| dc.contributor.author |
Biswal, B. |
|
| dc.contributor.author |
Mallick, D. |
|
| dc.contributor.author |
Bag, B. |
|
| dc.date.accessioned |
2018-10-01T12:26:29Z |
|
| dc.date.available |
2018-10-01T12:26:29Z |
|
| dc.date.issued |
2016 |
|
| dc.identifier.citation |
Organic & Biomolecular Chemistry, 14(7), 2016: 2241-2248 |
|
| dc.identifier.issn |
1477-0520 |
|
| dc.identifier.uri |
http://ore.immt.res.in/handle/2018/2264 |
|
| dc.description |
DST, New Delhi [SB/EMEQ-226/2013] |
|
| dc.description.abstract |
Two six-membered spirocyclic rhodamine derivatives containing substituted pyrroles (1 and 2) were shown to exhibit preferential dual mode 'turn-on' signaling responses in the presence of Hg2+ ions through complexation mediated spiro-ring opening. Although the rate of spiro-ring opening mediated through complexation is much slower in these probes in comparison to their five membered analogues, they exhibited a comparable sensitivity in metal ion detection. |
|
| dc.language |
en |
|
| dc.publisher |
Royal Society Of Chemistry |
|
| dc.relation.isreferencedby |
SCI |
|
| dc.rights |
Copyright [2016]. All efforts have been made to respect the copyright to the best of our knowledge. Inadvertent omissions, if brought to our notice, stand for correction and withdrawal of document from this repository. |
|
| dc.subject |
Chemical Sciences |
|
| dc.title |
Signaling preferences of substituted pyrrole coupled six-membered rhodamine spirocyclic probes for Hg2+ ion detection |
|
| dc.type |
Journal Article |
|
| dc.affiliation.author |
CSIR-IMMT, Bhubaneswar 751013, Odisha, India |
|