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Lower Rim 1,3-Di{bis(2-picolyl)}amide Derivative of Calix[4]arene (L) as Ratiometric Primary Sensor toward Ag(+) and the Complex of Ag(+) as Secondary Sensor toward Cys: Experimental, Computational, and Microscopy Studies and INHIBIT Logic Gate Properties of L

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Title Lower Rim 1,3-Di{bis(2-picolyl)}amide Derivative of Calix[4]arene (L) as Ratiometric Primary Sensor toward Ag(+) and the Complex of Ag(+) as Secondary Sensor toward Cys: Experimental, Computational, and Microscopy Studies and INHIBIT Logic Gate Properties of L
 
Creator JOSEPH, R
RAMANUJAM, B
ACHARYA, A
RAO, CP
 
Subject ion-selective electrodes
phosphate diester transesterification
basic-amino-acids
silver ion
binding-properties
l-lysine
water
recognition
cysteine
calixarenes
 
Description A structurally characterized lower rim 1,3-di{bis(2-picolyl)}amide derivative of calix[4]arene (L) exhibits high selectivity toward Ag(+) by Forming it 1:1 complex, among nine other biologically important metal ions, viz., Na(+), K(+), Mg(2+), Ca(2+), Mn(2+), Fe(2+), Co(2+), Ni(2+), and Zn(2+), its studied by fluorescence, absorption, and (1)H NMR spectroscopy. The 1:1 complex formed between L and Ag(+) has been further proven on the basis of ESI mass spectrometry and has been shown to have art association constant, K(a), of 11117 +/- 190 M(-1) based on fluorescence data. L acts as it primary ratiometric sensor toward Ag(+) by switch-on fluorescence and exhibits a lowest detectable concentration of 450 ppb. DFT computational studies carried out in mimicking thie formation of a 1:1 complex between L and Ag(+) resulted in it tetrahedral complex wherein the nitrogens of all four pyridyl moieties present on both arms are being coordinated. Whereas these pyridyls are located farther apart in the crystal structure, appropriate dihedral changes are induced in the arms in the presence of silver ion in order to form a coordination complex. Even the nanostructural features obtained in TEM clearly differentiates L from its Ag(+) complex. The in situ prepared silver complex of L detects Cys ratiometrically among the naturally occurring amino acids to a lowest concentration of 514 ppb by releasing L from the complex followed by formation of the cysteine complex of Ag(+). These were demonstrated on the basis of emission,absorption, (1)H NMR,and ESI mass spectra. The INH logic gate has also been generated by choosing Ag(+) and Cys as input and by monitoring the Output signal at 445 nm that originates from the excimer emission of L in the presence of Ag(+). Thus L is a potential primary sensor toward Ag(+) and is it secondary sensor toward Cys.
 
Publisher AMER CHEMICAL SOC
 
Date 2011-07-14T10:33:09Z
2011-12-26T12:48:20Z
2011-12-27T05:40:43Z
2011-07-14T10:33:09Z
2011-12-26T12:48:20Z
2011-12-27T05:40:43Z
2009
 
Type Article
 
Identifier JOURNAL OF ORGANIC CHEMISTRY, 74(21), 8181-8190
0022-3263
http://dx.doi.org/10.1021/jo901676s
http://dspace.library.iitb.ac.in/xmlui/handle/10054/3933
http://hdl.handle.net/10054/3933
 
Language en