Design, synthesis and photophysical aspects of 1, 2, 3-triazole appended Schiff base functionalized silanes and silatranes. (1st September 2021)
- Record Type:
- Journal Article
- Title:
- Design, synthesis and photophysical aspects of 1, 2, 3-triazole appended Schiff base functionalized silanes and silatranes. (1st September 2021)
- Main Title:
- Design, synthesis and photophysical aspects of 1, 2, 3-triazole appended Schiff base functionalized silanes and silatranes
- Authors:
- Singh, Gurjaspreet
Priyanka,
Sushma,
Diksha,
Mohit,
Suman,
Kaur, Jashan Deep
Saini, Anamika
Satija, Pinky - Abstract:
- Abstract : This article represents the synthesis of 1, 2, 3 triazoles allied Schiff base functionalized silanes and silatranes. The silane 5a and silatrane 6a were investigated for their photophysical potential via absorption and emission spectroscopy and found selective for Sn(ii ). Abstract : Organosilicon chemistry is appraised as the trunk of coalescence and structural manoeuvres of moieties. Schiff base compounds are popular auxiliary scaffolds having vast applications in the fields of biological activities, organic synthesis, sensing, catalysis and agriculture. Here, in this article we have presented the synthesis, structural elucidation and photophysical aspects of 1, 2, 3-triazole allied Schiff base functionalized silanes (5a–5d ) and silatranes (6a–6d ). A two-step approach was followed to synthesize the desired products and the compounds were confirmed by NMR ( 1 H and 13 C) and mass spectrometry. The silane 5a and silatrane 6a were investigated by density functional theory and their photophysical potential via absorption and emission spectroscopy. The probes were found to be specific and selective only for Sn 2+ metal ions. The limit of detection values were found to be 0.86 × 10 −8 M and 0.58 × 10 −8 M for 5a & 6a, respectively, from absorption spectroscopy. The limit of detection values from emission spectroscopy were calculated as 1.3 × 10 −9 M and 0.64 × 10 −9 M for 5a & 6a, respectively. Furthermore, the high binding efficiency of Sn(ii ) with sensors 5a & 6aAbstract : This article represents the synthesis of 1, 2, 3 triazoles allied Schiff base functionalized silanes and silatranes. The silane 5a and silatrane 6a were investigated for their photophysical potential via absorption and emission spectroscopy and found selective for Sn(ii ). Abstract : Organosilicon chemistry is appraised as the trunk of coalescence and structural manoeuvres of moieties. Schiff base compounds are popular auxiliary scaffolds having vast applications in the fields of biological activities, organic synthesis, sensing, catalysis and agriculture. Here, in this article we have presented the synthesis, structural elucidation and photophysical aspects of 1, 2, 3-triazole allied Schiff base functionalized silanes (5a–5d ) and silatranes (6a–6d ). A two-step approach was followed to synthesize the desired products and the compounds were confirmed by NMR ( 1 H and 13 C) and mass spectrometry. The silane 5a and silatrane 6a were investigated by density functional theory and their photophysical potential via absorption and emission spectroscopy. The probes were found to be specific and selective only for Sn 2+ metal ions. The limit of detection values were found to be 0.86 × 10 −8 M and 0.58 × 10 −8 M for 5a & 6a, respectively, from absorption spectroscopy. The limit of detection values from emission spectroscopy were calculated as 1.3 × 10 −9 M and 0.64 × 10 −9 M for 5a & 6a, respectively. Furthermore, the high binding efficiency of Sn(ii ) with sensors 5a & 6a was confirmed by the high association constants ( K a ) from the linear calibration curves as 4.6 × 10 6 M −1 and 0.15 × 10 7 M −1, respectively, for 5a & 6a . The Stern–Volmer plot was explored to calculate the Stern–Volmer constants ( K sv ), which were found to be 21.66 × 10 7 M −1 and 30.39 × 10 7 M −1 . A Job's plot confirmed the 1 : 1 stoichiometric ratio of host:guest in both 5a & 6a . … (more)
- Is Part Of:
- New journal of chemistry. Volume 45:Number 37(2021)
- Journal:
- New journal of chemistry
- Issue:
- Volume 45:Number 37(2021)
- Issue Display:
- Volume 45, Issue 37 (2021)
- Year:
- 2021
- Volume:
- 45
- Issue:
- 37
- Issue Sort Value:
- 2021-0045-0037-0000
- Page Start:
- 17356
- Page End:
- 17365
- Publication Date:
- 2021-09-01
- 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/d1nj03364f ↗
- 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:
- 19630.xml