Detectable Color Change Research Articles

A new indanone based dyes bearing dicyanomethylene and salicylidene moieties for selective detection cyanide anion and aromatic amines

Novel chemosensors that are indan-1-one dyes bearing salicylidene moiety were synthesized with good yields and characterized by FT-IR, 1H NMR, 13C NMR, and HRMS methods. Moreover, the molecular structure of 7 was characterization by X-ray and Environmental scanning electron microscopy (ESEM) analyses. The chemosensor potential of dyes were examined in a variety of basic conditions that include various anions, organic amines, and pH ranges by absorption and fluorescence spectra. The naked-eye detection of instant color changes was also observed. The deprotonation mechanism between dyes and anions was investigated by reversibility and 1H NMR studies. pKa values were determined in buffer solution with pH 6–11. Furthermore, organic amines were investigated and found they have two different interaction mechanism, deprotonation and addition. Density Functional Theory (DFT) were used for supporting the experimental results. In addition, the second-order nonlinear optical property of dyes were investigated and showed moderate μβ values.

A β-cyclodextrin-based supramolecular photonic crystal hydrogel biosensor with macroporous structures for naked-eye visual detection of cholesterol

Cholesterol (CHO) is an essential lipid in cell membranes and a precursor for vital living substances. Abnormal CHO levels can cause cardiovascular diseases. Therefore, simple and accurate monitoring of CHO levels is crucial for early diagnosis and effective management of cardiovascular diseases. Herein, we report a β-cyclodextrin-based supramolecular photonic crystal hydrogel (PCH) biosensor for naked-eye visual CHO detection. This sensor is composed of a poly(acrylamide-co-N-isopropylacrylamide-co-maleic anhydride-β-cyclodextrin) smart hydrogel with embedding Fe3O4 colloidal chains, which can translate CHO concentration signals into visually detectable color changes of the hydrogel. By carefully selecting a macromolecular crosslinker, a macroporous structure of the hydrogel was achieved, significantly enhancing CHO responsiveness. Molecular docking provides detailed information about the binding mode between MAH-β-CD and CHO. The cyclohexanol portion and alkyl chain of CHO molecule are inserted into MAH-β-CD cavity, driven primarily by hydrophobic interactions. Moreover, this sensor demonstrates excellent regenerability and could be facilely regenerated by washing using hot/cold water or acid solution. Furthermore, it is highly selective for CHO and is suitable for detecting actual human serums. Such a β-CD-based supramolecular PCH biosensor with visualization, excellent regenerability, and high sensitivity and selectivity toward CHO, provides a basis for clinical diagnosis of diseases relative to CHO abnormalities.

A Trianalyte µPAD for Simultaneous Determination of Iron, Zinc, and Manganese Ions.

In this work, a microfluidic paper-based analytical device (µPAD) for simultaneous detection of Fe, Zn, and Mn ions using immobilized chromogenic reagents Ferene S, xylenol orange, and 1-(2-pyridylazo)-2-naphthol, respectively, is presented. As the effective recognition of analytes via respective chromogens takes place under extremely different pH conditions, experiments reported in this publication are focused on optimization of the µPAD architecture allowing for the elimination of potential cross effects. The paper-based microfluidic device was fabricated using low-cost and well-reproducible wax-printing technology. For optical detection of color changes, an ordinary office scanner and self-made RGB-data processing program were applied. Optimized and stable over time, µPADs allow fast, selective, and reproducible multianalyte determinations at submillimolar levels of respective heavy metal ions, which was confirmed by results of the analysis of solutions mimicking real samples of wastewater. The presented concept of simultaneous determination of different analytes that required extremely different conditions for detection can be useful for the development of other multianalyte microfluidic paper-based devices in the µPAD format.

Stretchable Distributed Bragg Reflectors as Strain-Responsive Mechanochromic Sensors.

Mechanochromic materials exhibit color changes upon external mechanical stimuli, finding wide-ranging applications in colorimetric sensing, display technology, and anticounterfeiting measures. Many of these materials rely on fluorescence properties and therefore necessitate external optical or electrical excitation. However, for broader applicability, the detection of color changes by the naked eye only or without complicated detection instrumentation is highly desirable. Photonic crystals offer a promising avenue for attaining such performances. In this work, we present elastomeric distributed Bragg reflectors (DBRs) characterized by a series of photonic bandgaps exhibiting mechanochromic response from the near-infrared to the visible wavelengths. To achieve this, we engineered alternating thin films of a thermoplastic fluoropolymer and a styrene-butadiene copolymer using different elastomeric substrates to attain different behaviors. The reported system demonstrates a reversible and instantaneous shift of the photonic bandgaps in response to 100% strain in multiple deformation cycles. Comparing the DBR stress-strain response with the optical strain response confirms a mechanochromic sensitivity of ∼1.7-6.9 nm/% and ∼80 nm/MPa, with an optical Poisson's ratio in the range 0.3-0.7. All these properties are spectrally dependent, as demonstrated by exploiting the properties of different diffraction order photonic band gaps.

One-Pot Synthesis of Tannic Acid-Au Nanoparticles for the Colorimetric Determination of Hydrogen Peroxide and Glucose.

This study introduces a novel one-pot method employing tannic acid (TA) to synthesize stable gold nanoparticles (TA-AuNPs), which are characterized using transmission electron microscopy, X-ray powder diffraction, and Fourier transform infrared spectroscopy. We apply these TA-AuNPs in a newly developed colorimetric assay for hydrogen peroxide (H2O2) detection that utilizes the oxidation of iodide (I-) on TA-AuNPs, leading to a detectable yellow color change in the solution. The reaction kinetics are captured by the rate equation R = 0.217[KI]0.61[H2O2]0.69. The possible sensing mechanism was proposed through density functional theory calculations. At the optimum conditions, the proposed TA-AuNPs/I- system demonstrated a linear relationship between H2O2 concentration and absorbance intensity (λ = 350 nm) and achieved a limit of detection (LOD) of 7.33 μM. Furthermore, we expand the utility of this approach to glucose detection by integrating glucose oxidase into the system, resulting in a LOD of 10.0 μM. Application of this method to actual urine samples yielded spiked recovery rates ranging from 96.6-102.0% and relative standard deviations between 3.00-8.34%, underscoring its efficacy and potential for real-world bioanalytical challenges.

Investigating Ion-Coupled Electron Transfer of Conducting Polymers

After years of basic and applied studies of electron transfer in redox active films, the fundamentals of ion transfer during the exchange remain to be understood. Empirically, the processes are ion-transport limited. Using a conducting polymer as a model system, we aim to study the relationship between electron and ion transfer during redox switching.We work on electrochromic conducting polymers because of their observable and detectable color changes in addition to the current during the redox switching. Tracing optical signals can enhance the understanding of electrical signals from redox reactions. When a potential is applied to the electroactive polymer, its color will change from lighter to darker or vice versa. Keeping in mind that absorbances are additive, the ratio of the contents that make up the overall color of the polymer changes. This ratio change is directly proportional to the amount of matter under inter-conversion during the redox reaction.This study aims to explore the ion-electron mechanism in conductive polymers using the simultaneous Spectro-CV method. To achieve this, we conducted cyclic voltammetry at exceptionally high scanning rates, leveraging the conductive polymer's color-changing property. At these high rates, ion movement was restricted due to limited time for forward and backward motion, potentially reaching a point of stagnation. The investigation focused on whether the polymer would continue changing color, providing insights into ion-electron transfer. In addition, we are conducting EIS measurements alongside simultaneous Spectro-CV measurements and attempting to fit the impedance response of the polymer with an appropriate model. We aim to track the time constants provided by the polymer at different voltage values and understand the corresponding physical processes associated with these time constants. Additionally, we aim to use our EIS model to validate the desired redox current information obtained from optical data. We mathematically reach the faradaic portion of the total current with EIS and compare the results obtained from optical data.

Fluorescent Sensors Based on Lanthanide-Based Metal-Organic Frameworks via Devices and pH Response.

In light of the escalating industrial and environmental pollution, there is a pressing need for the development of novel materials capable of swiftly detecting pollutants. Here, we report the synthesis of five lanthanide metal-organic frameworks sharing a common structure, prepared via a hydrothermal method and denoted as [Ln2(H2DHBDC)2(phen)(H2O)6]n (where CUST-888 corresponds to Tb, CUST-889 corresponds to Eu, CUST-890 corresponds to Gd, CUST-891 corresponds to Dy, and CUST-892 corresponds to Nd). Notably, CUST-888 and CUST-889 exhibit discernible visual alterations in response to acidic and alkaline conditions. To assess their practical utility, luminescent test strips and light-emitting diode lights based on CUST-888 and CUST-889 were devised, enabling the visual detection of luminescence color changes induced by Hg2+, Cr2O72-, tetracycline, and 2,4,6-trinitrophenol. Furthermore, highlighters derived from CUST-888 and CUST-889 were designed, showcasing robust stability, adjustable color, and substantial potential for application in the realm of anticounterfeiting.

Sesame Detection in Food Using DNA-Functionalized Gold Nanoparticles: A Sensitive, Rapid, and Cost-Effective Colorimetric Approach.

Food safety control is a key issue in the food and agriculture industries. For such purposes, developing miniaturized analytical methods is critical for enabling the rapid and sensitive detection of food supplements, allergens, and pollutants. Here, a novel bioanalytical methodology based on DNA-functionalized gold nanoparticles (AuNPs) and colorimetric detection was developed to detect the presence of sesame (a major allergen) through sesame seed DNA as a target, in food samples. The presence of sesame DNA induces controlled nanoparticle aggregation/desegregation, resulting in a color change (from blue to red) proportional to sesame DNA concentration. The incorporation of multicomponent nucleic acid enzymes (MNAzymes) in this strategy has been carried out to perform an isothermal signal amplification strategy to improve the sensitivity of detection. Also, open-source software for color analysis was used to ensure an unbiased visual color-change detection, enhancing detection accuracy and sensitivity and opening the possibility of performing a simple and decentralized analyte detection. The method successfully detected the presence of sesame DNA in sesame seed, sesame oil, olive oil, and sunflower oil. In brief, the developed approach constitutes a simple and affordable alternative to perform a highly sensitive detection of DNA in food without complex methodologies or the requirement of expensive instrumentation.

Glucose detection: In-situ colorimetric analysis with double-layer hydrogel microneedle patch based on polyvinyl alcohol and carboxymethyl chitosan

Skin interstitial fluid (ISF) has emerged as a significant reservoir of biomarkers for disease diagnosis and prevention. Microneedle (MN) patches are regarded as an optimal platform for ISF extraction from the skin due to their non-invasive nature. However, challenges such as prolonged sampling durations and complex detection procedures impede timely metabolic analysis. In this investigation, we amalgamated MN technology with immobilized enzyme technology to fabricate a dual-layer MN patch integrating sampling and detection functionalities, thereby enabling in-situ colorimetric detection of hyperglycemia. The tip layer of the patch, comprising polyvinyl alcohol/carboxymethyl chitosan (PVA/CMCS) MN, was synthesized utilizing a chemical crosslinking approach for the first time, with glucose oxidase (GOx) being incorporated. The hydrophilicity of CMCS expedited the extraction process, facilitating the retrieval of approximately 10 mg of ISF within 10 min. The backing layer consisted of an immobilized polyvinyl alcohol-chitosan-horseradish peroxidase (PVA-CS-HRP) hydrogel film loaded with 3,3′, 5,5′-tetramethylbenzidine (TMB). Incorporating macromolecular polymer PVA and CS for HRP immobilization addressed the issue of poor stability associated with traditional natural enzymes, thereby enhancing the sensitivity of the reaction system. The in-situ colorimetric sensor facilitated minimally invasive ISF extraction and swift conversion of glucose levels into detectable color changes.

Instrumentation of novel optical sensor technology to detect the real-time electrolyte colour change in Li-on pouch cells

The need for new and improved diagnostic tools becomes paramount for Li-ion batteries in order to ensure their optimum performance along with their longevity and safety and there remain aspirational targets for Li-ion batteries regarding fast-charging, energy density, safety and lifetime that must be met to achieve further growth. The study of degradation mechanisms (such as electrolyte degradation, thermal runaway, gassing and cycling aging) at the cell level contributes significantly to the understanding of the aging phenomena and will enable improvements for future generations of LIBs. Among various indicators, the colour change of the electrolyte within Li-ion cells presents a largely unexplored avenue for assessing state of health and predicting early signs of degradation. This research proposes a new methodology for the development of an innovative optical sensor technology and its incorporation into a pouch cell. The sensor comprises of a photodiode and RGB LED, mounted on a single flexible PCB, capable of the real-time detection of electrolyte colour changes inside Li-ion pouch cells. Previous studies have identified electrolyte colour change as a potential marker for battery condition through various invasive testing methods; however, the proposed optical technique represents a step change in in-situ real-time diagnostics. This study elaborates on the process of developing and incorporating the sensors precisely into pouch cells and seeks to demonstrate the capability of these sensors to accurately detect alterations in the colour of the electrolyte as the cell ages, without having adverse effects on the cell's performance and offers the potential for direct correlation of electrolyte change with battery state of health.

Impact of plant-based nanoparticles synthesized from Carica papaya and Bryophyllum pinnatum against selected microorganisms

Plant-based nanoparticles offer sustainable, eco-friendly alternatives to conventional methods, promising antibacterial properties in the face of antibiotic resistance and addressing global health concerns. Five urine and stool samples were collected from the Benin Medical Centre in Benin City, Edo State, and sent to the Wellspring University Research Laboratory for microbiological analysis. Carica papaya and Bryophyllum pinnatum were used for fresh utilization by washing, weighing, and crushing their leaves, then mixing them with distilled water and heating at 85 °C and 60 °C for 60 minutes. Silver and copper nanoparticles (AgNPs and CuNPs) were synthesized using standard procedures. The NPs were preliminary validated by visual detection of color changes and characterized using a UV-visible spectrophotometer at 300 nm and Fourier transform infrared. The in vitro antimicrobial activity of plant-mediated NPs was investigated using five isolates: S. aureus, B. alvei, H. pylori, P. aeruginosa, and E. coli. The in vitro antimicrobial activity of plant-mediated NPs was investigated using five clinical strains displaying multiple resistance to antibiotics: S. aureus, B. alvei, H. pylori, P. aeruginosa, and E. coli. The agar-well diffusion method showed inhibition of the isolates by plant-mediated NPs but no inhibition by the plant extract alone. The study indicates that plant-mediated NPs exhibit promising antimicrobial activity, promoting sustainability and eco-friendliness, but further research is needed to assess their safety and efficacy in clinical settings. Keywords: nanoparticles, resistant, antimicrobial, plant-mediated, MAR index.

The Factors Contributed of incidence phlebitis cases with patients by using cannula in National Hospital Guido Valadares Dili, Timor Leste

Phlebitis is defined as inflammation of the vein wall where 2 complications that may develop as a result of phlebitis are: infection resulting from an accumulation of neutrophils; and thrombus, which may lead to complete occlusion of the vein. As healthcare professionals cannot look inside veins during IV therapy, they must rely on what they can see, feel and ask, i.e. detectable changes in skin color, texture, temperature and sensitivity, to identify the development of phlebitis. The absence of a good blood flow and the presence of a poor infusion rate have also been cited as clinical indicators of phlebitis Observation of the patient for clinical signs and symptoms of phlebitis is therefore the key to preventing serious venous damage. Health professional hands are a common of spreading microorganisms, thus very important for health workers followed one of precaution is to attention wash your hands of properly. Phlebitis is caused by chemical factors (type of net liquids), mechanical factors (insertion measures in place), and the most common factors (hand washing techniques including the factors of the patient's age), have been caused by phlebitis. The same results in some research conducted by some researchers show that the causes of phlebitis, among them, the types of liquidity and knowledge of nurses, type of therapy, and development of children, the location and the application of these measures were not yet put in place. The design of research is a quantitative study, with a cross-sectional approach. The sampling technique in this study was accicental sampling, with a sample of 56 respondents. The study was conducted on November 2022 in National Hospital Guido Valaradres Dili, Timor Lest. The result of study showed that the cannula factor influence the phlebitis of the correlations is 0.605 and significant P value is 0.000, time/duration using cannula factor influence the phlebitis of the results correlations is 0.633 and significant P value is 0.000 and the age factor influence the phlebitis of the correlations = 0.736 and significant P value is 0.000

A thiazole-based colorimetric and photoluminescent chemosensors for As3+ ions detection: Density functional theory, test strips, real samples, and bioimaging applications

A Schiff-base Ethyl (E)-2-(3-((2-carbamothioylhydrazono)methyl)-4-hydroxyphenyl)-4-methylthiazole-5-carboxylate (TZTS) dual functional colorimetric and photoluminescent chemosensor which includes thiazole and thiosemicarbazide has been synthesized to detect arsenic (As3+) ions selectively in DMSO: H2O (7:3, v/v) solvent system. The molecular structure of the probe was characterized via FT-IR, 1H, and 13C NMR & HRMS analysis. Interestingly, the probe exhibits a remarkable and specific colorimetric and photoluminescence response to As3+ ions when exposed to various metal cations. The absorption spectral changes of TZTS were observed upon the addition of As3+ ions, with a naked eye detectable color change from colorless to yellow color. Additionally, the chemosensor (TZTS) exhibited a new absorption band at 412 nm and emission enhancements in photoluminescence at 528 nm after adding As3+ ions. The limit of detection (LOD) for As3+ ions was calculated to be 16.5 and 7.19 × 10−9 M by the UV–visible and photoluminescent titration methods, respectively. The underlying mechanism and experimental observations have been comprehensively elucidated through techniques such as Job’s plot, Benesi-Hildebrand studies, and density functional theory (DFT) calculations. For practical application, the efficient determination of As3+ ions were accomplished using a spike and recovery approach applied to real water samples. In addition, the developed probe was successfully employed in test strip applications, allowing for the naked-eye detection of arsenic ions. Moreover, fluorescence imaging experiments of As3+ ions in the breast cancer cell line (MCF-7) demonstrated their practical applications in biological systems. Consequently, these findings highlight the significant potential of the TZTS sensor for detecting As3+ ions in environmental analysis systems.

A novel albumin-based supramolecular biosensor for ratiometric on-site determination of buprofezin

Buprofezin (BUP) is an effective insecticide against Homopteran and Thysanoptera pests. However, exposure to BUP may result in several harmful effects on the non-target organism including human body, such as hepatotoxicity and DNA damage. Therefore, development of a reliable analytical method for BUP holds paramount importance. This study presents a novel albumin-based supramolecular biosensor, DPP@ALB, designed for the sensitive detection of BUP in environmental matrices, including water, soil, and real food samples. The features of this biosensor include a fast response, high sensitivity, and visually detectable fluorescence color change, enabling on-site detection of BUP based on the portable paper strips and 3D-printed miniaturized testing system. Overcoming challenges associated with the low chemical reactivity of BUP, this supramolecular biosensor emerges as the very first fluorescent sensor for efficient and reliable monitoring of BUP with applications in broader areas of environmental analysis and food safety.

Portable multifunctional sensing platform for ratiometric H2O2 detection and photodynamic anti-bacteria using an AIE-featured electrospinning film

The development of portable flexible sensors for sensitive gas detection with antibacterial activity is of great significance for protecting human health and environment safety. In this paper, we designed a ratiometric sensing platform (PLA@RPEG@TBSN) for reliable and visual monitoring of gaseous H2O2 by electrospinning technology, which reveals self-antibacterial function and highly photostability simultaneously. By employing the aggregation-induced emission (AIE) active nanoparticles (TBSN) as fluorescent responder and Rose Bengal modified photosensitive polymer (RPEG) as reference unit, accurate ratiometric sensing process of PLA@RPEG@TBSN film was realized based on the specific peroxide-mediated reaction between TBSN and H2O2. The flexible film system demonstrated superiorsensingperformance toward H2O2 vapor, including excellent selectivity, visualized color change and low detection limit (7 ppb). Additionally, benefitting from the photodynamic activity of RPEG, the PLA@RPEG@TBSN film exhibited highly effective antibacterial performance (killing 84 % of bacteria). Moreover, the multifunctional wearable potential is supported by employing film sensor onto the protective mask, which reveals dual capabilities of ratio sensing and resistance bacteria aerosols, encouraging the application of the sensor in complex practical scenario.

Spectrophotometric analysis of the effectiveness of different dentin tubule occlusion techniques in preventing discoloration caused by photosensitizers used in photodynamic therapy

AimThe efficacy of Copal Varnish (CV), dentin bonding agent (DBA), Nd:YAG laser and Er:YAG laser, which occludes dentin tubules by different mechanisms, was investigated in order to prevent unwanted coloration caused by methylene blue (MB) and phthalocyanine used in photodynamic therapy (PDT). Materials and methods165 upper incisors included in the study. Root canals were prepared up to 30/0.6 size for all teeth using Protaper Next rotary files. Then the teeth were randomly divided into 2 main groups (n = 60); MB and phthalocyanine. Each main group was randomly divided into 5 subgroups (n = 15); Positive control, DBA, CV, Er:YAG and Nd:YAG. Root canals were filled with photosensitizers (PS) and activated after the dentin tubule occlusion method was applied to all teeth. Then, the residual PSs were removed by irrigation. Color measurements of the samples were carried out 5 different time periods. ResultsClinically detectable color change was observed in all groups except for the negative control (ΔE≥3.3). It was determined that the positive control using MB caused more unwanted coloration in the CV on the 30th and 90th days compared to the phthalocyanine used in the 90th day (p < 0.05). While none of the dentin tubule occlusion methods were superior to each other in preventing undesirable coloration caused by phthalocyanine, Er:YAG caused less unwanetd coloration than CV only on the 90th day in preventing unwanted coloration caused by MB (p < 0.05). ConclusionsAll dentin tubule occlusion methods used in the present study were effective in preventing some degree of unwanted discoloration. However, it was found that no technique could completely prevent unwanted coloration.

Simultaneous rapid detection of glycyrrhizin and sennoside A in Daiokanzoto samples by lateral flow immunoassay.

Glycyrrhizin (GLY) and sennoside A (SA) are characteristic bioactive marker compounds of the Kampo medicine Daiokanzoto. Their accurate detection in blends of Rhei rhizoma and Glycyrrhizae radix of several species (4:1 or 4:2) is essential for quality control and to ensure therapeutic efficacy. A rapid, efficient assay can significantly facilitate their detection. To establish a rapid qualitative assay for GLY and SA detection, a lateral flow immunoassay (LFA) was developed using specific monoclonal antibody (mAb) nanoparticles. This assay harnesses the competitive binding of mAb nanoparticles to the immobilized analytes on test strips and free analytes in the samples. Two conjugates for detecting GLY and SA, GLY-bovine serum albumin and SA-human serum albumin, were separately immobilized on the test zones of LFA strips. The detection mechanism is reliant on the visual detection of color changes in the test zones. When GLY and SA were present in samples, they contended with the immobilized conjugates on the strip to bind with the mAb nanoparticles and produced distinct color patterns in the test zones. The limits of detection of the assay for GLY and SA were both 3.13 μg/mL. The capability of the LFA was substantiated using plant samples and Daiokanzoto, and its alignment with indirect competitive ELISA results was confirmed. The introduced LFA is a groundbreaking procedure that offers a rapid, straightforward, and sensitive method for simultaneously detecting GLY and SA in Daiokanzoto samples. It is instrumental in ensuring product quality.

Visualizing fiber end geometry effects on stress distribution in composites using mechanophores.

Localized stress concentrations at fiber ends in short fiber-reinforced polymer composites (SFRCs) significantly affect their mechanical properties. Our research targets these stress concentrations by embedding nitro-spiropyran (SPN) mechanophores into the polymer matrix. SPN mechanophores change color under mechanical stress, allowing us to visualize and quantify stress distributions at the fiber ends. We utilize glass fibers as the reinforcing material and employ confocal fluorescence microscopy to detect color changes in the SPN mechanophores, providing real-time insights into the stress distribution. By combining this mechanophore-based stress sensing with finite element analysis (FEA), we evaluate localized stresses that develop during a single fiber pull-out test near different fiber end geometries-flat, cone, round, and sharp. This method precisely quantifies stress distributions for each fiber end geometry. The mechanophore activation intensity varies with fiber end geometry and pull-out displacement. Our results indicate that round fiber ends exhibit more gradual stress transfer into the matrix, promoting effective stress distribution. Also, different fiber end geometries lead to distinct failure mechanisms. These findings demonstrate that fiber end geometry plays a crucial role in stress distribution management, critical for optimizing composite design and enhancing the reliability of SFRCs in practical applications. By integrating mechanophores for real-time stress visualization, we can accurately map quantified stress distributions that arise during loading and identify failure mechanisms in polymer composites, offering a comprehensive approach to enhancing their durability and performance.

Detection of TNP and sulfite ions in an aqueous medium using a pyrazinium-based chemosensor

A pyrazinium-based fluorescent chemosensor exhibited effecient detection of TNP and sulfite ions in aqueous medium. The chemosensor with a visually detectable color change in the presence of sulfite was integrated with a smartphone.

An ICT-based highly fluorescent isoquinoline scaffold for selective Hg(II) detection in real-water samples: Development of a smart, low-cost RGB-Arduino electronic platform

Selective detection and quantification of Hg2+ ions is crucial to minimize health and environmental risks. Fluorescent organic small-molecule probes have been expeditiously utilized owing to their unique set of improved properties. However, isoquinoline core has not been extensively explored as a fluorescence platform partly due to synthetic challenges. Herein, a serendipitously discovered synthetic route to access a small yet highly functionalized novel isoquinoline-based probe, IQ is reported. The synthesis is achieved through the in-situ generation of ammonia, followed by intermolecular [5C + 1 N] aza-annulation reaction with a ketendithioacetal-based precursor, P-IQ. IQ displayed excellent recognition ability towards Hg2+ ions in H2O:ACN (99:1, v/v) via ICT-off fluorescent quenching behavior. Comparative FT-IR, 1H/13C NMR, mass spectral studies, and DFT analyses were carried out to validate the suggested mechanisms. Reversible studies confirm the secondary recognition effect of in-situ generated (IQ + Hg2+) complex on cysteine. The binding constant and LOD were estimated to be 3.7 × 104 M−1 and 0.86 µM, respectively. Further, IQ was utilized to evaluate the mercury ion content in real water samples demonstrating its effectiveness in water quality monitoring. The practical utility of IQ was further explored by developing TLC strips, Whatman filter-paper strips, and a low-cost, portable Arduino-based platform. Arduino microcontroller is interfaced with an RGB sensor to detect color changes and quantify mercury concentration w.r.t. RGB values.