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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.

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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.

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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.
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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.

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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
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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.

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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.

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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.

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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.

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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.

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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.

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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.
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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.

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11

Fang, Guiqian, Hao Wang, Zhancun Bian, Min Guo, Zhongyu Wu, and Qingqiang Yao. "A novel boronic acid-based fluorescent sensor for selectively recognizing Fe3+ ion in real time." RSC Advances 9, no. 35 (2019): 20306–13. http://dx.doi.org/10.1039/c9ra03978c.

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12

Wang, Hao, Guiqian Fang, Hongxiao Wang, et al. "A diboronic acid fluorescent sensor for selective recognition of d-ribose via fluorescence quenching." New Journal of Chemistry 43, no. 11 (2019): 4385–90. http://dx.doi.org/10.1039/c8nj06229c.

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Herein we reported a novel boronic acid-based water-soluble sensor. It decreased the fluorescence by 50% when combined with 0.0146 M of d-ribose, while increased or not changed obviously after binding to other carbohydrates.
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13

Stephenson-Brown, Alex, Hui-Chen Wang, Parvez Iqbal, et al. "Glucose selective Surface Plasmon Resonance-based bis-boronic acid sensor." Analyst 138, no. 23 (2013): 7140. http://dx.doi.org/10.1039/c3an01233f.

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14

Muthuchamy, N., A. Gopalan, and Kwang-Pill Lee. "Highly selective non-enzymatic electrochemical sensor based on a titanium dioxide nanowire–poly(3-aminophenyl boronic acid)–gold nanoparticle ternary nanocomposite." RSC Advances 8, no. 4 (2018): 2138–47. http://dx.doi.org/10.1039/c7ra09097h.

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A highly selective and sensitive enzymeless electrochemical glucose sensor was fabricated based on a novel ternary nanocomposite composed of titanium dioxide nanowire, poly(3-aminophenyl boronic acid) and gold nanoparticles.
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15

Ding, Yongling, Huadong Sun, Chunrong Ren, Mingchen Zhang, and Kangning Sun. "A Nonenzymatic Glucose Sensor Platform Based on Specific Recognition and Conductive Polymer-Decorated CuCo2O4 Carbon Nanofibers." Materials 13, no. 12 (2020): 2874. http://dx.doi.org/10.3390/ma13122874.

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CuCo2O4 decoration carbon nanofibers (CNFs) as an enzyme-free glucose sensor were fabricated via electrospinning technology and carbonization treatment. The CNFs with advantages of abundant nitrogen amounts, porosity, large surface area, and superior electrical conductivity were used as an ideal matrix for CuCo2O4 decoration. The resultant CuCo2O4–CNF hybrids possessed favorable properties of unique three-dimensional architecture and good crystallinity, accompanied by the CuCo2O4 nanoparticles uniformly growing on the CNF skeleton. To further enhance the selective molecular recognition capacit
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16

Dorledo de Faria, Ricardo Adriano, Hassan Iden, Luiz Guilherme Dias Heneine, Tulio Matencio, and Younès Messaddeq. "Non-Enzymatic Impedimetric Sensor Based on 3-Aminophenylboronic Acid Functionalized Screen-Printed Carbon Electrode for Highly Sensitive Glucose Detection." Sensors 19, no. 7 (2019): 1686. http://dx.doi.org/10.3390/s19071686.

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A highly sensitive glucose sensor was prepared by a one-step method using 3-aminophenyl boronic acid as a unit of recognition and a screen-printed carbon electrode (SPCE) as an electrochemical transducer. Scanning Electron Microscopy confirmed the success of the functionalization of the SPCE due to the presence of clusters of boronic acid distributed on the carbon surface. In agreement with the Electrochemical Impedance Spectroscopy (EIS) tests performed before and after the functionalization, Cyclic Voltammetry results indicated that the electroactivity of the electrode decreased 37.9% owing
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17

Chi, Lina, Jianzhang Zhao та Tony D. James. "Chiral Mono Boronic Acid As Fluorescent Enantioselective Sensor for Mono α-Hydroxyl Carboxylic Acids". Journal of Organic Chemistry 73, № 12 (2008): 4684–87. http://dx.doi.org/10.1021/jo8007622.

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18

Li, Meng, Haobo Ge, Rory L. Arrowsmith, et al. "Ditopic boronic acid and imine-based naphthalimide fluorescence sensor for copper(ii)." Chem. Commun. 50, no. 80 (2014): 11806–9. http://dx.doi.org/10.1039/c4cc03453h.

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19

Das, Debasmita, Dong-Min Kim, Deog-Su Park, and Yoon-Bo Shim. "A Glucose Sensor Based on an Aminophenyl Boronic Acid Bonded Conducting Polymer." Electroanalysis 23, no. 9 (2011): 2036–41. http://dx.doi.org/10.1002/elan.201100145.

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20

Yin, Mingyuan, Caiyun Zhang, Jing Li, Haijie Li, Qiliang Deng, and Shuo Wang. "Highly Sensitive Detection of Benzoyl Peroxide Based on Organoboron Fluorescent Conjugated Polymers." Polymers 11, no. 10 (2019): 1655. http://dx.doi.org/10.3390/polym11101655.

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The method capable of rapid and sensitive detection of benzoyl peroxide (BPO) is necessary and receiving increasing attention. In consideration of the vast signal amplification of fluorescent conjugated polymers (FCPs) for high sensitivity detection and the potential applications of boron-containing materials in the emerging sensing fields, the organoboron FCPs, poly (3-aminophenyl boronic acid) (PABA) is directly synthesized via free-radical polymerization reaction by using the commercially available 3-aminophenyl boronic acid (ABA) as the functional monomer and ammonium persulfate as the ini
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21

Lin, You-Rong, Chin-Chi Hung, Hsien-Yi Chiu, et al. "Noninvasive Glucose Monitoring with a Contact Lens and Smartphone." Sensors 18, no. 10 (2018): 3208. http://dx.doi.org/10.3390/s18103208.

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Diabetes has become a chronic metabolic disorder, and the growing diabetes population makes medical care more important. We investigated using a portable and noninvasive contact lens as an ideal sensor for diabetes patients whose tear fluid contains glucose. The key feature is the reversible covalent interaction between boronic acid and glucose, which can provide a noninvasive glucose sensor for diabetes patients. We present a phenylboronic acid (PBA)-based HEMA contact lens that exhibits a reversible swelling/shrinking effect to change its thickness. The difference in thickness can be detecte
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22

Boca, Sanda, Cosmin Leordean, Simion Astilean, and Cosmin Farcau. "Chemiresistive/SERS dual sensor based on densely packed gold nanoparticles." Beilstein Journal of Nanotechnology 6 (December 29, 2015): 2498–503. http://dx.doi.org/10.3762/bjnano.6.259.

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Chemiresistors are a class of sensitive electrical devices capable of detecting (bio)chemicals by simply monitoring electrical resistance. Sensing based on surface enhanced Raman scattering (SERS) represents a radically different approach, in which molecules are optically detected according to their vibrational spectroscopic fingerprint. Despite different concepts are involved, one can find in the literature examples from both categories reporting sensors made of gold nanoparticles. The same building blocks appear because both sensor classes share a common principle: nanometric interparticle g
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23

Lerner, Mitchell B., Nicholas Kybert, Ryan Mendoza, Romain Villechenon, Manuel A. Bonilla Lopez, and A. T. Charlie Johnson. "Scalable, non-invasive glucose sensor based on boronic acid functionalized carbon nanotube transistors." Applied Physics Letters 102, no. 18 (2013): 183113. http://dx.doi.org/10.1063/1.4804438.

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24

Seraj, Sanaz, Shohre Rouhani, and Farnoush Faridbod. "Naphthalimide-based optical turn-on sensor for monosaccharide recognition using boronic acid receptor." RSC Advances 9, no. 31 (2019): 17933–40. http://dx.doi.org/10.1039/c9ra01757g.

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A fluorogenic receptor/GO nano-platform. PET developed using a new designed functional gives amplified (OFF–ON) fructose sensing with a 35-fold response. Enhancement takes place during a fast selective GO desorption.
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25

Zhang, Yujian, Zhenfeng He, and Guowen Li. "A novel fluorescent vesicular sensor for saccharides based on boronic acid–diol interaction." Talanta 81, no. 1-2 (2010): 591–96. http://dx.doi.org/10.1016/j.talanta.2009.12.041.

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26

Qian, Siyu, Yuzhang Liang, Jie Ma, Yang Zhang, Jianzhang Zhao, and Wei Peng. "Boronic acid modified fiber optic SPR sensor and its application in saccharide detection." Sensors and Actuators B: Chemical 220 (December 2015): 1217–23. http://dx.doi.org/10.1016/j.snb.2015.06.107.

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27

Wu, Xin, Xuan-Xuan Chen, Bing-Nan Song, et al. "Direct sensing of fluoride in aqueous solutions using a boronic acid based sensor." Chem. Commun. 50, no. 90 (2014): 13987–89. http://dx.doi.org/10.1039/c4cc04542d.

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28

Schiller, Alexander, Ritchie A Wessling, and Bakthan Singaram. "A Fluorescent Sensor Array for Saccharides Based on Boronic Acid Appended Bipyridinium Salts." Angewandte Chemie 119, no. 34 (2007): 6577–79. http://dx.doi.org/10.1002/ange.200701888.

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29

Schiller, Alexander, Ritchie A Wessling, and Bakthan Singaram. "A Fluorescent Sensor Array for Saccharides Based on Boronic Acid Appended Bipyridinium Salts." Angewandte Chemie International Edition 46, no. 34 (2007): 6457–59. http://dx.doi.org/10.1002/anie.200701888.

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30

Melavanki, Raveendra M. "Fluorescence quenching of a biologically active boronic acid derivative by aniline in different solvents." Canadian Journal of Physics 96, no. 6 (2018): 603–9. http://dx.doi.org/10.1139/cjp-2017-0466.

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Boronic acid derivatives are novel biologically active fluorescent molecules with numerous applications in various fields. A study of their fluorescent properties reveals some information that can be utilized in sensor design. One such study is fluorescence quenching. Here fluorescence quenching of 2-methoxypyridin-3-yl-3-boronic acid (2MPBA) in different solvents of a wide range of polarities has been carried out at room temperature by steady state fluorescence measurements. Aniline is used as the quencher. The positive deviation observed in Stern–Volmer (S-V) plots is analyzed using differen
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31

Hosseinzadeh, Rahman, Maryam Mohadjerani, Mona Pooryousef, Abbas Eslami, and Saeed Emami. "A new boronic acid fluorescent sensor based on fluorene for monosaccharides at physiological pH." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 144 (June 2015): 53–60. http://dx.doi.org/10.1016/j.saa.2015.02.066.

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32

Kim, Dai Geun, Minjung Lee, and Taek Seung Lee. "A Glucose-Selective Fluorescent Water-Soluble Hyperbranched Polymer Sensor With Boronic Acid End Groups." Molecular Crystals and Liquid Crystals 519, no. 1 (2010): 54–61. http://dx.doi.org/10.1080/15421401003598090.

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33

Levonis, Stephan M., Milton J. Kiefel, and Todd A. Houston. "Comparing Self-Assembling and Covalent Fluorescent Boronolectins for the Detection of Free Sialic Acid." Australian Journal of Chemistry 64, no. 11 (2011): 1454. http://dx.doi.org/10.1071/ch11296.

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A self-assembling fluorescence sensor with boronic acid functionalities was tested for binding selectivity to the monosaccharide, sialic acid. Working from a previously reported system, a self-assembling system could form an imine in situ that enables a conjugated fluorophore to display a measurable change in fluorescence in the presence of monosaccharide. However, further examination showed that free sugars give a similar fluorescence response to just the m-aminophenylboronic acid moiety on its own. Still, such a self-assembly method may be applicable to cell surface saccharide sensing as ald
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34

Sato, Kiyoshi, Akiko Sone, Sadao Arai, and Takamichi Yamagishi. "Stilbazolium Boronic Acid/Borate - A New Stilbazolium Betaine Dye: An Optical Molecular Sensor for Monosaccharides." HETEROCYCLES 61, no. 1 (2003): 31. http://dx.doi.org/10.3987/com-03-s25.

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35

Higashi, Azumi, Naoya Kishikawa, Kaname Ohyama, and Naotaka Kuroda. "A simple and highly selective fluorescent sensor for palladium based on benzofuran-2-boronic acid." Tetrahedron Letters 58, no. 28 (2017): 2774–78. http://dx.doi.org/10.1016/j.tetlet.2017.06.005.

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36

Wang, Zhuo, Deqing Zhang, and Daoben Zhu. "A New Saccharide Sensor Based on a Tetrathiafulvalene−Anthracene Dyad with a Boronic Acid Group." Journal of Organic Chemistry 70, no. 14 (2005): 5729–32. http://dx.doi.org/10.1021/jo050682e.

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37

Tsuchido, Yuji, Nana Nodomi, Takeshi Hashimoto, and Takashi Hayashita. "Micelle-Type Sensor for Saccharide Recognition by Using Boronic Acid Fluorescence Amphiphilic Probe and Surfactants." Solvent Extraction and Ion Exchange 39, no. 5-6 (2021): 668–77. http://dx.doi.org/10.1080/07366299.2021.1876988.

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38

Tan, Wei, Zhuo Wang, Deqing Zhang, and Daoben Zhu. "A New Saccharides and Nnucleosides Sensor Based on Tetrathiafulvalene-anthracene Dyad with Two Boronic Acid Groups." Sensors 6, no. 8 (2006): 954–61. http://dx.doi.org/10.3390/s6080954.

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39

Wang, Qiusheng, Guangquan Li, Wenyi Xiao, Haixia Qi, and Guowen Li. "Glucose-responsive vesicular sensor based on boronic acid–glucose recognition in the ARS/PBA/DBBTAB covesicles." Sensors and Actuators B: Chemical 119, no. 2 (2006): 695–700. http://dx.doi.org/10.1016/j.snb.2006.01.030.

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40

Çelik, Filiz, Hakan Çiftçi, and Uğur Tamer. "A Glucose Selective Non-enzymatic Potentiometric Chitosan-Goldnanoparticle Nanocomposite Sensor Based on Boronic Acid-Diol Recognition." Electroanalysis 30, no. 11 (2018): 2696–703. http://dx.doi.org/10.1002/elan.201800372.

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41

James, Tony D., K. R. A. Samankumara Sandanayake, and Seiji Shinkai. "Novel photoinduced electron-transfer sensor for saccharides based on the interaction of boronic acid and amine." Journal of the Chemical Society, Chemical Communications, no. 4 (1994): 477. http://dx.doi.org/10.1039/c39940000477.

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42

Mayang, Yanchao, Xiwen He, Langxing Chen, and Yukui Zhang. "Detection of transferrin by using a surface plasmon resonance sensor functionalized with a boronic acid monolayer." Microchimica Acta 184, no. 8 (2017): 2749–57. http://dx.doi.org/10.1007/s00604-017-2275-3.

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43

Fang, Guiqian, Dongxue Zhan, Ran Wang, et al. "A highly selective and sensitive boronic acid-based sensor for detecting Pd2+ ion under mild conditions." Bioorganic & Medicinal Chemistry Letters 30, no. 17 (2020): 127397. http://dx.doi.org/10.1016/j.bmcl.2020.127397.

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44

Zhou, Yanli, Hui Dong, Lantao Liu, Jing Liu, and Maotian Xu. "A novel potentiometric sensor based on a poly(anilineboronic acid)/graphene modified electrode for probing sialic acid through boronic acid-diol recognition." Biosensors and Bioelectronics 60 (October 2014): 231–36. http://dx.doi.org/10.1016/j.bios.2014.04.012.

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45

Choi, Pu-Reun, Hyun Chul Kim, Sun Min Kim, and Eunhae Koo. "Fabrication and Characterization of Luminescence Film Sensor for Detecting Defects of Barrier Films." Journal of Nanomaterials 2016 (2016): 1–6. http://dx.doi.org/10.1155/2016/9128783.

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The most critical issue on flexible electronics such as organic solar-cell, OLEDs, and flexible display is the protection of the core active materials from the degradation by water and oxygen. The defect of barrier film is the main channel for the transmission of water and oxygen molecules. Herein, in order to monitor the defects of barrier films, we have developed anthracene boronic acid pinacol ester (ABAPE) sensor which is very sensitive to water vapor. When ABAPE film is exposed to water, it gives off fluorescence emission at 389 and 408 nm under excitation peak at 366 nm. Based on the flu
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46

Hattori, Yoshihide, Takuya Ogaki, Miki Ishimura, Yoichiro Ohta, and Mitsunori Kirihata. "Development and Elucidation of a Novel Fluorescent Boron-Sensor for the Analysis of Boronic Acid-Containing Compounds." Sensors 17, no. 10 (2017): 2436. http://dx.doi.org/10.3390/s17102436.

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47

Li, Jian, Ning Zhang, Qingqing Sun, Zhanming Bai, and Jianbin Zheng. "Electrochemical sensor for dopamine based on imprinted silica matrix-poly(aniline boronic acid) hybrid as recognition element." Talanta 159 (October 2016): 379–86. http://dx.doi.org/10.1016/j.talanta.2016.06.048.

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48

Ooyama, Yousuke, Kensuke Furue, Koji Uenaka, and Joji Ohshita. "Development of highly-sensitive fluorescence PET (photo-induced electron transfer) sensor for water: anthracene–boronic acid ester." RSC Advances 4, no. 48 (2014): 25330. http://dx.doi.org/10.1039/c4ra02265c.

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49

Iwami, Yuto, Hiroki Yamamoto, and Yasumasa Kanekiyo. "Multicolor Saccharide-analysis Sensor Arrays Based on Boronic Acid-containing Thin Films Combined with Various Anionic Dyes." Chemistry Letters 42, no. 10 (2013): 1214–16. http://dx.doi.org/10.1246/cl.130599.

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50

Heinrichs, Guido, Marc Schellenträger, and Stefan Kubik. "An Enantioselective Fluorescence Sensor for Glucose Based on a Cyclic Tetrapeptide Containing Two Boronic Acid Binding Sites." European Journal of Organic Chemistry 2006, no. 18 (2006): 4177–86. http://dx.doi.org/10.1002/ejoc.200600245.

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