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Chemosensing of ions has gained considerable attention by chemists. Insight into the mechanism involved between sensors and ions always fascinates researchers to develop economical, sensitive, selective, and robust sensors. This review comprehensively explores the mechanism of interaction between Imidazole sensors and anions. With most of the research concentrating only on fluoride and cyanide, this review has highlighted a large gap in various anions detection including SCN−, Cr2O72−, CrO42−, H2PO4−, NO2−, and HSO4−.This study also includes a critical analysis of different mechanisms and their respective limits of detection, with a discussion of the reported results. [ABSTRACT FROM AUTHOR]

Thiazole and its derivatives play an important role in biological and non-biological fields due to several structural and electronic behaviors associated with it. Thiazole derivatives act as chemosensors because they formed metal complexes upon interacting with various heavy metal ions like Cd2+, Co2+, Cr3+, Fe3+, Ag+, Al3+, Cu2+, Pd2+, Hg2+, Ni2+, Ga3+, In3+, Sn4+, Pb2+, Zn2+ as well as other cations. These metal ions are of prime importance from the environmental point of view with high. This review article focuses on the thiazole-based colorimetric as well as fluorometric sensor for the recognition of different heavy metal cations in various specimens like agricultural, biological, and environmental. It also summarizes the binding stoichiometry, detection limit, pH, structure, and practical application of the reported thiazole-based chemosensors. Further, the sensing performances, have been discussed and compared with some reported organic sensors. [ABSTRACT FROM AUTHOR]

This study focuses on developing and characterizing of fluorescent cellulose-based hydrogelsfor efficient chromium (Cr(VI)) adsorption. For this purpose, microcrystalline cellulose (MCC) was first surface-modified to achieve solubility using succinic anhydride. Cellulose succinate (CS) subsequently was grafted with a mixture of acrylic acid (AA) and acrylamide (AM), while N,N′-methylene-bis(acrylamide) (MBA) was added as crosslinker to obtain the final grafted and crosslinked hydrogels. To impart fluorescence and sensing capabilities, nitrogen-doped carbon quantum dots (N-CQDs) were synthesized via a microwave-assisted method using sugarcane bagasse, NaOH, and urea as precursors, and incorporated into the hydrogel. The resulting hydrogels demonstrated effective Cr(VI) adsorption, with optimal performance observed at 10% N–CQD loading. FTIR, SEM, rheological analysis, and TGA were employed for hydrogel characterization, while adsorption kinetics provided insights into the interaction mechanisms with Cr(VI). [ABSTRACT FROM AUTHOR]

Dynamic range is a crucial aspect in the development of fluorescent chemosensors. We aimed to address this issue using molecular logic gates. By creating an AND logic gate with two binding sites for the same type of ion, we increased the dynamic range of a sodium chemosensor while still using the same ionophore. Naphthalimide derivatives 1 and 2 were synthesized to test the plausibility of this application. Being an AND logic gate, the second molecule requires two Na+ ions, while molecule 1 requires a single ion for sensing. The application of this molecular logic gate is a useful method of altering the chemosensor range. [ABSTRACT FROM AUTHOR]

AbstractThe emergence of calixarenes as versatile compounds in recent years marks a significant advancement in scientific research. In the area of analytical chemistry, calixarenes have garnered attention for their utility as selective chemosensors, enabling the sensitive and specific detection of metal ions through colorimetric and fluorimetric methods. Moreover, calixarenes have found applications in bioimaging, where they serve as effective probes for visualizing biological structures and processes with high resolution and sensitivity. Additionally, recent studies have explored the anticancer properties of calixarenes, unveiling their potential as therapeutic agents for cancer treatment. This comprehensive review explores recent advancements in calixarenes chemistry, emphasizing their significance in the colorimetric and fluorimetric detection of metal ions. Additionally, it highlights the mechanisms involved in chemosensor design, providing insights into the underlying principles driving their efficacy. Furthermore, the application of calixarenes in bioimaging, particularly for visualizing cellular structures and processes, is discussed, showing their potential in biomedical research and diagnostics. The anticancer activity of calixarenes and their derivatives is also explored, shedding light on their promising role as therapeutic agents. Through an extensive examination of recent literature, this review provides valuable insights into the multifaceted applications of calixarenes and offers perspectives for future research directions. [ABSTRACT FROM AUTHOR]

Utility of pyrazoles and their derivatives in constructing ordered porous materials with physicochemical characteristics such as chemosensors has undoubtedly created much interest in developing newer frameworks. A variety of pyrazole based chemosensors are known for their remarkable photophysical, pH sensitivity, solvatochromic, ion detection, high quantum yields and nonlinear optical behavior. Many of the transition metals have shown beneficial biological effects in biological systems. There is always a need of continuous monitoring to maintain an adequate range of all and specifically for the toxic ones like mercury. Pyrazoline nanoparticle probes have been reported for sensing/detection of Hg2+ions. Pyridinyl pyrazoline and benzimidazolyl pyrazole derived sensors are more selective and sensitive towards Zn2+and Fe3+ ions respectively. Pyrazole derived metal organic frameworks (MOF's) have been reported for environmental monitoring and biological imaging. Keeping in view of the enormous synthetic and biological importance of pyrazoles, herein, we are presenting an overview on applications of pyrazoles in transition metal chemosensors. [ABSTRACT FROM AUTHOR]

Organic compounds display several electronic and structural features which enable their application in various fields, ranging from biological to non-biological. These compounds contain heteroatoms like sulfur, nitrogen and oxygen, which provide coordination sites to act as ligands in the field of coordination chemistry and are used as chemosensors to detect various metal ions. This review article covers different organic compounds including thiourea, Schiff base, pyridine, thiophene, coumarin, triazolyl pyrenes, imidazole, fluorescein, thiazole, tricarbocyanine, rhodanine, porphyrin, hydrazone, benzidine and other functional groups based chemosensors, that contain heteroatoms like sulfur, nitrogen and, oxygen for fluorimetric and colorimetric detection of Ag+ in different environmental, agricultural, and biological samples. Further, the sensing mechanism and performances of these chemosensors have been discussed, which could help the readers for the future design of highly efficient, selective, and sensitive chemosensors for the detection and determination of Ag+ ions. [ABSTRACT FROM AUTHOR]

This review provides an in-depth examination of recent progress in the development of chemosensors, with a particular emphasis on colorimetric and fluorescent probes. It systematically explores various sensing mechanisms, including metal-to-ligand charge transfer (MLCT), ligand-to-metal charge transfer (LMCT), photoinduced electron transfer (PET), intramolecular charge transfer (ICT), and fluorescence resonance energy transfer (FRET), and elucidates the mechanism of action for cation and anion chemosensors. Special attention is given to phenothiazine-based fluorescence probes, highlighting their exceptional sensitivity and rapid detection abilities for a broad spectrum of analytes, including cations, anions, and small molecules. Phenothiazine chemosensors have emerged as versatile tools widely employed in a multitude of applications, spanning environmental and biomedical fields. Furthermore, it addresses existing challenges and offers insights into future research directions, aiming to facilitate the continued advancement of phenothiazine-based fluorescent probes. [ABSTRACT FROM AUTHOR]

BTDs (2,1,3-benzothiadiazoles) are fluorescent heterocycles widely used in different applications, including biomarkers, sensing optical devices, OLEDs, organic transistors, and solar cells. This review mainly focuses on the current progress in the design of compounds derived from the BTD core, aiming for their use as chromogenic and/or fluorogenic devices for detecting anionic, cationic, and neutral analytes. Reactions and synthetic strategies that show the synthetic versatility of BTDs are initially presented, to provide a better understanding regarding the assembly of optical detection systems. The photophysical mechanisms of the detection are also described. A discussion is also presented on the target analytes for which the optical detection devices based on BTD were planned. The examples discussed here will offer the sensors community perspectives for developing new optical detection devices based on BTD for different types of analytes of importance for the most diverse areas of knowledge. [ABSTRACT FROM AUTHOR]

In recent years, European Union member states have hastened energy policy deliberations to address supply and sustainability concerns, placing a significant emphasis on nuclear energy as a means to achieve decarbonization goals. However, despite its significant role in power generation, nuclear energy faces significant challenges linked to fuel reprocessing and waste disposal, that hinder its broader expansion. In this context, the separation of technetium represents a concerning issue. Indeed, technetium's catalytic activity can impede the extraction of uranium, neptunium, and plutonium, affecting waste reprocessing efficiency. Additionally, the stable form of technetium in aerobic conditions, pertechnetate (TcO4−), poses risks of groundwater contamination due to its mobility and solubility. Hence, sensing and separation of TcO4− is imperative for both nuclear fuel processing and minimising radioactive contamination in the environment. However, the binding of TcO4− and its separation from contaminated solutions present challenges due to the acidic (or basic) waste components and the high ionic strength in real matrices. Supramolecular chemists have addressed these issues by designing receptors inspired by molecular recognition principles. This article explores recent advancements and future directions in TcO4− sensing and separation (using extraction and sorption) with a focus on molecular hosts. Metal‐organic receptors will also be discussed. [ABSTRACT FROM AUTHOR]

In recent years, European Union member states have hastened energy policy deliberations to address supply and sustainability concerns, placing a significant emphasis on nuclear energy as a means to achieve decarbonization goals. However, despite its significant role in power generation, nuclear energy faces significant challenges linked to fuel reprocessing and waste disposal, that hinder its broader expansion. In this context, the separation of technetium represents a concerning issue. Indeed, technetium's catalytic activity can impede the extraction of uranium, neptunium, and plutonium, affecting waste reprocessing efficiency. Additionally, the stable form of technetium in aerobic conditions, pertechnetate (TcO4−), poses risks of groundwater contamination due to its mobility and solubility. Hence, sensing and separation of TcO4− is imperative for both nuclear fuel processing and minimising radioactive contamination in the environment. However, the binding of TcO4− and its separation from contaminated solutions present challenges due to the acidic (or basic) waste components and the high ionic strength in real matrices. Supramolecular chemists have addressed these issues by designing receptors inspired by molecular recognition principles. This article explores recent advancements and future directions in TcO4− sensing and separation (using extraction and sorption) with a focus on molecular hosts. Metal‐organic receptors will also be discussed. [ABSTRACT FROM AUTHOR]

The widespread use of chromium in various fields has led to its significant presence in the environment, resulting in ecological and biological consequences. Chromium exists primarily in two valence states, Cr(III) and Cr(VI), each with distinct properties. While Cr(III) is essential in trace amounts for living organisms, elevated concentrations can be harmful. On the other hand, Cr(VI) is known for its toxicity, posing potential health risks, including carcinogenic effects. Therefore, the detection of Cr(III) and Cr(VI) ions is crucial in environmental, agricultural, and biological samples. This review explores the latest developments in O-, N- and S- donor ligands as colorimetric and fluorimetric sensors for the specific recognition of Cr(III) and Cr(VI). The article provides an in-depth analysis of the various design strategies, molecular structures, and sensing mechanisms employed in these chemosensors. Additionally, the review discusses the sensitivity, selectivity, and practical applications of these chemosensors in detecting chromium ions, highlighting their potential in environmental monitoring and analytical chemistry. The challenges and future prospects in this rapidly evolving field are also addressed. [ABSTRACT FROM AUTHOR]

Sensors play a critical role in the detection and monitoring of various substances present in our environment, providing us with valuable information about the world around us. Within the field of sensor development, one area that holds particular importance is the detection of small molecules. Small molecules encompass a wide range of organic or inorganic compounds with low molecular weight, typically below 900 Daltons including gases, volatile organic compounds, solvents, pesticides, drugs, biomarkers, toxins, and pollutants. The accurate and efficient detection of these small molecules has attracted significant interest from the scientific community due to its relevance in diverse fields such as environmental pollutants monitoring, medical diagnostics, industrial optimization, healthcare remedies, food safety, ecosystems, and aquatic and terrestrial life preservation. To meet the demand for precise and efficient monitoring of small molecules, this summary aims to provide an overview of recent advancements in sensing and quantification strategies for various organic small molecules including Hydrazine, Glucose, Morpholine, Ethanol amine, Nitrosamine, Oxygen, Nitro-aromatics, Phospholipids, Carbohydrates, Antibiotics, Pesticides, Drugs, Adenosine Triphosphate, Aromatic Amine, Glutathione, Hydrogen Peroxide, Acetone, Methyl Parathion, and Thiophenol. The focus is on understanding the receptor sensing mechanism, along with the electrical, optical, and electrochemical response. Additionally, the variations in UV–visible spectral properties of the ligands upon treatment with the receptor, fluorescence and absorption titration analysis for limit of detection (LOD) determination, and bioimaging analysis are discussed wherever applicable. It is anticipated that the information gathered from this literature survey will be helpful for the perusal of innovation regarding sensing strategies. [ABSTRACT FROM AUTHOR]

The pervasive presence of mercury in water and cosmetics poses significant health risks, necessitating the development of a method for the in-situ monitoring and extraction of mercury ions. This study introduces a novel approach utilizing Mesoporous Silica Nanotubes (MSNTs) with a unique worm-like structure, providing an expansive surface area ideal for the adsorption of a Hg2+ ion chromophore, N,N,N,N′-Tetramethyl-4,4′-diaminobenzophenone. This configuration enables rapid and visible detection of toxic mercury, with a color transition from yellow to green that is easily discernible by the naked eye. The sensitivity of the Mercury nano-sensor (MNS) is remarkably high, with a detection limit of 1.9 × 10-8 M as determined by digital image analysis, and 4.9 × 10-8 M via spectrophotometric methods—both well below the WHO guidelines for drinking water. The MNS’s low detection threshold, coupled with its reusability after simple regeneration, positions it as an effective tool for preliminary water testing. The findings suggest that the MNS, requiring only 10 mg for measurements, offers a promising solution for the real-time visualization of mercury ions, enhancing safety measures in water and cosmetic products.

Small molecules can display certain electronic and structural features that enable their use for metal-sensing applications in different fields. Of the reported metal sensors, there has been increasing interest in copper sensing in the past decade, given the biological importance of copper as well as its presence as a potential contaminant in water and fuels. Molecules used for copper(II) sensing generally consist of a fluorophore/chromophore and a ligand for selective metal ion recognition. This review article focuses on literature contributions since the year 2010 concerning small molecule copper(II) sensors that provide a naked-eye color response in solution. We present molecular structural features and sensing mechanisms for the colorimetric and fluorometric detection of copper(II) ions in different environmental, agricultural, and biological samples. In addition, the sensing performance of these chemosensors is compared and discussed, which could aid in the future design of chemosensors for copper(II). Finally, we outline the challenges and future prospects of fluorophore/chromophore–ligand chemistry in applications of small molecules for fluorometric and colorimetric assays of copper(II).

Three decades after A. P. de Silva’s seminal paper introduced the concept of logic gates at the molecular level, the field of molecular logic gates (MLGs) has witnessed significant advancements. MLGs are devices designed to perform logical operations, utilizing one or more physical or chemical stimulus signals (inputs) to generate an output response. Notably, MLGs have found diverse applications, with optical detection of analytes emerging as a notable evolution of traditional chemosensors. Organic synthesis methods are pivotal in crafting molecular architectures tailored as optical devices capable of analyte detection through logical functions. This review delves into the fundamental aspects and physical–chemical properties of MLGs, with a particular emphasis on synthetic strategies driving their design.

The ability to control the function and structure of some promising nanosystems using an external stimulus is attractive research to develop programmable and reconfigurable intelligent nanomaterials. The focal point of this review is the silicon-based nanoporous materials, and particularly the mesoporous silica materials (MSMs) class (pore size: 2–50 nm), due to their important intrinsic properties, such as high surface area, highly ordered nanostructure, narrow pore size distribution, various dimensions (one-dimensional, two-dimensional, and three-dimensional), and easily functionable. One of the most essential organic components that can be incorporated in MSMs is organic photochromic molecules (OPMs), such as azobenzene, stilbene, dithienylethenes, and spiropyrans. OPMs can be incorporated into MSMs, to form photochromic mesoporous organosilica materials (PMOMs), in two different ways: physical (non-covalent immobilization) or chemical (covalent immobilization) binding. PMOMs are considered smart nanomaterials because they have the ability to undergo reversible changes in the solid state when exposed to an external electromagnetic radiation. PMOMs have been the subject of many research studies during the last decade due to their potential applications, especially as chemosensors. This review discusses the main families of OPMs, their incorporation into MSMs using different methods, and the applications of some PMOMs as chemosensors.

In recent years, sensory polymers have evolved significantly, emerging as versatile and cost-effective materials valued for their flexibility and lightweight nature. These polymers have transformed into sophisticated, active systems capable of precise detection and interaction, driving innovation across various domains, including smart materials, biomedical diagnostics, environmental monitoring, and industrial safety. Their unique responsiveness to specific stimuli has sparked considerable interest and exploration in numerous applications. However, along with these advancements, notable challenges need to be addressed. Issues such as wearable technology integration, biocompatibility, selectivity and sensitivity enhancement, stability and reliability improvement, signal processing optimization, IoT integration, and data analysis pose significant hurdles. When considered collectively, these challenges present formidable barriers to the commercial viability of sensory polymer-based technologies. Addressing these challenges requires a multifaceted approach encompassing technological innovation, regulatory compliance, market analysis, and commercialization strategies. Successfully navigating these complexities is essential for unlocking the full potential of sensory polymers and ensuring their widespread adoption and impact across industries, while also providing guidance to the scientific community to focus their research on the challenges of polymeric sensors and to understand the future prospects where research efforts need to be directed. [ABSTRACT FROM AUTHOR]

Three decades after A. P. de Silva's seminal paper introduced the concept of logic gates at the molecular level, the field of molecular logic gates (MLGs) has witnessed significant advancements. MLGs are devices designed to perform logical operations, utilizing one or more physical or chemical stimulus signals (inputs) to generate an output response. Notably, MLGs have found diverse applications, with optical detection of analytes emerging as a notable evolution of traditional chemosensors. Organic synthesis methods are pivotal in crafting molecular architectures tailored as optical devices capable of analyte detection through logical functions. This review delves into the fundamental aspects and physical–chemical properties of MLGs, with a particular emphasis on synthetic strategies driving their design. [ABSTRACT FROM AUTHOR]

2,3-Bis[5-(pyren-1-yl)thiophen-2-yl]quinoxalines and 2,3-bis{5-[4-(9H-carbazol-9-yl)phenyl]thiophen-2-yl}pyrazino[2,3-f][1,10]phenanthroline were synthesized. One- and two-photon absorption and emission of the compounds were studied, the cross sections of the two-photon absorption were found to be equal to 101–476 GM in THF. Fluorescent responses of pyrene-containing fluorophores and dipyrido-annelated quinoxaline to nitroaromatic compounds and metal cations, respectively, were investigated. [ABSTRACT FROM AUTHOR]

A naphthylidene-diimine L2 was newly designed, and its structure was identified by elemental analysis and spectroscopic methods. The effect of temperature, acid–base and light on enol–keto tautomerism in this Schiff base was evaluated by colorimetry, UV–Vis and fluorescence spectroscopy. Under irradiation 365 nm, L2 emitted yellow, orange and strong green emission in pure, basic and aqueous DMSO media (v/v, 1/1), respectively. Its ionochromic behavior against various cations (Fe3+, Al3+, Cr3+, Cu2+, Co2+, Ni2+, Zn2+, Cd2+, Pb2+, Ba2+ and Ag+) and anions (F−, Cl−, CH3COO−, SO32–, S2O32−, HSO4−, H2PO4−, NO3−, CN−, and OH−) was investigated in aqueous DMSO media (v/v, 1/1) by UV–Vis and fluorescence experiments. Dark yellow color of L2 changed to colorless for Fe3+, Cr3+ and HSO4− ions, and turned to light yellow for Al3+ and Cu2+ ions, and to orange for CN− and OH− ions. According to UV–Vis data, the chemosensor displayed selective recognition towards Fe3+, Al3+, Cu2+, HSO4−, CN− and OH− with a 1:1 stoichiometric ratio. At the excitation wavelength of 365 nm, L2 gave strong yellowish white emission (λem = 445 and 539 nm) in the presence of Al3+, and the intensity increased about 12.5 times. On the other hand, the chemosensor displayed one emission band at 452 nm and 450 nm in the presence of CN− and OH− with 1.9 fold and 2.3 fold fluorescence enhancement, respectively. [ABSTRACT FROM AUTHOR]

This paper proposes a new, highly effective fluorescence test for Cr(VI) detection. This method utilizes a hydrogel composed of hydroxyethyl cellulose (HEC), nitrogen-doped carbon quantum dots (N–CQDs), and poly(co-acrylamido-2-methyl-1-propane sulfonic acid) (AMPS). The N–CQDs were successfully synthesized using a simple microwave method, and then conjugated with HEC and AMPS. The higher adsorption (99.41%) and higher reduction rate in H1 likely stems from both the presence of N–CQDs (absent in HB) and their increased free functional groups (compared to H2/H3, where N–CQDs block them). This facilitates the release (desorption) of Cr(VI) from the hydrogels, making it more available for reduction to the less toxic Cr(III). The fluorescent brightness of the HEC-N–CQDs-g-poly(AMPS) hydrogel increases gradually when Cr(VI) is added in amounts ranging from 15 to 120 mg/L. The fluorescent enhancement of the HEC-N–CQDs-g-poly(AMPS) hydrogel appeared to exhibit a good linear relationship with the 15–120 mg of the Cr(VI) concentration, with a detection limit of 0.0053 mg/L, which is lower than the standard value published by WHO. Our study found that the HEC-N–CQDs-g-poly(AMPS) hydrogel served effectively as a fluorescent probe for Cr(VI) detection in aqueous solutions, demonstrating high sensitivity. [ABSTRACT FROM AUTHOR]

Metal oxide ion-gated transistors (MOIGTs) have garnered significant attention within the sensing domain due to their potential for achieving heightened sensitivity while consuming minimal energy across diverse scenarios. By harnessing the advantageous combination of metal oxides' high carrier mobility and facile surface customization, coupled with the potent signal amplification capabilities of ion-gated transistors, MOIGTs offer a promising avenue for discerning biomolecules, overseeing chemical reactions, pH levels, as well as facilitating gas or light determination. Over the past few decades, the MOIGT field has made remarkable strides in refining device physics, enhancing material properties, showcasing robust sensing capabilities, and broadening its application spectrum. These advancements have simultaneously unveiled new challenges and opportunities, necessitating interdisciplinary expertise to fully unlock the commercial potential of MOIGTs. In this comprehensive review, we offer a snapshot of this swiftly evolving technology, delve into its current applications, and provide insightful recommendations for future directions in the coming decade. [ABSTRACT FROM AUTHOR]

Rhodamine chemosensors are extremely beneficial to identify and assess the quantity of iron ions (Fe3+) in environmental and biological samples. In the recent past, several rhodamine based chemosensors are specifically developed to detect Fe3+ ion. Among the ferrous and ferric ions, the ferric ion is expected to display more toxicity, if present, abundantly beyond the limit in the biological system. Similarly, ferric ion in the environment is also a major threat because it can affect both plant and animal kingdoms. The sources of ferric ion in the environment are through corrosion of pipes, supplemental pills from the counter, and municipal wastes. Therefore, specific detection of ferric ion is essential and rhodamine chemosensors play a crucial role in detecting such pollutants. The present review summarizes the rhodamine chemosensors that are recently developed to specifically identify ferric ion in both environmental and biological samples. Rhodamine chemosensors offer a cost-effective approach to detect the ferric ions distributed in various biological and environmental systems. [ABSTRACT FROM AUTHOR]

Extended organic polymers such as amorphous Covalent Organic Polymers (COPs) and crystalline Covalent Organic Frameworks (COFs) are emerging functional polymeric materials that have recently been shown promises as luminescent materials for chemosensing applications. A wide variety of luminescence COPs and COFs have been synthesized and successfully used as fluorescence-sensing materials for hazardous environmental pollutants and toxic contaminants. This review exemplifies various COPs and COFs-based fluorescence sensors for selective sensing of Fe(III) ions. The fluorescence sensors are sorted according to their structural features and each section provides a detailed discussion on the synthesis and fluorescence sensing ability of different COPs and COFs towards Fe(III) ions. Also, this review highlights the limitations of the existing organic polymer-based chemosensors and future perspectives on translating COPs and COFs-based fluorescence sensors for the practical detection of Fe(III) ions. [ABSTRACT FROM AUTHOR]

Conducting polymers (CPs) are conductive materials composed of organic polymers. CPs have excellent properties such as easy synthesis and effortless fabrication, tunable electrical property, high environmental stability, high mechanical and optical properties. These unique properties have attracted researchers to discover a wide variety of uses, such as batteries, solar cells, sensors, supercapacitors, electrochromic devices, and biochemical applications. Although CPs have many limitations in their pristine form, hybridization with other materials overcomes these limitations. Here in this review article, we discuss different CPs based chemosensors for colorimetric and fluorimetric detection and determination of noble metal ions (Ag+, Pd2+, Pt2+/4+, and Au3+) in different environmental, agricultural, and biological samples. Further, the sensing performances of these chemosensors have been compared and discussed. We hope this article will help the readers with the future design of CPs based optical sensor (colorimetric and fluorescent) for detecting noble metal cations. [ABSTRACT FROM AUTHOR]

Conducting polymers (CPs) are conductive materials composed of organic polymers. CPs have excellent properties such as easy synthesis and effortless fabrication, tunable electrical property, high environmental stability, high mechanical and optical properties. These unique properties have attracted researchers to discover a wide variety of uses, such as batteries, solar cells, sensors, supercapacitors, electrochromic devices, and biochemical applications. Although CPs have many limitations in their pristine form, hybridization with other materials overcomes these limitations. Here in this review article, we discuss different CPs based chemosensors for colorimetric and fluorimetric detection and determination of noble metal ions (Ag+, Pd2+, Pt2+/4+, and Au3+) in different environmental, agricultural, and biological samples. Further, the sensing performances of these chemosensors have been compared and discussed. We hope this article will help the readers with the future design of CPs based optical sensor (colorimetric and fluorescent) for detecting noble metal cations. [ABSTRACT FROM AUTHOR]

Antibiotics have successfully been developed and used widely in clinical therapeutics for many years to treat bacterial infections, resulting in their unregulated discharge into waterbodies, which adversely affects the flora and fauna. This triggers alarming health issues that ascertain the need to develop suitable sensors for the detection and removal of persitent antibiotic pollutants. Several reports have been made on lanthanide‐based luminescent metal‐organic frameworks (MOFs) as one of the best‐known chemosensors that render efficient and selective detection of antibiotics owing to their intrinsic luminescent response. Herein, the recent advancements in lanthanide‐based MOFs for recognizing antibiotics are reviewed with a detailed discussion on the mechanistic routes of detection. Also, the possible transitions between the energy levels of lanthanides and the unique photophysical attributes of lanthanide‐organic hybrids are critically assessed. Further, the performance of the reported chemosensors based on their detection range, the limit of detection, stability, reproducibility, and practical feasibility are extensively explored. These unique aspects of this review provide a solid prospect for designing innovative and ingenious fluorescent probes. [ABSTRACT FROM AUTHOR]

Thioureas and their derivatives are organosulfur compounds having excellent biological and non-biological applications. These compounds contain S- and N-, which are nucleophilic and allow for establishing inter-and intramolecular hydrogen bonding. These characteristics make thiourea moiety a very important chemosensor to detect various environmental pollutants. This article covers a broad range of thioureas and their derivatives that are used for highly sensitive, selective, and simple fluorimetric (turn-off and turn-on), and colorimetric chemosensors for the detection and determination of different types of anions, such as CN-, AcO-, F-, ClO- and citrate ions, etc., and neutral analytes such as ATP, DCP, and Amlodipine, etc., in biological, environmental, and agriculture samples. Further, the sensing performances of thioureas-based chemosensors have been compared and discussed, which could help the readers for the future design of organic fluorescent and colorimetric sensors to detect anions and neutral analytes. We hope this study will support the new thoughts to design highly efficient, selective, and sensitive chemosensors to detect different analytes in biological, environmental, and agricultural samples. [ABSTRACT FROM AUTHOR]

Rhodamine-based chemosensors have sparked considerable interest in recent years due to their remarkable photophysical properties, which include high absorption coefficients, exceptional quantum yields, improved photostability, and significant red shifts. This article presents an overview of the diverse fluorometric, and colorimetric sensors produced from rhodamine, as well as their applications in a wide range of fields. The ability of rhodamine-based chemosensors to detect a wide range of metal ions, including Hg+2, Al3+, Cr3+, Cu2+, Fe3+, Fe2+, Cd2+, Sn4+, Zn2+, and Pb2+, is one of their major advantages. Other applications of these sensors include dual analytes, multianalytes, and relay recognition of dual analytes. Rhodamine-based probes can also detect noble metal ions such as Au3+, Ag+, and Pt2+. They have been used to detect pH, biological species, reactive oxygen and nitrogen species, anions, and nerve agents in addition to metal ions. The probes have been engineered to undergo colorimetric or fluorometric changes upon binding to specific analytes, rendering them highly selective and sensitive by ring-opening via different mechanisms such as Photoinduced Electron Transfer (PET), Chelation Enhanced Fluorescence (CHEF), Intramolecular Charge Transfer (ICT), and Fluorescence Resonance Energy Transfer (FRET). For improved sensing performance, light-harvesting dendritic systems based on rhodamine conjugates has also been explored for enhanced sensing performance. These dendritic arrangements permit the incorporation of numerous rhodamine units, resulting in an improvement in signal amplification and sensitivity. The probes have been utilised extensively for imaging biological samples, including imaging of living cells, and for environmental research. Moreover, they have been combined into logic gates for the construction of molecular computing systems. The usage of rhodamine-based chemosensors has created significant potential in a range of disciplines, including biological and environmental sensing as well as logic gate applications. This study focuses on the work published between 2012 and 2021 and emphasises the enormous research and development potential of these probes. [ABSTRACT FROM AUTHOR]

Optical detection devices have become an analytical tool of interest in diverse fields of science. The search for methods to identify and quantify different compounds has transposed this curiosity into a necessity, since some constituents threaten the safety of life in all its forms. In this context, 30 years ago, Prof. Prasanna de Silva presented the idea of sensors as Molecular Logic Gates (MLGs): a molecule that performs a logical operation based on one or more inputs (analytes) resulting in an output (optical modification such as fluorescence or absorption). In this review, we explore the implementation of MLGs based on the interference of a second input (second analyte) in suppressing or even blocking a first input (first analyte), often resulting in INHIBIT-type gates. This approach is interesting because it is not related to attached detecting groups in the MLG but to the relation between the first and the second input. In this sense, flexible and versatile MLGs can be straightforwardly designed based on input selection. To illustrate these cases, we selected examples seeking to diversify the inputs (first analytes and interfering analytes), outputs (turn on, turn off), optical response (fluorescent/colorimetric), and applicability of these MLGs.

Dynamic range is a crucial aspect in the development of fluorescent chemosensors. We aimed to address this issue using molecular logic gates. By creating an AND logic gate with two binding sites for the same type of ion, we increased the dynamic range of a sodium chemosensor while still using the same ionophore. Naphthalimide derivatives 1 and 2 were synthesized to test the plausibility of this application. Being an AND logic gate, the second molecule requires two Na+ ions, while molecule 1 requires a single ion for sensing. The application of this molecular logic gate is a useful method of altering the chemosensor range.

BTDs (2,1,3-benzothiadiazoles) are fluorescent heterocycles widely used in different applications, including biomarkers, sensing optical devices, OLEDs, organic transistors, and solar cells. This review mainly focuses on the current progress in the design of compounds derived from the BTD core, aiming for their use as chromogenic and/or fluorogenic devices for detecting anionic, cationic, and neutral analytes. Reactions and synthetic strategies that show the synthetic versatility of BTDs are initially presented, to provide a better understanding regarding the assembly of optical detection systems. The photophysical mechanisms of the detection are also described. A discussion is also presented on the target analytes for which the optical detection devices based on BTD were planned. The examples discussed here will offer the sensors community perspectives for developing new optical detection devices based on BTD for different types of analytes of importance for the most diverse areas of knowledge.

Extended organic polymers such as amorphous Covalent Organic Polymers (COPs) and crystalline Covalent Organic Frameworks (COFs) are emerging functional polymeric materials that have recently been shown promises as luminescent materials for chemosensing applications. A wide variety of luminescence COPs and COFs have been synthesized and successfully used as fluorescence-sensing materials for hazardous environmental pollutants and toxic contaminants. This review exemplifies various COPs and COFs-based fluorescence sensors for selective sensing of Fe(III) ions. The fluorescence sensors are sorted according to their structural features and each section provides a detailed discussion on the synthesis and fluorescence sensing ability of different COPs and COFs towards Fe(III) ions. Also, this review highlights the limitations of the existing organic polymer-based chemosensors and future perspectives on translating COPs and COFs-based fluorescence sensors for the practical detection of Fe(III) ions.

Optical detection devices have become an analytical tool of interest in diverse fields of science. The search for methods to identify and quantify different compounds has transposed this curiosity into a necessity, since some constituents threaten the safety of life in all its forms. In this context, 30 years ago, Prof. Prasanna de Silva presented the idea of sensors as Molecular Logic Gates (MLGs): a molecule that performs a logical operation based on one or more inputs (analytes) resulting in an output (optical modification such as fluorescence or absorption). In this review, we explore the implementation of MLGs based on the interference of a second input (second analyte) in suppressing or even blocking a first input (first analyte), often resulting in INHIBIT-type gates. This approach is interesting because it is not related to attached detecting groups in the MLG but to the relation between the first and the second input. In this sense, flexible and versatile MLGs can be straightforwardly designed based on input selection. To illustrate these cases, we selected examples seeking to diversify the inputs (first analytes and interfering analytes), outputs (turn on, turn off), optical response (fluorescent/colorimetric), and applicability of these MLGs. [ABSTRACT FROM AUTHOR]

The extreme toxicity of nerve agents and the broad spectrum of their physical and chemical properties, enabling the use of these agents in a variety of tactical situations, is a continuing challenge in maintaining the knowledge and capability to detect them, as well as in finding new effective methods. Despite significant advances in the instrumentation of the analysis of nerve agents, relatively simple methods based on the evaluation of colour signals (absorption and fluorescence), in particular those using the cholinesterase reaction, continue to be of importance. This review provides a brief presentation of the current status of these simple methods, with an emphasis on military applications, and illustrates the high interest of the professional community in their further development. At the same time, it also contains some peculiarities (high reliability and durability, resistance to extreme climatic conditions, work in deployed means of protection, low purchase prices, economic availability especially in a state of war, etc.) that the authors believe research and development of simple methods and means for the detection of nerve agents should respect. [ABSTRACT FROM AUTHOR]

The advancement of optical chemosensors has achieved success with the advent of Supramolecular Chemistry. Unlike other scaffolds, the 1,8‐naphthalimide motif has emerged as an excellent fluorescent chemosensor due to its photophysical properties like thermostability, cytotoxicity, membrane permeability, selectivity, and sensitivity. The naphthalimide scaffold is distinctive in its ways of tracking biological analytes and diagnosing its role in various diseases. This review provides insight into current developments in the synthesis and designing of 1,8‐naphthalimide‐based chemosensors for the recognition of metal ions, its mechanistic approach for its sensitivity, selectivity, and practical applications in a real environment. We hope that this review will aid to develop a novel approach to sense toxic analytes in real water samples and improve real‐time applications. [ABSTRACT FROM AUTHOR]

Bearing in mind the interest in the development and application of amino acids/peptides as bioinspired systems for sensing, a series of new phenylalanine derivatives bearing thiosemicarbazone and hydrazone units at the side chain were synthesised and evaluated as fluorimetric chemosensors for ions. Thiosemicarbazone and hydrazone moieties were chosen because they are considered both proton-donor and proton-acceptor, which is an interesting feature in the design of chemosensors. The obtained compounds were tested for the recognition of organic and inorganic anions (such as AcO−, F−, Cl−, Br−, I−, ClO4−, CN−, NO3−, BzO−, OH−, H2PO4− and HSO4−) and of alkaline, alkaline-earth, and transition metal cations, (such as Na+, K+, Cs+, Ag+, Cu+, Cu2+, Ca2+, Cd2+, Co2+, Pb2+, Pd2+, Ni2+, Hg2+, Zn2+, Fe2+, Fe3+ and Cr3+) in acetonitrile and its aqueous mixtures in varying ratios via spectrofluorimetric titrations. The results indicate that there is a strong interaction via the donor N, O and S atoms at the side chain of the various phenylalanines, with higher sensitivity for Cu2+, Fe3+ and F− in a 1:2 ligand-ion stoichiometry. The photophysical and metal ion-sensing properties of these phenylalanines suggest that they might be suitable for incorporation into peptide chemosensory frameworks. [ABSTRACT FROM AUTHOR]

Organic compounds display several electronic and structural features which enable their application in various fields, ranging from biological to non-biological. These compounds contain heteroatoms like sulfur, nitrogen and, oxygen, which provide coordination sites to act as ligands in the field of coordination chemistry and are used as chemosensors to detect various metal ions. This review article covers different organic compounds including Schiff bases, thiourea, pyridine, rhodamine, triazole, pyrene, coumarin, imidazole, diaminomaleonitrile, naphthoxazole, pyrimidine, thiophene, thioether, and other functional groups based chemosensors that contain heteroatoms like sulfur, nitrogen and, oxygen for fluorimetric and colorimetric detection of Zn(II) ions in different environmental, agricultural, and biological samples. Further, the sensing performances of these chemosensors have been compared and discussed which could help the readers for the future design of organic fluorescent and colorimetric chemosensors for the detection of Zn(II) ions. We hope this study will support the new thoughts to design a simple, efficient, selective, and sensitive chemosensor for the detection of Zn(II) ions in different samples (environmental, agricultural, and biological). [ABSTRACT FROM AUTHOR]

Poly[4-(1′-pyrenyl)styrene was synthesized for the first time, its photophysical properties were explored, and among them, the fluorescence with a high absolute quantum yield was discovered. Data acquired using the fluorescent titration revealed the opportunity to detect model nitroaromatic explosives at detection limits varying in the range from 10−6 to 10−7 mol L−1. The results reported herein for the homopolymer were compared with the corresponding data for poly[styrene-co-4-(1′-pyrenyl)styrene] copolymer synthesized previously. [ABSTRACT FROM AUTHOR]

A selective sensing technique for HgII ions has been developed utilizing an amino acid based probe. The design, synthesis and efficacy of the chemosensor have been described. The probe (SALTYR) was successfully synthesized from a naturally occurring amino acid after sequential functional group modifications. Recognition studies were performed against a wide variety of metal cations and anions including real water samples. All the analyses were carried out utilizing UV–vis and fluorescence techniques with micromolar concentrations of the probe in HEPES buffer. The selectivity of the probe was found to be very specific for HgII with quenching of the fluorescence in a turn-off mechanism. The detection limit of the probe SALTYR was calculated and found to be 5.9 × 10−6 M. Quantum chemical calculations demonstrated the stability of the HgII complex in the context of binding energy. Furthermore, the change of the pattern of emission spectra has been rationalized with a logic gate model. A novel chemosensor has been designed and synthesized from a naturally occurring α-amino acid (l-tyrosine). Selective recognition of HgII has been achieved utilizing the chemosensing ability of the probe (SALTYR). The fluorescence intensity has been subsequently quenched showing a turn-off mechanism. [ABSTRACT FROM AUTHOR]