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This study investigates the solvatochromic behavior of a new D1 disperse dye, focusing on the 4-nitro-2-cyano-azo-Benzene-metaToluidine type. Using UV-visible spectroscopy, we analyze the dye's performance in single solvents and binary mixtures. Our analysis includes the evaluation of solvent polarity parameters and dye structure parameters, with emphasis on the longest wavelength intramolecular charge transfer absorption band. We identify nonlinear and linear patterns in the electronic transition energies plots with respect to solvent composition. Statistical analysis considers correlation coefficients, root mean squared error, mean absolute percentage error, and other parameters, providing insights into data accuracy and precision. This experimental and statistical study explores the absorption spectrum, wavelength characteristics, absorption energy, and polarity of a novel azo dye across various solvent and solute environments. These findings contribute to a comprehensive understanding of the dye's photophysical and photochemical properties, potentially enabling applications in optical sensors and advanced materials.

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Herein, a highly efficient colorimetric chemosensor incorporating ion-imprinted electrospun nanofiber was developed for the removal and detection of Cu2+ ions. In this regard, PVA/chitosan composites were used as the polymeric matrix, and 1-(2-pyridylazo)-2-naphthol was employed for complex formation. The prepared naked-eye sensor was characterized using Fourier transform infrared spectroscopy, energy-dispersive X-ray spectroscopy, scanning electron microscopy, atomic force microscopy, differential scanning calorimetry, thermogravimetric analysis, and X-ray diffraction analysis, revealing the morphological, structural, and molecular properties of the sensor. The results showed that the colorimetric chemosensor based on copper-imprinted nanofiber (Cu-INF) possesses higher selectivity for Cu2+ compared to interference ions. The selectivity coefficient (k) and relative selectivity coefficient (K') indicated the selective behavior of Cu-INF in the adsorption of Cu2+ in binary systems including Cu2+/Co2+, Cu2+/Ni2+, and Cu2+/Zn2+. Furthermore, the ion-imprinted nanofiber was used for the preconcentration of copper ions, demonstrating a high adsorption capacity of 128.205 mg g-1 for Cu2+. The equilibrium adsorption isotherm and adsorption kinetics of Cu2+ on Cu-INF followed the Freundlich adsorption isotherm and a pseudo-second-order model, respectively. The developed sensor exhibited a linear detection range of 5 × 10-8 - 2 × 10-7 M with a limit of detection (LOD) of 1.07 × 10-8 M for copper ions. The results indicated satisfactory adsorption and successful detection of Cu2+ at trace concentrations.

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A naphthalene diimide dye with two side amine arm was prepared. Uv-Vis and fluorescence spectroscopic techniques are used for their photophysical and solvatochromic characteristics in different solvents. The Lippert-Mataga plot for naphthalene diimide demonstrated a negative linear dependence by increasing polarity. Results showed naphthalene diimide is more polar in the ground than in the excited state. A quenching study was conducted for interacting the naphthalene diimide as a fluorophore and graphene oxide as a quencher. Fluorescence quenching-based platforms in nanoscale have been used in sensing systems. Raman, FTIR, Uv-Vis and fluorescence spectroscopic techniques were used to study the quenching mechanism. The results indicated that graphene plays an effective quencher against the naphthalene diimide, with a quenching efficiency 91%. The Stern-Volmer analysis results show a mix of static and dynamic quenching mechanisms. The binding constant of the quencher-fluorophore and the number of binding sites have been reported. Thermodynamic parameters of their interaction were evaluated. The negative values of the Gibbs free energy confirm that the complexation process is spontaneous. Meanwhile, the positive entropy value confirms that the favorable pathway process.

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During the past decades, carbon dots (CDs) as a kind of nanoparticles with interesting fluorescence properties have retained their place as one of the best bioimaging agents, although their effects on plants have been rarely studied. In this study, we synthesized two kinds of concentration-dependent multicolour CDs using two solvent approaches, phosphate-buffered saline (PBS) and ethanol 20%. We confirmed the nature of the CDs through Fourier transform infrared spectroscopy, atomic force microscopy, dynamic light scattering, zeta potential, X-ray powder diffraction, and high-resolution transmission electron microscopy. Afterwards, the cytotoxicity, phytotoxicity, and bioimaging of animal cells and plants using both synthesized CDs were examined. Eventually, PBS-based CDs were recommended during this study as an efficient bioimaging agent for animal cells and plants because of the appealing features of this CD, such as a small size range of less than 10 nm, surface charge with an average of -24 mV, a high quantum yield of 35.82%, the higher fluorescence intensity of ~400 a.u. for blue fluorescence light and 250 a.u. for green fluorescence light. Other features showing the superiority of PBS-based CDs include high photostability, low phytotoxicity (p ≤ 0.05 and p ≤ 0.01) and above all, there was no significant cytotoxicity at the concentration range of 500-7.81 µg/ml.

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It proved that the most destructive effects of the toxic Al3+ ion on the human nervous system and disease that are involved with this system, such as Alzheimer's. The development of solid-state electrodes is still in its infancy during the sensor-based detection methods for Al3+. Hence, in this study, a novel flexible ITO/PET-based electrochemical solid-state sensor was designed and constructed. Modification of the surface of electrode bedding was done by layer-by-layer (LbL) assembly of Mg-Al LDH. nanoplatelets along with alizarin red S (ARS) in an interconnected matrix film. In the molecular design of sensing base of the electrode, the electroactive organic units (ARS molecules) present in the ITO/PET-layered (ARS/LDHs)n matrix are involved in electrochemical reactions when exposed to the target molecule (Al3+ ion), so the electrochemical changes of the new formed Al-chelated system are detectable. This type of sensor is used for sensitive and selective detection of Al3+. The minimum sheet resistance, morphology and high electrocatalytic activity of the modified matrix film are obtained in the fifth cycle of LbL assembly technique. In this electrochemical sensor, both electrochemical and optical methods were detected with high sensitivity and selectivity of Al3+, so that in a cyclic voltammetry electrochemical method, the lower detection limit of 10.1 nM with a linear range of [0.2-120 µM] was obtained compared to the fluorescence-based optical method.

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Fluorescent molecularly imprinted polymer (FMIP) optosensor was utilized for the selective identification of 2,4-dichlorophenoxacetic acid (2,4-D) due to worldwide pollution caused by using herbicides in agricultural industry. In this regards, two derivatives of polymerizable 1,8-naphthalimide namely, 1,8-naphthalimide containing thiourea (NI) and diethyl amine tagged 1,8-naphthalimide (NII) were used as the receptors and 2,4-D was applied as a template. Also, precipitation polymerization was applied to prepare the fluorescent molecularly imprinted polymer (FMIP). The morphological, structural and thermal analysis was carried out using SEM, TEM, EDS, BET, FTIR, DSC and TGA for characterizing the fluorescent optosensor. The adsorption efficiency of FMIP and FNIP was studied using Langmuir, Freundlich, BET and Redlich Peterson isotherms. The results represented that the adsorption of 2,4-D on FMIP and FNIP agreed the Freundlich adsorption isotherm with correlation coefficient of 0.9935 and 0.9801, respectively. The prepared sensor was able for the selective determination of 2,4-D salt in the linear range of 5 × 10-7-1 × 10-3 M with a limit of detection of 16.8 nM. The present study revealed that the FMIP prepared by 1,8-naphthalimide derivative (NI) could potentially recognize the trace concentration of 2,4-D. Graphical Abstract Graphical abstract of flourescene switching mechanism in a fluorescent molecularly imprinted polymer sensor.

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A highly selective and sensitive fluorescent sensor for the determination of fructose is developed. The fluorescent sensor was prepared by incorporating a new naphthalimide dye with a planar structure as a selectophore and graphene oxide (GO) nanoplatelets as a quencher for rapid optical detection of fructose. The designed probe, made with the high fusion loop-containing dye, along with the GO nanoplatelets, detected fructose over the other monosaccharides very well. The proposed sensor displays a linear response range of 7 × 10-5 to 3 × 10-2 M with a low limit of detection of 23 × 10-6 M in solution at pH 7.4. This sensor shows a good selectivity towards fructose with respect to other saccharides. The proposed sensor was then applied to the determination of fructose in human plasma with satisfactory results.

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In this study, polydiacetylene (PDA) is embedded in electrospun polyvinylidene fluoride (PVDF) nanofibers for the preparation of mats with dual colorimetric and piezoelectric responses. The diacetylene monomers are self-assembled during the electrospinning process. The PDA-embedded PVDF nanofibers in the blue phase are obtained via photo-polymerization upon UV-light irradiation. The colorimetric transition of the nanofibers is studied as a function of temperature using a spectrophotometer. The morphology and crystal polymorphism of the nanofibers are investigated. The results show that the addition of PDA increases the diameter of the nanofibers due to the increase in the electrospinning solution viscosity. The results of Fourier transform infrared and wide angle X-ray diffraction demonstrate that PDA has the effect of inhibiting the growth of non-polar α-phase crystals, while promoting the growth of the polar ß-phase. However, the red phase of PDA-embedded PVDF exhibits a lower intensity of the ß-phase in comparison to that of the blue phase. In fact, the blue-to-red color transition of the PDA-embedded electrospun PVDF nanofibers is accompanied by the variation of piezoelectric signaling caused by variations in the ß-phase. This phenomenon creates great potential in commercial detection sensors in addition to their colorimetric detection properties.

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Graphene oxide is an efficient fluorescence quencher for various organic dyes. Herein the fluorescence quenching of graphene oxide has been carried out on a naphthalimide dye as a fluorescent probe model. The interaction between naphthalimide dye and graphene oxide was studied by UV-Vis and fluorescence spectroscopic techniques. The results indicated that graphene is a very efficient quencher for naphthalimide molecule. The Stern-Volmer analysis revealed that the remarkable quenching of graphene was based on a combined static and dynamic quenching mechanism and went through an energy transfer process. Graphical Abstract ᅟ.

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Nanocomposites with thermo and photo-switchable fluorescent properties were synthesized via mini-emulsion polymerization based on spiropyran and methyl methacrylate monomer. The photophysical behavior of fluorescence nanocomposites was investigated by fluorescence spectrophotometry in different temperature, UV-light and time of exposure. It was found that methyl methacrylate polymer is capable of acting as a protective layer and play a critical role in improving the photostability of colorants. The nanocomposites exhibited excellent fluorescent thermo-switching action with respect to the free spiro molecule. Graphical Abstract ᅟ.

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Allura red is a widely used food colorant, but there is debate on its potential security risk. In the present study, we found that degradation products of the dye were more potent agents with higher carbonic anhydrase inhibitory action than the parent dye. The mechanism by which the compounds inhibit the enzyme activity has been determined as competitive mode. In addition, the enzyme binding properties of the compounds were investigated employing different spectroscopic techniques and molecular docking. The analyses of fluorescence quenching data revealed the existence of the same binding site for the compounds on the enzyme molecule. The thermodynamic parameters of ligand binding were not similar, which indicates that different interactions are responsible in binding of the parent dye and degradation products to the enzyme. It appears that enzyme inhibition should be considered, more seriously, as a new opened dimension in food safety.

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The present work deals with the first attempt to study the removal of synthetic textile dye, reactive blue 19 (RB19), using the magnetic Fe3O4 nanoparticles modified by pyrrole (PPy@Fe3O4 MNPs) as an efficient adsorbent. The nanoadsorbent was synthesized using chemical co-precipitation. Scanning electron microscopy and FT-IR were used to characterize nanoparticles. Factors affecting the dye adsorption including the pH of the dye solution, amount of adsorbent and contact time were also further investigated. Sorption of the RB19 on PPy@Fe3O4 MNPs reached to equilibrium at contact time less than 10 min and fitted well to the Langmuir adsorption model with a maximum adsorption capacity of 112.36 mg g(-1). Experiments for adsorption kinetic were carried out and the data fitted well according to a pseudo-second-order kinetic model. Moreover, the MNPs were recovered with over than 90% efficiency using methanol as elution agent.

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The interaction of a food colourant, quinoline yellow (Qy), and bovine serum albumin (BSA) was investigated by spectrophotometry, spectrofluorometry, FT-IR and circular dichroism (CD) techniques. The experimental results indicated that the quenching mechanism of BSA by the dye was a static procedure. Various binding parameters were evaluated. The negative value of ΔH, negative value of ΔS and the negative value of ΔG indicated that van der Waals force and hydrogen bonding play major roles in the binding of Qy and BSA. Based on Forster's theory of non-radiation energy transfer, the binding distance, r, between the donor (BSA) and acceptor (Qy) was evaluated. The results of CD and UV-vis spectroscopy showed that this dye could bind to BSA and the conformation of BSA changed.

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A novel N-allyl-4-amino-substituted 1,8-naphthalimide dye, containing thiourea functional group with intense yellow-green fluorescence was successfully synthesized. Copolymerization was done with styrene. The photophysical characteristics of dye and its copolymer in solution and solid film were investigated in the presence of halide ions. The results reveal that the fluorescence emissions of the monomer dye and also its polymer were 'switched off' in the presence of fluoride ions. The dye showed spectral shifts and intensity changes in the presence of more fluoride ions which lead to detect certain fluoride concentrations of 10-150 mM at visible wavelengths. By adding the fluoride ions, green-yellow to purple color changes occurs and the green fluorescence emission quenches, all of which easily observed by naked eyes. These phenomena are essential for producing a dual responsive chemosensor for fluoride ions. The polymeric sensor, in the film state exhibited a fast response to the fluoride ions.

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A rapid, environmental friendly and low-cost method to prepare hydroxyapatite nanoparticles is proposed. In this method, hydroxyapatite is produced in a sonicated pseudo-body solution. The sonication time was found effective in the formation of the crystalline phase of nanoparticles. In our experimental condition, 15 min sonication resulted in the most pure hydroxyapatite phase. Also it was shown that growth temperature is a crucial factor and hydroxyapatite crystallizes only at 37 degrees C. The particles formed by sonication were generally smaller and more spherical than those obtained without sonication. Sonication increased the hydroxyapatite crystal growth rate up to 5.5 times compared to non-sonication condition. The comparison between the specific surface area of hydroxyapatite nanoparticles obtained by sonication and without sonication demonstrated that sonication increased the specific surface area from 63 m(2)/g to 107 m(2)/g and decreased the size of nanoparticles from 30 nm to 18 nm. Analysis on the pore structure demonstrated that the fractal structures obtained with and without sonication were considerably different.

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