Rhodamine 6G based efficient chemosensor for the trivalent metal ions (Al3+, Cr3+ and Fe3+) upon single excitation with applications in combinational logic circuits and memory devices

A new rhodamine 6G based chemosensor (L3), has been synthesized and characterized by 1H, 13C, IR and Mass spectroscopy studies. It exhibits an excellent selective and sensitive CHEF based recognition...

Depolarized Mitochondrial Membrane Potential and Protection with Duroquinone in Isolated Perfused Lungs from Rats Exposed to Hyperoxia

Dissipation of mitochondrial membrane potential (Δψm) is a hallmark of mitochondrial dysfunction. our objective was to use a previously developed experimental-computational approach to estimate tissue Δψm in intact lungs of rats exposed to hyperoxia, and to evaluate the ability of duroquinone (DQ) to reverse any hyperoxia-induced depolarization of lung Δψm. Rats were exposed to hyperoxia (>95% O2) or normoxia (room air) for 48 hrs, after which lungs were excised and connected to a ventilation-perfusion system. The experimental protocol consisted of measuring the concentration of the fluorescent dye rhodamine 6G (R6G) during three single-pass phases: loading, washing, and uncoupling, in which the lungs were perfused with and without R6G, and with the mitochondrial uncoupler FCCP, respectively. For normoxic lungs, the protocol was repeated with 1) rotenone (complex I inhibitor), 2) rotenone and either DQ or its vehicle (DMSO), and 3) rotenone, glutathione (GSH), and either DQ or DMSO added to the perfusate. Hyperoxic lungs were studied with and without DQ and GSH added to the perfusate. Computational modeling was used to estimate lung Δψm from R6G data. Rat exposure to hyperoxia resulted in partial depolarization (-33 mV) of lung Δψm, and complex I inhibition depolarized lung Δψm by -83 mV. Results also demonstrate the efficacy of DQ to fully reverse both rotenone-induced and hyperoxia-induced lung Δψm depolarization. This study demonstrates hyperoxia-induced Δψm depolarization in intact lungs, and the utility of this approach for assessing the impact of potential therapies such as exogenous quinones that target mitochondria in intact lungs.

Spectrofluorimetric Determination of Some N. Containing Medicines Using Rhodamine 6G as a Chromogenic Reagent

A sensitive spectrofluorimetric method has been developed for the analysis of some medicines containing primary, secondary, and tertiary amino groups, namely Diclofenac (DIC), Domperidone (DOM), Famotidine (FAM), and Propranolol (PRO), in their pure and medicinal forms. The method is based on the quenching of the fluorescence intensity of rhodamine 6G (R6G) through the formation of ion-pair complexes between the above medicines and the R-6G reagent, which is measured at 552 nm after excitation at 402 nm. The calibration graphs were rectilinear in the concentration ranges of 0.10- 9.00, 0.05-15.00, 0.10-14.0 and 0.05-5.00 µg mL-1 for above medicines respectively. The recovery (%) values were ranged between 99.45%- 100.97%. The detection limits ranged in the concentration of 0.243-0.754 µg/mL, and the limits of quantitation were 0.806- 2.420 µgmL-1 for all drugs. The method was successfully applied for the determination of these drugs in their pharmaceutical preparations.

The Sensitization of Scintillation in Polymeric Composites Based on Fluorescent Nanocomplexes

The sensitization of scintillation was investigated in crosslinked polymeric composite materials loaded with luminescent gold clusters aggregates acting as sensitizers, and with organic dye rhodamine 6G as the emitting species. The evolution in time of the excited states population in the systems is described by a set of coupled rate equations, in which steady state solution allowed obtainment of an expression of the sensitization efficacy as a function of the characteristic parameters of the employed luminescent systems. The results obtained indicate that the realization of sensitizer/emitter scintillating complexes is the strategy that must be pursued to maximize the sensitization effect in composite materials.

A hybrid random laser using dye with self-organised GaN nanorods

Self-organized GaN nanorods with population densities ranging between 0.1 and 0.5 m- 2 and average heights in the range 1.7 to 16.5 µm, prepared by metal-organic chemical vapor deposition, were used as scattering centres for random lasing by incorporating Rhodamine 6G liquid dye solutions as the gain media. A lasing threshold as low as 11.3 J/cm2 was obtained from samples with nanorod density above 0.3 m-2. The threshold depended on the nanorod density and diameter, but not the nanorod height. Lasing emission was observed at multiple angles, a clear indication of random lasing.

Narrow-band random Raman lasing from Rhodamine 6G assisted by cascaded stimulated Raman scattering effect

This study reports the first experimental observation of cascaded stimulated Raman scattering (SRS) generation in a colloidal disordered medium. Generation of the cascaded effect requires both a high Raman gain and pump power in the disordered medium. Here, to extend effective path lengths of photons into the Raman gain medium for producing additional SRS processes, ZnO microspheres with abundant nano-protrusions as suitable scattering centers are proposed. It is explained that nano-protrusions on the surface of the spheres can act as nano reflectors and significantly provide potent feedback in the disordered system. This provided feedback via nano-protrusions boosts cascaded SRS generation to allow the appearance of higher Raman signals of Rhodamine 6G dye solution at a low scatterer concentration of 5 mg/ml. The threshold for the formation of the first Raman signal is measured at about 60 mJ/pulse. Also, the evolution of Raman signals under several fixed pump pulses is examined to investigate the stability from pulse to pulse. Our findings provide promising perspectives for achieving the single-frequency laser sources and generate desirable wavelengths for specific applications.