 reactions with CN- ion was observed with the deprotonation and addition mechanisms at the same time. The mechanisms of reactions of chemosensor 4 with; CN-, F-, and AcO- were examined using H-1 NMR spectroscopy, and were also theoretically supported by DFT and TD-DFT calculations. In addition, the metal complexes of chemosensor 4 with Pd(II) and Pt(II) were also synthesized and all the synthesized compounds were characterized using general spectroscopic methods (FTIR, H-1/C-13 NMR, and mass spectrometry), magnetic susceptibilities, and conductivity measurements. Also, the molecular structure of 4 was determined using single crystal X-ray analysis. (C) 2016 Elsevier Ltd. All rights reserved.
Açıklama
Anahtar Kelimeler
Coumarin-thiazole, Schiff Base, Anion Detection, Fluorescence Turn-on Probe, DFT, TD-DFT Calculations, Pd(II)/Pt(II) Complexes
Kaynak
Tetrahedron
WoS Q Değeri
N/A
Scopus Q Değeri
Q3
Cilt
72
Sayı
39