1-Adamantanamine-based triazole-appended organosilanes as chromogenic "naked-eye" and fluorogenic "turn-on" sensors for the highly selective detection of Sn2+ ions. (23rd March 2022)
- Record Type:
- Journal Article
- Title:
- 1-Adamantanamine-based triazole-appended organosilanes as chromogenic "naked-eye" and fluorogenic "turn-on" sensors for the highly selective detection of Sn2+ ions. (23rd March 2022)
- Main Title:
- 1-Adamantanamine-based triazole-appended organosilanes as chromogenic "naked-eye" and fluorogenic "turn-on" sensors for the highly selective detection of Sn2+ ions
- Authors:
- Singh, Gurjaspreet
Kaur, Jashan Deep
Pawan,
Diksha,
Sushma,
Suman,
Shilpy,
Satija, Pinky
Singh, K. N. - Abstract:
- Abstract : 1-Adamantanamine based organosilanes 4a–d have been synthesized and possessed selectivity towards Sn 2+ ions only and serve as a colorimetric/fluorimetric dual-channel probe. The turn-on fluorescence has been marked on interaction with Sn 2+ ions. Abstract : The current investigation illustrates the design and facile synthesis of the 1-adamantanamine-based organosilanes 4a–d via a click silylation approach, and they were characterized well via NMR ( 1 H and 13 C) and mass spectroscopic techniques. All the synthesized organosilanes possessed preferential selectivity towards Sn 2+ ions in the presence of other relevant ions and served as colorimetric/fluorimetric dual-channel probes. The probes have been successfully employed as "naked-eye" sensors with a visible color change in daylight from transparent white to golden yellow upon binding with Sn 2+ ions. The enhancement in fluorescence is attributed to the inhibition of the PET process upon interaction with Sn 2+ ions. Furthermore, BH plots reveal the presence of strong binding with 1 : 1 stoichiometry in the physiological pH range. Moreover, the limits of detection when using 4a–d towards Sn 2+ found in this study are far lower than the WHO guidelines for drinking water. Interestingly, the chemosensor 4a has been successfully employed for performing recovery testing of Sn 2+ in real soil samples. Owing to these enticing features, this present protocol could enormously expedite the design and development ofAbstract : 1-Adamantanamine based organosilanes 4a–d have been synthesized and possessed selectivity towards Sn 2+ ions only and serve as a colorimetric/fluorimetric dual-channel probe. The turn-on fluorescence has been marked on interaction with Sn 2+ ions. Abstract : The current investigation illustrates the design and facile synthesis of the 1-adamantanamine-based organosilanes 4a–d via a click silylation approach, and they were characterized well via NMR ( 1 H and 13 C) and mass spectroscopic techniques. All the synthesized organosilanes possessed preferential selectivity towards Sn 2+ ions in the presence of other relevant ions and served as colorimetric/fluorimetric dual-channel probes. The probes have been successfully employed as "naked-eye" sensors with a visible color change in daylight from transparent white to golden yellow upon binding with Sn 2+ ions. The enhancement in fluorescence is attributed to the inhibition of the PET process upon interaction with Sn 2+ ions. Furthermore, BH plots reveal the presence of strong binding with 1 : 1 stoichiometry in the physiological pH range. Moreover, the limits of detection when using 4a–d towards Sn 2+ found in this study are far lower than the WHO guidelines for drinking water. Interestingly, the chemosensor 4a has been successfully employed for performing recovery testing of Sn 2+ in real soil samples. Owing to these enticing features, this present protocol could enormously expedite the design and development of chemosensors for the detection of Sn 2+ ions. … (more)
- Is Part Of:
- New journal of chemistry. Volume 46:Number 15(2022)
- Journal:
- New journal of chemistry
- Issue:
- Volume 46:Number 15(2022)
- Issue Display:
- Volume 46, Issue 15 (2022)
- Year:
- 2022
- Volume:
- 46
- Issue:
- 15
- Issue Sort Value:
- 2022-0046-0015-0000
- Page Start:
- 7055
- Page End:
- 7069
- Publication Date:
- 2022-03-23
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/d2nj00241h ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21901.xml