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Academic literature on the topic 'FLUORESCENCE CHEMOSENSORS'

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Published: 10 March 2023

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Journal articles on the topic "FLUORESCENCE CHEMOSENSORS"

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Ikeda, Hiroshi. "Diversely Responsive Turn-On Fluorescent Cyclodextrin Chemosensors: Guest Selectivities and Mechanism Insights." Chemosensors 8, no. 3 (July 1, 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, the mechanism of new CD chemosensors was investigated using nuclear magnetic resonance (NMR) spectroscopy and molecular mechanics calculations. The fluorescence intensity of NC0βCD and NC0γCD slightly decreased and largely increased, respectively, upon the addition of ursodeoxycholic acid as a guest. This is due to the fact that the fluorophore of NC0βCD moved away to the hydrophilic bulk water to form hydrogen bonds between the host and the guest, while the fluorophore of NC0γCD remained located at the primary hydroxy side of the γ-CD unit to form a stable inclusion complex with hydrogen bonds between the fluorophore and the guest. NC0αCD also acted as a turn-on chemosensor for small guests, which could not be detected by the previous CD chemosensors. The motion restriction of the fluorophore through the generation of inclusion complexes could also contribute to increase in fluorescence intensity.
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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 (February 6, 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 of chemosensors with analytes was substantiated through a combination of 1H NMR spectra, mass spectra, and DFT studies. The ‘turn-on’ nature of fluorescence sensing by the two chemosensors enabled the development of colorimetric detection, filter-paper-based test strips, and polystyrene film-based detection techniques.
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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 (October 1, 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: anthracene, crown ethers, saxitoxin, paralytic shellfish poison (PSP), binding constants; chemosensors.
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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 (October 25, 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, respectively, were characterized by 1H and 13C NMR and high-resolution mass spectrometry, and their photophysical and ion-responsive behaviours were investigated via absorption and fluorescence measurements. Chemosensors 1 and 2 displayed a rapid colorimetric response upon the addition of Cu2+, with a remarkable increase in the absorbance and fluorescence intensities. The addition of other metal ions caused no significant effects. Moreover, the resulting chemosensor-Cu2+ complexes revealed to be good probes for the sensing of Li+ with reversibility and low detection limits. The recognition ability of the new chemosensors was investigated by absorption and fluorescence titrations and competitive studies.
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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 (November 14, 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 sodium dodecyl sulfate (SDS, 20 mM, pH 7.5) solution with acetonitrile, 90:10 v/v. In acetonitrile solution, these probes had a fluorescence response for different cations but, most importantly, in SDS aqueous solution both compounds displayed a selective fluorescence response in the presence of palladium.
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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 (December 3, 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 limit of hypochlorite is 1.80 × 10−4 M in solution, and the visual detection limit is 1.27 µg/cm2 with the naked eye for the flexible paper-based chemosensor. The proposed flexible chemosensors show a good selectivity and sensitivity which has great potential for effective detection of hypochlorite anions without any spectroscopic instrumentation.
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Bai, Liping, Yuhang Xu, Guang Li, Shuhui Tian, Leixuan Li, Farong Tao, Aixia Deng, Shuangshuang Wang, and Liping Wang. "A Highly Selective Turn-on and Reversible Fluorescent Chemosensor for Al3+ Detection Based on Novel Salicylidene Schiff Base-Terminated PEG in Pure Aqueous Solution." Polymers 11, no. 4 (March 27, 2019): 573. http://dx.doi.org/10.3390/polym11040573.

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The development of highly selective and sensitive chemosensors for Al3+ detection in pure aqueous solution is still a significant challenge. In this work, a novel water-soluble polymer PEGBAB based on salicylidene Schiff base has been designed and synthesized as a turn-on fluorescent chemosensor for the detection of Al3+ in 100% aqueous solution. PEGBAB exhibited high sensitivity and selectivity to Al3+ over other competitive metal ions with the detection limit as low as 4.05 × 10−9 M. PEGBAB displayed high selectivity to Al3+ in the pH range of 5–10. The fluorescence response of PEGBAB to Al3+ was reversible in the presence of ethylenediaminetetraacetic acid (EDTA). Based on the fluorescence response, an INHIBIT logic gate was constructed with Al3+ and EDTA as two inputs. Moreover, test strips based on PEGBAB were fabricated facilely for convenient on-site detection of Al3+.
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Udhayakumari, Duraisamy. "Various Sensing Mechanisms for the Design of Naphthalimide based Chemosensors Emerging in Recent Years." Recent Innovations in Chemical Engineering (Formerly Recent Patents on Chemical Engineering) 13, no. 4 (June 2, 2020): 262–89. http://dx.doi.org/10.2174/2405520413666200217125754.

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In the design of novel fluorescent chemosensors, investigation of new sensing mechanisms between recognition and signal reporting units is of increasing interest. In recent years, a smart chemosensor probe containing a 1,8-naphthalimide moiety could be developed as a fluorescent and colorimetric sensor for toxic anions, metal ions, biomolecules, nitroaromatics, and acids and be further applied to monitor the relevant biological applications. In this field, several problems and challenges still exist. This critical review is mainly focused on various sensing mechanisms that have emerged in the past few years, such as Photo-Induced Electron Transfer (PET), Intramolecular Charge Transfer (ICT), Fluorescence Resonance Energy Transfer (FRET), Excited-State Intramolecular Proton Transfer (ESIPT), hydrogen bonding and displacement approach. The review concludes with some current and future perspectives, including the use of the naphthalimides for sensing anions, metal ions, biomolecules, nitroaromatics and acids and their potential uses in various fields.
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Peng, Xiao Jun. "Fluorescence Chemosensors Based on Intramolecular Charge Transfer and Intramolecular Energy Transfer." Advanced Materials Research 441 (January 2012): 783. http://dx.doi.org/10.4028/www.scientific.net/amr.441.783.

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Ratiometric fluorescent sensors which based on ICT mechanism permit signal rationing to detect target molecules by measuring the ratio of fluorescence intensities at two different wavelengths, which are autoemitted by sensors upon binding objects. The autoreferential function of relative changes of two fluorescence intensities may avoid the influences of many nontarget factors in the changes of monofluorescence intensity. Therefore, the design of ratiometric fluorescent sensors is of great current interest. Generally, Cd2+ and Zn2+ havevery similar chemical properties, so the discrimination of them is very difficult.In sensor 1, we chose boradiazaindacene (BODIPY) as the fluorophore because it absorbs and emits in the visible region with high quantum yield, large extinction coefficient and good photo-stability,and N, N-bis(pyridin-2-ylmethyl)benzenamine as Cd2+ receptor. A vinyl group between the receptor and BODIPY fluorophore can induce red-shifts in absorption and fluorescence spectra. When Cd2+ is added into the aqueous solution of 1, owing to the reduction of the electron-donating character of the receptor, the photophysical properties of BODIPY will consequently be changed. In fact, 1 can distinguish Cd2+ from Zn2+ and especially can be used in both general fluorescence microscopy and ratiometric fluorescence microscopy.
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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 (November 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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Dissertations / Theses on the topic "FLUORESCENCE CHEMOSENSORS"

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Cabell, Larry Allen. "Chemosensors and competition sensing assays /." Digital version accessible at:, 1999. http://wwwlib.umi.com/cr/utexas/main.

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Jin, Shan. "Development of Boronic Acid-Based Chemosensors." Digital Archive @ GSU, 2009. http://digitalarchive.gsu.edu/chemistry_diss/31.

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It is well known that boronic acids can bind with diols and can be further applied as chemosensors for biomolecules such as carbohydrates and dopamine. Carbohydrates are known to mediate a large number of biological and pathological events. Small and macromolecules capable of carbohydrate recognition have great potentials as research tools, diagnostics, vectors for targeted delivery of therapeutic and imaging agents, and therapeutic agents.
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Williams, James Anthony Gareth. "Luminescence behaviour of macrocycle metal complexes." Thesis, Durham University, 1995. http://etheses.dur.ac.uk/5313/.

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Luminescent complexes of lanthanide ions are of growing interest because the long lifetime of emission allows time-resolved detection procedures to be employed. A key step in the development of such systems lies in the preparation of highly luminescent complexes which display high stability in aqueous solution. A series of ligands based on 1,4,7,10-tetraazacyclododecane have been prepared, in which the nitrogen atoms are appended with coordinating phosphinate or amide groups, or a combination of both. The compounds obtained are octadentate ligands which form water-soluble lanthanide complexes of high stability. Complexes incorporating aryl groups in the pendent arms have been prepared and some display intense metal luminescence following excitation into the organic chromophores. A back energy transfer process occurs in the terbium complexes containing naphthyl or quinohnone groups. Measurements of the luminescence lifetimes in H(_2)O and H(_2)O show diat diere are no metal-bound water molecules in the tetrabenzylphosphinate complexes. Those incorporating one amide and three phosphinate groups display hydration states between 0 and 1. An attempt has been made to correlate this information with that obtained from an analysis of the nuclear magnetic resonance dispersion profiles of related gadolinium complexes. The complexes incorporating secondary amide groups display an additional deactivation pathway for the metal excited state involving energy transfer into N-H bonds. The luminescence behaviour of four macrocyclic tetraamide ligands incorporating naphthyl fluorophores has been studied. These compounds exhibit distinctive changes in luminescence in the presence of quenching (eg. Pb(^2+), Cu(^2+) and Ni(^2+)) and non- quenching ions (eg. Cd(^2+) and Zn(^2+)). This behaviour extends to non-aqueous solution. The protonated tetranaphthyl ligand forms an intramolecular excimer in which the excimer emission displays a sensitive dependence on the polarity of die solvent.
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Fan, Li-juan. "Design, synthesis and photophysics of fluorescence "turn-on" conjugated polymer chemosensors." Diss., Online access via UMI:, 2006.

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Sargenti, Azzurra <1986&gt. "Study of Magnesium Homeostasis and Intracellular Compartmentalization in Human Cells by Fluorescent Chemosensors and Synchrotron X-Ray Fluorescence." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2016. http://amsdottorato.unibo.it/7496/1/Sargenti_Azzurra_tesi.pdf.

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In this study, we investigated the analytical capabilities of DCHQ5, a new fluorescent chemosensor, belonging to the family of diaza-crown-hydroxyquinolines, for the quantitative assessment of total intracellular magnesium content, and its biological applications. We performed a comparative study of DCHQ5 and DCHQ1, the latter being the mother probe of the series, which showed preliminary encouraging results comparable to atomic absorption spectroscopy. We demonstrated that DCHQ5 is able to accurately quantify the total amount of Mg in a very “small” cellular population, by using a simple spectrofluorimetric assay. Furthermore, DCHQ5 demonstrated to be a versatile tool for different applications: its higher intracellular retentions allow to perform cytofluorimetric assays and two-photon confocal microscopy on whole and viable cells; its photochemical characteristic make it excitable in both UV and visible spectra, and the presence of different lifetimes allow to perform fluorescence life time imaging of intracellular Mg. DCHQ5 was also exploited for studying the involvement of magnesium in the commitment of human adipose-derived mesenchymal stem cells (hASCs) with a mixture of hyaluronic, butyric and retinoic acids (HBR). We found that in normal magnesium availability, hASCs precommitment is associated by an increase of total magnesium content during time and by a block in the G2/M phase of the cell cycle. Moreover, our results demonstrated that magnesium deprivation triggers multilineage enrichments of HBR-induced preconditioning of hASCs. The second part of this research was aimed at comparing single cells elemental analysis performed with synchrotron-based fluorescence and cell population analysis carry out by DCHQ5. We exploited innovative techniques of x-ray fluorescence microscopy by using a multimodal approach in order to achieve within the cells the spatial distribution of the concentration of magnesium and fundamental light elements for life. The combination of classical and innovative analytical techniques can shed new light in the comprehension of magnesium homeostasis.
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Sargenti, Azzurra <1986&gt. "Study of Magnesium Homeostasis and Intracellular Compartmentalization in Human Cells by Fluorescent Chemosensors and Synchrotron X-Ray Fluorescence." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2016. http://amsdottorato.unibo.it/7496/.

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In this study, we investigated the analytical capabilities of DCHQ5, a new fluorescent chemosensor, belonging to the family of diaza-crown-hydroxyquinolines, for the quantitative assessment of total intracellular magnesium content, and its biological applications. We performed a comparative study of DCHQ5 and DCHQ1, the latter being the mother probe of the series, which showed preliminary encouraging results comparable to atomic absorption spectroscopy. We demonstrated that DCHQ5 is able to accurately quantify the total amount of Mg in a very “small” cellular population, by using a simple spectrofluorimetric assay. Furthermore, DCHQ5 demonstrated to be a versatile tool for different applications: its higher intracellular retentions allow to perform cytofluorimetric assays and two-photon confocal microscopy on whole and viable cells; its photochemical characteristic make it excitable in both UV and visible spectra, and the presence of different lifetimes allow to perform fluorescence life time imaging of intracellular Mg. DCHQ5 was also exploited for studying the involvement of magnesium in the commitment of human adipose-derived mesenchymal stem cells (hASCs) with a mixture of hyaluronic, butyric and retinoic acids (HBR). We found that in normal magnesium availability, hASCs precommitment is associated by an increase of total magnesium content during time and by a block in the G2/M phase of the cell cycle. Moreover, our results demonstrated that magnesium deprivation triggers multilineage enrichments of HBR-induced preconditioning of hASCs. The second part of this research was aimed at comparing single cells elemental analysis performed with synchrotron-based fluorescence and cell population analysis carry out by DCHQ5. We exploited innovative techniques of x-ray fluorescence microscopy by using a multimodal approach in order to achieve within the cells the spatial distribution of the concentration of magnesium and fundamental light elements for life. The combination of classical and innovative analytical techniques can shed new light in the comprehension of magnesium homeostasis.
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Finkelmeier, Nils. "Synthesis and Fluorescence Properties of Anthracene Derivatives and their Metal Complexes." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2013. http://hdl.handle.net/11858/00-1735-0000-0023-994A-7.

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Paul, Uchenna Prince. "Fluorescence Detectors for Proteins and Toxic Heavy Metals." Diss., CLICK HERE for online access, 2004. http://contentdm.lib.byu.edu/ETD/image/etd416.pdf.

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Akdeniz, Ali. "Sensing of Enantiomeric Excess in Chiral Carboxylates." Bowling Green State University / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1465223828.

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Fang, Albert Geeson. "Development of novel fluorescent chemosensors /." Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 2004. http://wwwlib.umi.com/cr/ucsd/fullcit?p3138822.

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Books on the topic "FLUORESCENCE CHEMOSENSORS"

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1957-, Czarnik Anthony W., American Chemical Society. Division of Organic Chemistry., and American Chemical Society Meeting, eds. Fluorescent chemosensors for ion and molecule recognition. Washington, DC: American Chemical Society, 1993.

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Czarnik, Anthony W., ed. Fluorescent Chemosensors for Ion and Molecule Recognition. Washington, DC: American Chemical Society, 1993. http://dx.doi.org/10.1021/bk-1993-0538.

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Wu, Luling, Adam C. Sedgwick, Xiao-Peng He, and Tony D. James. Fluorescent Chemosensors. Royal Society of Chemistry, The, 2023.

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Wu, Luling, Adam C. Sedgwick, Xiao-Peng He, and Tony D. James. Fluorescent Chemosensors. Royal Society of Chemistry, The, 2023.

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Wu, Luling, Adam C. Sedgwick, Xiao-Peng He, and Tony D. James. Fluorescent Chemosensors. Royal Society of Chemistry, The, 2023.

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Book chapters on the topic "FLUORESCENCE CHEMOSENSORS"

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Parola, A. Jorge, João C. Lima, Carlos Lodeiro, and Fernando Pina. "Water-soluble Fluorescent Chemosensors: in Tune with Protons." In Springer Series on Fluorescence, 117–49. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/4243_2007_003.

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Nandhikonda, Premchendar, Zhi Cao, and Michael D. Heagy. "Theme and Variation on N-Aryl-1, 8-Napthalimides: Minimal Modification to Red-Shifted Fluorescence and Applications in Fluorescent Chemosensors." In Reviews in Fluorescence 2009, 303–19. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-9672-5_11.

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Goretzki, Gudrun, Peter V. Bonnesen, Reza Dabestani, and Gilbert M. Brown. "Fluorophores as Chemosensors Based on Calix[4]arenes and Three Different Fluorescence Reporters." In ACS Symposium Series, 12–33. Washington, DC: American Chemical Society, 2006. http://dx.doi.org/10.1021/bk-2006-0943.ch002.

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Parkesh, Raman, Emma B. Veale, and Thorfinnur Gunnlaugsson. "Fluorescent Detection Principles and Strategies." In Chemosensors, 229–52. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118019580.ch12.

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Niko, Yosuke, and Shigeru Watanabe. "Fluorescent Chemosensors." In Progress in the Science of Functional Dyes, 377–408. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-33-4392-4_11.

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Fahrni, Christoph J. "Design of Cation-Selective Synthetic Fluorescent Indicators." In Chemosensors, 371–94. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118019580.ch18.

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Valeur, B., F. Badaoui, E. Bardez, J. Bourson, P. Boutin, A. Chatelain, I. Devol, B. Larrey, J. P. Lefèvre, and A. Soulet. "Cation-Responsive Fluorescent Sensors." In Chemosensors of Ion and Molecule Recognition, 195–220. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-3973-1_15.

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Akkaya, Engin U. "Squaraine-Based Long Wavelength Fluorescent Chemosensors for Ions." In Chemosensors of Ion and Molecule Recognition, 177–88. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-3973-1_13.

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Yoon, J., N. E. Ohler, D. H. Vance, W. D. Aumiller, and A. W. Czarnik. "A Fluorescent Chemosensor with Selectivity for Hg(II)." In Chemosensors of Ion and Molecule Recognition, 189–94. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-3973-1_14.

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Ueno, Akihiko. "Fluorescent Cyclodextrins as Chemosensors for Molecular Recognition." In Molecular Recognition and Inclusion, 77–84. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5288-4_8.

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Conference papers on the topic "FLUORESCENCE CHEMOSENSORS"

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Kovalev, Igor S., Leila K. Sadieva, Olga S. Taniya, Victoria M. Yurk, Artem S. Minin, Dmitry S. Kopchuk, Grigory V. Zyryanov, et al. "Pyrene-based lipophilic/biphilic chemosensors for the fluorescence “turn-off” detection of nitroanalytes in aqueous media." In MODERN SYNTHETIC METHODOLOGIES FOR CREATING DRUGS AND FUNCTIONAL MATERIALS (MOSM2020): PROCEEDINGS OF THE IV INTERNATIONAL CONFERENCE. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0068657.

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Prodi, L., L. S. Dolci, M. Montalti, N. Zaccheroni, G. Farruggia, G. Andreani, E. Carpenè, et al. "New fluorescent chemosensors for magnesium ions in living cells." In Biomedical Optics 2006, edited by Samuel Achilefu, Darryl J. Bornhop, and Ramesh Raghavachari. SPIE, 2006. http://dx.doi.org/10.1117/12.645783.

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Wren, Stephen P., Tong Sun, and Kenneth T. V. Grattan. "A fluorescent optical fibre chemosensor for mercury detection." In International Conference on Optical Fibre Sensors (OFS24), edited by Hypolito J. Kalinowski, José Luís Fabris, and Wojtek J. Bock. SPIE, 2015. http://dx.doi.org/10.1117/12.2194588.

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Zaremba, Oleg, Sergey Kovalenko, Viktor Gusarov, and Pavlo Nikolaienko. "Rapid way to fluorescent cholic-based chemosensor precursors." In The 15th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00661.

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Nguyen, T. Hien, Stephen P. Wren, Tong Sun, and Kenneth T. V. Grattan. "Fluorescent optical fibre chemosensor for the detection of mercury." In SPIE BioPhotonics Australasia, edited by Mark R. Hutchinson and Ewa M. Goldys. SPIE, 2016. http://dx.doi.org/10.1117/12.2243054.

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Mutovska, Monika, and Yulian Zagranyarski. "Fluorescent and colorimetric chemosensors for cations based on 1,8-naphthalimide core." In RAD Conference. RAD Centre, 2022. http://dx.doi.org/10.21175/rad.sum.abstr.book.2022.11.1.

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Fu, Y. Y., L. Q. Shi, D. F. Zhu, C. He, D. Wen, C. M. Deng, Q. G. He, H. M. Cao, and J. G. Cheng. "Fluorene-thiophene-based thin-film fluorescent chemosensor for methamphetamine vapor." In TRANSDUCERS 2011 - 2011 16th International Solid-State Sensors, Actuators and Microsystems Conference. IEEE, 2011. http://dx.doi.org/10.1109/transducers.2011.5969267.

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Jones, Jr., Wayne E., Clifford Murphy, Yan Zhang, Vivian Ferry, and Scott Gilje. "Selective detection of transition metal ions by an array of functionalized fluorescent conjugated polymer chemosensors." In Environmental and Industrial Sensing, edited by Tuan Vo-Dinh and Stephanus Buettgenbach. SPIE, 2002. http://dx.doi.org/10.1117/12.456948.

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Yoon, Juyoung, and Anthony W. Czarnik. "Fluorescent chemosensors that signal carbohydrates in aqueous solution: a novel mechanism for signal transduction is required and found." In Fibers '92, edited by Robert A. Lieberman. SPIE, 1993. http://dx.doi.org/10.1117/12.143499.

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Narakathu, Binu B., Massood Z. Atashbar, Fasil A. Abebe, Carla S. Eribal, and Ekkehard Sinn. "8.2.5 Detection of Zn2+ Ions Using a Novel Chemosensor Based on Coumarin Schiff-base Derivatives by Electrochemical and Fluorescence Spectroscopy." In 14th International Meeting on Chemical Sensors - IMCS 2012. AMA Service GmbH, Von-Münchhausen-Str. 49, 31515 Wunstorf, Germany, 2012. http://dx.doi.org/10.5162/imcs2012/8.2.5.

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Reports on the topic "FLUORESCENCE CHEMOSENSORS"

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Guttinger, Kimberly. Multi-Dimensional Analysis of Fluorescent Chemosensor Data. Portland State University Library, January 2015. http://dx.doi.org/10.15760/honors.194.

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Shepodd, Timothy J., Thomas Zifer, James Ross McElhanon, and Larry A. Rahn. Biological detection and tagging using tailorable, reactive, highly fluorescent chemosensors. Office of Scientific and Technical Information (OSTI), November 2006. http://dx.doi.org/10.2172/895704.

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Kawakami, J., R. T. Bronson, G. Xue, J. S. Bradshaw, and R. M. Izatt. Characterization of Bis-8-hydroxyquinoline-Armed Diazatrithia-16-crown-5 and Diazadibenzo-18-crown-6 Ligands as Fluorescent Chemosensors for Zinc. Fort Belvoir, VA: Defense Technical Information Center, June 2002. http://dx.doi.org/10.21236/ada406097.

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