Stokes Shift Research Articles

Up-conversion materials for solid-state lighting

AbstractConventional phosphor-converted white LEDs (WLEDs), using (Stokes) down-conversion light emission, suffer from a red deficiency that increases the Color Temperature towards “cool white light” above 5000 K. The present work describes a phosphor-Up-converted WLED approach that wishes to overcome this issue by achieving white light generation (WLG) through Up-conversion photoluminescence (UCPL), without energy losses due to Stokes shift and excited by a 980 nm LED instead of the more expensive blue LEDs. The UC materials include thin films of lanthanide (Ln)-doped aluminosilicate glass multilayers, alternating (Ln)-doped aluminosilicate and titania films in the form of 1-D photonic crystals and Ln ion-implanted materials. Sol-gel (SG) processing has been used as a low-cost high purity processing method to prepare titania, as well as aluminosilicate films containing Er3+, Tm3+ and Yb3+, for WLG and possible application as WLED materials. The total Ln content varied from a high of 22 mol% to as low as 5.8 mol%. The materials prepared have been characterized by UV-Vis-NIR (using a variable angle specular reflection accessory), plus FTIR and UCPL spectroscopies. The UC light emission was analyzed with the help of CIE chromaticity diagrams. Graphical abstract

Near-infrared probes based on the phenanthridinium for dynamic monitoring of viscosity fluctuations during mitophagy

Abnormal changes in the mitochondrial microenvironment can cause a variety of diseases. Consequently, based on the twisted intramolecular charge transfer (TICT) theory, three hemicyanine fluorescent probes 1a-c were designed and developed by linking the phenanthridine group with different electron donor groups for the dynamic detection of mitochondrial viscosity in this paper. They have the advantages of near-infrared emission, excellent pH stability and viscosity sensitivity. Optical experiments showed that the maximum absorption and emission wavelengths of the probes in different solvents located at 411 − 529 nm and 623 − 684 nm with large Stokes shifts of 133 – 230 nm. In addition, when the viscosity increased from 0.89 cP to 856 cP, their fluorescence intensities in glycerol enhanced by 115-fold, 83-fold and 303-fold compared with water, respectively. The fluorescence intensities of probes showed excellent fit to the Forster Hoffmann equation, and exhibited nearly OFF-ON response to viscosity. Moreover, the probe 1a with good photostability and low cytotoxicity could target mitochondria. It was verified that 1a also could detect variation in mitochondrial viscosity during autophagy by modelling starvation and drug-induced (rapamycin and nystatin) in HeLa cells. Therefore, this study provides a useful probe for the analysis of mitophagy process in HeLa cells by the viscosity variation of mitochondria.

Role of Dark States and Stokes Shift Simulations for Tetraphenylpyrazine Compared to Other Donor-Acceptor Photosensitizers.

An excellent agreement for simulated and measured absorption and emission spectra is found for four donor-acceptor aromatic molecules (tetraphenylpyrazine, tetraphenylethene, distirylanthracene and hexaphenylsilole) whose derivatives serve as solid state photosensitizers. After comparing several hybrid TDDFT functionals, EOM-CCSD, and experiments, the best agreement was found with TD-B3LYP and double zeta basis sets (6-31G** and def2-SVP) for one molecule in gas phase. A full characterisation of twelve to twenty electronic excited states was performed in every system. Symmetry-forbidden bands are found in the absorption spectra by sampling fifty to hundred geometries from a Wigner distribution. The density of states in the region 2-6 eV was also analysed, showing a very packed region of excited states and suggesting that dark electronic states may play a role in the dynamics of some of the photoexcited systems. Further calculations were done with QM/xTB at geometries extracted from previously published X-ray data to evaluate the influence of the environment on the excitations of the four aggregated molecular crystals.

A Carbazole-based Fluorescent Probe with AIE Performance and a Large Stokes Shift for Peroxynitrite Detection and Imaging in Live Cells.

A carbazole-based fluorescent probe YCN with AIE performance and a large Stokes shift (242nm) shift was synthesized by attaching 4-acetonitrile pyridine to the 3-phenylaldehyde butylcarbazole. Its structure was characterized by 1H NMR, 13C NMR and MS. Probe YCN has high selectivity and sensitivity toward ONOO-. The addition of ONOO- to the probe YCN solution results in a noticeable color change from pale yellow to colorless under natural light, and a fluorescent color change from bright orange-yellow to bright yellow-green under a 365nm UV lamp, which can be distinguished by the naked eye. The research results on the reaction mechanism showed that when YCN reacted with ONOO-, -C = C- was oxidized and broken into -CHO, and the ICT effect was significantly inhibited, resulting in changes in UV absorption and fluorescence emission phenomenon. The recognition mechanism was verified by 1H NMR, mass spectrometry (MS) and density function theory (DFT) calculations. The experiments of live cells imaging suggested that compound YCN can be used as a fluorescent probe for the detection of ONOO- in HeLa cells. This result indicates that YCN has potential application prospects in the biological aspects.

Storehouse of Peculiar Supramolecular Architecture: Probing the Charge-Transfer Phenomenon and Effect of Altering the pH in a Meta-Oriented Single Donor-Double Acceptor Fluorophore.

The investigation of excited-state intramolecular charge transfer (ESICT) has been a fascinating area of research. Although the ESICT events have been studied mostly for para-disubstituted donor-acceptor type molecules, the meta-oriented donor-acceptor type molecules have also shown tremendous potential as ESICT active molecules. In the current work, a small fluorescent probe diethyl 5-amino isophthalate (DE-5A-IPA) was investigated as a potential model to investigate ESICT events in the solution as well as solid phase. DE-5A-IPA was synthesized easily starting from commercially available 5-amino isophthalic acid in excellent yield. In the solid state, differing extents of CH···π-type binding led to formation of fully planar and puckered "cyclobutane" mimic supramolecular architecture, as evidenced from the crystal structure analysis. In addition, the single crystal structure of DE-5A-IPA shows that the donor (-NH2) and acceptor (-CO2Et) are situated in the same plane, thereby assuring the prerequisites of a through-space charge transfer. DE-5A-IPA undergoes noticeable Stokes shift (in cm-1) when the polarity of the medium was changed (4820 cm-1 in hexane; 9375 cm-1 in water). The excited-state dipole moment (μe) was calculated to be 4.0 units higher than the ground-state dipole moment (μg). DE-5A-IPA had an appreciable quantum yield (0.10 ± 0.03 to 0.27 ± 0.04). The ESICT phenomenon was also investigated by ground- and excited-state structural calculations using Gaussian 16 software. The excited-state lifetime measured by the time correlated single photon counting technique was found to vary with the polarity of the solvent, thereby providing further support to the ESICT phenomenon being operative in DE-5A-IPA. Taking advantage of the -NH2 group (which is susceptible to protonation) in DE-5A-IPA, steady state and time-resolved photodynamics were investigated in solutions of varying pH values. Interestingly, the emission quantum yields as well as the emission lifetime increase with an increase in pH value, thereby establishing DE-5A-IPA as a pH-sensitive probe. The current findings shall boost the understanding of meta-oriented ESICT enabled compounds in terms of their excited-state photophysics.

An intramolecular charge transfer based fluorescent probe for imaging of OCl–

The discovery and utilization of new fluorescent chromophore is indispensable to exploit high performance probes for biological research. Stokes shift is one of the most important properties of chromophore accounting for super-resolution fluorescence imaging. Intramolecular charge transfer (ICT) is one of the fundamental mechanisms for fluorescence that accompanied by large Stokes shifts. Based on the conformational changes between ground and excited states, ICT models can be divided into two types: conformation-steady ICT, whose conformation remains unchanged, and conformation-changeable ICT, which is characterized by the rotation of the chromophore around an axis upon excitation. Herein, we report a new chromophore whose donor and acceptor parts took a butterfly geometry with a dihedral angle of 21° in ground state and a planar conformation upon photo excitation. The bent conformation might be ascribed to the extra conjugated double bond, which made the coplanarity of the chromophore in ground state get worse. The chromophore shows a remarkable Stokes shift over 150 nm and a high fluorescence quantum yieldof 0.62. The limit of detection is 41 nM, which enabled the imaging of basal as well as induced OCl– in different cells. Moreover, the pronounced spectroscopic properties ensure the in vivo monitoring of OCl– in arthritic mice. This finding would shed light on the exploitation of small molecule probes based on new fluorescence chromophore for precise biological imaging.

Green florescent carbon dots synthesized from various household green wastes for detection of parathion methyl pesticide

The purpose of the current study was to examine the use of green household wastes, such as lemon peel, bottle gourd peel (BG), culinary banana peel, and sugarcane bagasse, as a source for synthesizing carbon dots (C-dots) and to determine how the composition of the material affected the functional characteristics of the C-dots and its interaction behaviour for detection of pesticide. The synthesized C-dots showed green fluorescence with varying particle sizes and red shifting fluorescence with more than 100 nm Stokes shift, indicating time and excitation dependent luminescence behaviour. C-dots produced from bottle gourd (BG) peel had a positive impact on the functional characteristics with a maximum emission of 514 nm and excitation of 410 nm. The SAED and TEM pattern confirmed its amorphous structure. The hydronium ion diameter and the quantum yield were 0.99 nm and 3.1 % respectively. Contributing towards food safety, the synthesized C-dots from BG showed significant behaviour in the detection of parathion methyl (MP) like organophosphorus pesticide (OP) as it conjugated with iron and 1 ppm of parathion methyl, which exhibited “Turn-Off-On” fluorescence behaviour with noticeable changed in intensity and act as a promising qualitative tool for detection of parathion methyl in real sample. The intensity of FL and concentration of OP is directly proportional which is established by the investigated OP in vegetable, fruit and water samples. The significance of iron and MP-OP was also investigated in the presence of other metal ions and pesticides and showed that the C-dots synthesized probe solution was reliable and sensitive towards the detection of MP-OP in real samples.

A naphthimide based fluorescent probe for the detection of thiophenols and its application in actual water and food

Thiophenol (PhSH) and its derivatives are widely employed as common industrial raw materials, while they also pose high toxicity for animals and aquatic organisms. Herein, a novel fluorescent probe P1 was constructed, based on photo-induced electron transfer (PET) mechanism, using naphthimide as the fluorophore and 7-nitrobenzoxadiazole as the recognizing group. Probe P1 exhibited an “Off-On” fluorescence recognition response to PhSH by nucleophilic substitution reaction. The probe displayed advantageous properties for the recognition of PhSH, including a chromogenic response, high selectivity, fast response (< 90 s), and a large Stokes shift (150 nm). In addition, probe P1 exhibited a good linear response to PhSH within the range of 0-9 μM, and the limit of detection (LOD) is 21 nM. Furthermore, probe P1 has been successfully applied for the efficient and rapid PhSH detection in environmental water and actual food samples.

A FRET probe based on flavonol-benzothiazole for the detection of viscosity and SO2 derivatives

Sulfur dioxide (SO2) and viscosity play important roles in living organisms, and abnormal levels of them are associated with many diseases. Hence, a bifunctional fluorescence probe (E)-3-(2-(4-(4-(4-(6-fluoro-3-hydroxy-4-oxo-4H-chromen-2-yl)benzoyl)piperazin-1-yl)styryl)benzo-[d]thiazol-3-ium-3-yl)propane-1-sulfonate (HFBT) with fluorescence resonance energy transfer (FRET) properties was successfully constructed by using 3-hydroxyflavonol as the energy donor and benzothiazole sulphonate derivatives as the energy acceptor, and it can be used for the detection of SO2 derivatives (HSO3−/HSO32−) and viscosity. HFBT exhibits a large Stokes shift (245 nm), high resonance energy transfer efficiency (95.56 %), and excellent selectivity, anti-interference and low limit of detection (LOD = 0.057 μM) for HSO3−. The fluorescence intensity of HFBT at 608 nm gradually increases with the increase of viscosity. Interestingly, a visual HSO3− detection platform was successfully constructed and applied to the quantitative detection of HSO3− in food. Additionally, HFBT was successfully applied to imaging endogenous and exogenous HSO3− in cells. The successful development of HFBT provides an effective tool for the detection and imaging of HSO3− in food and cells.

Excitonic origin of the optical properties of CsPbBr3

The optical properties of CsPbBr3 are studied with temperature dependent spectroscopic techniques. The samples are obtained from a method that has 10 % Pb waste compared with conventional ones. The dependence with temperature between 30 K and room temperature of the optical transmittance and photoluminescence is measured. Near bandgap optical properties are governed by structures originated in free excitons. Using the Elliott model for excitonic absorption, the dependence with temperature of bandgap energy and exciton binding energy are obtained. Both increase with temperature increase. Also, the width of the excitonic absorption and the inter-band absorption, which is assimilated to Urbach energy, were studied. Several models are used to extract parameters from these data. The excitonic absorption width follows the Segall model giving an exciton optical phonon interaction as the dominant term at room temperature. From several fittings, an effective optical phonon energy between 23 and 32 meV is obtained. The Urbach energy at 30 K reaches 10 meV which is related to a good crystalline quality of the samples. Several experimental results show that the origin of the photoluminescence is produced by direct recombination of free excitons. The first one is the similarity of the temperature dependence of photoluminescence width with the one of excitonic absorption. The second one is based in the activation energies obtained from the dependence of the integrated photoluminescence with temperature, one of which coincides with Excitonic Biding Energy. The third one is related to the dependence of the Stokes Shift with temperature which corresponds to the Gurioli model of excitonic thermalization. The last one comes from the dependence of the time resolved photoluminescence. Using rate equations, a radiative and non-radiative monomolecular time constant between 32 and 50 ns and an exciton-exciton annihilation rate constant between 1.0 and 6.0 × 10−7 cm3/s are obtained.

Novel BODIPY-based NIR fluorescent probe with appropriate Stokes shift for diagnosis and treatment evaluation of epilepsy via imaging ONOO− fluctuation

Epilepsy is a chronic brain disorder characterized by recurrent seizures that has severely threatened human health. Cumulative research achievements uncover that the pathological progression of epilepsy is closely related to peroxynitrite (ONOO−). In this work, we first constructed BODIPY dye containing pyridine group and indoline group to make it have the donor-acceptor structure, thus achieving NIR emission wavelength (740 nm) and appropriate Stokes shift (80 nm). Based on the BODIPY dye, the novel probe BDP-NIR-Fa was developed that displayed good specificity, faster response speed (60 s), and high signal to noise ratio (247-fold) for monitoring ONOO−. Based on these excellent properties, BDP-NIR-Fa was able to trace endogenous/exogenous ONOO− fluctuations in living cells and mice without interference from other reactive oxygen species. Most importantly, BDP-NIR-Fa could visualize the changes of endogenous ONOO− with remarkable temporal-spatial resolution in KA-induced seizures cell and mice models, that furnishing a potentially forceful tool for diagnosing epilepsy. Finally, BDP-NIR-Fa successfully realized imaging the concentration reduction of ONOO− in epilepsy model during the treatment by an antiepileptic drug. Therefore, the present work provided a reliable approach to investigate the diagnosis and therapy of epilepsy via imaging ONOO− fluctuation.

Development of Donor-acceptor-type Molecules and Their Application as Analytical Reagents

π-Extended donor-acceptor (D-A)-type molecules, which bear both electron-donor and electron-acceptor substituents on the backbone, exhibit unique optical properties, such as bathochromic shifts in absorption and emission, large Stokes shifts, solvatochromic behavior, and fluorescence quenching in polar solvents. These unique properties are attributed to intramolecular charge transfer (ICT) or twisted intramolecular charge transfer (TICT) in the ground and excited states. This review article introduces three types of D-A-type molecules that are used as detection reagents for (1) methanol, (2) amino acids during solid-phase peptide synthesis (SPPS), and (3) amines present in the biological environment. For methanol detection, D-A-type fluorophores with basic guanidine moieties were developed to differentiate between methanol (MeOH) and ethanol (EtOH) based on the small difference in their pKa values (ΔpKa=0.4). Selective protonation of the guanidine moiety in methanol disrupts the D-A structure, allowing emission in the resultant polar environment. Similarly, an acid-base reaction between the hydrogen chloride (HCl) salts of the D-A-type molecules and amines is applied to detect amines during SPPS. In this method, a colorless solution of an HCl salt of the D-A-type molecule is deprotonated by amines, forming a yellow solution. This is the first reported quantitative and non-destructive colorimetric method for detecting amines. Finally, a turn-on-type amine-labeling reagent was developed for the nucleophilic aromatic substitution (SNAr) reaction. This new reagent enables protein staining of living cells with a large Stokes shift and without solvent-polarity-dependent fluorescence quenching.

Fluorescence and colorimetric dual-mode sensing of copper ions and fingerprint visualization by benzimidazole derivatives

In this paper, the molecular fluorescence probe H containing an imidazole structure was designed and synthesized by forming a ring between two amino groups and one aldehyde group. The synthesized probe H exhibits a Stokes shift of 144 nm with fluorescence emission at 555 nm and excitation at 411 nm. The fluorescence of probe H was quenched by the addition of Cu2+ and accompanied a red-shift of ultraviolet–visible (UV–Vis) absorption spectrum. Probe H reveals good selectivity and high sensitivity to Cu2+ in the fluorescence and UV–Vis absorption spectrum. And the limit of detection (LOD) for Cu2+ by fluorescence and UV–Vis spectrum methods were 0.14 nmol L−1 and 1.34 μmol L−1, respectively. The binding ratio of probe H and Cu2+ is 1:1 according to the Job’s plot equation. High resolution mass spectrometry (HRMS) and density function theory (DFT) calculations proved that the solvent acetonitrile and anionic chloride ion participated in the formation of H-Cu2+ complex. Furthermore, the established fluorescence analytical method was successfully applied for the detection of Cu2+ and spiked recovery experiments in tap water and mineral water. In addition, the probe exhibited outstanding solid-state fluorescence because of its excellently planar structure, and displayed a secondary fingerprint structure in the application of fingerprint detection.

Fluorescence switching of triarylamine-based polyamides with pendant pyrene units and its application in electrochromic smart displays

The pyrene group was directly connected to the triarylamine (TAA) unit through a benzene bridge via the Suzuki reaction to successfully prepare the diamine monomer. A series of new polyamides (PAs) based on TAA units were prepared by polycondensation. The PAs exhibited good solution processability and high thermal stability with the char yield in excess of 53% at 800°C in air atmosphere. In solvents with different polarities, these PAs showed solvatochromic effect and large stokes shift. Strongly photoluminescent PAs have a sensitive stimulus response to explosive and hazardous gas, and its fluorescence is easily turned off by the addition of trinitrophenol (TNP) and hydrogen chloride (HCl). And achieve fluorescence switching between exposure to HCl and ammonia (NH3) gas. The PAs exhibited a reversible color response in the electrochemical oxidation process, with no significant degradation in current and transmittance after 200 cycles. The sandwich structure multicolor electrochromic device can achieve electrochromic performance applied by different voltages.

Red fluorescent AIE bioprobes with a large Stokes shift for droplet-specific imaging and fatty liver diagnosis

Lipid droplets (LDs) as spherical dynamic subcellular organelles, play an important role in various cellular functions such as protein degradation, lipid metabolism, energy storage, signal transduction, and membrane formation. Abnormal function of LDs will lead to a series of diseases and hence monitoring the status of LDs is particularly important. In this study, we synthesized a water-insoluble red fluorescent emitting small molecule fluorescent probe (TPE-TCF), which exhibited aggregation-induced emission (AIE) properties and enabled highly selective real-time imaging of LDs (Pearson’s R value was 0.90). More interestingly, this probe was able to track the dynamic processes of LDs in living cells, including lipophagy, and monitor fatty liver disease in mice. Therefore, TPE-TCF with red fluorescence emission, good biocompatibility, large Stokes shift, AIE properties, LDs imaging, and fatty liver recognition capabilities can be practically used in more LDs-related diseases.

Self–Trapped Exciton versus Band–Edge Electron Transitions: Insights of the Factors Affecting the Optical Properties of Lead–Free Sn–Halide Perovskites

AbstractLead–free Sn–halide perovskites (Sn–HPs) are attractive photomaterials due to their lower toxicity, and some of them with higher stability against moisture and water, compared to their Pb‐based analogous. Interestingly, Sn‐HPs can exhibit two types of optical characteristics: the first scenario is known as band‐edge electron transitions [or band‐to‐band (b‐b) emission], where accumulated electrons in the conduction band recombine with holes in the valence band, providing a close separation between the absorption edge/photoluminescence (PL) peak (small Stokes shift). The second scenario is denominated as self‐trapped exciton (STE), where intraband gap energy states are formed to trap photocarriers generated in the perovskite, producing a broadband PL and a large Stokes shift. These optical features have been suitable for developing prominent devices, but there is no consolidated explanation about the key factors influencing the emergence of b–b emission or STE in Sn‐HPs, mainly the presence of these PL mechanisms in a particular perovskite system. This review highlights how the chemical composition, structural defects, and synthetic procedures are pivotal to producing Sn‐HPs with specific b–b or STE features. This will allow the preparation of Sn‐HPs with better quality/stability, and facile modulation of their PL properties, expanding their future applicability in LCD technologies.

Synthesis of low-dimensional metal halide CsAgCl2 for X-ray scintillation applications

Low-dimensional metal halides, which possess efficient luminescent properties, have garnered significant interest in the fields of optoelectronics and radiation detection. This study introduces novel lead-free silver-based metal halide material, CsAgCl2 microcrystals (MCs). These MCs have a one-dimensional atomic chain structure and a unique [AgCl5]4- tetragonal shared triangular configuration. CsAgCl2 MCs exhibit excellent performance as X-ray scintillators due to their bright broadband yellow emission and fast decay time in the microsecond range. The large Stokes shift of 350 nm is produced by self-trapped exciton emission. In X-ray scintillation applications, CsAgCl2 MCs demonstrate a high light yield of 13280 photons/MeV and a wide range of linear scintillation response. It is noteworthy that the CsAgCl2 MCs maintain good stability under both atmospheric conditions and continuous X-ray irradiation. The sample was used in an X-ray imaging screen, which clearly presented the X-ray projection image of a wooden stick. As a result, this research not only contributes to the collection of lead-free metal halide scintillators but also indicates that CsAgCl2 MCs have a wide range of future applications and potential in areas such as medical imaging, scientific research, and diagnostic and detection technologies.

A ratiometric fluorescent probe based on phenothiazine and quinazolinone for rapid detection of ClO− and its application

A novel fluorescent probe (BPQ-1) with large conjugated system (phenothiazine was conjugated with quinazolinone) was synthesized. BPQ-1 showed a remarkable ratiometric fluorescence response to ClO− within 10 s, and achieved large stokes shift (168 nm), high sensitivity (LOD = 16.7 nM) and excellent selectivity. Among the analytes to be detected, there is a significant change from bright yellow fluorescence to cyan fluorescence only when ClO− is added to BPQ-1. Through density functional theory calculation and mass spectrometry experiments, the fluorescence response mechanisms of the BPQ-1 are given. In addition, BPQ-1 has been successfully applied to the detection of ClO− in real water samples and test strips for detecting ClO− with different concentrations have been prepared. In particular, the probe has been successfully applied to the fluorescence imaging of exogenous ClO− in living cells.

Quantum Dot Reporters Designed for CRISPR-Based Detection of Viral Nucleic Acids.

Diagnostic methods based on CRISPR technology have shown great potential due to their highly specific, efficient, and sensitive detection capabilities. Although the majority of the current studies rely on fluorescent dye-quencher reporters, the limitations of fluorescent dyes, such as poor photostability and small Stokes shifts, urgently necessitate the optimization of reporters. In this study, we developed innovative quantum dot (QD) reporters for the CRISPR/Cas systems, which not only leveraged the advantages of high photoluminescence quantum yield and large Stokes shifts of QDs but were also easily synthesized through a simple one-step hydrothermal method. Based on the trans-cleavage characteristics of Cas12a and Cas13a, two types of QD reporters were designed, the short DNA strand and the hybridization-based QD reporters, achieving the detection of DNA and RNA at the pM level, respectively, and validating the performance in the analysis of clinical samples. Furthermore, based on the unique property of QDs that allowed multicolor emission under one excitation, the application potential for simultaneous detection of diseases was further investigated. Taken together, this work proposed novel QD reporters that could be applied to the various CRISPR/Cas systems, providing a new toolbox to expand the diagnosis of bioanalytical and biomedical fields.

A novel fluorescent probe for fast detection of sulfur dioxide derivatives in water, soil, food samples and its applications in biological imaging

Sulfur dioxide (SO2) has a wide range of applications in food additives and industrial production, and it is one of the main substances that form acid rain, causing serious harm to ecosystems and human health. Hence, it is necessary to construct an effective tool to quickly and accurately detect SO2 derivatives in environmental, food, and biological samples. In this study, fluorescent probe NPMQ was built to detect SO2 derivatives from nopinone with the merits of superior water solubility, high sensitivity (12nM), excellent specificity, large Stokes shift (180nm), and rapid response time (within 5s). NPMQ was used to qualitatively and quantitatively detect SO2 derivatives in environmental water, soil and food samples. In addition, an electrospinning film was prepared with the probe NPMQ to image SO2 derivatives, and test strips are capable of rapidly, sensitively, and selectively detecting SO2 derivatives with the naked eye. Moreover, the probe NPMQ was used to visualize endogenous SO2 derivatives in Arabidopsis thaliana under Cd2+ stress. Furthermore, the probe NPMQ was employed to image exogenous and endogenous SO2 derivatives in living Hela, HepG-2 cells, and zebrafish. This study develops an effective tool for monitoring SO2 derivatives in the environmental, food, and biological systems.