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Academic literature on the topic 'Chemosensori'

Author: Grafiati

Published: 10 March 2023

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Journal articles on the topic "Chemosensori"

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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 chemosensors.

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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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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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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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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 (February 28, 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 emission bands centered around 553-644 nm at an excitation of 280 nm. We found that the only 2Pz3 chemosensors showed quenching phenomena with a significant decrease in its emission intensity of 100% for exposure in 5 minutes with irreversible performance. Interestingly, we also found that the shifting of the emission center due to the disruption of metal-metal interaction performed by chemosensor 2Pz5 resulting in the best detection performance of methanol and ethanol (∆λ= 60 nm) and propanol (∆λ = 22 nm) showing autonomous recovery within 15 minutes. Based on the findings, the specific balance, such as rigidity and amphiphilicity in the molecular design of chemosensors, is important for the detection of vapors via supramolecular interactions.

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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 (July 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 mechanism of interaction between the S2 and CN– ions has been confirmed by the 1H NMR titration experiments. Furthermore, the detection limits of chemosensor S2 towards F– and CN– ions were found to be 3.7 and 1.2 μmol/L, respectively.

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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 (January 15, 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 summarized the application of calixarenes as the supramolecular chemosensor agent for detecting metal ions, anions, biomolecules, and neutral molecules through fluorescent spectroscopy to give brief information on the design and development of the chemosensor field. This review updates the world with the application of calixarene derivatives as fluorescent chemosensors and challenges researchers to design and develop better chemosensor agents in the future.

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Huang, Qing, Qiao Li, Hai-Li Zhang, Wei Zhu, Wen-Juan Qu, Qi Lin, Hong Yao, You-Ming Zhang, and Tai-Bao Wei. "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 (April 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 chemosensors were fabricated for convenient and efficient detection of Hg2+.

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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 (November 13, 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 environmental and medicinal relevance, this work reports the synthesis and characterization of two heterocyclic aldehydes based on the thieno[3,2-b]thiophene core, by Suzuki coupling, as well as the synthesis of the corresponding precursors. Preliminary chemosensory studies for the synthesized heterocyclic aldehydes in the presence of selected cations were also performed, in solution, in order to determine their potential application as optical chemosensors.

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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 (December 22, 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 fluorescent signaling units. The discussion focuses on the design, synthesis, and physicochemical properties of this type of fluorescent chemosensors in order to analyze the applications associated to the sensing of metal ions, anions, and neutral molecules of environmental and/or biological interest. To facilitate a quick access and overview of all the chemosensors covered in this review, a summary table of the chemosensor structures and analytes, with all the corresponding references, is also presented.

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Dissertations / Theses on the topic "Chemosensori"

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PIERSANTI, LUCA. "Nuovi chemosensori ottici aventi un derivato benzossazolico come unità sensibile." Doctoral thesis, Urbino, 2015. http://hdl.handle.net/11576/2628889.

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Samuelsen, Chad L. "Chemosensory processing in the amygdala." Tallahassee, Florida : Florida State University, 2009. http://etd.lib.fsu.edu/theses/available/etd-09212009-161414/.

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Thesis (Ph. D.)--Florida State University, 2009.
Advisor: Michael Meredith, Florida State University, College of Arts and Sciences, Dept. of Biological Science. Title and description from dissertation home page (viewed on May 4, 2010). Document formatted into pages; contains xv, 131 pages. Includes bibliographical references.

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Olofsson, Jonas. "Gender differences in chemosensory function." Licentiate thesis, Umeå University, Department of Psychology, 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-22533.

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This thesis consists of two studies, in which gender differences in nasal chemosensory function are investigated. The first study assesses odor identification ability in a populationbased sample, varying from 45 to 90 yrs, screened for cognitive impairment and severe olfactory dysfunction. Results show that women are generally better than men at identifying odors, but there is no significant interaction of gender by age. Although odoridentification is influenced by semantic memory and cognitive speed, these cognitivefactors are unlikely to cause the observed gender difference in odor identification. The second study investigates chemosensory perception in men and women by assessing eventrelatedbrain potentials, and perceptual ratings for an odorant, which varies inconcentration and olfactory/irritating properties. The results display a generally larger cortical response in women than in men, beginning from about 350 ms after stimulus onset. Women report higher perceived intensity and npleasantness at the highest stimulus concentration, and a steeper psychophysical function, than do men. The results indicatethat stronger cortical responses of nasal chemosensory stimuli provide a neural basis for stronger supra-threshold perception in women than in men, which might enhance odor identification performance. The nature and causes of these gender-differences in nasal chemosensory function are discussed.

This thesis for the licenciate degree is based on the following studies:Larsson, M., Nilsson, L-G., Olofsson, J.K., & Nordin, S. (2004). Demographic and cognitive predictors of odor identification: Evidence from a population-based study.Chemical Senses, 29, 547-554.Olofsson, J.K., & Nordin, S. (2004). Gender differences in chemosensory perception andevent-related potentials. Chemical Senses, 29, 629-637.

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Roberts, Craig Dane. "cAMP Signaling in Chemosensory Transduction." Scholarly Repository, 2008. http://scholarlyrepository.miami.edu/oa_dissertations/161.

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cAMP is a second messenger in a variety of chemosensory receptors, including taste buds and glucose-sensitive pancreatic beta-cells. cAMP is modulated during taste transduction, yet the significance of cAMP changes and the taste cell types in which they occur (Type I glial-like; Type II Receptor; Type III Presynaptic) remain unclear. I developed techniques to image real-time changes in intracellular cAMP in taste cells using genetically-encoded cAMP reporters. This FRET-based reporter permits one to measure single-cell cAMP levels with excellent spatial and temporal resolution (Zaccolo & Pozzan 2002, Science 295:1711). Using a biolistic approach I have transfected rat fungiform taste buds with cAMP reporter plasmids. Focal application of bitter tastant to living fungiform tastebuds in situ produced a decrease in [cAMP]i within individual taste receptor cells. These results are qualitatively similar to previous biochemical measurements from homogenized taste tissue (Yan et al. 2001, Am J Physiol Cell Physiol 280:C742) but are now allowing us to examine the cAMP response in individual, identified cells. I next explored the effect of elevating cAMP on calcium levels, using Fura-2 imaging of isolated mouse vallate taste buds. Elevating [cAMP]i in taste buds evoked calcium responses in presynaptic/Type III taste cells, which do not express GAD1. cAMP induced responses were generated by calcium influx. Using pharmacological antagonists, I determined that the calcium influx triggered by cAMP is through L-type calcium channels, whereas influx following depolarization is primarily through P/Q-type calcium channels. Consistent with these data, single cell RT-PCR showed that the L-type subunit (alpha 1C) was expressed primarily in GAD-negative Presynaptic cells, while the P/Q-type (alpha 1A) was expressed in all Presynaptic cells. Thus, cAMP may modulate the function of synapses in some taste cells. Finally, we have developed a mouse strain expressing a cAMP reporter in a tissue-specific and tetracycline-inducible manner. We crossed this mouse with another strain expressing tet-activator in beta cells of the pancreas. Such islets responded to increasing concentrations of glucose (5.5 to 35mM) with an increase in cAMP levels. The half maximum of 9mM glucose for the cAMP response corresponds well with reported glucose concentrations that elicit insulin release from whole islets. Stimulating pancreatic islets with glucose is known to drive calcium influx into beta-cells. When we simultaneously imaged both second messengers, we found that cAMP changes precede and are independent of calcium changes. In conclusion, these studies have outlined novel potential functions for cAMP signaling in the transduction of both primary tastant and plasma glucose information. In addition, the flexibility of the tet-system will enable cAMP reporter expression in numerous cell types, including those which mediate gustatory transduction.

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Stephens, Bonnie Baggett. "Chemosensory Responses in Azospirillum brasilense." Digital Archive @ GSU, 2006. http://digitalarchive.gsu.edu/biology_diss/11.

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The ability to swim and navigate the surrounding environment confers an advantage to motile bacteria, allowing the occupation of niches that are optimum for survival and growth. Bacteria are too small to sense their environment spatially, so they must sense the environment temporally by comparing the past and present environments and altering their motility accordingly. Chemotaxis systems coordinate flagellar motility responses with temporal sensing of the environment. Chemotaxis is proposed to be involved in plant root colonization by directing soil bacteria toward root exudates of various cereals, promoting growth. The nitrogen-fixing alpha-proteobacterium Azospirillum brasilense utilizes chemotaxis to navigate its environment by integrating various environmental signals into a chemotaxis signal transduction pathway. In chemotaxis, transducers receive environmental sensory information and transmit the signal to the histidine kinase CheA, which relays the signal to the response regulator CheY. A novel chemotaxis transducer, Tlp1, has been identified and characterized as an energy sensor by constructing a tlp1 mutant and performing behavioral and root colonization assays. In order to adapt to changing environmental conditions, chemotactic microorganisms must employ a molecular “memory” comparing present environmental conditions to ones previously experienced and resetting the chemotaxis transducer to a prestimulatory status. A recently identified chemotaxis operon revealed a methyltransferase CheR and methylesterase CheB, comprising an adaptation system, suggesting that A. brasilense undergoes methylation-dependent taxis responses, contrary to previous reports. Chemotaxis and methanol release assays suggest that adaptation by methylation in locomotor behavior involves the presence of other unknown methylation systems, and the contribution of CheR and CheB to chemotactic and aerotactic responses is complex. There is growing evidence that chemotaxis-like signal transduction pathways control a myriad of other cellular processes regulated in a temporal fashion. This would convey an advantage to cells by allowing modulation of cellular processes based on slight changes in environmental conditions and provide checkpoints for energetically consuming processes. Mutations in components of the chemotaxis-like signal transduction system revealed differences in cell size and exopolysaccharide production. This work shows that the signal transduction pathway of A. brasilense modulates cell length in response to changes in nutrient conditions, independently of growth rate.

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Dujols, Virginie Elisabeth. "Rhodamine & anthracene-based chemosensors /." The Ohio State University, 1996. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487941504294111.

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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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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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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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Lau, Hsien Lee. "Chemosensory context conditioning in Caenorhabditis elegans." Thesis, University of British Columbia, 2010. http://hdl.handle.net/2429/25779.

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These studies were designed to investigate how environmental cues are associated during a non-associative learning process by studying chemosensory context conditioning for habituation in the nematode Caenorhabditis elegans. In chemosensory context conditioning for habituation animals that are trained and tested in the presence of either a taste or smell context cue show greater retention of habituation to tap stimuli when compared to animals trained and tested in different environments. This thesis is based on the work of Rankin (2000), in which taste (sodium acetate) context conditioning of habituation, extinction and latent inhibition of the cue were demonstrated. Here, I have shown context conditioning for an olfactory chemosensory cue (diacetyl) and dissociated the taste and smell pathways for this form of learning. odr-7 worms, with non-functional AWA olfactory chemosensory neuron (that detects diacetyl), showed short-term context conditioning to the taste but not to smell; the reverse was true for osm-3 worms with non-functional taste chemosensory neurons. This dissociation allows me to distinguish learning genes from genes involved in the detection of taste or smell. I also demonstrated long-term associative memory (24h) for context conditioning; context conditioning did not enhance normal long-term habituation, however, it produced memory in a training procedure that normally does not produce memory. My results showed that glr-1 (an AMPA-type ionotropic glutamate receptor subunit) and nmr-1 (an NMDA-type ionotropic glutamate receptor subunit) mutant worms did not show either short- or long-term context conditioning. To identify one site of plasticity, I showed that NMR-1 in the RIM interneurons was critical to produce short-term olfactory context conditioning. These studies lay the foundation to elucidate the cellular mechanisms of non-associative and associative learning for both short- and long-term memory, and may provide insights into how interneurons integrate information from multiple sensory systems.

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Books on the topic "Chemosensori"

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Wang, Binghe, and Eric V. Anslyn, eds. Chemosensors. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118019580.

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Schild, Detlev, ed. Chemosensory Information Processing. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-75127-1.

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NATO Advanced Research Workshop on Information Processing of Chemical Sensory Stimuli in Biological and Artificial Systems (1989 Göttingen, Germany). Chemosensory information processing. Berlin: Springer-Verlag, 1989.

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A, Simon Sidney, and Nicolelis Miguel A. L, eds. Methods in chemosensory research. Boca Raton, FL: CRC Press, 2002.

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Chemosensors: Principles, strategies, and applications. Hoboken, N.J: Wiley, 2011.

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Anslyn, Eric V., and Binghe Wang. Chemosensors: Principles, strategies, and applications. Hoboken, N.J: Wiley, 2011.

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Desvergne, J. P., and A. W. Czarnik, eds. Chemosensors of Ion and Molecule Recognition. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-3973-1.

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P, Desvergne J., Czarnik Anthony W. 1957-, North Atlantic Treaty Organization. Scientific Affairs Division., and NATO Advanced Research Workshop on Chemosensors of Ion and Molecule Recognition (1996 : Bonas, France), eds. Chemosensors of ion and molecule recognition. Dordrecht: Kluwer Academic, 1997.

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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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Korsching, Sigrun, and Wolfgang Meyerhof, eds. Chemosensory Systems in Mammals, Fishes, and Insects. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-69919-4.

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Book chapters on the topic "Chemosensori"

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Gibb, Bruce C. "Van Der Waals Interactions and the Hydrophobic Effect." In Chemosensors, 3–18. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118019580.ch1.

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Wang, Hui, Yan Chen, and Weihong Tan. "Aptamer Selection, Phage Display, and Sensor Development." In Chemosensors, 191–209. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118019580.ch10.

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Yamaguchi, Hiroyasu, Tomoki Ogoshi, and Akira Harada. "Sensor Development Using Existing Scaffolds." In Chemosensors, 211–26. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118019580.ch11.

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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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Heagy, Michael D. "New Fluorophore Design." In Chemosensors, 253–73. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118019580.ch13.

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Bicker, Kevin L., Sheryl L. Wiskur, and John J. Lavigne. "Colorimetric Sensor Design." In Chemosensors, 275–95. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118019580.ch14.

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Bayly, Simon R., George Z. Chen, and Paul D. Beer. "Electrochemical Detection." In Chemosensors, 297–328. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118019580.ch15.

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Liu, Yang, Archana Jaiswal, Mark A. Poggi, and W. David Wilson. "Surface Plasmon Resonance and Quartz Crystal Microbalance Methods for Detection of Molecular Interactions." In Chemosensors, 329–44. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118019580.ch16.

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Anzenbacher, Pavel, and Manuel A. Palacios. "Array-Based Sensors." In Chemosensors, 345–68. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118019580.ch17.

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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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Conference papers on the topic "Chemosensori"

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Sousa, Rui P. C. L., Susana P. G. Costa, Rita B. Figueira, and Maria Manuela M. Raposo. "Synthesis and Chemosensory Studies of a Heterocyclic Thiosemicarbazone as a New Tributyltin Optical Chemosensor." In International Electronic Conference on Synthetic Organic Chemistry. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13540.

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McMeniman, Conor. "Chemosensory basis of malaria transmission." In 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.90188.

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Gutierrez-Osuna, R., N. Powar, and P. Sun. "Chemosensory adaptation in an electronic nose." In Proceedings 2nd Annual IEEE International Symposium on Bioinformatics and Bioengineering (BIBE 2001). IEEE, 2001. http://dx.doi.org/10.1109/bibe.2001.974433.

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4

Lieberzeit, Peter A., A. Rehman, B. Najafi, A. Mujahid, and Franz L. Dickert. "Acoustic chemosensors for real-life environments." In 2008 IEEE International Frequency Control Symposium. IEEE, 2008. http://dx.doi.org/10.1109/freq.2008.4623033.

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Tutov, Mikhail, Aleksandr Nazirov, Aleksandr Sergeev, and Aleksandr Mironenko. "Dendrimeric rhodamine-derived chemosensor for Au3+." In Asia-Pacific Conference on Fundamental Problems of Opto- and Microelectronics 2017, edited by Roman V. Romashko, Yuri N. Kulchin, and Jyh-Chiang Jiang. SPIE, 2019. http://dx.doi.org/10.1117/12.2315110.

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Boeker, Peter, T. Haas, B. Diekmann, P. Schulze Lammer, Matteo Pardo, and Giorgio Sberveglieri. "Continuous Odour Measurement with Chemosensor Systems." In OLFACTION AND ELECTRONIC NOSE: Proceedings of the 13th International Symposium on Olfaction and Electronic Nose. AIP, 2009. http://dx.doi.org/10.1063/1.3156635.

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Ueno, Akihiko, Hiroshi Ikeda, and Taiyo Aoyagi. "Signal transduction in chemosensors of modified cyclodextrins." In BiOS '97, Part of Photonics West, edited by Richard B. Thompson. SPIE, 1997. http://dx.doi.org/10.1117/12.273523.

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Lehmann, Hartmut, Sven Brueckner, Jens Kobelke, Guenter Schwotzer, Kay Schuster, and Reinhardt Willsch. "Toward photonic crystal fiber based distributed chemosensors." In Bruges, Belgium - Deadline Past. SPIE, 2005. http://dx.doi.org/10.1117/12.623667.

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Vaknin, Ady. "The dynamics in the bacterial chemosensory arrays." In INTERNATIONAL CONFERENCE ON ANALYSIS AND APPLIED MATHEMATICS (ICAAM 2014). AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4893507.

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Maria, Letizia De, Nunzio Cennamo, Luigi Zeni, Fabio Scatiggio, and Maria Pesavento. "Optical chemosensors for transformers’oil degradation monitoring:case studies." In 2018 AEIT International Annual Conference. IEEE, 2018. http://dx.doi.org/10.23919/aeit.2018.8577418.

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Reports on the topic "Chemosensori"

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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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Greenberg, E. P. Electrophysiological and Genetic Analysis of Chemosensory Mechanisms in Spirochaeta Aurantia. Fort Belvoir, VA: Defense Technical Information Center, May 1988. http://dx.doi.org/10.21236/ada197188.

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Savage, Paul B., Ning Su, Jerald S. Bradshaw, Reed M. Izatt, and Luca Prodi. N,N-Bis-(8-hydroxy-5-nitroquinolin-7-ylmethyl)diaza-18-crown-6, a Chemosensor for Mercury Ions. Fort Belvoir, VA: Defense Technical Information Center, March 2000. http://dx.doi.org/10.21236/ada375273.

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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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