Abstract
Calixarenes, which have a great place in supramolecular chemistry, have become the most prominent macrocyclic compounds in synthetic organic chemistry due to their easy synthesis and functionalization. In this study, p-tert-butyl calix[4]arene dihydrazide derivative was synthesized and then reacted with 3-oxo-3,4-dihydro-2 H-benzo[b][1,4] thiazin-2-ylideneacetyl chloride to prepare new calixarene based chromophore compound 4. The structure of the synthesized compound was elucidated by spectroscopic methods such as 1H NMR 13C NMR and FT-IR spectroscopy. Chromogenic and fluorescence properties of compound 4 were evaluated. It was observed from both studies that compound 4 was Co2+ selective and shows fluorescence Switched-off behavior. Stoichiometry, binding constant and the detection limit were calculated. The stoichiometry between compound 4 and Co2+ was found to be 1:1. The binding constant value (K) was calculated as 666.67 M− 1 using Benesi–Hildebrand equation, while the detection limit for Co2+ ion was calculated as 0.0465 µM.
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We would like to thank The Research Foundation of Selcuk University (SUBAP-Grant Number: 18201144) for their financial support of this work.
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Fatimah Fateh: Conceptualization, Methodology, Investigation, Visualization.
Ayse Yildirim: Conceptualization, Methodology, Investigation, Visualization.
Asif Ali Bhatti: Conceptualization, Investigation, Writing - Review & Editing.
Mustafa Yilmaz: Conceptualization, Supervision, Funding acquisition, Resources, Writing - Review & Editing.
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Fateh, F., Yildirim, A., Bhatti, A.A. et al. A New Benzothiazin-functionalized Calix[4]arene-based Fluorescent Chemosensor for the Selective Detection of Co2+ Ion. J Fluoresc 31, 1075–1083 (2021). https://doi.org/10.1007/s10895-021-02745-w
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DOI: https://doi.org/10.1007/s10895-021-02745-w