
Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/2304
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DC Field | Value | Language |
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dc.contributor.author | Khullar, S. | - |
dc.contributor.author | Mandal, S.K. | - |
dc.date.accessioned | 2020-11-27T04:44:17Z | - |
dc.date.available | 2020-11-27T04:44:17Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | New Journal of Chemistry, 42(8), pp. 6315-6321 | en_US |
dc.identifier.other | https://doi.org/10.1039/C8NJ00728D | - |
dc.identifier.uri | https://pubs.rsc.org/ru/content/articlelanding/2018/nj/c8nj00728d#!divAbstract | - |
dc.identifier.uri | http://hdl.handle.net/123456789/2304 | - |
dc.description | Only IISERM authors are available in the record. | - |
dc.description.abstract | A new methyl red (MR) based silatrane was synthesized in high yield by the transesterification reaction of methyl red-amidopropyltrimethoxysilane 1 (MR-APTMS) and trisisopropanolamine. Single crystal X-ray diffraction analysis was used to deduce the structure of silatrane 2 which was also supported by NMR (1H, 13C) spectroscopy, mass spectrometry, FTIR, UV-Vis and DFT studies. Silatrane 2 when surveyed for cation recognition ability with a library of metal ions in CH3CN/H2O (9:1, v/v) was found to act as an excellent UV-Vis probe for the selective recognition of Hg2+in vitro. Also, quantum mechanical calculations of the interaction complex [MR-APS-Hg]2+3 using DFT at the B3LYP level in conjunction with the LanL2DZ basis set determined the geometric and the stability parameters of the surveyed interaction. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.subject | Methyl red | en_US |
dc.subject | Trisisopropanolamine | en_US |
dc.subject | Silatrane derivative | en_US |
dc.title | Selective mercury ion recognition using a methyl red (MR) based silatrane sensor | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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