A Carbazole-based Fluorescent Turn-off Chemosensor for Iron (II/III) Detection in a Dimethyl Sulfoxide.

We designed a novel carbazole-based chemosensor from 2-(N-hexylcarbazol-3'-yl)-pyridine-5-carbaldehyde which was named probe 7b. The main purpose of this study is to investigate whether metal ions in liquid media can be detected with probe 7b. The details were presented in this paper. First, the molecular absorption and fluorescence properties of probe 7b were characterized by spectrophotometers. Then, several methods were applied to check its sensing properties. The results showed that probe 7b has a sense towards Fe3+ ion than other interfering metal ions. The selectivity and sensitivity of probe 7b towards Fe3+ were very satisfactory to use in applications. Also, it was observed that when aqueous Fe3+ ion solutions were added to probe 7b in dimethyl sulfoxide (DMSO), the fluorescence intensity of probe 7b decreased. This situation (turn-off of emission) is due to the paramagnetic effect between probe 7b and Fe3+ ions. The limit of detection (LOD) value was found as 1.38 nM for probe 7b. This value is very small to compete with its counterparts in the literature. A real sample experiment indicated that probe 7b can detect Fe3+ ions more than other ions in real media, too. As a result, it was deduced that probe 7b is a very strong candidate to use in sensor technology.

Safranin T- SDS- GO ternary system: A fluorescent pH sensor.

Graphene oxide (GO), one of the popular materials in recent years, has been synthesized according to the modified Hummers' method. Stable dispersions of different amounts of negatively charged GO were prepared in aqueous media. The GO/dye composites were prepared in deionized water by a simple method with the positively charged Safranin T compound (SfT), which is known to have strong fluorescence properties. By changing the GO/dye ratio, it was obtained stable composites in aqueous media. It was investigated the interaction of SfT with GO in an aqueous solution under the critical micelle concentration (CMC), at the CMC and above the CMC by adding sodium dodecyl sulfate (SDS). It was clarified the formation of GO-SfT composites by using spectroscopic techniques. In these composites, the effect of GO layers on the SfT's photophysical properties was examined by absorption and fluorescence spectroscopy techniques. The change in the quenching effect of GO was monitored both adding a stabilizing electrolyte (NaCl) to the media and changing the pH of the medium. The evaluation was on the probability of the GO-SfT-SDS ternary system being a pH sensing biological sensor material. As a result of this study, it was thought that the GO-SfT-SDS system could be functionalized as a fluorescent pH sensor by taking advantage of GO's sensitivity to pH.

Photophysical and photodynamic properties of Pyronin Y in micellar media at different temperatures.

In this study, photophysics and photodynamical properties of Pyronin Y (PyY) in different liquid media were investigated. Interactions of PyY, which is a positively charged pigment compound pertaining to the xanthene derivatives with surfactants possessing distinct charges, were determined by using the molecular absorption and fluorescence spectroscopy techniques. It was observed that band intensities of absorption and fluorescence spectra belonging to PyY increase in proportion to the water when compared to three micelle systems, cetyltrimethylammonium bromide (CTAB), sodium dodecyl sulfate (SDS) and Triton X-100 (TX-100). This suggests that interactions in micelle systems are different from those in deionized water, and solvation and surface interactions modify. It is determined that the strongest interaction occurs between PyY dye and SDS, anionic surfactant, and this interaction arises from the electrostatic forces. Calculated photophysical parameters indicated that the microenvironment of PyY in SDS micelle is different to that of other systems. In temperature studies, it was reported that increasing the temperature of the samples increased non-radiative transitions. Steady-state fluorescence anisotropy values were calculated by using fluorescence intensities of PyY compound in pre-micellar, micellar and post-micellar systems. Once the PyY fluorescence probe is added to the surfactant containing solutions below the critical micelle concentrations, the measured anisotropy values were found to be low because the probe remains in the deionized water phase. When the surfactant concentration of the medium becomes closer to the critical micelle concentrations, the steady-state anisotropy value prominently increases. This is because of the restrictions on the rotational diffusion of the probe in micellar solution. It is observed that positively charged PyY shows a higher affinity to the negatively charged SDS compared with the positively charged CTAB and neutral TX-100 surfactants. This can be explained by Coulombic interactions.

Photophysics and photodynamics of Pyronin Y in n-alcohols.

The photophysical properties and photodynamics of Pyronin Y (PyY) dye compound in seven polar protic solvents (n-alcohols) were examined as a function of temperature by using UV-visible, steady-state and time-resolved fluorescence spectroscopy techniques. To understand dye-solvent interactions, photophysical parameters including Stokes' shifts, fluorescence quantum yields and fluorescence lifetimes were determined. To examine the effect of solvent polarity, the difference between the ground state dipole moment and the excited state dipole moment was determined. For this purpose, the multiple regression analysis and the Kamlet-Taft technique were used. Moreover, photodynamic parameters, rotational relaxation times and steady-state anisotropy were calculated. The result showed that the specific interactions of PyY with the solvent molecules take place through hydrogen bonding. As the hydrocarbon chain of the alcohols gets longer, photophysical parameters diminish, probably because of weaker hydrogen bonding. Furthermore, it was found out that the dipole moment of excited states (µe ) is higher than that of the ground state (µg ). In addition, Brownian motions increased with the increasing temperature that weakened the fluorescence character of PyY. It was also revealed that the rotation of PyY increased with a prolonged hydrocarbon chain of alcohol series, due to the lesser extent of hydrogen bonding.

Biophysical influence of coumarin 35 on bovine serum albumin: Spectroscopic study.

The binding mechanism and protein-fluorescence probe interactions between bovine serum albumin (BSA) and coumarin 35 (C35) was investigated by using UV-Vis absorption and fluorescence spectroscopies since they remain major research topics in biophysics. The spectroscopic data indicated that a fluorescence quenching process for BSA-C35 system was occurred. The fluorescence quenching processes were analyzed using Stern-Volmer method. In this regard, Stern-Volmer quenching constants (KSV) and binding constants were calculated at different temperatures. The distance r between BSA (donor) and C35 (acceptor) was determined by exploiting fluorescence resonance energy transfer (FRET) method. Synchronous fluorescence spectra were also studied to observe information about conformational changes. Moreover, thermodynamics parameters were calculated for better understanding of interactions and conformational changes of the system.

Rhodamine 101-graphene oxide composites in aqueous solution: the fluorescence quenching process of rhodamine 101.

The interaction of rhodamine 101 (Rh101) with graphene oxide (GO) in aqueous dispersion was examined using advanced spectroscopic techniques. Rh101-GO composites in water were easily prepared by mixing an aqueous solution of both components since GO sheets interacted with the cationic dyes via π-π and electrostatic cooperative interactions. In the composites, the fluorescence of Rh101, which was a well-known laser dye with a high fluorescence quantum yield, could be efficiently quenched by GO. The quenching mechanism of Rh101 by GO sheets was evaluated by the Stern-Volmer (SV) equation and the time-resolved fluorescence studies. The results revealed that the fluorescence quenching of Rh101 by GO in the aqueous dispersion is due to the static quenching mechanism. The formation of the Rh101-GO composites at various pH values was spectroscopically monitored, and the spectroscopic results revealed that the composites were formed at the pH values studied except in the strong acidic media (pH ≈ 2). The interaction of Rh101 with GO in aqueous solution was spectroscopically followed in the presence of SDS (sodium dodecyl sulphate) at the surfactant concentrations above and below the CMC (critical micelle concentration). The fluorescence studies revealed that the fluorescence of Rh101 in the aqueous solution remarkably increased at the surfactant concentration forming the micelle of SDS.