dc.contributor.author |
Tayade, K. |
|
dc.contributor.author |
Kaur, A. |
|
dc.contributor.author |
Tetgure, S. |
|
dc.contributor.author |
Chaitanya, G. K. |
|
dc.contributor.author |
Singh, N. |
|
dc.contributor.author |
Kuwar, A. |
|
dc.date.accessioned |
2016-08-04T06:37:45Z |
|
dc.date.available |
2016-08-04T06:37:45Z |
|
dc.date.issued |
2016-08-04 |
|
dc.identifier.uri |
http://localhost:8080/xmlui/handle/123456789/174 |
|
dc.description.abstract |
The (13E,19E)-N1′,N3′-bis[4-(diethylamino)-2-hydroxybenzylidene]malonohydrazide (L) has been developed for the detection of Th4+ ions using dual channel signalling system. The UV–vis absorbance and fluorescence spectroscopic data revealed the formation of L–Th4+ complex in 1:1 equilibrium. The density functional theory (DFT) also confirms the optimum binding cavity for the recognition of metal ion. The binding constant computed from different mathematical models for an assembly of L–Th4+. The detection limit of L for Th4+ recognition is to a concentration down to 0.1 μM (0.023 μg g−1). The present sensing system is also successfully applied for the detection of Th4+ ion present in soil near nuclear atomic plants. |
en_US |
dc.language.iso |
en_US |
en_US |
dc.subject |
Ratiometric fluorescent sensor |
en_US |
dc.subject |
Tetravalent thorium ion (Th4+) |
en_US |
dc.subject |
Real sample analysis |
en_US |
dc.title |
Fluorogenic ratiometric dipodal optode containing imine-amide linkages: Exploiting subtle thorium (IV) ion sensing |
en_US |
dc.type |
Article |
en_US |