Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/6403
Title: Aza-crown ether tethered with benzothiazole: Synthesis and optical spectral studies
Authors: Mashraqui, Sabir H
Dhaval, Vashi
Subramanian, S
Khan, Tabrez B
Keywords: Aza-crown fluoroionophore;optical spectral studies;intramolecular charge transfer;protonation;metal-ion complexation
Issue Date: Mar-2006
Publisher: CSIR
IPC Code: Int.Cl.7 C 07 D
Abstract: Synthesis of a new fluoroionophore 2 encompassing aza-phenyl-crown and benzothiazole is described. The UV-Vis spectra of 2 are not altered with change in solvent polarity indicating the absence of solvatochromism. However, the fluorescence spectra are progressively red shifted in more polar solvents on account of increasing charge transfer character of the excited state. In the presence of trifluoroacetic acid (TFAA), protonation of benzothiazole nitrogen results in the red shift of the absorption spectra. Contrary to expectation, the emission spectra suffers blue shift in the presence of TFAA. Presumably, the emission for the case 2+H+ occurs from higher vibrational energy levels which accounts for the blue shift. Unfortunately, selected alkali or alkaline earth metals ions examined for metal sensing applications have failed to induce significant perturbations either in the absorption or emission spectra. This may be attributed to poor electronic communication between the crown-bound metal ions and the benzothiazole fluorophore due to steric encumbrance between the ortho-substituted benzothiazole chromophore and the phenyl aza-crown moiety.
Page(s): 815-819
URI: http://hdl.handle.net/123456789/6403
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.45B(03) [March 2006]

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