Water dispersed fluorescent organic aggregates for the picomolar detection of ClO4− in water, soil and blood serum and the attogram detection of ClO4− in the solid state by a contact mode method. Issue 31 (19th July 2016)
- Record Type:
- Journal Article
- Title:
- Water dispersed fluorescent organic aggregates for the picomolar detection of ClO4− in water, soil and blood serum and the attogram detection of ClO4− in the solid state by a contact mode method. Issue 31 (19th July 2016)
- Main Title:
- Water dispersed fluorescent organic aggregates for the picomolar detection of ClO4− in water, soil and blood serum and the attogram detection of ClO4− in the solid state by a contact mode method
- Authors:
- Kumar, Rahul
Sandhu, Sana
Singh, Prabhpreet
Kumar, Subodh - Abstract:
- Abstract : An aggregation–disaggregation based molecular probe allows the detection of 10 pM ClO4 − in solution and 6 × 10 −18 g cm −2 ClO4 − in the solid state by a contact mode method with a selectivity of ∼10 000 over other inorganic anions. Abstract : Fluorescent organic aggregates (FOAs) ofCS-1 have been used for the fluorescence based selective estimation of ClO4 − ions.CS-1 undergoes self-aggregation to form FOAs ( ϕ = 0.35) with a diameter of 140 ± 50 nm in aqueous medium. Dynamic light scattering and field emission scanning electron microscopy studies reveal that FOAs ofCS-1 undergo further aggregation to form larger particles upon addition of ClO4 − (10 pM–1 nM concentration) but at higher concentrations of ClO4 − ions, these FOAs undergo dis-aggregation to give finally a molecularly dissolved complex ofCS-1 and ClO4 − . This ClO4 − induced aggregation–dis-aggregation process of FOAs ofCS-1 is associated with super-amplified fluorescence quenching following two domains of non-linear complexation with K sv values of 2.42 × 10 8 M −1 and 3.59 × 10 5 M −1 and variation in the lifetime measurements of FOAs ofCS-1 at different concentrations of ClO4 − . The lowest limit of detection is 10 pM in solution and 6 × 10 −18 g cm −2 in the solid state by a contact mode method with a selectivity of ∼10 000 over other inorganic anions and allows the quantitative measurement of ClO4 − ions using front surface steady state fluorescence of paper strips coated withCS-1 . FOAs ofCS-1Abstract : An aggregation–disaggregation based molecular probe allows the detection of 10 pM ClO4 − in solution and 6 × 10 −18 g cm −2 ClO4 − in the solid state by a contact mode method with a selectivity of ∼10 000 over other inorganic anions. Abstract : Fluorescent organic aggregates (FOAs) ofCS-1 have been used for the fluorescence based selective estimation of ClO4 − ions.CS-1 undergoes self-aggregation to form FOAs ( ϕ = 0.35) with a diameter of 140 ± 50 nm in aqueous medium. Dynamic light scattering and field emission scanning electron microscopy studies reveal that FOAs ofCS-1 undergo further aggregation to form larger particles upon addition of ClO4 − (10 pM–1 nM concentration) but at higher concentrations of ClO4 − ions, these FOAs undergo dis-aggregation to give finally a molecularly dissolved complex ofCS-1 and ClO4 − . This ClO4 − induced aggregation–dis-aggregation process of FOAs ofCS-1 is associated with super-amplified fluorescence quenching following two domains of non-linear complexation with K sv values of 2.42 × 10 8 M −1 and 3.59 × 10 5 M −1 and variation in the lifetime measurements of FOAs ofCS-1 at different concentrations of ClO4 − . The lowest limit of detection is 10 pM in solution and 6 × 10 −18 g cm −2 in the solid state by a contact mode method with a selectivity of ∼10 000 over other inorganic anions and allows the quantitative measurement of ClO4 − ions using front surface steady state fluorescence of paper strips coated withCS-1 . FOAs ofCS-1 find applications in the determination of ClO4 − in tap water, soil and also blood serum. ProbeCS-2, which differs fromCS-1 in lacking three methyl groups on the m -phenylene spacer, shows poor sensitivity (LOD 1.6 μM) towards ClO4 − . DFT studies ofCS-1 andCS-2 and their complexes with ClO4 − reveal the effect of methyl substituents on their geometries. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 4:Issue 31(2016)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 4:Issue 31(2016)
- Issue Display:
- Volume 4, Issue 31 (2016)
- Year:
- 2016
- Volume:
- 4
- Issue:
- 31
- Issue Sort Value:
- 2016-0004-0031-0000
- Page Start:
- 7420
- Page End:
- 7429
- Publication Date:
- 2016-07-19
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Optical materials -- Research -- Periodicals
Electronics -- Materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tc# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6tc01891b ↗
- Languages:
- English
- ISSNs:
- 2050-7526
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 418.xml