Fluorescence Quantum Yield Research Articles

Design and Construction of Highly Luminescent Transparent Woody Materials Exhibiting Unique Fluorescence-Enhanced Staining Effects for Visualization of Intrinsic Microporous Networks.

Luminescent wood materials are an emerging class of biomass hybrid host materials owing to the hierarchical porous structure and functionalization versatility. The fluorescence properties are largely dependent on exogenous fluorophores, which are, however, often plagued by notorious aggregation effects. In this work, an efficient strategy for the preparation of luminescent transparent wood materials is developed by incorporating tetraphenylethylene-derived aggregation-induced emission (AIE)-active fluorophores during a delignification-backfill transparency process. These wood hybrids showed unexpected luminescence enhancement that significantly increased the fluorescence quantum yield of the fluorophores up to 99%, much higher than that of the fluorophores in other states such as crystalline solids or doped in a polymer substrate. Mechanistic investigations reveal that in situ polymerization of prepolymerized methyl methacrylate in delignified microporous wood frames produces high molecular weight ordered PMMA polymers, resulting in a rigid molecular environment that improves the luminescence efficiency of TPE-based fluorophores at the interfaces of PMMA polymer and cell walls. By confocal laser scanning microscopy (CLSM), this excellent fluorescence staining capability was furthermore utilized to visualize the intrinsic porous network of wood in three dimensions over a large volume with submicrometer resolution, thus providing an alternative approach to the study of structure-function relationships in such wood hybrids.

Mercury (Hg2+) Sensing Using Coumarin-Derived Fluorescent Chemo-Sensors: An Intuitive Development from 2015 to 2023.

Mercury is known as a highly toxic metal that is poisonous even if present in a trace amount. Generally, it enters in the food chain (especially fish) and water resources via different pathways and leads to harmful effects. Owing to the detrimental nature of the metal, traditionally several methods were employed by researchers for regular monitoring of the mercury metal ions. However, these methods are associated with many limitations like high cost of technical expertise, and intricacy of the detection procedure. So, using these methods to detect mercury ions in real time is challenging. Therefore, in recent years fluorescent-based analytical tools emerged rapidly. Among the various fluorescent organic scaffolds, coumarin has been scorching, owing to quick response, light stability, high sensitivity, good selectivity, excellent fluorescence intensity, and fluorescence quantum yield. This review provides a deep dive into the coumarin-derived chemo-sensors development throughout 2015-2023. We anticipate that the review will assist to broad scientific community as a reference document to design more interesting sensors.

General Post-Regulation Strategy of AIEgens' Photophysical Properties for Intravital Two-Photon Fluorescence Imaging.

Fluorogens with aggregation-induced emission (AIEgens) are promising agents for two-photon fluorescence (TPF) imaging. However, AIEgens' photophysical properties are fixed and unoptimizable once synthesized. Therefore, it is urgent and meaningful to explore an efficient post-regulation strategy to optimize AIEgens' photophysical properties. Herein, a general and efficient post-regulation strategy is reported. By simply tuning the ratio of inert AIEgens within binary nanoparticles (BNPs), the fluorescence quantum yield and two-photon absorption cross-section of functional AIEgens are enhanced by 8.7 and 5.4 times respectively, which are not achievable by conventional strategies, and the notorious phototoxicity is almost eliminated. The experimental results, theoretical simulation, and mechanism analysis demonstrated its feasibility and generality. The BNPs enabled deep cerebrovascular network imaging with ≈1.10mm depth and metastatic cancer cell detection with single-cell resolution. Furthermore, the TPF imaging quality is improved by the self-supervised denoising algorithm. The proposed binary molecular post-regulation strategy opened a new avenue to efficiently boost the AIEgens' photophysical properties and consequently TPF imaging quality.

Synthesis of uniform sized ZnS quantum dots using hydrodynamic cavitation and their characterization

As representative non-toxic cadmium-free quantum dots (QDs), ZnS QDs with high quantum efficiency, super stability and excellent biocompatibility had attracted wide attention in the fields of photocatalysis, solar cells and biomedicine. In this study, hydrodynamic cavitation (HC) technology was applied to the preparation of ZnS QDs. By adjusting HC device parameters, water soluble ZnS QDs with small particle size, narrow particle size distribution range, high absorbance, high luminous efficiency and high quantum yield were prepared. The morphology, size distribution, element composition and optical properties of ZnS QDs were studied by various characterization methods. ZnS QDs with average particle size of 1.48 nm, fluorescence quantum yield of 34.07% and Stokes shift of 112 nm were obtained. In addition, the mechanism of preparation of ZnS QDs by using HC method was also studied. It is hoped that this HC technology can provide a new idea for large-scale preparation of ZnS QDs with excellent properties.

Tetraphenylethylene tethered 1-(pyridine-2-yl)imidazo[1,5-a]pyridine: Synthesis, aggregation induced emission, copper(II) ion detection and imaging of latent fingerprint

The development of aggregation induced emissive probe with high sensitivity and selectivity for Cu2+ ions is a fascinating research in biomedical sciences. In this context, we have successfully synthesized an aggregation induced emissive probe for the selective detection of Cu2+ ions by incorporating a 1-(pyridine-2-yl)imidazo[1,5-a]pyridine arm in the tetraphenylethylene framework. The aggregates have been characterized using pivotal microscopic and photophysical measurements. The results exhibits that the aggregates have a spherical shape with an average size of 90 nm and a fluorescence quantum yield of ∼23 %. The aggregated fluorescent probe exhibited an excellent selectivity towards Cu2+ ions with a detection limit of 83 nM and presented a good efficacy over diverse environmental water samples. Furthermore, the quenching type is delineated as static due to complexation followed by deaggregation which was supported by dynamic light scattering and Tyndall effect experiments. In addition, the high solid state emissive property of the probe makes it a potential candidate for latent fingerprint analysis to gather level 2 and 3 information thereby playing a substantial role in forensic investigations.

Self-assembled dipeptide confined in covalent organic polymers for fluorescence sensing of tryptamine in fermented meat products.

Diphenylalanine(FF)-Zn self-assembly (FS) confined in covalent organic polymers (FS@COPs) with efficient fluorescence was synthesizedfor fluorescence sensing of biogenic amines, which was one of the most important indicators for monitoring food freshness. FS@COPs combined excellent biodegradability of self-assembled dipeptide with chemical stability, porosity and targeted site recognition of COPs. With an optimal excitation wavelength of 360 nm and an optimal emission wavelength of 450 nm, FS@COPs could be used as fluorescence probes to rapidly visualize and highly sensitive determination of tryptamine (Try) within 15 min, and the linear range was from 40 to 900 μg L-1 with a detection limit of 63.08 μg kg-1. Importantly, the FS@COPs showed a high fluorescence quantum yield of 11.28%, and good stability, solubility, and selectivity, which could successfully achieve the rapid, accurate and highly sensitive identification of Try. Furthermore, we revealed the mechanism of FS@COPs for fluorescence sensing of targets. The FS@COPs system was applied to the fluorescence sensing of Try in real samples and showed satisfactory accuracy of 93.02%-105.25%.

Biomass-derived sensor for selective detection of Fe(III) ions in non-aqueous environments

Eco-friendly biomass-derived nanocarbons have gained considerable attention for detecting metallic pollutants, such as iron, in the environment. In addition, fluorescence probes are in high demand due to the growing need for iron detection in various organic solvents. Herein, we synthesize luminescent biomass-derived carbon nanoparticles (BMCNPs) from Kalanchoe pinnata plant leaves using a simple single-step solvothermal method. The synthesized BMCNPs emit red fluorescence in non-aqueous environments (organic solvents) and exhibit excellent fluorescence stability and solubility in both aqueous and non-aqueous media. The quenching of fluorescence emissions from BMCNPs in non-aqueous medium, facilitated by the addition of Fe(III) ions, demonstrates the ability of BMCNPs to serve as probes for detecting trace quantities of iron impurities. Experimental results confirm that the fluorescence from the BMCNPs is influenced by a ligand-to-metal charge transfer-assisted dynamic quenching mechanism. The proposed sensor is suitable for the real-time detection of iron in organic solvents, where iron contamination occurs due to the corrosion of iron metal. The fluorescence quantum yield of the probe is determined to be ∼11 %. The detection limit for Fe(III) in N,N-dimethylformamide using the synthesized probe is determined to be 1.9 µM. This study provides a platform for detecting Fe(III) ions in non-aqueous media. The proposed probe overcomes the limitation of Fe(III) ion-specific aqueous solubility, enabling the detection of Fe(III) ions in non-aqueous media due to the solubility and red emission specificity of BMCNPs in non-aqueous environments.

Comprehensive Review of Synthesis, Optical Properties and Applications of Heteroarylphosphonates and Their Derivatives.

This review focuses on optical properties of compounds in which at least one phosphonate group is directly attached to a heteroaromatic ring. Additionally, the synthesis and other applications of these compounds are addressed in this work. The influence of the phosphonate substituent on the properties of the described compounds is discussed and compared with other non-phosphorus substituents, with particular attention given to photophysical properties, such as UV-Vis absorption and emission, fluorescence quantum yield and fluorescence lifetime. Considering the presence of heteroatom, the collected material was divided into two parts, and a review of the literature of the last thirty years on heteroaryl phosphonates containing sulfur and nitrogen atoms in the aromatic ring was conducted.

Tetraphenylethylene-based conjugated polymers with valine-containing side chains: Aggregation-induced emission, helical self-assembly, complexation-induced circularly polarized luminescence

Realizing high circularly polarized luminescence (CPL) in polymer system is an important but challenging task. Herein, we provide a strategy for designing conjugated polymers with high CPL performance upon the complexation with mandelic acids. Two tetraphenylethylene (TPE)-based conjugated polymers, l-P1 and d-P1, were synthesized by Sonogashira polycoupling reactions between the TPE-containing diethynyl monomer and dibromo aryl monomers carrying valine methyl ester groups. Both the polymers showed aggregation-induced emission (AIE) properties and the capabilities to self-assemble into regular helical nanostructures on nanoscale and fluorescent microfibers on microscale. They exhibited weak circular dichroism (CD) signals; upon the complexation with R/S-mandelic acids, their CD absorption and fluorescence emission can be efficiently enhanced. The composite films of l/d-P1 and R/S-mandelic acids exhibited excellent complexation-induced CPL properties with the absolute luminescence dissymmetric factor (glum) up to 0.01 and the fluorescence quantum yield up to 26.8%; the glum values showed little dependence on their emission wavelength. Various types of carboxyl acids have been screened and only mandelic acids show significantly chiroptical induction. The specific interaction between mandelic acids and l/d-P1 also makes the latter promising candidates for the enantioselective recognition of chiral organic molecules.

Selective detection of MnO4- in non-standard explosives by nitrogen-doped carbon quantum dots-copper complexes (NCQDs@Cu)

Nitrogen-doped carbon quantum dots (NCQDs) with bright yellow fluorescence (quantum yield of 27.3 %) were synthesized via a solvothermal method using 2,3-diaminopyridine as the carbon and nitrogen source and ethanol as the solvent. Subsequently, the NCQDs were reacted with Cu2+ in an aqueous solution, forming nitrogen-doped carbon quantum dots-copper complexes (NCQDs@Cu) with great potential for selective determination of MnO4- ions. The aqueous solution of NCQDs@Cu exhibiting a very weak fluorescence (quantum yield of 2.2 %) demonstrated a significant enhancement (quantum yield of 10.0 %) upon interaction with MnO4-(Turn-on). Furthermore, this enhancement remained unaffected by the interfering conventional or unconventional explosives, inorganic ions, and oxidants. Moreover, a good linear relationship existed between the fluorescence intensity of the NCQDs@Cu and the concentration of the permanganate ions in a range of 0 to 5 μmol/L with a detection limit of 32.4 nmol/L. Additionally, the study investigated the underlying principles of the detection mechanism using advanced technologies such as X-ray photoelectron spectroscopy(XPS), The Fourier-transform infrared (FTIR), ultraviolet visible spectrometer (UV–Vis), fluorescence spectrometer and other methods. Finally, the NCQDs@Cu were successfully applied for detecting MnO4- in simulated and actual unconventional explosives, demonstrating a good correlation with standard methods. Therefore, the developed NCQDs@Cu can be used for rapid on-site inspection in explosive incident scenarios. This new method of using carbon dots-metal complexes as fluorescent probes will also provide new ideas for researchers.

Synthesis and properties of a visual fluorescence-enhanced HClO/ClO- probe

Hypochlorite ion (ClO-/HClO) is a reactive oxygen species that plays a vital role in biological systems and daily life. The accurate detection of ClO- is critical for disease prevention and environmental monitoring. Therefore, it is necessary to develop highly sensitive probes. In this study, we report a visual fluorescence-enhanced HClO/ClO- probe CN-TPE-PEG1900, which was obtained by grafting poly (ethylene glycol) monomethyl ether 1900 with tetraphenylethylene (TPE) as the fluorescent parent. The fluorescence intensity of a solution containing CH3OH/H2O (30 μM, v/v, 1/4, PBS, pH = 7.4) and the probe CN-TPE-PEG1900 was increased by 9 times at 525 nm due to the presence of ClO-. The color of the probe CN-TPE-PEG1900 solution changed from yellow to colorless after reaction with ClO-. The limit of detection (LOD) of the probe CN-TPE-PEG1900 was 5.48 × 10–8 mol/L. In addition, it had a high fluorescence quantum yield of 51.27 %, a large Stokes shift of 165 nm, good water solubility, and high water sample recovery rates. The calculated data, 1H NMR, mass spectrometry, DLS, and SEM results were combined to deduce the recognition mechanism of the probe CN-TPE-PEG1900 for ClO-. Thus, the presence of ClO- facilitated the cleavage of the double bond in CN-TPE-PEG1900, thereby separating the water-soluble poly (ethylene glycol) chain from TPE through oxidative cleavage. Moreover, this led to the formation of TPE-CHO, which was less water-soluble and more prone to aggregation, resulting in fluorescence enhancement at 525 nm. Meanwhile, the process also caused a blue shift in the emission wavelength and a change in the color of the probe solution.

Erythrocyte nano-ghosts with dual optical and magnetic resonance characteristics.

Fluorescent organic dyes provide imaging capabilities at cellular and sub-cellular levels. However, a common problem associated with some of the existing dyes such as the US FDA-approved indocyanine green (ICG) is their weak fluorescence emission. Alternative dyes with greater emission characteristics would be useful in various imaging applications. Complementing optical imaging, magnetic resonance (MR) imaging enables deep tissue imaging. Nano-sized delivery systems containing dyes with greater fluorescence emission as well as MR contrast agents present a promising dual-mode platform with high optical sensitivity and deep tissue imaging for image-guided surgical applications. We have engineered a nano-sized platform, derived from erythrocyte ghosts (EGs), with dual near-infrared fluorescence and MR characteristics by co-encapsulation of a brominated carbocyanine dye and gadobenate dimeglumine (Gd-BOPTA). We have investigated the use of three brominated carbocyanine dyes (referred to as BrCy106, BrCy111, and BrCy112) with various degrees of bromination, structural symmetry, and acidic modifications for encapsulation by nano-sized EGs (nEGs) and compared their resulting optical characteristics with nEGs containing ICG. We find that asymmetric dyes (BrCy106 and BrCy112) with one dibromobenzene ring offer greater fluorescence emission characteristics. For example, the relative fluorescence quantum yield ( ) for nEGs fabricated using of BrCy112 is -fold higher than nEGs fabricated using the same concentrations of ICG. The dual-mode nEGs containing BrCy112 and Gd-BOPTA show a nearly twofold increase in their as compared with their single optical mode counterpart. Cytotoxicity is not observed upon incubation of SKOV3 cells with nEGs containing BrCy112. Erythrocyte nano-ghosts with dual optical and MR characteristics may ultimately prove useful in various biomedical imaging applications such as image-guided tumor surgery where MR imaging can be used for tumor staging and mapping, and fluorescence imaging can help visualize small tumor nodules for resection.

Nitrogen-Doped Carbon Quantum Dots with Photoactivation Properties for Ultraviolet Ray Detection.

Photoactivation is a phenomenon that could enhance the photoluminescence (PL) and photostability upon UV/vis light exposure, which is usually observed in CdSe/ZnS quantum dots (QDs). However, the photoactivation phenomenon has been scarcely reported in fluorescent carbon quantum dots (CQDs). Herein, the nitrogen-doped carbon quantum dots (N-CQDs) were prepared through a facile solvothermal approach with naphthalenetracarboxylic dianhydride and serine as precursors. Upon simple UV light irradiation for 10 min, the fluorescence quantum yield (QY) of N-CQDs could increase up to 10-fold. Based on this phenomenon, the N-CQDs were explored as an ultraviolet (UV) light sensor to assess the intensity of ultraviolet radiation in sunlight and indirectly evaluate the UV-blocking efficiency of various sunscreen products. Thus, this contribution not only provided an insight into developing a low-cost UV detector but also opened a door for the development of carbon quantum dots with converse-photobleaching properties.

Synthesis, enantiomeric separation and (chir)optical properties of [7]helicene derivatives for OLED applications. A comprehensive experimental and computational investigation

A two–step photochemical process was employed to synthesize new racemic [7]helicenes with appropriate functional groups, resulting in an overall yield of 61 % to 74 %. These helical species showed good solubility in common solvents and confirmed structurally through various spectroscopic methods. In solution, they exhibited strong absorption (λabs = 250–500 nm) and blue light emission with a fluorescence quantum yield (Φ) ranging from 7 % to 26 %. Experimental analysis of their HOMO and LUMO energy levels highlighted an irreversible electrochemical behavior and a band gap (Eg–el) of 2.60 eV to 2.64 eV. The helicenes were successfully separated by chiral HPLC, yielding P and M–enantiomers in high optical purity (>98.5 % up to >99.5 % ee) that demonstrated substantial optical rotations (e.g., +3700–5000 for the P–enantiomer at λ = 589 nm) and notable electronic circular dichroism (ECD) signals. Density functional theory (DFT) was undertaken to establish connections between diverse structure-properties relationships and precisely replicate the experimental findings. Ultimately, these helical species, with notable performance in emission, electrochemical behavior, and thermal stability, can effectively serve as blue-emitting chiral dopants in OLED devices and as hole-transport units.

π-π conjugated PDI supramolecular regulating the photoluminescence of imine-COFs for sensitive smartphone visual detection of levofloxacin

As the contamination and enrichment in food chain of levofloxacin (LV) antibiotics have caused a significant threat to life safety, the instant detection of LV has become an urgent need. Here, a PDI-functionalized imine-based covalent organic framework (PDI-COF300) was prepared by the electrostatic self-assembly method as fluorescent probe for smartphone visual detection of LV, which exhibited excellent fluorescence quantum yield (82.68%), greater stability, high sensitivity with detection limit of 0.303 μM. Based on the results of molecular docking and Stern-Volmer equation, the LV detection by PDI-COF300 was mainly a static quenching process through π-π stacked hydrophobic interactions and fluorescence resonance energy transfer. Besides, PDI-COF300 was applied to LV detection in environmental medium and milk samples with recoveries from 85.56% to 108.34% and relative standard deviations <2.70%. This work also provided a new general strategy for using PDI-COF in smartphone devices and fluorescent papers for LV fluorescence detection and microanalysis.

Exploiting Mixed Valence Charge Transfer for Electrochromic and Electrofluorochromic Use.

An asymmetric mixed valence fluorophore with two different electron rich termini was investigated as a dual-role active material for electrochromism and electrofluorochromism. The fluorescence quantum yield (Φfl) and emission wavelength of the fluorophore were dependent on solvent polarity. The quantum yield of the material in an electrolyte gel, on a glass substrate and in a device was 40 %, 20 % and 13 % respectively. The fluorophore further underwent two near-simultaneous electrochemical oxidations. The first oxidation resulted in a 1000 nm red shift in the absorption to broadly absorb in the NIR, corresponding to the intervalence charge transfer (IVCT). Whereas the second oxidation led to a perceived green color at 715 nm with the extinction of the NIR absorbing IVCT. Owing to the dissymmetry of the fluorophore along with its two unique oxidation sites, the IVCT gives rise to a mixed valence transfer charge (MVCT). The coloration efficiency of the fluorophore in both solution and a device was 1433 and 200 cm2 C-1, respectively. The fluorescence intensity could be reversibly modulated electrochemically. The photoemission intensity of the fluorophore was modulated with applied potential in an operating electrochromic/electrofluorochromic device. Both the dual electrochromic and the electrofluorochromic behavior of the fluorophore were demonstrated.

Asparagus officinalis Herb-Derived Carbon Quantum Dots: Luminescent Probe for Medical Diagnostics.

The utilization of natural materials for the synthesis of highly fluorescent carbon quantum dots (CQDs) presents a sustainable approach to overcome the challenges associated with traditional chemical precursors. Here, we report the synthesis of novel S,N-self-doped CQDs (S,N@CQDs) derived from asparagus officinalis herb. These S,N@CQDs exhibit 16.7 % fluorescence quantum yield, demonstrating their potential in medical diagnostics. We demonstrate the efficacy of S,N@CQDs as luminescent probes for the detection of anti-pathogenic medications metronidazole (MTZ) and nitazoxanide (NTZ) over concentration ranges of 0.0-180.0 μM (with a limit of detection (LOD) of 0.064 μM) and 0.25-40.0 μM (LOD of 0.05 μM), respectively. The probes were successfully applied to determine MTZ and NTZ in medicinal samples, real samples, and spiked human plasma, with excellent recovery rates ranging from 99.82 % to 103.03 %. Additionally, S,N@CQDs demonstrate exceptional efficacy as diagnostic luminescent probes for hemoglobin (Hb) detection over a concentration range of 0-900 nM, with a minimal detectability of 9.24 nM, comparable to commercially available medical laboratory diagnostic tests. The eco-friendly synthesis and precise detection limits of S,N@CQDs meet necessary analytical requirements and hold promise for advancing diagnostic capabilities in clinical settings. This research signifies a significant step towards sustainable and efficient fluorescence-based medical diagnostics.

Benzo-Crown-Ether Functionalized O-BODIPY Probes for Cations - A Selective Fluorescent Probe for Ba2.

Herein, we report the synthesis and sensing characteristics of 4,4'-methoxy-substituted BODIPY fluorescent probes (O-BODIPYs) 3, 4 and 5 equipped with differently sized benzo-crown ethers (cf. Scheme 1, 3 (benzo-15-crown-5), 4 (benzo-18-crown-6) and 5 (benzo-21-crown7)). O-BODIPYs 3, 4 and 5 exhibited in comparison to their known F-BODIPY analogues 3a, 4a and 5a (cf. Scheme 1) an improved solubility in aqueous medium and higher fluorescence quantum yields. Fluorometric study in aqueous solutions of 3, 4 and 5 in the presence of different cations show cation induced fluorescence enhancements (FE). Compared to the benzo-crown ether substituted F-BODIPY analogues 3a, 4a and 5a, we found for the free O-BODIPYs 3, 4 and 5 higher fluorescence quantum yields (φf) but lower cation induced FEs. We show that in aqueous medium the fluorescence quenching process (OFF switching), a photoinduced electron transfer, in O-BODIPYs 3, 4 and 5 is less effective and consequently sensitive and selective ON switching of the fluorescence by cations, too. Albeit these observations the novel benzo-21-crown-7 equipped fluorescent probe 5 exhibits a good fluorometric Ba2+ selectivity and Ba2+ sensitivity in conjunction to their aqueous solubility.

Studies of Anticancer Activities In Vitro and In Vivo for Butyltin(IV)-Iridium(III) Imidazole-Phenanthroline Complexes with Aggregation-Induced Emission Properties.

Organotin(IV) and iridium(III) complexes have shown good application potential in the field of anticancer; however, the aggregation-caused quenching (ACQ) effect induced by high concentration or dose has limited the research on their targeting and anticancer mechanism. Then, a series of aggregation-induced emission (AIE)-activated butyltin(IV)-iridium(III) imidazole-phenanthroline complexes were prepared in this study. Complexes exhibited significant fluorescence improvement in the aggregated state because of the restricted intramolecular rotation (RIR), accompanied by an absolute fluorescence quantum yield of up to 29.2% (IrSn9). Complexes demonstrated potential in vitro antiproliferative and antimigration activity against A549 cells, following a lysosomal-mitochondrial apoptotic pathway. Nude mouse models further confirmed that complexes had favorable in vivo antitumor and antimigration activity in comparison to cisplatin. Therefore, butyltin(IV)-iridium(III) imidazole-phenanthroline complexes possess the potential as potential substitutes for platinum-based drugs.

Holistic analysis of a gliding arc discharge using 3D tomography and single-shot fluorescence lifetime imaging

Gliding arc plasmas, a versatile form of non-thermal plasma discharges, hold great promise for sustainable chemical conversion in electrified industrial applications. Their relatively high temperatures compared to other non-thermal plasmas, reactive species generation, and efficient energy transfer make them ideal for an energy-efficient society. However, plasma discharges are transient and complex 3D entities influenced by gas pressure, mixture, and power, posing challenges for in-situ measurements of chemical species and spatial dynamics. Here we demonstrate a combination of innovative approaches, providing a comprehensive view of discharges and their chemical surroundings by combining fluorescence lifetime imaging of hydroxyl (OH) radicals with optical emission 3D tomography. This reveals variations in OH radical distributions under different conditions and local variations in fluorescence quantum yield with high spatial resolution from a single laser shot. Our results and methodology offer a multidimensional platform for interdisciplinary research in plasma physics and chemistry.