Search Results (52)

Electronic devices with polyurethane electronic packaging have been stored in Chinese tropical marine atmosphere environments for 10 years. The long-term natural aging mechanism was studied by comparing the appearance inspection, molecular structure, elemental content, and chemical functional groups of the surface and interior of polyurethane electronic potting. The results indicated that, despite evident chemical aging and physical changes in the encapsulant material, it continued to effectively protect the internal electronic devices, maintaining their performance within an acceptable range. The interior polyurethane potting of electronic devices was white, but the surface turned yellow with noticeable color change. On the surface, the content of tolylene diisocyanate was greatly decreased. The peak heights of the internal carbamate groups located at 1708 cm⁻¹ and 1529 cm⁻¹ were significantly higher than those at the surface. In addition, the internal C element content for the carbamate group at 289.5 eV was higher than that of the surface. It can be inferred that, under ambient temperature and trace oxygen conditions, the urethane groups on the polyurethane electronic potting surface undergo aging reactions. These groups slowly oxidize into the quinoid structure of the chromophore, causing the surface to turn yellow. Despite this discoloration, the potting still protects electronic devices. Therefore, polyurethane electronic potting is ideal for the long-term sealed storage of electronic devices. Full article

This study researches the impact of diclofenac (DCF) oxidation via UV/H₂O₂ on water quality, focusing on aromaticity and color changes. The process effectively degrades DCF and its intermediates through hydroxyl radical attack on the aromatic structure, leading to the formation of oxidized by-products. Initially, chromophoric compounds such as quinones and conjugated intermediates cause a yellow coloration, which diminishes as mineralization progresses. Turbidity remains below 1 NTU, aligning with European water quality standards. Aromaticity initially increases due to the stable intermediates (e.g., catechols and hydroquinones) but decreases as advanced oxidation cleaves aromatic rings. Kinetic modeling shows that DCF degradation follows first-order kinetics, while aromatic intermediates degrade via fractional-order kinetics (~0.3), indicating a non-linear relationship with concentration. The formation of chromophore compounds follows first-order kinetics, whereas their degradation transitions to zero-order kinetics when hydroxyl radicals are abundant. The study highlights the environmental relevance of these transformations, as aromatic intermediates like anilines and phenols, which contribute to water toxicity, are ultimately converted into less hazardous compounds (e.g., carboxylic acids and inorganic ions). Experimental validation confirms that degradation kinetics depend on hydrogen peroxide concentration, underscoring the potential of UV/H₂O₂ for water purification and pollutant removal. Full article

A novel method for the spectrophotometric determination of trace amounts of molybdenum has been developed. This method utilizes a centrifuge-less cloud point extraction (CL-CPE) in a mixed micellar (MM) system containing a nonionic surfactant (Triton X-114) and an ionic liquid (Aliquat^® 336, A336). The chromophore chelating reagent employed was 4-nitrocatechol (4NC, H₂L). This work marks its first application as a CPE reagent. Under the optimal conditions, Mo(VI) forms a yellow ternary complex with 4NC and A336, which can be represented by the formula (A336⁺)₂[MoO₂L₂]. The method possesses the following characteristics: limit of detection (LOD) of 3.2 ng mL⁻¹, linear range of 10.8–580 ng/mL, absorption maximum of 435 nm, molar absorptivity coefficient of 3.34 × 10⁵ L mol⁻¹ cm⁻¹, and Sandell’s sensitivity of 0.29 ng cm⁻². The method has been successfully employed for the determination of molybdenum in reference standard steel samples, bottled mineral water, and a molybdenum-containing dietary supplement. Full article

The delimitation of an ecotone is an important reference for ecosystem conservation; however, the assessment of a marine ecotone from an ecological point of view represents a knowledge gap. The Yellow River Estuary (YRE) serves as both spawning and feeding grounds for numerous economically important organisms. Delineating the boundary of YRE and assessing the boundary change have great importance in maintaining its ecosystem health. This study attempts to apply a Moving Split Window (MSW) to determine marine boundary in YRE. Level 2 remote sensing satellite data spanning from 2012 to 2020 sourced from the Geostationary Ocean Color Imager (GOCI) were utilized. Chlorophyll-a, Chromophoric Dissolved Organic Matter (CDOM), and Total Suspended Solids (TSS) were employed as variables, with Squared Euclidean Distance (SED) serving as the determinant for identifying the marine ecological ecotone within the Yellow Estuary and its adjacent waters. Results indicate the following: (1) SED values exhibit distinct peaks and valleys, facilitating the accurate identification of marine ecotones via MSW. (2) Evident ecotones are observable in both the gate and coastal regions. (3) The influence range of TSS on the gate spans between 10 km and 14 km. In synthesis, the ensuing conclusions are drawn: MSW proves to be a reliable method for quantitatively determining ecotones in marine environments. Furthermore, MSW introduces a novel approach to the delineation of marine ecotones. Full article

The market demand for black polyimide (BPI) has grown hugely in the field of flexible copper-clad laminates (FCCLs) as a replacement for transparent yellow polyimide. The 3,6-bis(thiophen-2-yl)diketopyrrolopyrroles (TDPP) derivative is recognized for its high molar extinction coefficient. In this research, we have synthesized a diamine monomer named 3,6-bis[5-(4-amino-3-fluorophenyl)thiophen-2-yl]-2,5-bis(2-ethylhexyl)pyrrolo[4,3-c]pyrrole-1,4-dione (DPPTENFPDA), featuring a TDPP unit attached by fluorinated benzene rings. The subsequent reaction of DPPTENFPDA with pyromellitic dianhydride (PMDA) yielded an inherent BPI (DPPTENFPPI). By introducing chromophores derived from TDPP, the light absorption spectrum of DPPTENFPPI was broadened and red-shifted, thereby achieving full absorption within the visible spectrum and producing a highly black color that has a cut-off wavelength (λ_cut) of 717 nm and a CIE-Lab coordinate L* of 0.86. Additionally, DPPTENFPPI exhibited a low coefficient of thermal expansion (CTE) and remarkable thermal and electrical performance. Density functional theory calculations were conducted to explore the electronic nature of DPPTENFPPI. The outcomes revealed that the excellent light absorption of DPPTENFPPI predominantly originates from the transition from HOMO to LUMO + 1 within the chromophore moiety. The FCCL made from DPPTENFPPI films has high solder heat resistance and peel strength. This research contributes valuable insights into the structure and design of high-performance intrinsically black PIs for microelectronics applications. Full article

Sulfamethoxazole (SMX) is an antibiotic that is extensively used in veterinary medicine, and its occurrence in wastewater and surface water can reach up to 20 μg/L. SMX is categorized as a pollutant of emerging concern by the US EPA due to its persistence and effects on humans and the environment. In this study, photo-Fenton technology is proposed for the removal of SMX. Aqueous solutions of SMX (50.0 mg/L) are treated in a 150 W UV photoreactor, using [Fe²⁺]₀ = 0.5 mg/L and varying [H₂O₂]₀ = 0–3.0 mM. During the reaction, colour (AU) was assessed along with SMX (mg/L), turbidity (NTU), and TC (mg/L). SMX degrades to aromatic intermediates with chromophoric groups, exhibiting colour (yellow to brown) and turbidity. As these intermediates are mineralized into CO₂ and H₂O, the colour and turbidity of the water lose intensity. Using a molar ratio of 1 mol SMX:10 mol H₂O₂, the maximum degradation of aromatic species takes place (71% elimination), and colourless water with turbidity < 1 NTU is obtained. A kinetic modelling for aromaticity loss and colour formation as a function of the oxidant concentration has been proposed. The application of this model allows the estimation of oxidant amounts for an efficient removal of SMX under environmentally friendly conditions. Full article

Thermal green protein Q66E (TGP-E) has previously shown increased thermal stability compared to thermal green protein (TGP), a thermal stable fluorescent protein produced through consensus and surface protein engineering. In this paper, we describe the protein crystal structure of TGP-E to 2.0 Å. This structure reveals alterations in the hydrogen bond network near the chromophore that may result in the observed increase in thermal stability. We compare the very stable TGP-E protein to the structure of a yellow mutant version of this protein YTP-E E148D. The structure of this mutant protein reveals the rationale for the observed low quantum yield and directions for future protein engineering efforts. Full article

In this study, fully aromatic polyether sulfones were developed, bearing blue, yellow, and orange–red π-conjugated semiconducting units. Carbazole-, anthracene-, and benzothiadiazole-based fluorophores are copolymerized with a diphenylsulfone moiety. A diphenylpyridine comonomer was additionally utilized, acting as both a solubilizing unit and a weak blue fluorescent group. Using this rationale, fluorescent polyarylethers with high molecular weights, up to 70 kDa, were developed, showing film formation ability and high thermal stability, while preserving excellent solubility in common organic, nonvolatile, and nonchlorinated solvents. Fine-tuning of the emission color was achieved through subtle changes of the comonomers’ type and ratio. Single-chromophore-bearing copolymers emitted in the blue or the yellow region of the visible spectrum, while the dual-chromophore-bearing terpolymers emitted throughout the visible spectrum, resulting in white light emission. Solutions of 20 wt% in polar aprotic solvents at ambient conditions allowed the deposition of fluorescent copolyethers and printing from non-chlorinated solvents. All polyethers were evaluated for their structural and optoelectronic properties, and selected copolymers were successfully used in the emitting layer (EML) of organic light-emitting diode (OLED) devices, using either rigid or flexible substrates. Remarkable color stability was displayed in all cases for up to 15 V of bias voltage. The Commission Internationale de L’Eclairage (CIE) of the fabricated devices is located in the blue (0.16, 0.16), yellow (0.44, 0.50), or white region of the visible spectrum (0.33, 0.38) with minimal changes according to the ratio of the comonomers. The versatile methodology toward semiconducting polyethersulfones for polymer light-emitting diodes (PLEDs) developed herein led to the scaled-up production of luminescent polymers of up to 25 g of high-molecular-weight single batches, demonstrating the effectiveness of this approach as a straightforward tool to facilitate the synthesis of flexible and printable EMLs for large-area PLED coverage. Full article

A thiourea-based colorimetric sensor incorporating polyethyleneimine (PEI) and chromophoric nitrophenyl groups was synthesized and utilized for detecting various anions. Structural characterization of the sensor was accomplished using FTIR and 1H-NMR spectroscopy. The sensor’s interactions and colorimetric recognition capabilities with different anions, including CI⁻, Br⁻, I⁻, F⁻, NO₃⁻, PF₆⁻, AcO⁻, H₂PO₄⁻, PO₄³⁻, and SO₄²⁻, were investigated via visual observation and UV/vis spectroscopy. Upon adding SO₄²⁻, F⁻, and AcO⁻ anions, the sensor exhibited distinct color changes from colorless to yellow and yellowish, while other anions did not induce significant color alterations. UV/vis spectroscopic titration experiments conducted in a DMSO/H₂O solution (9:1 volume ratio) demonstrated the sensor’s selectivity toward SO₄²⁻, F⁻, and AcO⁻. The data revealed that the formation of the main compounds and anion complexes was mediated by hydrogen bonding, leading to signal changes in the nitrophenyl thiourea-modified PEI spectrum. Full article

A series of stimuli-responsive fluorescent hydrogels were successfully synthesized via micelle radical copolymerization of hydrophilic acrylamide (AM), hydrophobic chromophore terpyridine-based monomer (TPY), and N-isopropylacrylamide (NIPAM). These hydrogels presented blue emissions (423–440 nm) under room temperature, which is caused by the π-π* transition of the conjugated structures. Once the ambient temperature was increased to 55 °C, the fluorescence color changed from blue (430 nm) to pink (575 nm) within 10 min, subsequently to yellow (535 nm), and eventually back to pink. The thermal-responsive properties are attributed to the transition of the TPY units from unimer to dimer aggregation via the intermolecular charge transfer complex at high temperatures. The hydrogels showed pH-responsive properties. The emission peak of the hydrogel exhibited a blue shift of ~54 nm from neuter conditions to acidic conditions, while a 6 nm red shift to an alkaline environment was observed. The hydrogels demonstrated an obvious change in fluorescence intensity and wavelength upon adding different metal ions, which is caused by the coordination between the terpyridine units incorporated on the backbones and the metal ions. As a consequence, the hydrogels presented a sharp quenching fluorescence interaction with Fe²⁺, Fe³⁺, Cu²⁺, Hg²⁺, Ni²⁺, and Co²⁺, while it exhibited an enhanced fluorescence intensity interaction with Sn²⁺, Cd²⁺, and Zn²⁺. The microstructural, mechanical, and rheological properties of these luminescent hydrogels have been systematically investigated. Full article

Skin yellowness is a hallmark of dull or unhealthy skin, particularly among Asians. Previous research has indicated a link between skin glycation and skin yellowness. However, the specific glycated chemicals contributing to yellowish skin appearance have not been identified yet. Using HPLC-PDA-HRMS coupled with native and artificially glycated human epidermal explant skin, we identified intensely yellow colored glycated chromophores “(1R, 8aR) and (1S, 8aR)-4-(2-furyl)-7-[(2-furyl)-methylidene]-2-hydroxy-2H,7H,8AH-pyrano-[2,3-B]-pyran-3-one” (abbreviated as AGEY) from human skin samples for the first time. The abundance of AGEY was strongly correlated with skin yellowness in the multiple skin explant tissues. We further confirmed the presence of AGEY in cultured human keratinocytes and 3D reconstructed human epidermal (RHE) models. Additionally, we demonstrated that a combination of four cosmetic compounds with anti-glycation properties can inhibit the formation of AGEY and reduce yellowness in the RHE models. In conclusion, we have identified specific advanced glycation end products with an intense yellow color, namely AGEY, in human skin tissues for the first time. The series of study results highlighted the significant contribution of AGEY to the yellow appearance of the skin. Furthermore, we have identified a potential cosmetic solution to mitigate AGEY formation, leading to a reduction in yellowness in the in vitro RHE models. Full article

Extensive research has been dedicated to the solution-processable white organic light-emitting diodes (WOLEDs), which can potentially influence future solid-state lighting and full-color flat-panel displays. The proposed strategy based on WOLEDs involves blending two or more emitting polymers or copolymerizing two or more emitting chromophores with different doping concentrations to produce white light emission from a single layer. Toward this direction, the development of blends was conducted using commercial blue poly(9,9-di-n-octylfluorenyl2,7-diyl) (PFO), green poly(9,9-dioctylfluorenealt-benzothiadiazole) (F8BT), and red spiro-copolymer (SPR) light-emitting materials, whereas the synthesized copolymers were based on different chromophores, namely distyryllanthracene, distyrylcarbazole, and distyrylbenzothiadiazole, as yellow, blue, and orange–red emitters, respectively. A comparative study between the two approaches was carried out to examine the main challenge for these doping systems, which is ensuring the proper balance of emissions from all the units to span the entire visible range. The emission characteristics of fabricated WOLEDs will be explored in terms of controlling the emission from each emitter, which depends on two possible mechanisms: energy transfer and carrier trapping. The aim of this work is to achieve pure white emission through the color mixing from different emitters based on different doping concentrations, as well as color stability during the device operation. According to these aspects, the WOLED devices based on the copolymers of two chromophores exhibit the most encouraging results regarding white color emission coordinates (0.28, 0.31) with a CRI value of 82. Full article

Antoine Janot and Paul Gout were 18th-century master dyers who specialised in the piece-dyeing of fine wool broadcloths manufactured in Languedoc (southern France) for exportation to the Levant. They wrote treatises, similarly entitled Mémoires de Teinture (Memoirs on Dyeing), illustrated with dozens of dyed textile samples. Janot’s is dated 1744, and Gout’s is dated 1763. These books are full of extremely valuable information, which is unique to its time: the books are composed of carefully described recipes for every colour, each originally preceded by a sample swatch. The yellows of both master dyers made from weld (Reseda luteola L.), belonging to recipes described as Jaune (yellow), were reproduced. The influence of the ingredients, in both the mordanting and dyeing baths, was assessed, and the timings for both baths, which in many recipes are not clear, were tested. This provided key knowledge on the technological processes for dyeing with weld from these 18th c. French masters. The resulting reference samples were preliminarily analysed by a multi-analytical approach. Their chromatic specifications, expressed in the CIEL*a*b*, were compared with those in the Mémoires. Moreover, the influence of the recipe on the percentages of the chromophores was assessed by HPLC-DAD. It was found that the bran and tartar in the mordanting bath influence the final obtained colour and that lime is essential to obtain a bright yellow. Full article

This work examines the effect of thermal modification temperature (180, 200, and 220 °C) in comparison with reference (untreated) samples on selected optical properties of six tropical wood species—Sp. cedar (Cedrala odorata), iroko (Chlorophora excelsa), merbau (Intsia spp.), meranti (Shorea spp.), padouk (Pterocarpus soyauxii), and teak (Tectona grandis). The main goal is to expand the existing knowledge in the field of wood thermal modification by understanding the related degradation mechanisms associated with the formation of chromophoric structures and, above all, to focus on the change in the content of extractive substances. For solid wood, the CIELAB color space parameters (L*, a*, b*, and ΔE*), yellowness (Y), ISO brightness, and UV-Vis diffuse reflectance spectra were obtained. Subsequently, these wood samples were extracted into three individual solvents (acetone, ethanol, and ethanol-toluene). The yields of the extracted compounds, their absorption spectra, and again L*, a*, b*, ΔE*, and Yi parameters were determined. With increasing temperatures, the samples lose brightness and darken, while their total color difference grows (except merbau). The highest yield of extractives (mainly phenolic compounds, glycosides, and dyes) from thermally modified samples was usually obtained using ethanol. New types of extractives (e.g., 2-furaldehyde, lactones, formic acid, some monomer derivatives of phenols, etc.) are already created around a temperature of 180 °C and may undergo condensation reactions at higher temperatures. For padouk, merbau, teak, and partially iroko modified at temperatures of 200 and 220 °C, there was a detected similarity in the intensities of their UV-Vis DR spectra at the wavelength regions corresponding to phenolic aldehydes, unsaturated ketones, quinones, stilbenes, and other conjugated carbonyl structures. Overall, a statistical assessment using PCA sorted the samples into five clusters. Cluster 3 consists of almost all samples modified at 200 and 220 °C, and in the other four, the reference and thermally modified samples at 180 °C were distributed. The yellowness of wood (Y) has a very high dependence (r = 0.972) on its brightness (L*) and the yellowness index of the extractives in acetone Yi(Ac), whose relationship was described by the equation Y = −0.0951 × Y(Ac) + 23.3485. Full article

The versatile functions of fluorescent proteins (FPs) as fluorescence biomarkers depend on their intrinsic chromophores interacting with the protein environment. Besides X-ray crystallography, vibrational spectroscopy represents a highly valuable tool for characterizing the chromophore structure and revealing the roles of chromophore–environment interactions. In this work, we aim to benchmark the ground-state vibrational signatures of a series of FPs with emission colors spanning from green, yellow, orange, to red, as well as the solvated model chromophores for some of these FPs, using wavelength-tunable femtosecond stimulated Raman spectroscopy (FSRS) in conjunction with quantum calculations. We systematically analyzed and discussed four factors underlying the vibrational properties of FP chromophores: sidechain structure, conjugation structure, chromophore conformation, and the protein environment. A prominent bond-stretching mode characteristic of the quinoidal resonance structure is found to be conserved in most FPs and model chromophores investigated, which can be used as a vibrational marker to interpret chromophore–environment interactions and structural effects on the electronic properties of the chromophore. The fundamental insights gained for these light-sensing units (e.g., protein active sites) substantiate the unique and powerful capability of wavelength-tunable FSRS in delineating FP chromophore properties with high sensitivity and resolution in solution and protein matrices. The comprehensive characterization for various FPs across a colorful palette could also serve as a solid foundation for future spectroscopic studies and the rational engineering of FPs with diverse and improved functions. Full article