Ipsit Hauli

Thiophene anchored coumarin derivative as a turn-on fluorescent probe for Cr3+: cell imaging and speciation studies.

A thiophene-coumarin hybrid molecule, (6E)-6-((thiophen-2-yl)methyleneamino)-2H-chromen-2-one (TMC) has been prepared and its single crystal X-ray structure is reported. TMC can selectively detect Cr(3+) in presence of other common cations. Both TMC and its Cr(3+) complex are well characterized by different spectroscopic techniques like (1)H NMR, QTOF-MS ES(+), FTIR and elemental analysis as well. TMC exhibits fluorescence enhancement upon binding Cr(3+) in CH(3)CN-HEPES buffer (0.02 M, pH 7.4) (4:6, v/v) medium. Detection limit of the method is 1 × 10(-6)M. Binding constant is estimated with the Benesi-Hildebrand method and the value 8 × 10(4) indicates a fairly strong interaction between TMC and Cr(3+). Speciation studies have been performed in a fast and environment friendly way using least sample volume, less hazardous chemicals and solvents. Cr(3+) assisted restricted rotation around the imine bond and inhibited photo-induced electron transfer from the N,S-donor sites to the coumarin unit are responsible for fluorescence enhancement. TMC is capable to detect intracellular Cr(3+) in living cells.

Nickel(II)-induced excimer formation of a naphthalene-based fluorescent probe for living cell imaging.

Ni(2+)-induced intramolecular excimer formation of a naphthalene-based novel fluorescent probe, 1-[(naphthalen-3-yl)methylthio]-2-[(naphthalen-6-yl)methylthio]ethane (L), has been investigated for the first time and nicely demonstrated by excitation spectra, a fluorescence lifetime experiment, and (1)H NMR titration. The addition of Ni(2+) to a solution of L (DMSO:water = 1:1, v/v; λ(em) = 345 nm, λ(ex) = 280 nm) quenched its monomer emission, with subsequent enhancement of the excimer intensity (at 430 nm) with an isoemissive point at 381 nm. The fluorescence lifetime of free L (0.3912 ns) is much lower than that of the nickel(2+) complex (1.1329 ns). L could detect Ni(2+) as low as 1 × 10(-6) M with a fairly strong binding constant, 2.0 × 10(4) M(-1). Ni(2+)-contaminated living cells of plant origin could be imaged using a fluorescence microscope.

Interaction of soft donor sites with a hard metal ion: crystallographically characterized blue emitting fluorescent probe for Al(III) with cell staining studies

A naphthalene based compound, 1-((E)-(2-(2-(phenylthio)ethylthio)phenylimino)methyl)naphthalen-2-ol (L2) has been synthesized and characterized by FTIR, 1H NMR, mass spectra and single crystal X-ray structure analysis. L2 shows a blue shift with a large fluorescence enhancement in the presence of Al3+ which is attributed to a chelation-enhanced fluorescence (CHEF) effect with inhibition of an intramolecular charge transfer (ICT) process and cis/trans isomerization. L2 binds to Al3+ with 2 : 1 stoichiometry (mole ratio) with an association constant (Ka) of 0.15 × 104 M−1/2. The detection limit for Al3+ is 5 × 10−8 M in DMSO/H2O (1 : 2, v/v). L2 can efficiently detect intracellular Al3+ under fluorescence microscope

Vanillin-coumarin hybrid molecule as an efficient fluorescent probe for trace level determination of Hg(II) and its application in cell imaging

An efficient Hg(2+) selective fluorescent probe (vanillin azo coumarin, VAC) was synthesized by blending vanillin with coumarin. VAC and its Hg(2+) complex were well characterized by different spectroscopic techniques like (1)H NMR, QTOF-MS ES(+), FTIR and elemental analysis as well. VAC could detect up to 1.25 μM Hg(2+) in aqueous methanol solution through fluorescence enhancement. The method was linear up to 16 μM of Hg(2+). Negative interferences from Cu(2+), Ni(2+), Fe(3+), and Zn(2+) were eliminated using EDTA as a masking agent. VAC showed a strong binding to Hg(2+) ion as evident from its binding constant value (2.2×10(5)), estimated using Benesi-Hildebrand equation. Mercuration assisted restricted rotation of the vanillin moiety and inhibited photoinduced electron transfer from the O, N-donor sites to the coumarin unit are responsible for the enhancement of fluorescence upon mercuration of VAC. VAC was used for imaging the accumulation of Hg(2+) ions in Candida albicans cells.