Hossein Tavalali; Abolfath Parhami; Mohammad Ali Karimi; Jamshid Askari
Abstract
In this study, a novel mixed ligand (Dithizone-Co(II)-Alizarin red S: DTZ-Co-ALR-) ensemble is designed and developed ultra-sensitive, and highly selective to UV-Vis absorption and for naked-eye detection of Arginine (Arg), and Glutathione (GSH). The out coming high sensitivity and selectivity for new ...
Read More
In this study, a novel mixed ligand (Dithizone-Co(II)-Alizarin red S: DTZ-Co-ALR-) ensemble is designed and developed ultra-sensitive, and highly selective to UV-Vis absorption and for naked-eye detection of Arginine (Arg), and Glutathione (GSH). The out coming high sensitivity and selectivity for new receptor (DTZ-Co(II)-ALRs-Arg) was attained by adding Glutathione. The indicator is released due to its displacement from the mixed ligand (DTZ-Co-ALRs-Arg) by Glutathione and the change in absorbance may be due to the further complexation of GSH with the additional coordination sites present in the Arg bonded with the mixed ligand (DTZ-Co-ALRs). The label-free DTZ-Co-ALRs receptor provided sensitive and selective detection of L-Arginine, and Glutathione with detection limits of 0.03, and 0.009µmol L-1, respectively. The protocol especially offers high selectivity for the determination of Arg, and GSH among amino acids found in real samples. Moreover, the investigation of the logic behavior of the proposed DTZ-Co-ALRs receptor indicated its capability of functioning as an INHIBIT-type colorimetric chemosensor with the chemical inputs and UV-Vis absorbance signal as the output. This mixed ligand receptor could also behave as a molecular “keypad lock” with the correct sequential addition of Arg and GSH inputs.
Hossein Tavallali; Gohar Deilamy-Rad; Abolfath Parhami; Sajedeh Lohrasbi
Volume 3, Issue 2 , September 2016, , Pages 76-87
Abstract
A new diazo based, Congo-Red-Cu , was developed to act as an ‘Off–On’ reversible fluorescent probe for CN− detection. The changes in solvent composition has been shown greatly effective on selectivity of anion sensing through eliminate of sulfite interference. Increasing the amount ...
Read More
A new diazo based, Congo-Red-Cu , was developed to act as an ‘Off–On’ reversible fluorescent probe for CN− detection. The changes in solvent composition has been shown greatly effective on selectivity of anion sensing through eliminate of sulfite interference. Increasing the amount of ethanol up to 5% (v/v) cause a dramatic development in selectivity of CN−via inhibitory effect on sulfite interferent. The chemosensing behavior of the CR-Cu has been demonstrated through fluorescence, absorption, visual color changes and FT-IR studies. This chemosensor (CR-Cu) has been shown a significant visible color change and displays a remarkable fluorescent switch on in the presence of CN− ions. The ‘in situ’ prepared CN− complexes of CR-Cu shows high “Turn-Off” selectivity toward CO32− over the other anions. The detection limits for CN− were 90 and 20 nM for colorimetric and fluorometric methods respectively, that is far lower than the WHO guideline of 1.9 µM. The complex of CN− with CR-Cu also displayed ability to detect up to 15 nM CO32− among other competing anions through a fast response time of less than 30 s which is much lower than most recently reported chemosensor probes. It has been possible to build an INHIBIT logic gate for two binary inputs viz., CN− and CO32− by monitoring the fluorescence emission band at 446 nm as output. The development of fluorometric an ‘‘Off–On’’ reversible switch for three chemical inputs Cu2+, CN− and CO32− ions and mimics a molecular level keypad lock.
