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Inhomogeneity in single molecule electron transfer at the surface of lipid in a single vesicle has been explored by single molecule spectroscopic technique. In our study we took Di-methyl aniline (DMA), as the electron donor (D) and three different organic dyes as acceptor. These dyes are C153, C480 and C152 and they reside in different regions in the vesicle depending upon their preference of residence. For each probe, we found fluctuations in the single-molecule fluorescence decay, which are attributed to the variation in the reactivity of interfacial electron transfer. We found a non-exponential auto-correlation fluctuation of the intensity of the probe, which is ascribed to the kinetic disorder in the rate of electron transfer. We have also shown the power law distribution of the dark state (off time), which obeys the levy's statistics. We found a shift in lifetime distribution for the probe (C153) from 3.9 ns to 3.5 ns. This observed quenching is due to the dynamic electron transfer. We observed the kinetic disorderness in the electron transfer reaction for each dye. This source of fluctuation in electron transfer rate may be ascribed to the inherent fluctuation, occurring on the time scale of ~ 1.1 ms (for C153) of the vesicle, containing lipids. [ABSTRACT FROM AUTHOR]

Fluorescent organic dyes play an essential role in the creation of new "smart" materials. Fragments and functional groups capable of free rotation around single bonds can significantly change the fluorescent organic dye's electronic structure under analyte effects, phase state transitions, or changes in temperature, pressure, and media polarity. Dependencies between steric and electronic structures become highly important in transition from a solution to a solid-state. Such transitions are accompanied by a significant increase in the dye molecular structure's rigidity due to supramolecular associates' formation such as H-bonding, π···π and dipole–dipole interactions. Among those supramolecular effects, H-bonding interactions, first of all, lead to significant molecular packing changes between loose or rigid structures, thus affecting the fluorescent dye's electronic states' energy and configuration, its fluorescent signal's position and intensity. All the functional groups and heteroatoms that are met in the organic dyes seem to be involved in the control of fluorescence via H-bonding: C-H···N, C-H···π, S = O···H-C, P = O···H, C-H···O, NH···N, C − H···C, C − H···Se, N–H···O, C − H···F, C-F···H. Effects of molecular packing of fluorescent organic dyes are successfully used in developing mechano-, piezo-, thermo- fluorochromes materials for their applications in the optical recording of information, sensors, security items, memory elements, organic light-emitting diodes (OLEDs) technologies. [ABSTRACT FROM AUTHOR]

In the present work, CdTe/ZnS high luminescence quantum dots (QDs) were synthesized by a facile, fast, one-pot, and room temperature photochemical method. Synthesized QDs were characterized by different structural and optical analyses such as X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), Fourier transform-infrared spectroscopy (FT-IR), Raman, photoluminescence (PL) and UV–visible (UV–vis) spectroscopies. The results confirmed the successful growth of the ZnS shell and formation of CdTe/ZnS core/shell structure. CdTe/ZnS prepared QDs indicated a PL quantum yield of about 51%. These high luminescence QDs were used for detection of Hg2+ ions in aqueous media, as catalyst for photodegradation of different organic dyes, and as antibacterial material for the inhibition of bacterial growth. PL intensity of the CdTe/ZnS QDs was completely quenched after addition of 1 m molar Hg2+in to the media. Photocatalyst activity of CdTe/ZnS QDs was studied by rhodamine b, methylene blue, and methylene orange as organic dyes under both the sun and UV illuminations, and results showed that CdTe/ZnS QDs had the best photocatalyst activity for methylene blue degradation under UV irradiation and radical scavenger results indicated that electrons have a main role in photodegradation of methylene blue dye by CdTe/ZnS QDs under UV illumination. Antibacterial effects of CdTe/ZnS QDs evaluated by Minimum Inhibitory Concentration (MIC), and Minimum Bactericidal Concentration (MBC) methods against two strains of bacteria. The results of the antibacterial test showed that CdTe/ZnS could inhibit bacterial growth in Bacillus cereus (Gram-positive) and Escherichia coli (Gram-negative G) bacteria. [ABSTRACT FROM AUTHOR]

This research explores the synthesis, characterization, and application of Vanadium Pentoxide nanoparticles (V2O5 NPs), focusing on their efficacy in the photocatalytic degradation of organic dyes under visible light. Utilizing a co-precipitation method, we synthesized V2O5 NPs characterized by an orthorhombic crystal structure with a consistent average particle size of 28 nm. The optical properties of V2O5 NPs, including their band gap, were thoroughly investigated to understand their light absorption capabilities, which are crucial for photocatalytic activity. In our study, Methyl Violet (MV) dye was employed as a model organic pollutant to assess the photocatalytic performance of the nanoparticles. Under visible light irradiation, the V2O5 nanoparticles demonstrated an exceptional photocatalytic degradation efficiency, achieving up to 85% degradation of the MV dye within 100 min. This high level of efficiency is attributed to the nanoparticles’ ability to effectively absorb visible light and generate electron-hole pairs, thereby facilitating a robust degradation process. Further analysis revealed that the photocatalytic activity led to the generation of reactive oxygen species (ROS) such as superoxide and hydroxyl radicals, which are integral to the dye degradation mechanism. These ROS play a critical role in breaking down the dye molecules, significantly contributing to the overall effectiveness of the photocatalytic process. The results of this study highlight the potential of V2O5 nanoparticles as a sustainable and effective photocatalytic material for environmental remediation applications, particularly in the treatment of wastewater containing organic dyes. This research not only advances our understanding of the photocatalytic properties of V2O5 nanoparticles but also demonstrates their practical application in addressing environmental pollution through innovative and efficient degradation of hazardous substances. [ABSTRACT FROM AUTHOR]

A novel cyanine 3 (Cy3)-based bio-conjugated sensor has been developed to detect target DNA or extracted RNA from COVID -19 samples using the fluorescence resonance energy transfer (FRET) experiment. A special sequence of the COVID -19 genome was selected as a complementary DNA (target DNA) part. The opposite chain of this target sequence was designed in 2 parts; one part was attached to the Cy3 organic dye (capture DNA or Cy3- DNA), and the other part was attached to the BHQ2 molecule (quencher DNA or BHQ2- DNA). The Cy3 molecule acts as a donor pair, and BHQ2 acts as an acceptor pair in the FRET experiment. The capture DNA and quencher DNA can form a sandwiched complex in the presence of target DNA. The formation of the entitled sandwiched hybrid causes the decrement of emission intensity of the Cy3 donor in bio-conjugated Cy3-DNA via energy transfer from Cy3 (as a donor) to BHQ2 (as an acceptor). Indeed, in the presence of non-complementary DNA, the pairing of DNA strands does not occur, the FRET phenomenon does not exist, and therefore fluorescence intensity of Cy3 does not decrease. Moreover, this biosensor was successfully applied to analyze real samples containing extracted RNA of COVID -19 prepared for the reverse transcriptase-polymerase chain reaction (RT-PCR) test, and the results were promising. [ABSTRACT FROM AUTHOR]

Ruthenium-based metal complex dyes have been employed extensively in dye-sensitized solar cells (DSSCs) as photosensitizers, but the cost and toxicity of metal complexes have promoted the development of metal-free organic dyes. The present investigation deals with the synthesis of hemicyanine and Dicyanoisophorone (DCI) based dyes adopting the D-π-A strategy, and their application on sensitization of nano-crystalline ZnO electrodes by appending the carboxyl (COOH) anchoring group as a pendant on the primary skeleton of dyes. Dyes have been characterized by UV, FTIR, and NMR spectroscopic studies. Absorption maxima (λmax) were found in the region 416-551 nm while emission wavelength (λem) was observed in the range 575-685 nm. Cyclic voltammetry and DFT calculations were used to estimate redox potential and band gap energies of dyes. [ABSTRACT FROM AUTHOR]

Hot-band absorption and anti-Stokes emission properties of an organic fluorescent dye, Alexa Fluor 568, were characterized and compared with those of Rhodamine 101. The comparison of the properties (e.g., quantum efficiency, spectral distribution, thermal properties, and fluorescence lifetime) between the two dyes confirms that both dyes undergo the same process when excited in the red spectral region. Possible undesirable crosstalk effects and applications in dSTORM microscopy were demonstrated and discussed. [ABSTRACT FROM AUTHOR]

We have developed a colorimetric chemosensor based on an anionic organic dye, commercially available nuclear fast red (NFR) and a cationic polyelectrolyte, poly(diallyldimethylammonium chloride) (PDADMAC) for detection of Hg2+ in aqueous solution at physiological conditions. Upon addition of Hg2+, a bathchromic shift in the absorption was observed concomitantly with color change from pink to reddish violet which was easily detectable by the naked eye, while such a change was not observed for NFR alone, indicating that PDADMAC played an important role in detecting Hg2+. This investigation can propose the simple and valuable construction method for a novel chemosensor by mixture of a water-soluble organic dye and an oppositely charged polyelectrolyte. [ABSTRACT FROM AUTHOR]

The design and development of the fluorescence reporting molecules for the trace recognition of the metallic ions in the aqueous, mixed organic aqueous media, environmental specimen, living things e.g., body fluids, serum, urine etc is the evergreen research area. Among several methodologies utilized for these purposes, the fluorescent techniques have wonderful impact in the era of metal sensor development due to their acclamatory features of non-invasive detection process and appreciable sensitivity. The utilization of small organic molecules for the sensation of metallic ions through the fluorescent techniques harvested the wonderful results having some interesting features of chromogenic response on metal binding, robustness in the preparation and applicability to establish the metallic accumulation level inside the live cells via bioimaging studies. The detailed knowledge and background about the several reported chemosening strategies have the utmost importance in order to understand or to design the novel molecules for metal sensing purposes. The objective of the presents review was to compile the best ever used copper sensing strategies via fluorescent means in the running decade. We have summarized the values of optical positions of the spectral lines, spectral shifting upon metal binding, binding/association/dissociation constants, chromogenic changes in the reaction mixture, proposed complexation mechanism of the ligand with the copper, ligand sensitivities toward the copper recognition, binding stoichiometries and the detailed bioimaging results where applicable. [ABSTRACT FROM AUTHOR]

The commercially available natural organic dye, carminic acid (CA), an anthraquinone derivative bearing hydroxyl and carboxyl groups as recognition sites was found to be a colorimetric probe for Pb in perfect aqueous solution under neutral conditions with specific selectivity and high sensitivity. Upon addition of Pb, the absorption maximum of CA showed a large red shift, and the resulted color change from red to purple could be easily identified even by the naked eye. The chemical stoichiometric ratio between CA and Pb was determined to be 1:2 through Job plot, Pb titration, and kinetic experiments. Moreover, other environmental relevant metal ions induced no or minimal spectral and color changes. The reversibility of Pb to CA with EDTA even through several cycles was established for practical applications. The results indicated that CA can be a good candidate for simple, convenient and reversible colorimetric detection of Pb in aqueous solution even though it was hard to be applied to determine Pb on the water testing by US EPA. [ABSTRACT FROM AUTHOR]

Aqueous solutions with Rhodamine dye, and fluorescently labeled polymer samples of fibrin and collagen were mixed with aqueous dispersions of cerium oxide, lanthanum oxide, iron (II) oxide nanoparticles, and OxyFluor, a commonly used reagent for suppressing photobleaching. From time dependent studies of the fluorescence from these samples, we observed that the dyes in samples containing rare earth oxide nanoparticles exhibited significantly slower rates of fluorescence decay compared to control samples without additives, or containing OxyFluor or iron oxide nanoparticles. We posit that this may be related to the oxygen free radical scavenging properties of rare earth oxides. [ABSTRACT FROM AUTHOR]

Microwave-assisted synthesis, photophysical and electrochemical properties of thermal-stable naphthalene benzimidazoles and naphthalimides are studied in this paper. Microwave-assisted synthesis of naphthalene benzimidazoles provide higher yields than the conventional thermal synthesis. Comparative photophysical properties of naphthalene benzimidazoles and naphthalimides are revealed that conjugation of electron-donating group onto naphthalimide moiety increases fluorescence quantum yields. Fluorophore-solvent interactions are also investigated using Lippert-Mataga equation for naphthalimides and naphthalene benzimidazoles. Thermal stabilities of naphthalene benzimidazoles are better than naphthalimides due to increased aromaticity. The experimental E levels of naphthalene benzimidazoles are found to be between 3.15 and 3.28 eV. Therefore, naphthalene benzimidazole derivatives consisting of anchoring groups are promising materials in organic dye sensitized solar cells. [ABSTRACT FROM AUTHOR]

This paper presents the synthesis of organic dye molecules embedded silica nanoparticles by Stöber method and their applications as fluorescence probes in cell imaging. By modifying the surface of fluorescent silica nanoparticles (FSNs) with amino, biologically functionalized and monodisperse FSNs can be obtained. In this work, FSNs were conjugated with monoclonal anti-Carcinoembryonic Antigen (anti-CEA) antibody via covalent binding. The antibody-conjugated FSNs can be used to label the SPCA-1 cells successfully, demonstrating that the application of FSNs as fluorescence probes in fluorescence imaging and bioassay would be feasible. [ABSTRACT FROM AUTHOR]

Very limited number of parameters is available for fluorescence sensing and imaging. The changes of intensity are of low analytical value due to the absence of internal reference. Anisotropy and lifetime sensing have their own limitations. In this respect the λ-ratiometric (based on intensity ratios at two or more wavelengths) recording of spectral changes becomes more popular. Because the spectral changes are connected directly with the variations of interaction energies this approach is seen as the most universal method to study intermolecular interactions. It is applicable for different sensor formats and for obtaining analytical information from cell images. Here we critically analyze different approaches in λ-ratiometric sensing that use single and double fluorescence emitters and are based on different mechanisms producing spectroscopic change. Very promising is the exploration of mechanisms that allow obtaining ratiometric response from a single dye. [ABSTRACT FROM AUTHOR]

Suitable chemical strategy is a useful approach on the tuning color and photoluminescence of organic dyes. This paper presented tuning novel branched p-nitro-stilbene derivatives efficiently with a new chemical strategy through variation of chemical bridged bond. Linking bonds played significant effects on the absorption and fluorescence spectroscopy of the branched p-nitro-stilbene derivatives. A change from "D-π-A" to "A-π-A" chemical structural characteristics occurred for the branched p-nitro-stilbene derivatives as ester bond was attached. This led to not only large hypsochromic shift of the maximal absorption wavelength of the branched p-nitro-stilbene derivatives, but considerable reduction of the fluorescence intensity. While in contrast, the branched p-nitro-stilbene derivatives with ether bond exhibited longer wavelength absorption and much stronger fluorescence emission in modest polar solvent. The cyclic voltammograms of these branched p-nitro-stilbene derivatives were determined. Different electrochemistry processes were observed for the branched p-nitro-stilbene derivatives with various linking bonds. The energies of frontier orbital of the branched p-nitro-stilbene derivatives were estimated from their corresponding redox potentials. Molecular geometry optimization of the branched p-nitro-stilbene derivatives was performed, and the electron density distribution of frontier orbital was analyzed. Thermal stabilities of these branched nitrostilbene derivatives were investigated via the analysis of the differential scanning calorimetry (DSC) and thermograving (TGA) curves. This paper presented strong evidences that the absorption and fluorescence spectroscopy of the branched stilbene derivatives could be mediated efficiently by chemical strategy. [ABSTRACT FROM AUTHOR]

The control of the spontaneous emission (SE) rate of dye molecules (4-dicyanomethylene-2-methyl-6-p-dimethylaminostyryl-4H-pyran (DCM) and Coumarin 523 (C523)) embedded in the Porous Silicon (PS) matrix has been studied using picosecond resolved fluorescence decay and polarization studies. We have shown that the SE rates of the two organic dyes embedded in the PS matrix depend on the relative positions of the emission maxima of the dyes with respect to electronic band gap energy of the PS matrix. We have also explored that the electronic band gap of the host PS matrix can easily be tuned by partial oxidation of the PS and the nature of SE of the embedded dyes can be tuned accordingly. The demonstrated retardation or enhancement of the spontaneous photon emission may enable the application of fluorescent organic molecules in PS matrix in several quantum optical devices including the realization of single photon sources. [ABSTRACT FROM AUTHOR]

Abstract  A CdSe–ZnS quantum dot (QD) has been surface functionalised with 1-(2-mercapto-ethyl)-3-phenyl-thiourea in the fluorophore–spacer–receptor format typical of Photoinduced Electron Transfer (PET) based organic dye sensors. The resulting QD conjugate was tested for selectivity toward the tetrabutylammonium salts of fluoride, chloride, bromide, hydrogen sulfate and acetate. Addition of fluoride, chloride and acetate ions resulted in an approximate 90% quenching of the original fluorescence intensity, while bromide and hydrogen sulfate had almost no effect. The observed quench was attributed to an increase in the reduction potential of the receptor upon anion binding resulting in an increase in PET from the excited QD to the receptor and a concomitant reduction in fluorescence intensity. The selectivity and sensitivity were comparable to an analagous organic dye based sensor where a similar receptor was bound to an anthracene fluorophore. Thus a modular approach is evident where a receptor used in an organic dye based sensor can be adapted and successfully used with QD’s. [ABSTRACT FROM AUTHOR]

Spectral-luminescence characteristics of Yb3+ and Nd3+ ions in water solutions of their complexes with some organic dyes of sulfophenylphthalexones group have been considered. Complexes can be efficiently excited with visible light (λexc = 532 nm). 4f-Luminescence as a result of energy transfer from the dye moiety to the lanthanide ion was shown. Complexation of new polydentate ligand L of sulfophenylphthalexones type increases the luminescence lifetimes because of the reduced solvation of the ion by water. They were determined as 12.60 μs for complex Yb-L and 1.45 μs for Nd-L. [ABSTRACT FROM AUTHOR]