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1

Ying, Liang, and Yu Chun-Wei. "A Chemosensor for Fe3+ Detection Derived from Pyrene." Academic Journal of Chemistry, no. 73 (August 20, 2022): 42–46. http://dx.doi.org/10.32861/ajc.73.42.46.

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It is of great significance to find a suitable method to detect Fe3+ due to its essential role in human and animal health. Artificial chemosensors have been a suitable method in view of simple preparation, fast response, et al. [Aim]: A selective Fe3+ chemosensor was designed. [Method]: A novel Fe3+-selective chemosensor was rationally designed based on pyrene derivative by the introduction of benzoyl hydrazine. [Results] The proposed chemosensor presented good selectivity for Fe3+ in presence of other common metal ions. [Conclusions]: The proposed idea can be used for reference to enrich chem
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2

Ikeda, Hiroshi. "Diversely Responsive Turn-On Fluorescent Cyclodextrin Chemosensors: Guest Selectivities and Mechanism Insights." Chemosensors 8, no. 3 (2020): 48. http://dx.doi.org/10.3390/chemosensors8030048.

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Chemosensors have attracted considerable attention among the numerous strategies for detecting organic molecules in water. A turn-off mechanism was previously employed for the construction of a cyclodextrin (CD) chemosensor. This mechanism is greatly effective but has several shortcomings. In order to overcome these shortcomings, new fluorescent chemosensors NC0αCD, NC0βCD, and NC0γCD, which were (7-nitrobenz-2-oxa-1,3-diazol-4-yl)amine-modified α-CD, β-CD, and γ-CD, respectively, were prepared. Their guest selectivities were different from those of previously reported CD chemosensors. Here, t
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3

Mao, Hua, John B. Thorne, Jennifer S. Pharr, and Robert E. Gawley. "Effect of crown ether ring size on binding and fluorescence response to saxitoxin in anthracylmethyl monoazacrown ether chemosensors." Canadian Journal of Chemistry 84, no. 10 (2006): 1273–79. http://dx.doi.org/10.1139/v06-093.

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Convenient macrocyclization synthetic routes for the preparation of different-sized monoaza anthracylmethyl crown ether chemosensors (15-crown-5, 18-crown-6, 21-crown-7, 24-crown-8, and 27-crown-9) are described. Evaluation of these crowns as chemosensors for saxitoxin revealed that the larger crowns have moderately higher binding constants, with the 27-crown-9 chemosensor having the largest binding constant (2.29 × 105 (mol/L)–1). Fluorescence enhancements of 100% were observed at saxitoxin concentrations of 5 µmol/L, which is close to the detection limit in mouse bioassay.Key words: anthrace
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4

Goyal, Hina, Ibrahim Annan, Deepali Ahluwalia, Arijit Bag, and Rajeev Gupta. "Discriminative ‘Turn-on’ Detection of Al3+ and Ga3+ Ions as Well as Aspartic Acid by Two Fluorescent Chemosensors." Sensors 23, no. 4 (2023): 1798. http://dx.doi.org/10.3390/s23041798.

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In this work, two Schiff-base-based chemosensors L1 and L2 containing electron-rich quinoline and anthracene rings were designed. L1 is AIEE active in a MeOH-H2O solvent system while formed aggregates as confirmed by the DLS measurements and fluorescence lifetime studies. The chemosensor L1 was used for the sensitive, selective, and reversible ‘turn-on’ detection of Al3+ and Ga3+ ions as well as Aspartic Acid (Asp). Chemosensor L2, an isomer of L1, was able to selectively detect Ga3+ ion even in the presence of Al3+ ions and thus was able to discriminate between the two ions. The binding mode
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5

Ghazalli, Nur Fatiha Nur, Nurul Husna Sabran, Juan Matmin, Mohamad Azani Jalani, and Hendrik Oktendy Lintang. "Phosphorescent Vapochromic Responses of Copper(I) Complex Bearing Pyrazole Ligands for Detection of Alcohol Derivatives." Malaysian Journal of Fundamental and Applied Sciences 18, no. 1 (2022): 138–47. http://dx.doi.org/10.11113/mjfas.v18n1.2560.

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The methodical study of trinuclear copper(I) metal complexes phosphorescent vapochromic chemosensor via metal-metal interactions for sensing various volatile organic compounds has piqued the interest of many researchers. Herein, we highlighted the performance of chemosensors trinuclear copper(I) pyrazolate complexes (2Pz1‒2Pz5) with different molecular design short alkyl side chains from the respective pyrazole ligands. The synthesized complexes had demonstrated a high phosphorescent sensing capacity of various alcohol derivatives. Due to weak metal-metal interactions, the complexes give emiss
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6

Koralli, Panagiota, and Dionysios E. Mouzakis. "Advances in Wearable Chemosensors." Chemosensors 9, no. 5 (2021): 99. http://dx.doi.org/10.3390/chemosensors9050099.

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In this review, the latest research on wearable chemosensors is presented. In focus are the results from open literature, mainly from the last three years. The progress in wearable chemosensors is presented with attention drawn to the measuring technologies, their ability to provide robust data, the manufacturing techniques, as well their autonomy and ability to produce power. However, from statistical studies, the issue of patients’ trust in these technologies has arisen. People do not trust their personal data be transferred, stored, and processed through the vastness of the internet, which
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7

Sousa, Rui P. C. L., Raquel C. R. Gonçalves, Susana P. G. Costa, Rita B. Figueira, and Maria Manuela M. Raposo. "Heterocyclic Aldehydes Based on Thieno[3,2-b]thiophene Core: Synthesis and Preliminary Studies as Ion Optical Chemosensors." Cells 3, no. 1 (2020): 88. http://dx.doi.org/10.3390/ecsoc-24-08092.

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Heterocyclic aldehydes show a variety of optical properties and the versatility of their reactivity allows them to yield a wide range of more complex compounds, with application in areas such as medicinal, materials and supramolecular chemistry. The biological and environmental relevance of certain molecules and ions turns them into targets for the design of molecular recognition systems. Recently, heterocyclic aldehydes have been reported in the literature as ion chemosensors. Following the group’s work on optical chemosensors, for the detection and quantification of ions and molecules with e
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8

Verdejo, Begoña, Mario Inclán, María Paz Clares, Irene Bonastre-Sabater, Mireia Ruiz-Gasent, and Enrique García-España. "Fluorescent Chemosensors Based on Polyamine Ligands: A Review." Chemosensors 10, no. 1 (2021): 1. http://dx.doi.org/10.3390/chemosensors10010001.

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Polyamine ligands are water-soluble receptors that are able to coordinate, depending on their protonation degree, either metal ions, anionic, or neutral species. Furthermore, the presence of fluorescent signaling units allows an immediate visual response/signal. For these reasons, they can find applications in a wide variety of fields, mainly those where aqueous media is necessary, such as biological studies, wastewater analysis, soil contamination, etc. This review provides an overview of the recent developments in the research of chemosensors based on polyamine ligands functionalized with fl
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9

Albu, Camelia, Ana Chira, Gabriel-Lucian Radu, and Sandra A. V. Eremia. "Advances in Cost-Effective Chemosensors for Sustainable Monitoring in Food Safety and Processing." Chemosensors 13, no. 3 (2025): 113. https://doi.org/10.3390/chemosensors13030113.

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Cost-effective chemosensors have become an indispensable tool for sustainable monitoring in food safety and processing, where there is an urgent need for affordable, efficient, and real-time analytical solutions. This review discusses recent advances in low-cost chemosensor technologies, highlighting developments in materials, miniaturization, and integration into portable and accessible platforms. The focus is on applications for detecting contaminants, monitoring quality, and ensuring safety in food production and processing. This review also addresses the challenges related to sensor sensit
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10

Martins, Cátia D. F., Patrícia M. R. Batista, M. Manuela M. Raposo, and Susana P. G. Costa. "Crown Ether Benzoxazolyl-Alanines as Fluorimetric Chemosensors for the Detection of Palladium in Aqueous Environment." Chemistry Proceedings 3, no. 1 (2020): 5. http://dx.doi.org/10.3390/ecsoc-24-08310.

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Palladium has wide application in different contexts and, as a consequence, high levels of palladium in the environment have been reported, representing a risk to human health. Considering the interest to develop more selective and sensitive chemosensors for this analyte, two novel benzoxazolyl-alanine derivatives bearing a crown ether moiety were studied as potential fluorimetric chemosensors for palladium detection. Preliminary chemosensory studies for these unnatural amino acids in the presence of selected metal cations were performed in acetonitrile solution and in aqueous mixtures of sodi
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Queirós, Carla, Vítor A. S. Almodôvar, Fábio Martins, Andreia Leite, Augusto C. Tomé, and Ana M. G. Silva. "Synthesis of Novel Diketopyrrolopyrrole-Rhodamine Conjugates and Their Ability for Sensing Cu2+ and Li+." Molecules 27, no. 21 (2022): 7219. http://dx.doi.org/10.3390/molecules27217219.

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The search for accurate and sensitive methods to detect chemical substances, namely cations and anions, is urgent and widely sought due to the enormous impact that some of these chemical species have on human health and on the environment. Here, we present a new platform for the efficient sensing of Cu2+ and Li+ cations. For this purpose, two novel photoactive diketopyrrolopyrrole-rhodamine conjugates were synthesized through the condensation of a diketopyrrolopyrrole dicarbaldehyde with rhodamine B hydrazide. The resulting chemosensors 1 and 2, bearing one or two rhodamine hydrazide moieties,
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Leathers, Kyle W., Brenden T. Michaelis, and Matthew A. Reidenbach. "Interpreting the Spatial-Temporal Structure of Turbulent Chemical Plumes Utilized in Odor Tracking by Lobsters." Fluids 5, no. 2 (2020): 82. http://dx.doi.org/10.3390/fluids5020082.

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Olfactory systems in animals play a major role in finding food and mates, avoiding predators, and communication. Chemical tracking in odorant plumes has typically been considered a spatial information problem where individuals navigate towards higher concentration. Recent research involving chemosensory neurons in the spiny lobster, Panulirus argus, show they possess rhythmically active or ‘bursting’ olfactory receptor neurons that respond to the intermittency in the odor signal. This suggests a possible, previously unexplored olfactory search strategy that enables lobsters to utilize the temp
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13

Mohammadi, Asadollah, and Jeyran Jabbari. "Simple naked-eye colorimetric chemosensors based on Schiff-base for selective sensing of cyanide and fluoride ions." Canadian Journal of Chemistry 94, no. 7 (2016): 631–36. http://dx.doi.org/10.1139/cjc-2016-0039.

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The present work describes the design and synthesis of simple colorimetric chemosensors based on Schiff-base for highly selective sensing of cyanide and fluoride ions. The chemosensor S2, containing an electron withdrawing group (EWG), displayed selective sensing properties for both cyanide and fluoride ions. The interaction of S2 with F– and CN– ions provides remarkable colorimetric responses from yellow to purple, enabling naked-eye sensing without any spectroscopic instrumentation. The mechanism of anion binding with chemosensor S2 showed one-to-one stoichiometry by Job’s plot. The mechanis
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14

Gou, Gao Zhang, He Ping Yan, Shi Juan Xu, Na Wu, Bo Zhou, and Wei Liu. "1,8-Naphthyridine Modified Rhodamine B Derivatives: Turn-On Colorimetric Sensor for Cu2+." Advanced Materials Research 881-883 (January 2014): 1079–82. http://dx.doi.org/10.4028/www.scientific.net/amr.881-883.1079.

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A 1,8-naphthyridine modified rhodamine B derivative, one Cu2+-selective chemosensors was designed, synthesized and characterized, which display a high selectivity for Cu2+among environmentally and biologically relevant metal ions. It can detect Cu2+in aqueous solution selectively with a dramatic colour change from colorless to magenta. The detection mechanism involves a ring-opening process as a consequence of metal complex formation. Jobs plots study indicated that the chemosensor chelated Cu2+with 2:1 stoichiometry.
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15

Huang, Qing, Qiao Li, Hai-Li Zhang, et al. "A novel fluorometric chemosensor based on imidazo[4,5-b]phenazine-2-thione for ultrasensitive detection and separation of Hg2+ in aqueous solution." Canadian Journal of Chemistry 100, no. 4 (2022): 280–84. http://dx.doi.org/10.1139/cjc-2021-0244.

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We synthesized and developed 1,3-dihydro-2H-imidazo[4,5-b]phenazine-2-thione as a ratiometric chemosensor for Hg2+ recognition in a DMSO/H2O (v/v = 9:1) binary solution. We rationally introduced the phenazine imidazole group as the fluorophore and the thione moiety as the recognition site to bind Hg2+. Interestingly, the chemosensor showed an ultrasensitive response to Hg2+, and the lowest limit of detection was 0.167 nM. In addition, it can also separate Hg2+ from aqueous solutions with excellent ingestion capacity, with an adsorption ratio of up to 96%. Furthermore, ion test strips based on
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16

Acikgoz, Orhan, and Christopher Abelt. "Use of Molecular Logic Gates for the Tuning of Chemosensor Dynamic Range." Molecules 29, no. 18 (2024): 4330. http://dx.doi.org/10.3390/molecules29184330.

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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 al
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17

Dr., Vinayak Vishram Kadam. "Recent Trends in Chemosensors: A Review." International Journal of Innovative Research in Engineering & Multidisciplinary Physical Sciences 12, no. 1 (2024): 1–8. https://doi.org/10.5281/zenodo.10541952.

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Chemosensors are analytical devices or substances that are designed to detect and measure the presence of specific chemical compounds in the environment. These compounds can include gases, liquids, or solids. Chemosensors are chemical structures that respond to chemical stimuli by changing their color, fluorescence, or other electrical signal into a form that is easy to detect. The development of chemosensors for gas detection and monitoring has garnered substantial attention recently because of the significance of gases in biological and ecological systems. Thus, one of science's major object
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18

Priyangga, Krisfian Tata Aneka, Yehezkiel Steven Kurniawan, Keisuke Ohto, and Jumina Jumina. "Review on Calixarene Fluorescent Chemosensor Agents for Various Analytes." Journal of Multidisciplinary Applied Natural Science 2, no. 1 (2022): 23–40. http://dx.doi.org/10.47352/jmans.2774-3047.101.

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Calixarenes are well-known supramolecular host molecules with versatile applications. Over the past decades, hundreds of selective and sensitive detections of several analytes have been reported by employing calixarenes as the chemosensor agent. The detection and quantification of metal ions and anions are crucial as heavy metal ions are harmful to living organisms, while monitoring anions is pivotal in the environmental samples. On the other hand, detecting and quantifying biomolecules and neutral molecules are critical due to their irreplaceable role in human health. In this review, we summa
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Obaiah, G. O., M. A. Abdulzahra, A. Tewari, et al. "Selective Sensing and Determination of Cu2+ Ions in Environmental Samples with Newly Prepared Quinoline based Chemosensors and Confirmation of Results using DFT Molecular Modelling." Asian Journal of Chemistry 36, no. 7 (2024): 1571–78. http://dx.doi.org/10.14233/ajchem.2024.31456.

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An efficient turn-off-fluorescence chemosensing method has been developed to detect Cu2+ ions in a variety of samples. Two new quinoline-based chemosensors (QC1 and QC2) have been prepared under the condensation reaction of 8-quinolinecarboxylic acid with derivatives of L-valine. The synthesized chemosensors were characterized by spectroscopic techniques such as 1H NMR, UV, IR, HRMS and CHNS. The HOMO-LUMO orbitals and energy-minimized structures of the chemosensors were developed. The interaction of metal ions with chemosensors and stable structures of complexes were investigated using DFT. T
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Tang, Zeyi, Tianrui Cui, Houfang Liu, et al. "Wearable Chemosensors in Physiological Monitoring." Chemosensors 11, no. 8 (2023): 459. http://dx.doi.org/10.3390/chemosensors11080459.

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The development of flexible electronic technology has led to significant advancements in wearable sensors. In the past decades, wearable chemosensors have received much attention from researchers worldwide due to their high portability, flexibility, lightweight, and adaptability. It allows real-time access to the user’s physiological status at the molecular level to analyze their health status. Therefore, it can be widely used in the field of precision medicine. This review introduces the sensing mechanisms of wearable chemosensors and recent progress in wearable sweat and interstitial fluid-b
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Xie, Puhui, Fengqi Guo, Changshan Li, and Yue Xiao. "A new chemosensor based on rhodamine 101 hydrazone for Cu (II) in the red region." Canadian Journal of Chemistry 89, no. 11 (2011): 1364–69. http://dx.doi.org/10.1139/v11-111.

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A new chemosensor based on the spirolactam form of rhodamine 101 hydrazone (III) is found to exhibit a reversible colorimetric response toward Cu2+ in aqueous solutions in a selective, sensitive and rapid manner because of a formation of a Cu(II)-III complex. The dominating absorption maximum at 584 nm is uniquely red-shifted among rhodamine chemosensors toward Cu2+. The fluorescence of III can be detected in a low concentration of Cu2+. The results revealed that III is a good colorimetric sensor to Cu2+ in the red region.
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Fernandes, Rikitha S., Nitinkumar S. Shetty, Priyanka Mahesha, and Santhosh L. Gaonkar. "A Comprehensive Review on Thiophene Based Chemosensors." Journal of Fluorescence 32, no. 1 (2021): 19–56. http://dx.doi.org/10.1007/s10895-021-02833-x.

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AbstractThe recognition and sensing of various analytes in aqueous and biological systems by using fluorometric or colorimetric chemosensors possessing high selectivity and sensitivity, low cost has gained enormous attention. Furthermore, thiophene derivatives possess exceptional photophysical properties compared to other heterocycles, and therefore they can be employed in chemosensors for analyte detection. In this review, we have tried to explore the design and detection mechanism of various thiophene-based probes, practical applicability, and their advanced models (design guides), which cou
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Jeon, Hyokyung, Hwahui Ryu, Inho Nam, and Dong-Youn Noh. "Heteroleptic Pt(II)-dithiolene-based Colorimetric Chemosensors: Selectivity Control for Hg(II) Ion Sensing." Materials 13, no. 6 (2020): 1385. http://dx.doi.org/10.3390/ma13061385.

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Hg2+ ions can accumulate in the natural environment and in organisms, where they cause damage to the central nervous system. Therefore, the detection of Hg2+ ions is essential for monitoring environmental contamination and human health. Herein, we demonstrate a simple method for tuning chemosensor signal ratios that significantly increased chemosensor selectivity for Hg2+ detection. Selectivity tuning was accomplished for chemosensors of the type (diphosphine)Pt(dmit), bearing the two different terminal groups 1,2-bis(diphenylphosphino)ethane (dppe) and 1,2-bis[bis(pentafluorophenyl)phosphino]
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Zhou, Meng, Hui Sun, Shuai Chen, et al. "Chemosensors for H2O2 Detection: Principles, Active Materials, and Applications." Chemosensors 13, no. 2 (2025): 54. https://doi.org/10.3390/chemosensors13020054.

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Hydrogen peroxide (H2O2), a common oxidant present in the environment, food, and biological systems, has wide-ranging applications. While H2O2 is generally considered non-toxic, prolonged or repeated exposure to high concentrations can be harmful, making its accurate detection crucial in environmental monitoring, food safety, healthcare, and other fields. This review delves into the recent advancements in H2O2 detection methods, with a particular focus on chemosensors. We comprehensively summarize the fundamental principles of various chemosensor principles (e.g., colorimetric, fluorescence, c
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Rani, Poonam, Kashmiri Lal, and Rahul Shrivastava. "Tris-Triazole Based Chemosensors for Selective Sensing of Pb2+ Ions." Asian Journal of Chemistry 31, no. 11 (2019): 2443–47. http://dx.doi.org/10.14233/ajchem.2019.22076.

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A series of novel tris-trizole based neutral chemosensors (4a-c) have been synthesized via click reaction and characterized by various spectral techniques. All the synthesized triazoles were evaluated for their ion binding properties towards various cations (Cu2+, Zn2+, Ca2+, Co2+, Cd2+, Hg2+, Pb2+ and Ni2+) by UV-visible titration experiments. It was observed that the addition of Pb2+ ions to compound 4a led to significant changes in UV-visible spectrum and a new UV band was observed at 262 nm. Further, the Job′s plot confirmed the formation of 1:1 complex between compound 4a and Pb2+. The sy
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Wu, Qin, Tao Tao, Yunxia Zhao, and Wei Huang. "A Flexible Chemosensor Based on Colorimetric and Fluorescent Dual Modes for Rapid and Sensitive Detection of Hypochlorite Anion." Sensors 21, no. 23 (2021): 8082. http://dx.doi.org/10.3390/s21238082.

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A flexible chemosensor has been developed based on colorimetric and fluorescent dual modes using tetraphenylethylene-centered tetraaniline (TPE4A) for rapid and sensitive detection of hypochlorite anion. The fluorescent probe TPE4A exhibits a unique aggregation-induced emission (AIE) character which is proved by a blue shift of the fluorescent peak from 544 to 474 nm with the water equivalents increasing. With the addition of hypochlorite in solution, the absorbance of the probe changes and the responding fluorescence color can be observed to change from light green to purple. The detection li
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Esteves, Cátia I. C., Maria Manuela M. Raposo, and Susana P. G. Costa. "New Amino Acid-Based Thiosemicarbazones and Hydrazones: Synthesis and Evaluation as Fluorimetric Chemosensors in Aqueous Mixtures." Molecules 28, no. 21 (2023): 7256. http://dx.doi.org/10.3390/molecules28217256.

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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
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Kim, Sook Kyung, Dong Hoon Lee, Jong-In Hong, and Juyoung Yoon. "Chemosensors for Pyrophosphate." Accounts of Chemical Research 42, no. 1 (2009): 23–31. http://dx.doi.org/10.1021/ar800003f.

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Lee, Jong-Heun, and Hyung Gi Byun. "Chemosensors and chemoreception." Analytical and Bioanalytical Chemistry 406, no. 16 (2014): 3929. http://dx.doi.org/10.1007/s00216-014-7671-5.

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Sedgwick, Adam C., and Tony D. James. "Virtual Issue: Chemosensors." ChemistryOpen 7, no. 3 (2018): 215–16. http://dx.doi.org/10.1002/open.201800027.

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Rodrigues, João M. M., Andreia S. F. Farinha, Zhi Lin, José A. S. Cavaleiro, Augusto C. Tome, and Joao P. C. Tome. "Phthalocyanine-Functionalized Magnetic Silica Nanoparticles as Anion Chemosensors." Sensors 21, no. 5 (2021): 1632. http://dx.doi.org/10.3390/s21051632.

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Anionic species are one of the most common pollutants in residual and freshwaters. The presence of anthropogenic anions in water drastically increases the toxicity to living beings. Here, we report the preparation of a new optical active material based on tri(tosylamino)phthalocyanines grafted to ferromagnetic silica nanoparticles for anion detection and removal. The new unsymmetrical phthalocyanines (Pcs) proved to be excellent chemosensors for several anions (AcO−, Br−, Cl−, CN−, F−, H2PO4−, HSO4−, NO2−, NO3−, and OH−) in dimethyl sulfoxide (DMSO). Furthermore, the Pcs were grafted onto magn
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Rokhmah, Nevi Faizatu, Muhammad Idham Darussalam Mardjan, and Bambang Purwono. "Synthesis of Vanillin-Azine as Colorimetric Chemosensor of Sulfide Anion." Indonesian Journal of Chemistry 22, no. 6 (2022): 1490. http://dx.doi.org/10.22146/ijc.71569.

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Vanillin-azine (VA), (4,4'-((1E,1'E)-hydrazine-1,2-diylidenebis(methane-lylidene))bis(2-methoxyphenol) has been synthesized from vanillin and tested as anion colorimetric chemosensors for sulfide anion. The VA was obtained from a condensation reaction between vanillin and hydrazine hydrate with a mol ratio of 2:1 mol for 24 h at room temperature. The structure was elucidated using FTIR, GC-MS, 1H-NMR, and 13C-NMR spectrometers. The VA compound was examined as a colorimetric chemosensor for sulfide anion over several anions of CN−, F−, Cl−, Br−, I−, N3−, CH3COO−, and NO3−. The structure of the
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Ta, Daniel D., and Sergei V. Dzyuba. "Squaraine-Based Optical Sensors: Designer Toolbox for Exploring Ionic and Molecular Recognitions." Chemosensors 9, no. 11 (2021): 302. http://dx.doi.org/10.3390/chemosensors9110302.

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Small molecule-based chromogenic and fluorogenic probes play an indispensable role in many sensing applications. Ideal optical chemosensors should provide selectivity and sensitivity towards a variety of analytes. Synthetic accessibility and attractive photophysical properties have made squaraine dyes an enticing platform for the development of chemosensors. This review highlights the versatility of modular assemblies of squaraine-based chemosensors and chemodosimeters that take advantage of the availability of various structurally and functionally diverse recognition motifs, as well as utiliz
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Matmin, Juan, Nur Fatiha Ghazalli, Fazira Ilyana Abdul Razak, Hendrik O. Lintang, and Mohamad Azani Jalani. "Supramolecular Interactions in Aromatic Structures for Non-Optical and Optical Chemosensors of Explosive Chemicals." Solid State Phenomena 317 (May 2021): 202–7. http://dx.doi.org/10.4028/www.scientific.net/ssp.317.202.

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The scientific investigation based on the molecular design of aromatic compounds for high-performance chemosensor is challenging. This is because their multiplex interactions at the molecular level should be precisely determined before the desired compounds can be successfully used as sensing materials. Herein, we report on the molecular design of chemosensors based on aromatic structures of benzene as the organic motif of benzene-1,3,5-tricarboxamides (BTA), as well as the benzene pyrazole complexes (BPz) side chain, respectively. In the case of BTA, the aromatic benzene acts as the centre to
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Manjira, Mukherjee, and Chattopadhyay Pabitra. "Chemosensors based on diazole derivatives." Journal of Indian Chemical Society Vol. 94, Jul 2017 (2017): 715–44. https://doi.org/10.5281/zenodo.5604911.

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Department of Chemistry, The University of Burdwan , Golapbag, Burdwan-713 104, West Bengal, India <em>E-mail</em> : pabitracc@yahoo.com <em>Manuscript received 02 May 2017, accepted 08 May 2017</em> The heterocyclic diazole compounds and their derivatives not only exhibit a wide range of pharmacological activity but also can act as bioagent and revolve around its ability to bond to various guests as host. Hence it is useful in designing chemosensors. This review summarizes the most recent and relevant advances in this area.
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M. Sujatha, K. Mrudula Devi, Abhishek Kumar Tripathi, et al. "ROBUST AND SELECTIVE ANALYSIS OF THE Co2+ IONS USING NEWLY PREPARED QUINOLINE-BASED CHEMOSENSORS AND DFT OPTIMIZATION." RASAYAN Journal of Chemistry 18, no. 03 (2025): 1451–58. https://doi.org/10.31788/rjc.2025.1839309.

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A chemosensing method focused on sensitivity, selectivity, and reproducibility has been developed to identify Co2+ ions in various materials. Two new chemosensors (QHZ and QEDA) have been prepared by introducing the strong ligand groups (hydrazine and ethylenediamine) into quinoline molecules and characterized with spectroscopic techniques. High turn-off-fluorescence sensitivity, specifically to Co2+ ions, was demonstrated by both chemosensors. The fluorescence emission of QHZ and QEDA was at 507 and 502 nm, respectively, and they demonstrated outstanding photoluminescence properties. The sens
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Lintang, Hendrik Oktendy, Nur Fatiha Ghazalli, and Leny Yuliati. "Supramolecular Phosphorescent Trinuclear Copper(I) Pyrazolate Complexes for Vapochromic Chemosensors of Ethanol." Indonesian Journal of Chemistry 17, no. 2 (2017): 191. http://dx.doi.org/10.22146/ijc.22553.

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We highlight that by using supramolecular single crystals of phosphorescent trinuclear copper(I) pyrazolate complexes with different molecular structures (2A-E), vapochromic chemosensors were successfully designed for sensing ethanol with high sensing capability. These complexes 2A-E were synthesized from non-side chain, 3,5-dimethyl, 3,5-bis(trifluoromethyl), 3,5-diphenyl and 4-(3,5-dimethoxybenzyl)-3,5-dimethyl pyrazole ligands (1A-E) in 83, 97, 99, 88 and 85% yields, respectively. All complexes showed emission bands centered at 553, 584, 570 and 616 nm upon an excitation at 280 nm for compl
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Kumudhavalli, D., and Ayyakannu Arumugam Napoleon. "A Mini Review on Arsenic and Cadmium Ion Detection Using Fluorescent-Colorimetric Sensors." ECS Transactions 107, no. 1 (2022): 16833–42. http://dx.doi.org/10.1149/10701.16833ecst.

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Heavy metals with high atomic numbers, mass, and density are five times greater than water. They are naturally occurring elements and widely distributed in the environment due to their numerous applications like agricultural, industrial, domestic, technological, and medical fields increasing issues about their potential impact on the environment and human health. In this mini review, we focused on cadmium and arsenic metals. Cadmium is also the non-essential toxic heavy metal element found naturally in the earth's crust, and it is easily affected by plants’ movements through the food cycle and
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Park, Jong-Kwon, Junhyeop Shin, Seohyeon Jang, et al. "Rational Design of Fluorescent/Colorimetric Chemosensors for Detecting Transition Metal Ions by Varying Functional Groups." Inorganics 10, no. 11 (2022): 189. http://dx.doi.org/10.3390/inorganics10110189.

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In recent decades, concerns about increasing biological and environmental contamination have necessitated the development of chemosensors with high selectivity, sensitivity, and cost-effectiveness. In principle, the sensing performance can be affected by the functional group(s) of receptor, the charge of the metal ion(s), and the electron configuration of the sensing molecule(s)e and metal ion(s). Fine controlling of the substituents can influence the electron density of the receptor to enhance the binding affinity to metal ions, which is an effective way to improve the photophysical propertie
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Wang, Yujiao, Xiaojun Wang, Wenyu Ma, Runhua Lu, Wenfeng Zhou, and Haixiang Gao. "Recent Developments in Rhodamine-Based Chemosensors: A Review of the Years 2018–2022." Chemosensors 10, no. 10 (2022): 399. http://dx.doi.org/10.3390/chemosensors10100399.

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Chemosensors based on traditional fluorescent dyes have always contributed to the development of chemical sensor areas. In this review, the rhodamine-based chemosensors’ improvements and applications from 2018 to 2022 are discussed, mainly focusing on cations (metal ions and H+), anions (CN−, F−, etc.), and small bio-functional molecules’ (thiols, amino acids, etc.) detection. Specifically, this review highlights the detection target, detection limit, detection solution system, detection mechanism, and performance of the rhodamine-based sensors. Although these rhodamine-based sensors are well
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Medintz, Igor L. "Chemosensors Comes of Age." Chemosensors 9, no. 2 (2021): 22. http://dx.doi.org/10.3390/chemosensors9020022.

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Giannetti, Ambra, and Markéta Bocková. "Optical Chemosensors and Biosensors." Chemosensors 8, no. 2 (2020): 33. http://dx.doi.org/10.3390/chemosensors8020033.

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Xu, Zhaochao, Juyoung Yoon, and David R. Spring. "Fluorescent chemosensors for Zn2+." Chemical Society Reviews 39, no. 6 (2010): 1996. http://dx.doi.org/10.1039/b916287a.

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Bren, Vladimir A. "Fluorescent and photochromic chemosensors." Russian Chemical Reviews 70, no. 12 (2001): 1017–36. http://dx.doi.org/10.1070/rc2001v070n12abeh000667.

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Bren, V. A., O. S. Popova, I. E. Tolpygin, V. A. Chernoivanov, Yu V. Revinskii, and A. D. Dubonosov. "New ionochromic azomethinimine chemosensors." Russian Chemical Bulletin 64, no. 3 (2015): 668–71. http://dx.doi.org/10.1007/s11172-015-0916-4.

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Kryshtal, R. G., A. V. Medved, V. V. Shemet, and V. E. Zemlyakov. "Electronically tunable SAW chemosensors." Electronics Letters 35, no. 8 (1999): 676. http://dx.doi.org/10.1049/el:19990440.

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Mancin, Fabrizio, Enrico Rampazzo, Paolo Tecilla, and Umberto Tonellato. "Self-Assembled Fluorescent Chemosensors." Chemistry - A European Journal 12, no. 7 (2006): 1844–54. http://dx.doi.org/10.1002/chem.200500549.

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Sun, Kien Wen. "Chemosensors for Ion Detection." Chemosensors 11, no. 9 (2023): 499. http://dx.doi.org/10.3390/chemosensors11090499.

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Yang, Tingyu, Jinglei Qin, Jinling Zhang, et al. "Recent Progresses in NIR-II Luminescent Bio/Chemo Sensors Based on Lanthanide Nanocrystals." Chemosensors 10, no. 6 (2022): 206. http://dx.doi.org/10.3390/chemosensors10060206.

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Fluorescent bio/chemosensors are widely used in the field of biological research and medical diagnosis, with the advantages of non-invasiveness, high sensitivity, and good selectivity. In particular, luminescent bio/chemosensors, based on lanthanide nanocrystals (LnNCs) with a second near-infrared (NIR-II) emission, have attracted much attention, owing to greater penetration depth, aside from the merits of narrow emission band, abundant emission lines, and long lifetimes. In this review, NIR-II LnNCs-based bio/chemo sensors are summarized from the perspectives of the mechanisms of NIR-II lumin
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Yadav, Pramod Kumar. "Search for Chemosensors for Fluoride Ions: A Highly Promising Area of Research." Academic Voices: A Multidisciplinary Journal 4 (March 28, 2015): 42–44. http://dx.doi.org/10.3126/av.v4i0.12356.

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In recent times, chemosensors for fluoride ions have attracted a great deal of attention. Fluoride ions play an important role in many biological, industrial and environmental processes and are associated with diseases like Alzeimer’s disease. This paper covers imidazole, indole, azo-phenol and benzohydrazide based chemosensors for F-ion with synthesis and detection methods.DOI: http://dx.doi.org/10.3126/av.v4i0.12356Academic Voices Vol.4 2014: 42-44
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