Search Results (67)

Light-responsive hydrogel-based oscillators typically exhibit small oscillation amplitudes because solvent diffusion is intrinsically slow, and their dependence on external periodic light modulation further results in limited amplitude, poor stability, and insufficient autonomy. Inspired by the trigger and sliding mechanism of the ancient crossbow, this study introduces an innovative system that integrates a sliding-block mechanism with time-delay feedback, breaking from conventional approaches that rely on hydrogel inertia or external modulation, within a purely theoretical and simulation-based framework. By establishing a nonlinear dynamic model coupling solvent diffusion, photoisomerization, and optical attenuation, this research shows through numerical simulations that the system can exhibit two distinct modes under constant illumination: a stable state and a self-sustained oscillatory state. The model predicts that the oscillation frequency can be flexibly tuned by varying key parameters, including the crosslinking density, Flory–Huggins interaction parameters of the spiropyran and hydrophilic polymer, ring-opening reaction rate, light intensity, fraction of light-sensitive molecules, and sliding displacement, whereas the initial absorption coefficient has only a minor influence. The slider displacement is also identified as an effective means to regulate the oscillation amplitude. Furthermore, the expansion force at the container bottom is predicted to oscillate synchronously with the hydrogel’s volume change. This theoretical framework represents a paradigm shift from “static small deformation” to “dynamic large-amplitude oscillation”, significantly enhancing the mechanical responsiveness of the material. This work provides a novel and controllable strategy for the conceptual design of autonomous light-driven micromechanical systems. Full article

This work investigates the use of two photoactive polymers, functionalized with quantum dots (QDs) (ZnS and CdTe/ZnS), to develop optical sensing hydrogel films through their interactions. It examines their responses to light stimulation for potential biological applications. The optical and morphological properties of the films were studied, revealing photoactive surfaces. The photoactive copolymers were synthesized based on poly(maleic anhydride-alt-2-methyl-2-butene), P(MAn-alt-2MB), and poly(maleic anhydride-alt-1-octadecene), P(MAn-alt-OD), by attaching the photochromic agent, 1-(2-hydroxyethyl)-3,3-dimethylindoline-6-nitrobenzo pyran (SP). Subsequently, QD nanoparticles (ZnS or CdTe/ZnS NPs) were incorporated into the polymer solutions in the presence of a crosslinker agent, and were then spin-coated onto glass substrates under suitable conditions to produce porous-patterned films. These films were created using a one-step bio-inspired process called the breath figure (BF) method. SEM images of QD-containing samples show a photoactive porous surface resulting from a synergistic interaction between the components. The reversibility of these macroscopic properties results from photoinduced transformations at the molecular level. The light-emitting properties of the films were characterized by blue and violet fluorescence under UV light. Advances in film-forming techniques enable the creation of functional structures with important applications, such as microstructured hydrogel films for biological uses. Full article

Stimuli-responsive materials based on renewable biopolymers are highly attractive for developing sustainable chemical sensors. Here, two spiropyran derivatives (SP1 and SP2) were synthesized and covalently grafted onto cellulose, yielding the functional materials Cel-SP1 and Cel-SP2. Cellulose was selected as a biocompatible, biodegradable, and renewable support able to provide a stable, hydrogen-bond-rich microenvironment for chromic responses. Raman spectroscopy confirmed successful esterification, while SEM-EDS analyses revealed preserved cellulose morphology and the incorporation of nitrogen-rich spiropyran moieties. Both materials exhibited pronounced solvatochromic and pH-dependent behaviors in the solid state. Diffuse reflectance measurements revealed distinct bathochromic or hypsochromic shifts depending on solvent polarity and specific solute–matrix interactions, with DMF and DMSO producing the strongest responses. Under acidic vapors, both materials generated new absorption bands consistent with the formation of protonated merocyanine species, whereas basic vapors promoted partial or full reversion to the spiropyran form. Cel-SP1 and Cel-SP2 also displayed solvent- and pH-dependent luminescence, with Cel-SP2 showing a markedly higher sensitivity to protonation. Prototype solvent strips and acid/base vapor indicators demonstrated fast, naked-eye, reversible chromic transitions. These results highlight spiropyran-modified cellulose as an effective, renewable platform for dual solvent and acid/base vapor sensing. Full article

Spiropyran (SP)–Merocyanine (MC) systems represent versatile molecular switches, with their open–closed equilibrium can be finely tuned by their structural characteristics. In this study, we combined conformational sampling, DFT (Density Functional Theory) calculations to rationalize the distinct behaviors of two recently synthesized derivatives: SP1/MC1 and SP3/MC3. While SP1 primarily exists in the colorless, non-fluorescent SP form, MC3 remains stabilized in the colored, open MC state, displaying intense emission. Our results reveal that allyl and benzyl substituents impose conformational constraints that limit interconversion, while hydroxyl substitution and solvent polarity modulate the relative stability of the SP and MC isomers. Full article

We fabricated dye-sensitized solar cells (DSSCs) co-sensitized with the organic dye YD2 and a spiropyran derivative (SPNO₂), a photochromic molecule capable of reversible isomerization under light irradiation. Upon UV exposure, SPNO₂ converts from its closed spiropyran (SP) form to the open photomerocyanine (PMC) form, which absorbs visible light and changes the optical properties of the photoelectrode. Spectroscopic analysis showed an 18% decrease in transmittance at 540 nm after UV irradiation and a 10% increase following visible light exposure. These changes were accompanied by a 0.5% increase in power conversion efficiency (η) after 5 min of UV irradiation, and a 0.83% decrease after 10 min of visible light. Although direct electron injection from PMC into TiO₂ appears inefficient, the enhanced performance is attributed to Förster resonance energy transfer (FRET) from PMC to YD2. This photoresponsive behavior highlights a co-sensitization strategy that combines dynamic optical control and efficient energy transfer. Our findings demonstrate a promising approach to designing smart DSSCs with externally tunable photovoltaic properties using photochromic sensitizers. Full article

The low fluorescence quantum efficiency of hydrophilic modified spiropyran in hydrogel matrices cannot be naturally improved during photoresponsive operation, which significantly limits their practical applications.In this study, a hybrid hydrogel system integrating metal plasmon resonance-enhanced fluorescence effects is designed through copolymerization of N,N′-bis(acryloyl)cystamine-modified Au nanoparticles (Au NPs), hydrophilic graft-modified spiropyran molecules, and N-isopropylacrylamide. This approach successfully achieves a spiropyran-based fluorescent hydrogel sensor with enhanced fluorescence intensity. Furthermore, an inverted pyramid-structured surface is engineered on the hydrogel using a template-assisted strategy, combining anti-reflection optical effects with plasmonic enhancement mechanisms. Molecular modification facilitated the integration of spiropyran and Au NPs into the hydrogel molecular chains, enhancing the dispersion of Au NPs within the hydrogel matrix and preventing fluorescence quenching from direct contact between Au NPs and spiropyran. Additionally, the anti-reflection effect of the hydrogel surface microstructure and the plasmon resonance effect of Au NPs were crucial in boosting the sensor’s fluorescence. Finally, the fluorescence intensity of the hydrogel increased by 10.2 times. In addition, under the action of excitation light, this sensor exhibited dual responsiveness of colorimetry and fluorescence, allowing for the sensing of heavy metal ions. The limit of detection for Zn²⁺ is as low as 0.803 μM, and the hydrogel exhibited more than 10 cycles of photo-isomerization and ion responsiveness. Full article

The photosensitive properties of smart photoactive polymers give them a wide range of potential applications across various fields. This study focuses on designing polymeric systems that incorporate hydrophilic polymers, with the primary goal of adapting these materials for biological applications. Specifically, it aims to contribute to the development of photochromic materials for optical processing, utilizing both molecular and macromolecular components. Additionally, this study evaluates the effectiveness of photoactive polymers in photodynamic therapy (PDT). It details the synthesis and characterization of photoactive copolymers derived from maleic anhydride (MAn) combined with vinyl monomers such as 2-methyl-2-butene (MB) and 1-octadecene (OD), as well as the organic compound 1-(2-hydroxyethyl)-3,3-dimethylindoline-6-nitrobenzopyran (SP). The two novel optically active alternating polymeric systems, poly(maleic anhydride-alt-octadecene) and poly(maleic anhydride-alt-2-methyl-2-butene), were functionalized with SP through an esterification process in a 1:1 monomer feed ratio, using pyridine as a catalyst. This methodology incorporated approximately 100% of the photoactive molecules into the main acrylic chain to prepare the alternating copolymers. These copolymers were characterized by UV-visible, FTIR, and 1H-NMR spectroscopy and analysis of their optical and thermal properties. When exposed to UV light, the photoactive polymer films can develop a deep blue color (566 nm in the absorption spectra). Finally, the study also assesses their capacity for photodynamic antimicrobial action in organic film. Notably, the photoactive P(MAn-alt-2MB)-PS significantly enhances the photodynamic antimicrobial activity of the photosensitizer Ru(bpy) against two bacterial strains of Staphylococcus aureus, reducing the minimum inhibitory concentration (MIC) from 2 µg/mL to 0.5 µg/mL. Therefore, 4 times less photosensitizer is required when mixed with the photoactive polymer to inhibit the growth of antibiotic-sensitive and -resistant bacteria. Full article

Spiropyran has an attractive and mysterious fluorescence switch and dual-color conversion characteristics, as it exhibits both aggregation-caused quenching (ACQ) in solvents and fluorescence enhancement in polymer matrices. The explanation for this phenomenon has always been of great controversy. Hence, the solvent effect on the emission of spiropyran (SP) was investigated in 16 solvents. By means of molecular orbital theory and the Jablonski diagram, several special parameters (e.g., Hansen solubility parameters and viscosity) were selected for this analysis, with excellent goodness of fit. Subsequently, the main factors that affected the blue shift, red shift, and luminescence efficiency of the emission of the ring-opened form merocyanine (MC) were found to be the hydrogen bonding and polarity, aggregation effect, and viscosity, respectively. A newly modified Jablonski diagram was proposed to clarify the emission behaviors of spiropyran influenced by solvent polarity and isomerization. Meanwhile, the solvent effect could also be extended to a solid polymer matrix (six kinds of polyethylene glycol (PEG) with different molecular weights), which is proposed to be defined as the generalized solvent effect. Accordingly, we have demonstrated that the unique fluorescence properties of spiropyran are dominated by the generalized solvent effect. The security information storage capacity of the simulated quick response (QR) code sensor combined with SP for anti-counterfeiting was significantly improved to six dimensions in taking advantage of the former theoretical analysis. Full article

Background/Objectives: This study explores the potential of using elevated levels of blood double-stranded RNA (dsRNA) as a diagnostic tool for severe fever with thrombocytopenia syndrome (SFTS) infection. Methods: Blood samples from SFTS patients were collected, dsRNA was purified, and total dsRNA expression was quantitatively analyzed using a spiropyran-based method. Comparative analysis was performed using blood samples from healthy individuals and scrub typhus patients with similar symptoms. Results: The results revealed that individuals infected with SFTS had significantly higher total blood dsRNA levels compared to healthy or scrub typhus controls. The dsRNA-based method also has potential for assessing infection severity based on dsRNA levels. Conclusions: These findings suggest that total dsRNA expression can serve as a quick and convenient method to differentiate SFTS from other non-viral conditions with similar clinical presentations. This method shows promise as a novel diagnostic tool. Full article

Due to their ability to reversibly isomerize under the influence of external stimuli, spiropyrans represent the most interesting class of organic photochromic molecules. The photochromic properties of the isomeric forms of spiropyrans differ significantly from each other, which makes it possible to use these photochromes as sensors, optoelectronic and holographic devices, memory elements, etc. Also, an undoubted advantage of spiropyrans compared to other classes of organic photochromes is the relative ease of their preparation and chemical transformation. At the same time, modification of the structure of spiropyrans by introducing various functional groups opens up great synthetic possibilities for obtaining new photochromic molecules with various spectral-kinetic characteristics. In the development of research aimed at expanding the boundaries of the use of spirophotochromic compounds, in order to obtain new light-controlled materials with different characteristics, as well as to study the influence of functional groups in the spirophotochromic molecule on the spectral and photochromic properties, we have synthesized a new spiropyran. In this work, we synthesized a new salt of photochromic spiropyran containing various functional groups (–CHO, –NO₂, –OCH₃, –(CH₂)₅N(CH₃)₂*HBr), capable of reversibly responding to external influences. Photoinduced transformations and the spectral and kinetic characteristics of the synthesized compound were studied. Full article

We developed dye-sensitized solar cells (DSSCs) using 1,5-carboxy-2-[[3-[(2,3-dihydro-1,1-dimethyl-3-ethyl-1H-benzo[e]indol-2-ylidene)methyl]-2-hydroxy-4-oxo-2-cyclobuten-1-ylidene]methyl]-3,3-dimethyl-1-octyl-3H-indolium and 1,3,3-trimethyl indolino-6′-nitrobenzopyrylospiran. The DSSCs incorporate photochromic molecules to regulate photoelectric conversion properties. We irradiated photoelectrodes adsorbed with SQ2/SPNO₂ using both UV and visible light and observed the color changes in these photoelectrodes. Following UV irradiation, the transmittance at 540 nm decreased by 20%, while it increased by 15% after visible light irradiation. This indicates that SPNO₂ on the DSSCs is photoisomerized from the spiropyran form (SP) to the photomerocyanine (PMC) form under UV light. The photoelectric conversion efficiency (η) of the DSSCs increased by 0.15% following 5 min of UV irradiation and decreased by 0.07% after 5 min of visible light irradiation. However, direct electron injection from PMC seems challenging, suggesting that the mechanism for improved photoelectric conversion in these DSSCs is likely due to Förster resonance energy transfer (FRET) from PMC to the SQ2 dye. The findings suggest that the co-sensitization of DSSCs by PMC-SQ2 and SQ2 alone, facilitated by their respective photoabsorption, results in externally responsive and co-sensitized solar cells. This study provides valuable insights into the development of advanced DSSCs with externally controllable photoelectric conversion properties via the strategic use of photochromic molecules and energy transfer mechanisms, advancing future solar energy applications. Full article

In daily life, counterfeit and substandard products, particularly currency, medicine, food, and confidential documents, are capable of bringing about very serious consequences. The development of anti-counterfeiting and authentication technologies with multilevel securities is a powerful means to overcome this challenge. Among various anti-counterfeiting technologies, fluorescent anti-counterfeiting technology is well-known and commonly used to fight counterfeiters due to its wide material source, low cost, simple usage, good concealment, and simple response mechanism. Spiropyran is favored by scientists in the fields of anti-counterfeiting and information encryption due to its reversible photochromic property. Here, we summarize the current available spiropyran-based fluorescent materials from design to anti-counterfeiting applications. This review will be help scientists to design and develop fluorescent anti-counterfeiting materials with high security, high performance, quick response, and high anti-counterfeiting level. Full article

Shape-shifting polymers usually require not only reversible stimuli-responsive ability, but also strong mechanical properties. A novel shape-shifting photochromic hydrogel system was designed and fabricated by embedding hydrophobic spiropyran (SP) into double polymeric network (DN) through micellar copolymerisation. Here, sodium alginate (Alg) and poly acrylate-co-methyl acrylate-co-spiropyran (P(SA-co-MA-co-SPMA)) were employed as the first network and the second network, respectively, to realise high mechanical strength. After being soaked in the CaCl₂ solution, the carboxyl groups in the system underwent metal complexation with Ca²⁺ to enhance the hydrogel. Moreover, after the hydrogel was exposed to UV-light, the closed isomer of spiropyran in the hydrogel network could be converted into an open zwitterionic isomer merocyanine (MC), which was considered to interact with Ca²⁺ ions. Interestingly, Ca²⁺ and UV-light responsive programmable shape of the copolymer hydrogel could recover to its original form via immersion in pure water. Given its excellent metal ion and UV light stimuli-responsive and mechanical properties, the hydrogel has potential applications in the field of soft actuators. Full article

The most important area of modern pharmacology is the targeted delivery of drugs, and one of the most promising classes of chemical compounds for creating drugs of this kind are the photochromic spiropyrans, capable of light-controlled biological activity. This work is devoted to the synthesis and study of the photochromic properties of new triphenylphosphonium salts of spiropyrans. It was found that all the synthesized cationic spiropyrans have high photosensitivity, increased resistance to photodegradation and the ability for photoluminescence. Full article

In this paper, the relaxation isomerization properties of a spiropyran-doped poly(methyl methacrylate) (PMMA) UV light-responsive dynamic material are presented. The polar liquid (acetonitrile) and solid (PMMA matrix) medium may contain two merocyanine isoforms of the selected spiropyran. A complex equilibrium of the colored and colorless spiropyran isoforms resulted in specific transformations of the absorption spectra during the relaxation process. Bands at 522 nm and 580 nm characterized the absorption of the fabricated dynamic material in the ground (non-activated) state in the visible range. The presence of colored and colorless isoforms of spiropyran incorporated into the PMMA matrix using Raman spectroscopy was revealed. The photosensitive polymer samples were irradiated with a UV LED (365 nm and 390 nm) under various temperatures (0–30 °C). Spectral changes within the relaxation process demonstrated their complex dynamics. Surprisingly, the photodegradation of the dynamic material was estimated at about 25% (using 390 nm) and 7% (using 365 nm) after eight photoswitch cycles for one isoform, and no fatigue after an additional one (using 390 nm) was discovered. The presented light-responsive material is of interest for UV sensors and new hybrid material design. Full article