Relevant bibliographies by topics / Aromatic boronic acid sensors

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Academic literature on the topic 'Aromatic boronic acid sensors'

Author: Grafiati
Published: 7 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "Aromatic boronic acid sensors"

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Li, Tao, Yu-Jing Sheng, Xiao-Li Sun, et al. "Novel NBN-Embedded Polymers and Their Application as Fluorescent Probes in Fe3+ and Cr3+ Detection." Polymers 14, no. 10 (2022): 2025. http://dx.doi.org/10.3390/polym14102025.

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The isosteric replacement of C═C by B–N units in conjugated organic systems has recently attracted tremendous interest due to its desirable optical, electronic and sensory properties. Compared with BN-, NBN- and BNB-doped polycyclic aromatic hydrocarbons, NBN-embedded polymers are poised to expand the diversity and functionality of olefin polymers, but this new class of materials remain underexplored. Herein, a series of polymers with BNB-doped π-system as a pendant group were synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization from NBN-containing vinyl monome
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Xiao, Can, Victor Izquierdo-Roca, and Pilar Rivera-Gil. "Real Time and Spatiotemporal Quantification of pH and H2O2 Imbalances with a Multiplex Surface-Enhanced Raman Spectroscopy Nanosensor." ACS Materials Au 3, no. 2 (2023): 164–75. https://doi.org/10.1021/acsmaterialsau.2c00069.

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Oxidative stress is involved in many aging-related pathological disorders and is the result of defective cellular management of redox reactions. Particularly, hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), is a major byproduct and a common oxidative stress biomarker. Monitoring its dynamics and a direct correlation to diseases remains a challenge due to the complexity of redox reactions. Sensitivity and specificity are major drawbacks for H<sub>2</sub>O<sub>2</sub>&nbsp;sensors regardless of their readout. Luminiscent boronate-based probes such as 3-mercaptophenylboronic acid (3-MPBA) are eme
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Wang, Wei, Xingming Gao, and Binghe Wang. "Boronic Acid-Based Sensors." Current Organic Chemistry 6, no. 14 (2002): 1285–317. http://dx.doi.org/10.2174/1385272023373446.

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Zhang, Chen, and Kenneth S. Suslick. "Syntheses of boronic-acid-appended metalloporphyrins as potential colorimetric sensors for sugars and carbohydrates." Journal of Porphyrins and Phthalocyanines 09, no. 09 (2005): 659–66. http://dx.doi.org/10.1142/s1088424605000770.

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Boronic-acid-based dyes have been widely studied in the past decade as potential sensors for sugars and carbohydrates, owing to the strong interaction of boronic acid and diols. In this work, two boronic-acid-appended metalloporphyrins were synthesized by new routes and tested as potential sugar and carbohydrate sensors. Boronic acid substituents were attached either to a β-pyrrolic position ((2-dihydroxylboryl-5,10,15,20-tetraphenylporphyrinato)zinc(II), 1) or to the meso-position ((10-dihydroxylboryl-5,15-diphenylporphyrinato)zinc(II), 2) of the porphyrin core. These complexes were tested as
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Williams, George T., Jonathan L. Kedge, and John S. Fossey. "Molecular Boronic Acid-Based Saccharide Sensors." ACS Sensors 6, no. 4 (2021): 1508–28. http://dx.doi.org/10.1021/acssensors.1c00462.

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Hattori, Yoshihide, Miki Ishimura, Youichirou Ohta, et al. "Detection of boronic acid derivatives in cells using a fluorescent sensor." Organic & Biomolecular Chemistry 13, no. 25 (2015): 6927–30. http://dx.doi.org/10.1039/c5ob00753d.

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Zhang, Xiao-tai, Guang-jian Liu, Zhang-wei Ning, and Guo-wen Xing. "Boronic acid-based chemical sensors for saccharides." Carbohydrate Research 452 (November 2017): 129–48. http://dx.doi.org/10.1016/j.carres.2017.10.010.

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Sibrian-Vazquez, Martha, Jorge O. Escobedo, Mark Lowry, and Robert M. Strongin. "Progress toward red and near-infrared (NIR) emitting saccharide sensors." Pure and Applied Chemistry 84, no. 11 (2012): 2443–56. http://dx.doi.org/10.1351/pac-con-11-11-06.

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Red-shifted and near-infrared (NIR)-active rhodamine analogs and their boronic acid derivatives were synthesized and studied. These latter compounds function as fluorogenic NIR active substrates for sugar sensing. The effects of benzannulation and boronic acid functionalization on fluorophore optical and sensing properties are described.
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Bian, Zhancun, Aiqin Liu, Ying Li, et al. "Boronic acid sensors with double recognition sites: a review." Analyst 145, no. 3 (2020): 719–44. http://dx.doi.org/10.1039/c9an00741e.

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Herein, boronic acid-based sensors containing two recognition sites were summarized systematically. By two recognition sites working synergistically, the binding affinity and selectivity of sensors improve significantly.
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Zhai, Wenlei, Brette M. Chapin, Akina Yoshizawa, et al. "“Click-fluors”: triazole-linked saccharide sensors." Organic Chemistry Frontiers 3, no. 8 (2016): 918–28. http://dx.doi.org/10.1039/c6qo00171h.

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Dissertations / Theses on the topic "Aromatic boronic acid sensors"

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Wang, Hui-Chen. "Selective boronic acid fluorescent sensors for saccharide detection." Thesis, University of Bath, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.582865.

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Boronic acids in orgamc chemistry are extensively used as building blocks in coupling reactions. Moreover, boronic acids also act as Lewis acids which enable them to easily form reversible covalent complexes with sugars, amino acids and other Lewis base donors. Taking this unique characteristic that two phenylboronic acids separated by a six-carbon amino linker are especially selective for D-glucose. The major part of this research is to modify boronic acid sensors with various fluorophores and material supports, not just for saccharide detection, but also for other applications such as protei
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Ni, Weijuan. "Development of Boronic Acid-Based Spectroscopic Sensors for Saccharides." NCSU, 2004. http://www.lib.ncsu.edu/theses/available/etd-01052004-165857/.

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Boronic acid functional group is used widely as a recognition moiety for the development of sensors for saccharides, due to its unique strong and reversible interaction with diols. The fluorescence and/or UV spectroscopic method are the easiest and most common methods to signal the binding event of these receptors (boronic acid compounds) with saccharides. This dissertation consists of three major parts. First, a series of fluorescent diboronic acid compounds with an anthracene PET (photoinduced electron transfer) system were designed and synthesized (Chapter 1). These compounds can be used as
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Zhai, Wenlei. "'Click-fluors' : boronic acid-based saccharide sensors via CuAAC reaction." Thesis, University of Birmingham, 2017. http://etheses.bham.ac.uk//id/eprint/7197/.

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A series of mono- and bis-boronic acid compounds were synthesised via copper-catalysed azide-alkyne cycloaddition (CuAAC) reactions. The conditions of the CuAAC reaction were optimised across a range of substrates. In chapter 2, the saccharide binding capacity of the synthesised mono-boronic acids (1\(^s\)\(^t\) and 2\(^n\)\(^d\) generation "click-fluors") were studied by fluorescence spectroscopy and isothermal titration calorimetry (ITC). The fluorescence studies of the synthesised boronic acids binding with D-fructose indicated that the triazole ring - boron acid distance has an obvious eff
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Bosch, Laurence Isabelle. "Design synthesis and evaluation of novel boronic acid based fluorescent sensors." Thesis, University of Bath, 2004. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.398432.

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Kaur, Gurpreet. "Synthesis of Boronic Acid Based Sensors for Glucose and Sialic Acid and Synthesis of Novel and Selective PDE4 Enzyme Inhibitors." Digital Archive @ GSU, 2006. http://digitalarchive.gsu.edu/chemistry_diss/9.

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The boronic acid functional group is known to bind compounds with the diol group tightly and reversibly in aqueous environment and has been used as a recognition moiety for the design of carbohydrate sensors. The first chapter of the dissertation studies the synthesis and substitution effect on the affinity and selectivity of a known boronic acid-based glucose sensor. In such a sensor design effort, the availability of a signaling event, whether it is fluorescence or UV, is crucial. The second chapter studies the detailed mechanism on how a well-known fluorescent boronic acid compound change
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Sun, Xiaolong. "Design, synthesis and evaluation of fluorescent sensors for the detection of saccharide and reactive oxygen species." Thesis, University of Bath, 2015. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.669030.

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Reactive oxygen species (ROS) and reactive nitrogen species (RNS), saccharide (i.e. monosaccharide, disaccharide and polysaccharide), are continuously generated, transformed and consumed in the living systems. As a consequence of their significant value towards human health in aerobic life, it is very important and has drawn much attention in the chemical and biological sensing of the species. It is our long-standing interest in the recognition of monosaccharide (e.g. glucose) through exploration of various boronate-based fluorescence probes, thus, based on the previous work, we started on the
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Levonis, Stephan Michael. "Design and Synthesis of Boronolectin Fluorescence Sensors." Thesis, Griffith University, 2012. http://hdl.handle.net/10072/365998.

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This thesis reports on the use of the element boron in organic chemistry. Its role in catalysis, as well as its broad utility when in the form of a boronic acid functional group is demonstrated. Boric acid and boronic acids have applications in numerous kinds of chemical reactions as catalysts. Boric acid is demonstrated in this work to catalyse the esterification of a- hydroxycarboxylic acid starting materials, including carbohydrates, typically in excellent yield. A series of reactions were conducted to demonstrate the utility and limitations of this technique. Included in this work is the s
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Murugan, Thiruppathi, and 莫西儒. "Oxygen and boronic acid functionalized screen printed carbon electrode for electrochemical sensors." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/rp8uxs.

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博士<br>國立中興大學<br>化學系所<br>106<br>This thesis describes the oxygen, boronic acid functionalization of screen printed carbon electrode (SPCE) and utilization of those functional moieties for versatile sensor applications. In-situ generated oxygen functionalities along with edge/defect sites of preanodized SPCE (SPCE*) is used for metal free oxidation of poly aromatic hydrocarbons (PAHs). In later sections, we report preparation of stimuli responsive boronic acid based probes on SPCE via both electrochemical as well as chemical routes. In the electrochemical method, 4-Aminophenylboronic acid (4-APB
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Metola, Pedro. "Boronic acids : structural and mechanistic studies and application as macromolecular sensing systems." Thesis, 2013. http://hdl.handle.net/2152/28345.

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Boronic acids, particularly those that carry an ortho-aminomethyl group, have been extensively utilized in the field of molecular recognition in recent years thanks to their ability to reversibly bind to a wide variety of polyol substrates. They have been shown to form cyclic boronate esters rapidly upon reaction with 1,2- and 1,3-diols, catechols, carbohydrates and hydroxycarboxylic acids, making them attractive as potential sensing units. While they have found broad application in this forum, the mechanism by which they work is still up for debate. This work begins in Chapter 1 with a review
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Neethirajan, Sureshraja. "DEVELOPMENT OF A POLYANILINE BORONIC ACID (PABA) CARBON DIOXIDE (CO2) SENSOR FOR USE IN THE AGRI-FOOD INDUSTRY." 2009. http://hdl.handle.net/1993/3214.

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In the agri-food industry, carbon dioxide sensors can be used for process control, monitoring quality, and assessing safety. A carbon dioxide sensor was developed using poly aniline boronic acid (PABA) conducting polymer as the electrically conductive region of the sensor for use in the agri-food industry and was demonstrated for use in detecting incipient or ongoing spoilage in stored grain. The developed sensor dynamically detected up to 2455 ppm CO2 concentration levels. The performance of the sensor in measurements of low concentrations of dissolved CO2 was characterized using standard sol
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Book chapters on the topic "Aromatic boronic acid sensors"

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James, Tony D. "Boronic Acid-Based Receptors and Sensors for Saccharides." In Boronic Acids. Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527606548.ch12.

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Yang, Xiaochuan, Yunfeng Cheng, Shan Jin, and Binghe Wang. "Boronic Acid-Based Receptors and Chemosensors." In Artificial Receptors for Chemical Sensors. Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527632480.ch6.

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Fossey, John S., and Tony D. James. "Boronic Acid Based Modular Fluorescent Saccharide Sensors." In Reviews in Fluorescence. Springer New York, 2009. http://dx.doi.org/10.1007/978-0-387-88722-7_5.

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Sivaev, Igor B., and Vladimir I. Bregadze. "Boronic Acid-Based Sensors for Determination of Sugars." In Boron-Based Compounds. John Wiley & Sons, Ltd, 2018. http://dx.doi.org/10.1002/9781119275602.ch2.3.

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Taber, Douglass. "Substituted Benzenes: The Alvarez-Manzaneda Synthesis of (-)-Taiwaniquinone G." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0065.

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Continuing efforts toward the direct functionalization of aromatic C-H bonds, Nobutaka Fujii and Hiroaki Ohno of Kyoto University described (Chem. Commun. 2009, 3413) a Pd-mediated protocol for the ortho hydroxylation of aryl tetrahydropyrimidines such as 1. To use a boronic acid as an activating/directing group, Michinori Suginome, also of Kyoto University, devised (J. Am. Chem. Soc. 2009, 131, 7502) the pyrazolylpyridyl derivative 3. The product 4 could be returned to the boronic acid or carried on to the borate ester, in each case with recovery of the directing group. Eiichi Nakamura of the
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Taber, Douglass F. "Substituted Benzenes: The Kirsch Synthesis of Cybrodol." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0063.

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Stephen L. Buchwald of MIT established (J. Am. Chem. Soc. 2010, 132, 14076) a Pd-catalyzed protocol for conversion of an aryl triflate 1 to the halide 2. Jie Wu of Fudan University prepared (Tetrahedron Lett. 2010, 51, 6646) aromatic halides from the corresponding carboxylic acids. Yong-Chua Teo of Nanyang Technological University described (Tetrahedron Lett . 2010, 51, 3910) the Mn-mediated conversion of 3 to 5, suggesting a benzyne intermediate. Takanori Shibata of Waseda University effected (Synlett 2010, 2601) the direct Ru-mediated coupling of aryl halides with amines, and Paul Helquist o
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Taber, Douglass F. "Preparation of Benzene Derivatives: The Yu/Baran Synthesis of (+)-Hongoquercin A." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0061.

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Lutz Ackermann of the Georg-August-Universität Göttingen oxidized (Org. Lett. 2013, 15, 3484) the anisole derivative 1 to the phenol 2. Melanie S. Sanford of the University of Michigan devised (Org. Lett. 2013, 15, 5428) complementary condi­tions for either para acetoxylation of 3, illustrated, to give 4, or meta acetoxylation. Lukas J. Goossen of the Technische Universität Kaiserlautern developed (Synthesis 2013, 45, 2387) conditions for the cascade alkoxylation/decarboxylation of 5 to give 6. Cheol-Hong Cheon of Korea University showed (J. Org. Chem. 2013, 78, 12154) that the boronic acid of
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Conference papers on the topic "Aromatic boronic acid sensors"

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Wang, Fang, Yang Zhang, Zigeng Liu, et al. "Detection of glycoprotein using fiber optic surface plasmon resonance sensors with boronic acid." In 25th International Conference on Optical Fiber Sensors, edited by Youngjoo Chung, Wei Jin, Byoungho Lee, John Canning, Kentaro Nakamura, and Libo Yuan. SPIE, 2017. http://dx.doi.org/10.1117/12.2265366.

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Li, Guangquan, Ting Jiang, Xiao Zhang, Qiusheng Wang, and Guowen Li. "A new fluorescent vesicular sensor for saccharides based on boronic acid-diol recognition on the interfaces of vesicles." In 2007 IEEE Sensors. IEEE, 2007. http://dx.doi.org/10.1109/icsens.2007.4388467.

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Hashemi, P., A. Afkhami, and H. Bagheri. "P1BS.7 - An impedimetric immunosensor based on magnetic graphene nanoribbons modified by boronic acid for sensitive label-free detection of lymphoma cancer cells." In 17th International Meeting on Chemical Sensors - IMCS 2018. AMA Service GmbH, Von-Münchhausen-Str. 49, 31515 Wunstorf, Germany, 2018. http://dx.doi.org/10.5162/imcs2018/p1bs.7.

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Andrade, Karine N. de, Amanda R. P. Costa, Rodolfo I. Teixeira, et al. "Photophysical characterization of 3-acyl-4-quinolones." In VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol202006.

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4-quinolones derivatives can present fluorescent properties, depending on their substituents and on the chemical environment (e.g., acidic medium), allowing their application as ion sensors. We theoretically evaluated the photophysical properties of previously synthesized 3-acyl-4-quinolones to verify how different substituents (R1=H, NH2 and R2 = OEt, OH, NHPh) affect their absorption profiles and the emission profile of a reference compound, PB3. All DFT and TD-DFT calculations were performed at B3LYP-D3/6-311++G(d,p) level and continuum polarization model for simulated acetonitrile as solve
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Sandoval, J., J. Faustinelli, J. Granadillo, et al. "Patented Surface Automatic Valve to Maximize the Recovery of Light Oil, Condensate, and Gas from Depleted Reservoirs with Minimum Manpower Interaction and Without External Energy to be Operated." In SPE Annual Technical Conference and Exhibition. SPE, 2023. http://dx.doi.org/10.2118/214961-ms.

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Abstract This Surface Automatic Valve (SAV) is designed to recover and optimize the production from light oil, condensate, and gas in depleted reservoirs, which are no longer economically viable with the current technologies on the market. It is manufactured in stainless steel allowing operation in wells with acid and aromatic crudes. The valve's operation demands little maintenance and additionally reduces the exposure of personnel to unsafe or geographically difficult to access fields. The completion design, surface pressures and choke valve use are the initial components analyzed when deter
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