Relevant bibliographies by topics / Boronic acid sensor

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Boronic acid sensor'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Boronic acid sensor.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Boronic acid sensor"

1

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Bian, Zhancun, Guiqian Fang, Ran Wang, Dongxue Zhan, Qingqiang Yao, and Zhongyu Wu. "A water-soluble boronic acid sensor for caffeic acid based on double sites recognition." RSC Advances 10, no. 47 (2020): 28148–56. http://dx.doi.org/10.1039/d0ra00980f.

Full text
Abstract:
Herein, the specific recognition of caffeic acid by the double sites boronic acid sensor 5c is reported. The synergistic effect of the two recognition sites greatly improves the binding affinity and selectivity of the sensor.
APA, Harvard, Vancouver, ISO, and other styles
3

Fang, Guiqian, Hao Wang, Zhancun Bian, et al. "2-(4-Boronophenyl)quinoline-4-carboxylic acid derivatives: Design and synthesis, aggregation-induced emission characteristics, and binding activity studies for D-ribose with long-wavelength emission." Journal of Chemical Research 44, no. 3-4 (2019): 152–60. http://dx.doi.org/10.1177/1747519819893642.

Full text
Abstract:
Long-wavelength fluorescent sensors with large Stokes shifts show useful applications in chemical biology and clinical laboratory diagnosis. We have recently reported [4-(4-{[3-(4-boronobenzamido)propyl]carbamoyl}quinolin-2-yl)phenyl]boronic acid that can selectively recognize d-ribose in a buffer solution of pH 7.4. However, the short emission wavelength (395 nm) and aggregation-caused quenching effect are not conducive to applications as a sensor. Novel diboronic acid compounds are synthesized using 2-(4-boronophenyl)quinoline-4-carboxylic acid as the building block and p-phenylenediamine as
APA, Harvard, Vancouver, ISO, and other styles
4

Hattori, Yoshihide, Miki Ishimura, Yoichiro Ohta, Hiroshi Takenaka, and Mitsunori Kirihata. "Visualization of Boronic Acid Containing Pharmaceuticals in Live Tumor Cells Using a Fluorescent Boronic Acid Sensor." ACS Sensors 1, no. 12 (2016): 1394–97. http://dx.doi.org/10.1021/acssensors.6b00522.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Wang, Chunlei, Qi Wang, Min Zhong, and Xianwen Kan. "Boronic acid based imprinted electrochemical sensor for rutin recognition and detection." Analyst 141, no. 20 (2016): 5792–98. http://dx.doi.org/10.1039/c6an01294a.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Zhou, Yanli, Huijie Huangfu, Jie Yang, Hui Dong, Lantao liu, and Maotian Xu. "Potentiometric analysis of sialic acid with a flexible carbon cloth based on boronate affinity and molecularly imprinted polymers." Analyst 144, no. 21 (2019): 6432–37. http://dx.doi.org/10.1039/c9an01600g.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Badhulika, Sushmee, Chaker Tlili, and Ashok Mulchandani. "Poly(3-aminophenylboronic acid)-functionalized carbon nanotubes-based chemiresistive sensors for detection of sugars." Analyst 139, no. 12 (2014): 3077–82. http://dx.doi.org/10.1039/c4an00004h.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Fabre, Bruno, and Laurent Taillebois. "Poly(aniline boronic acid)-based conductimetric sensor of dopamine." Chemical Communications, no. 24 (2003): 2982. http://dx.doi.org/10.1039/b311198a.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Kim, Soyeon, Huie Zhu, Ali Demirci, Shunsuke Yamamoto, Tokuji Miyashita, and Masaya Mitsuishi. "Cyclosiloxane polymer bearing dynamic boronic acid: synthesis and bottom-up nanocoating." Polymer Chemistry 10, no. 38 (2019): 5228–35. http://dx.doi.org/10.1039/c9py00855a.

Full text
Abstract:
Boronic acid-containing polycyclosiloxane showed unique self-assembly nanofilm formation (6 nm film thickness) on various substrates and provided film-based metal ion sensor capability through dynamic covalent bonding.
APA, Harvard, Vancouver, ISO, and other styles
10

Miao, Yanming, Maoqing Yang, and Guiqin Yan. "Self-assembly of phosphorescent quantum dots/boronic-acid-substituted viologen nanohybrids based on photoinduced electron transfer for glucose detection in aqueous solution." RSC Advances 6, no. 11 (2016): 8588–93. http://dx.doi.org/10.1039/c5ra19911e.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Boronic acid sensor"

1

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

Full text
Abstract:
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.
APA, Harvard, Vancouver, ISO, and other styles
2

Cheng, Yunfeng. "Development of Boronic Acid Flurescent Reporters, Boronic Acid-Modified Thymidine Triphosphates for Sensor Design and Antagonists of Bacterial Quorum Sensing in Vibrio Harveyi." Digital Archive @ GSU, 2011. http://digitalarchive.gsu.edu/chemistry_diss/58.

Full text
Abstract:
Carbohydrates are known to play important roles in a large number of physiological and pathological processes. Conceivably, “binders” of carbohydrates of biological importance could be used as diagnostic and therapeutic agents. Currently, lectins are the major available tools in research for carbohydrate recognition. However, the available lectins often have cross-reactivity issues, along with the high costs and stability issues. Therefore, there is a critical need to develop alternatives (lectin mimics). In this regard, there have been very active efforts in developing different “binders”, su
APA, Harvard, Vancouver, ISO, and other styles
3

Fowle, Chris. "Carbohydrate directed photoaffinity labelling." Thesis, University of Bath, 2018. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.760976.

Full text
Abstract:
Glycoproteins have diverse and essential roles within biological systems. They are formed by enzymatic addition of saccharides to proteins during, or shortly after, translation. However, saccharides can also react with proteins non-enzymatically, a process termed glycation, which can cause impaired function and improper folding. Glycated proteins further react to form advanced glycation end-products, which have been implicated in the pathogenesis and progress of many diseases. Due to this pathological effect, glycation has been studied as a potential biomarker of these diseases. Photoaffinity
APA, Harvard, Vancouver, ISO, and other styles
4

Yang, Xiaochuan. "Design and Synthesis of Boronic Acid-Modified Nucleotides for Fluorescent Sensing and Cell Imaging." Digital Archive @ GSU, 2009. http://digitalarchive.gsu.edu/chemistry_diss/39.

Full text
Abstract:
With the rapidly increasing interest in the field of glycomics, which is the comprehensive study of the roles carbohydrates play in a living system, urgent need for developing quick and highly selective carbohydrate sensors is growing. The boronic acid group, with its electron-deficient structure (6 valence electrons with an open shell), acts as a Lewis acid with high intrinsic affinity towards Lewis bases such as fluoride, cyanide and hydroxyl groups. Specifically, formation of a 5- or 6- membered ring between the boronic acid moiety and a1,2- or 1,3-diol in aqueous solution has been fully ex
APA, Harvard, Vancouver, ISO, and other styles
5

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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
6

Ni, Weijuan. "Development of Boronic Acid-Based Spectroscopic Sensors for Saccharides." NCSU, 2004. http://www.lib.ncsu.edu/theses/available/etd-01052004-165857/.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
7

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/.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
8

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Ni, Nanting. "Application of Boronic Acids in Medicinal Chemistry (Inhibitors, Sensors)." Digital Archive @ GSU, 2010. http://digitalarchive.gsu.edu/chemistry_diss/34.

Full text
Abstract:
It is well known boronic acids have its unique chemistry and related applications in organic synthesis. The boronic acid functionally group also plays very important roles in medicinal chemistry and chemical biology. For example, boronic acids have been developed as potential therapeutic agents, chemical biology tools. All these applications are directly related to the unique electronic and chemical properties of the boronic acid group. Herein, several application of boronic acids have been studied: 1) several groups of compounds were found as bacterial quorum sensing inhibitors; 2) a boronate
APA, Harvard, Vancouver, ISO, and other styles
10

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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
More sources

Book chapters on the topic "Boronic acid sensor"

1

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Lambert, Tristan H. "Functional Group Interconversion." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0006.

Full text
Abstract:
David Milstein at the Weizmann Institute of Science reported (Angew. Chem. Int. Ed. 2013, 52, 6269) the unusual deamination of amine 1 to alcohol 3 catalyzed by ruthenium complex 2. In the reverse sense, Qing Xu at Wenzhou University found (Adv. Synth. Cat. 2013, 355, 73) that the conversion of benzyl alcohol (4) to sulfonamide 5 was catalyzed by benzaldehyde and catalytic potassium carbonate. Gold(I) catalysis was utilized (Chem. Commun. 2013, 49, 4262) by Ai-Lan Lee at Heriot-Watt University for the direct etherification of allylic alcohol 6 with isopropanol to produce 7. Tobias Ritter at Harvard demonstrated (J. Am. Chem. Soc. 2013, 135, 2470) that the reagent PhenoFluor (9) developed in his laboratory displays astonishing selectivity for the late-stage deoxyfluorination of complex alcohols and polyols, including glucopyranoside 8 to produce 10. A Mitsunobu protocol for the conversion of alcohol 11 to ester 13 using catalytic amounts of the hydrazide 12 and iron(II) phthalocyanine was developed (Angew. Chem. Int. Ed. 2013, 52, 4613) by Tsuyoshi Taniguchi at Kanazawa University. We reported (Org. Lett. 2013, 15, 38) a Mitsunobu-like inversion of alcohol 14 to mesylate 16 catalyzed by diphenylcyclopropenone 15. Domingo Gomez Pardo and Janine Cossy at ESPCI Paris Tech found (Org. Lett. 2013, 15, 902) that the reagent XtalFluor-E (18) was effective for the coupling of N-Boc proline (17) and phenylglycine ethyl ester (19) without epimerization to furnish the dipeptide 20. The conversion of primary amide 21 to secondary amide 23 via cross-coupling with boronic acid 22 was reported (Org. Lett. 2013, 15, 2314) by Donald A. Watson at the University of Delaware. Catalysis of the Lossen rearrangement of hydroxamide 24 to carbamate 26 using N-methylimidazole (25), which helped to minimize side products, was reported (Org. Lett. 2013, 15, 602) by Scott J. Miller at Yale University. Keiji Maruoka at Kyoto University demonstrated (Angew. Chem. Int. Ed. 2013, 52, 5532) that propionaldehyde (27) could be converted under simple conditions to N-Boc aminal 28, which served as a convenient source for the in situ generation of the corresponding highly useful N-Boc imine.
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Boronic acid sensor"

1

Seeleang, Boonrasri, Songpol Ongwattanakul, Chamras Promptmas, Sakoolkan Boonruang, Waleed S. Mohammed, and Romuald Jolivot. "Boronic acid Functionalized Guided Mode Resonance Sensor for HbA1c Detection." In 2018 11th Biomedical Engineering International Conference (BMEiCON). IEEE, 2018. http://dx.doi.org/10.1109/bmeicon.2018.8609979.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Cooper, Christopher R., and Tony D. James. "Fluorescent sensors based on boronic acids." In BiOS '99 International Biomedical Optics Symposium, edited by Joseph R. Lakowicz, Steven A. Soper, and Richard B. Thompson. SPIE, 1999. http://dx.doi.org/10.1117/12.347553.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Silmi, Nadiatus, Tribidasari A. Ivandini, and Asijati W. Endang. "Hypochlorous Acid Sensor using Boron-Doped Diamond Electrode in Physiological pH Solution." In 2018 3rd International Seminar on Sensors, Instrumentation, Measurement and Metrology (ISSIMM). IEEE, 2018. http://dx.doi.org/10.1109/issimm.2018.8727635.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Jia, W., and V. K. Dhir. "Experimental Study of Bubble Dynamics and Concentration Variation in the Presence of Boron in the Liquid." In ASME 2002 International Mechanical Engineering Congress and Exposition. ASMEDC, 2002. http://dx.doi.org/10.1115/imece2002-33225.

Full text
Abstract:
Accumulation of neutron absorber (boron or boron compounds) within the porous crud layer on the fuel rods in the cores of pressured water reactors (PWR) results in the so-called axial offset anomaly (AOA). There is practically little information on the gradients of neutron absorber concentration near a nucleation site on the cladding surface during the growth of a bubble. The objective of the present work is to study bubble dynamics and associated concentration field of aqueous boron. As a first step in solving the complete problem, dynamics of single bubble was studied under pool boiling cond
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Boronic acid sensor' for particular source types:
Journal articles Dissertations / Theses
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography