硼酸类化学传感器的研究进展

doi:10.6023/cjoc201709037

有机化学 ›› 2018, Vol. 38 ›› Issue (5): 1035-1051.DOI: 10.6023/cjoc201709037 上一篇下一篇

所属专题：元素有机化学合辑2018-2019；荧光探针-生物传感合辑；有机超分子化学合辑

综述与进展

硼酸类化学传感器的研究进展

王浩^a,b,c,d, 王凯^a,b,c,d, 孙捷^a,b,c,d, 方桂迁^a,b,c,d, 姚庆强^a,b,c,d, 吴忠玉^a,b,c,d

a 济南大学山东省医学科学院医学与生命科学学院济南 250200;
b 山东省医学科学院药物研究所济南 250062;
c 国家卫生部生物技术药物重点实验室济南 250062;
d 山东省罕少见病重点实验室济南 250062

收稿日期:2017-09-22 修回日期:2017-12-22 发布日期:2018-01-03
通讯作者: 姚庆强,E-mail:yao_imm@163.com;吴忠玉,E-mail:u_med@foxmail.com E-mail:yao_imm@163.com;u_med@foxmail.com
基金资助:
山东省自然科学基金（No.ZR2014YL035）资助项目.

Research Progress of Boronic Acid in Chemsensors

Wang Hao^a,b,c,d, Wang Kai^a,b,c,d, Sun Jie^a,b,c,d, Fang Guiqian^a,b,c,d, Yao Qingqiang^a,b,c,d, Wu Zhongyu^a,b,c,d

a School of Medicine and Life Sciences University of Jinan-Shandong Academy of Medical Sciences, Jinan 250200;
b Institute of Materia Medica, Shandong Academy of Medical Sciences, Jinan 250062;
c Key Laboratory for Biotech-Drugs Ministry of Health, Jinan 250062;
d Key Laboratory of Rare and Uncommon Diseases of Shandong Province, Jinan 250062

Received:2017-09-22 Revised:2017-12-22 Published:2018-01-03
Contact: 10.6023/cjoc201709037 E-mail:yao_imm@163.com;u_med@foxmail.com
Supported by:
Project supported by the Shandong Provincial Natural Science Foundation (No. ZR2014YL035).

文章分享

摘要/Abstract

检测和识别体内某些物质，例如唾液酸化LewisA/X，能够为疾病的诊断、治疗、预后、分子示踪及深入研究相关疾病机理等方面提供重要参考.因此，开发高选择性、高灵敏度的化学传感器具有重要价值.苯基硼酸化合物由于其特殊结构，能够与糖、儿茶酚胺以及氟化物、氰化物等路易斯碱相互作用，使得其能够作为传感器用于相关物质的荧光识别和检测；且此类化合物具有高选择性、高效能、分析速度快等优点.近几年，将硼酸与纳米粒子、量子点等新材料相结合，设计出性能更加优越的硼酸传感器.综述了硼酸类化合物在传感器方面的研究进展.

关键词: 硼酸, 化学传感器, 荧光, 糖, 电化学

The detection and fluorescent identification of some substances such as sLea/x in vivo can provide important reference for the diagnosis, treatment and prognosis of disease, molecular tracing and further research on the mechanism of related diseases. Therefore, the development and discovery of high selectivity and high sensitivity chemsensors is of great value. Due to the special structure, phenyl boronic acid compounds could interact and bind with sugar, catecholamine containing catechol structure, fluoride or alkali cyanide. So boronic acids could be develeped as fluorescence sensors selectively for related substances, while have the advantages of high selectivity, high efficiency, rapid analysis and so on. In recent years, boronic acid has been functioned with new materials such as nanoparticles and quantum dots to design novel sensors for better performance. In this paper, the recent progress in the study of boronic acid compounds in sensors is reviewed.

Key words: boronic acid, chemsensor, fluorescence, carbohydrate, electrochemistry

引用此文

王浩, 王凯, 孙捷, 方桂迁, 姚庆强, 吴忠玉. 硼酸类化学传感器的研究进展[J]. 有机化学, 2018, 38(5): 1035-1051.

Wang Hao, Wang Kai, Sun Jie, Fang Guiqian, Yao Qingqiang, Wu Zhongyu. Research Progress of Boronic Acid in Chemsensors[J]. Chin. J. Org. Chem., 2018, 38(5): 1035-1051.

导出引用 EndNote|Reference Manager|ProCite|BibTeX|RefWorks

分享此文

参考文献

[1] Hu, X.; Wang, Y.; Liu, H.; Wang, J.; Tan, Y., Wang, F.; Tan, W. Chem. Sci. 2017, 8, 466.
[2] Verly, I. R. N.; Kuilenburg, A. B. P. V.; Abeling, N. G. G. M. Eur. J. Cancer 2017, 235.
[3] Bergenstal, R. M.; Bailey, T. S.; Rodbard, D.; Ziemen, M.; Guo, H.; Muehlen-Bartmer, I.; Ahmann, A. J. Diabetes Care 2017, 40, 554.
[4] Rojas, L. J.; Taracila, M. A.; Papp-Wallace, K. M.; Bethel, C. R.; Caselli, E.; Romagnoli, C.; Bonomo, R. A. Antimicrob. Agents Chemother. 2016, 60, 1751.
[5] Whyte, G. F.; Vilar, R.; Woscholski, R. ChemBioChem 2013, 6, 161.
[6] Nishiyabu, R.; Shimizu, A. Chem. Commun. 2016, 52, 9765.
[7] Imperio, D.; Del Grosso, E.; Fallarini, S.; Lombardi, G.; Panza, L. Org. Lett. 2017, 19, 1678.
[8] Guan, Y.; Zhang, Y. Chem. Soc. Rev. 2013, 42, 8106.
[9] Wu, X.; Chen, X. X.; Jiang, Y. B. Analyst 2017, 142, 1403.
[10] Wang, L.; Zhang, J.; Kim, B.; Peng, J.; Berry, S. N.; Ni, Y.; Chang, Y. T. J. Am. Chem. Soc. 2016, 138, 10394.
[11] Wu, S.; Guo, H.; Wang, L.; Xin, Y.; Cheng, Y.; Fan, W. Sens. Actuators, B 2017, 245, 11.
[12] Tanaka-Okamoto, M.; Mukai, M.; Takahashi, H.; Fujiwara, Y.; Ohue, M.; Miyamoto, Y. Glycobiology 2017, 27, 400.
[13] Springsteen, G.; Wang, B. Tetrahedron 2002, 58, 5291.
[14] Springsteen, G.; Wang, B. Chem. Commun. 2001, 17, 1608.
[15] James, T. D.; Shinkai, S. In Host-Guest Chemistry, Vol. 218, Ed.:Penadés, S., Springer-Verlag, Berlin, 2002, p. 159.
[16] Zhai, W.; Male, L.; Fossey, J. S. Chem. Commun. 2017, 53, 2218.
[17] Li, H.; Yang, C.; Zhu, X. Spectrochim. Acta, Part A 2017, 180, 199.
[18] Hosseinzadeh, R.; Mohadjerani, M.; Pooryousef, M. Spectrochim. Acta, Part A 2015, 144, 53.
[19] Teichert, J. F.; Mazunin, D.; Bode, J. W. J. Am. Chem. Soc. 2013, 135, 113.
[20] Basiruddin, S. K.; Swain, S. K. Mater. Sci. Eng., C 2016, 58, 103.
[21] Solís-Delgado, L. E.; Ochoa-Terán, A.; Yatsimirsky, A. K. Anal. Lett. 2016, 49, 2301.
[22] Hansen, J. S.; Hoeg, J. T.; Christensen, J. B. Tetrahedron 2017, 73, 3010.
[23] Karaku?, E.; Üçüncü, M.; Eanes, R. C.; Emrullaho?lu, M. New J. Chem. 2013, 37, 2632.
[24] Wang, X. K.; Peng, Y.; Tao, H. R.; Zhou, F. F.; Zhang, C.; Su, F.; Xie, W. J. Huazhong Univ. Sci.-Med. 2017, 37, 343(in Chinese). (王小康, 彭燕, 陶浩冉, 周芬芳, 张弛, 苏飞, 谢伟, 华中科技大学学报, 2017, 37, 343.)
[25] Trinchera, M.; Aronica, A.; Dall'Olio, F. Biol. 2017, 6, 16.
[26] Chang, M. H.; Chang, C. N. Tetrahedron Lett. 2014, 55, 4437.
[27] Suazette, R. Sci. China:Chem. 2010, 53, 3.
[28] Xu, X. D.; Cheng, H.; Chen, W. H.; Cheng, S. X.; Zhuo, R. X.; Zhang, X. Z. Sci. Rep. 2013, 3, 2679.
[29] Chu, Y.; Wang, D.; Wang, K.; Liu, Z. L.; Weston, B.; Wang, B. Bioorg. Med. Chem. Lett. 2013, 23, 6307.
[30] Varki, A.; Gagneux, P.; Ann, N. Y. Acad. Sci. 2012, 1253, 16.
[31] Dan, W.; Ozhegov, E.; Lin, W.; Zhou, A.; Nie, H.; Yu, L. Glycoconjugate J. 2016, 33, 725.
[32] Zhang, X.; Chen, B.; He, M.; Zhang, Y.; Peng, L.; Hu, B. Analyst 2016, 141, 1286.
[33] Matsumoto, A.; Stephenson-Brown, A. J.; Khan, T. Chem. Sci. 2017, 8, 6165.
[34] Yang, L.; Zhu, S.; Hang, W.; Wu, L.; Yan, X.; Chem, A. Anal. Chem. 2009, 81, 2555.
[35] Miyata, K.; Christie, R. J.; Kataoka, K. React. Funct. Polym. 2011, 71, 227.
[36] Perdicchio, M.; Ilarregui, J. M.; Verstege, M. I.; Cornelissen, L. A.; Schetters, S. T.; Engels, S.; van Berkel, L. A. Proc. Natl. Acad. Sci. U. S. A. 2016, 113, 3329.
[37] Xu, Y.; Sette, A.; Sidney, J.; Gendler, S. J.; Franco, A. Immunol. Cell Biol. 2005, 83, 440.
[38] Matsumoto, A.; Cabral, H.; Sato, N.; Kataoka, K.; Miyahara, Y. Angew. Chem., Int. Ed. 2010, 49, 5494.
[39] Deshayes, S.; Cabral, H.; Ishii, T.; Miura, Y.; Kobayashi, S.; Yamashita, T.; Kataoka, K. J. Am. Chem. Soc. 2013, 135, 15501.
[40] Zhang, L.; Yu, C.; Gao, R.; Niu, Y. Y.; Li, Y. L.; Chen, J.; He, J. L. Biosens. Bioelectron. 2016, 92, 434.
[41] Zhang, L.; Yu, C.; Gao, R. Biosens. Bioelectron. 2017, 92, 434.
[42] Erickson, J. M.; Messer, T. M.; Scand, J. Plast. Reconstr. Surg. 2013, 38, 1638.
[43] Richy, F.; Bruyere, O.; Ethgen, O.; Cucherat, M.; Henrotin, Y.; Reginster, J. Y. Arch. Intern. Med. 2003, 163, 1514.
[44] Wandel, S.; Jüni, P.; Tendal, B.; Nüesch, E.; Villiger, P. M.; Welton, N. J.; Trelle, S. Br. Med. J. 2010, 341, 4675.
[45] Hwang, J. S.; Kwon, M. Y.; Kim, K. H.; Lee, Y.; Lyoo, I. K.; Kim, J. E.; Han, I. O. J. Biol. Chem. 2017, 292, 1724.
[46] Singh, G.; Alekseeva, L.; Alekseev, V.; Goriachev, D.; Barinov, A.; Nasonov, E.; Pyanykh, S. Ann. Rheum. Dis. 2016, 75, 852.
[47] Reginster, J. Y.; Cooper, C.; Bruyère, O. Curr. Med. Res. Opin. 2016, 32, 1771.
[48] Kantor, E. D.; Zhang, X.; Wu, K.; Signorello, L. B.; Chan, A. T.; Fuchs, C. S.; Giovannucci, E. L. Int. J. Cancer. 2016, 139, 1949.
[49] Saegnipanthkul, S.; Waikakul, S.; Rojanasthien, S.; Totemchokyakarn, K.; Srinkapaibulaya, A.; Chin, T. C.; Lwin, M. Int. J. Rheum. Dis. 2017, 1.
[50] Tran, T. M.; Alan, Y.; Glass, T. E. Chem. Commun. 2015, 51, 7915.
[51] Suk, K. T.; Kim, H. S.; Kim, M. Y.; Kim, J. W.; Uh, Y.; Jang, I. H.; Baik, S. K. J. Korean Med. Sci. 2010, 25, 399.
[52] Huey, E. D.; Putnam, K. T.; Grafman, J. Neurology 2006, 66, 17.
[53] Beck, G. C.; Brinkkoetter, P.; Hanusch, C.; Schulte, J.; van Ackern, K.; van der Woude, F. J.; Yard, B. A. Crit. Care 2004, 8, 485.
[54] Rye, D. B. Neurology 2004, 63, S2.
[55] Nagatsu, T. Cell. Mol. Neurobiol. 2017, 1, 535.
[56] Jenkins, P. O.; Mehta, M. A.; Sharp, D. J. Brain 2016, 139, 2345.
[57] Ali, S. R.; Ma, Y.; Parajuli, R. R.; Balogun, Y.; Lai, W. Y. C.; He, H. Anal. Chem. 2007, 79, 2583.
[58] Nikolajsen, R. P. H.; Hansen, Å. M. Anal. Chim. Acta 2001, 449, 1.
[59] Seto, D.; Maki, T.; Soh, N.; Nakano, K.; Ishimatsu, R.; Imato, T. Talanta 2012, 94, 36.
[60] Wu, Z.; Li, M.; Fang, H.; Wang, B. Bioorg. Med. Chem. Lett. 2012, 22, 7179.
[61] Wu, Z.; Yang, X.; Xu, W.; Wang, B.; Fang, H. Drug Discoveries Ther. 2012, 6, 238.
[62] Chaicham, A.; Sahasithiwat, S.; Tuntulani, T.; Tomapatanaget, B. Chem. Commun. 2013, 49, 9287.
[63] Jun, E. J.; Liu, H.; Choi, J. Y.; Lee, J. Y.; Yoon, J. Sens. Actuators, B 2013, 176, 611.
[64] Ptak, T.; M?ynarz, P.; Dobosz, A.; Rydzewska, A.; Prokopowicz, M. J. Mol. Struct. 2013, 1040, 59.
[65] Liu, S.; Y. Shi, F.; Zhao, X.; Chen, L.; Su, X. Biosens. Bioelectron. 2013, 47, 379.
[66] Ma, Y.; Zhao, Y.; Zhang, F. Sens. Actuators, B 2017, 241, 735.
[67] Yang, Z. R.; Wang, M. M.; Wang, X. S. Anal. Chem. 2017, 89, 1930.
[68] Xu, Z.; Kim, S. K.; Han, S. J.; Lee, C.; Kociok-Kohn, G.; James, T. D.; Yoon, J. Eur. J. Org. Chem. 2009, 18, 3058.
[69] Swamy, K. M. K.; Lee, Y. J.; Lee, H. N.; Chun, J.; Kim, Y.; Kim, S. J.; Yoon, J. J. Org. Chem. 2006, 71, 8626.
[70] Wu, X.; Chen, X. X.; Song, B. N.; Huang, Y. J.; Ouyang, W. J.; Li, Z.; Jiang, Y. B. Chem. Commun. 2014, 50, 13987.
[71] Solís-Delgado, L. E.; Ochoa-Terán, A.; Yatsimirsky, A. K. Anal. Lett. 2016, 49, 2301.
[72] Mohammadpour, Z.; Safavi, A.; Omidvar, A.; Mohajeri, A.; Mobaraki, N.; Shamsipur, M. J. Fluorine Chem. 2016, 190, 12.
[73] Guan, R.; Chen, H.; Cao, F.; Cao, D.; Deng, Y. Inorg. Chem. Commun. 2013, 38, 112.
[74] Jose, D. A.; Elstner, M.; Schiller, A. Chem.-Eur. J. 2013, 19, 14451.
[75] Yoon, J. W.; Jeong, H.; Lee, M. H. Bull. Korean Chem. Soc. 2017, 38, 329.
[76] KyungáKwon, S.; NaáLee, H. Chem. Commun. 2008, 45, 5915.
[77] Chen, X.; Li, H.; Jin, L. Tetrahedron Lett. 2014, 55, 2537.
[78] Higashi, A.; Kishikawa, N.; Ohyama, K. Tetrahedron Lett. 2017, 58, 2774.
[79] Rhee, S. G. Science 2006, 312, 1882.
[80] Lin, M. T.; Beal, M. F. Nature 2006, 443, 787.
[81] Dai, H.; Lü, W.; Zuo, X.; Zhu, Q.; Pan, C.; Niu, X.; Chen, X. Biosens. Bioelectron. 2017, 95, 131.
[82] Reverte, M.; Vaissiere, A.; Boisguerin, P. ACS Sens. 2016, 1, 970.
[83] Chen, Z.; Tian, Z.; Kallio, K. J. Am. Chem. Soc. 2016, 138, 4900.
[84] Rios, N.; Piacenza, L.; Trujillo, M. Free Radical Biol. Med. 2016, 101, 284.
[85] Du, Ý, L.; Ni, N.; Li, M.; Wang, B. Tetrahedron Lett. 2010, 51, 1152.
[86] Du, L.; Li, M.; Zheng, S.; Wang, B. Tetrahedron Lett. 2008, 49, 3045.
[87] Li, J.; Sun, Q.; Mao, Y. J. Electroanal. Chem. 2017, 794, 1.
[88] Wu, S.; Guo, H.; Wang, L. Sens. Actuators, B 2017, 245, 11.
[89] Dervisevic, M.; Çevik, E.; ?enel, M. J. Electroanal. Chem. 2016, 776, 18.
[90] Silva-Carrillo, C.; Reynoso-Soto, E. A.; Paraguay-Delgado, F. J. Electroanal. Chem. 2017, 164, B86.
[91] Guo, S.; Chen, J.; Cai, B. Y. Mater. Chem. Front. 2017, 1, 61.
[92] Wang, W.; Kong, L.; Zhu, J. J. Colloid Interface Sci. 2017, 498, 1.
[93] Jiang, G.; Zhu, W.; Shen, X. Microchim. Acta 2017, 1, 1.
[94] Cheng, T.; Zhu, S.; Zhu, B. J. Sep. Sci. 2016, 39, 1347.
[95] Na, W.; Liu, H.; Wang, M. Microchim. Acta 2017, 184, 1463.
[96] Gu, S.; Ma, K.; Kong, J. Int. J. Electrochem. Sci. 2017, 12, 5092.
[97] Abellán-Llobregat, A.; Jeerapan, I.; Bandodkar, A. Biosens. Bioelectron. 2017, 91, 885.
[98] Wu, S.; Guo, H. Wang, L. Sens. Actuators, B 2017, 245, 11.
[99] Takahashi, S.; Suzuki, I.; Nishiyama, T. Bumseki Kagaku 2016, 65, 751.
[100] Zhou, Y.; Dong, H.; Liu, L. Biosens. Bioelectron. 2015, 64, 442.
[101] Gao, P.; Wang, Z.; Yang, L. Electrochim. Acta 2015, 151, 370.
[102] Wang, Q.; Kaminska, I.; Niedziolka-Jonsson, J. Biosens. Bioelectron. 2013, 50, 331.
[103] Thearle, R. A.; Latiff, N. M.; Sofer, Z. Electroanalysis 2017, 29, 45.
[104] Zhou, X.; Gao, X.; Song, F. Appl. Surf. Sci. 2017, 423, 810.
[105] Lawrence, K.; Nishimura, T.; Haffenden, P.; Mitchels, J. M.; Sakurai, K.; Fossey, J. S. Marken, F. New J. Chem. 2013, 37, 1883.
[106] Suzuki, J.; Shida, N.; Inagi, S. Electroanalysis 2016, 28, 2797.
[107] Yin, H.; Zhou, Y.; Yang, Z. Sens. Actuators, B 2015, 221, 1.
[108] Wang, C.; Zholudov, Y. T.; Nsabimana, A., Xu, G.; Li, J. Anal. Chim. Acta 2016, 937, 39.
[109] Wang, C.; Wang, Q.; Zhong, M.; Kan, X. Analyst 2016, 141, 5792.
[110] Zhong, M.; Teng, Y.; Pang, S.; Yan, L.; Kan, X. Biosens. Bioelectron. 2015, 64, 212.
[111] Ooyama, Y.; Uenaka, K.; Matsugasako, A.; Harima, Y.; Ohshita, J. RSC Adv. 2013, 3, 23255.
[112] Zheng, J.; Zhang, M.; Guo, X.; Wang, J.; Xu, J. Sens. Actuators, B 2017, 250, 8.
[113] Sun, X.; Zhai, W.; Fossey, J. S.; James, T. D. Chem. Commun. 2016, 52, 3456.
[114] Wang, X.; Yuan, Z. F.; Fan, J.; Karch, K. R.; Ball, L. E.; Denu, J. M.; Garcia, B. A. Mol. Cell. Proteomics 2016, 15, 2462.
[115] Abdellaoui, S.; Corgier, B. C.; Mandon, C. A.; Doumèche, B.; Marquette, C. A.; Blum, L. J. Electroanalysis 2013, 25, 671.
[116] Nübel, G.; Sorgenfrei, F. A.; Jäschke, A. Methods 2017, 117, 14.
[117] Geninatti, C. S.; Alberti, D.; Szabo, I.; Aime, S.; Djanashvili, K. Angew. Chem. 2013, 52, 1161.
[118] Wang, W.; Yin, R.; Zhang, M.; Yu, R.; Hao, C.; Zhang, L.; Jiang, T. J. Med. Chem. 2017, 60, 2840.
[119] Munusamy, S. K.; Thirumoorthy, K.; Muralidharan, V. P. Sens. Actuators, B 2017, 244, 175.

硼酸类化学传感器的研究进展

Research Progress of Boronic Acid in Chemsensors

PDF

可视化

摘要/Abstract

引用此文

分享此文

参考文献

相关文章 15

编辑推荐

相关统计

本文评价

[1]	邹发凯, 王能中, 姚辉, 王慧, 刘明国, 黄年玉. 1β-/3R-芳基硫代糖的区域与立体选择性合成[J]. 有机化学, 2024, 44(2): 593-604.
[2]	吴思敏, 唐嘉欣, 周于佳, 徐学涛, 张昊星, 王少华. 2β-Acetoxyferruginol去醋酸基骨架衍生物抑制α-葡萄糖苷酶活性研究[J]. 有机化学, 2024, 44(2): 613-621.
[3]	张莹珍, 江丹丹, 李娟华, 王菁菁, 刘昆明, 刘晋彪. 高选择性硒代半胱氨酸荧光探针的构建策略及成像[J]. 有机化学, 2024, 44(1): 41-53.
[4]	杨维清, 葛宴兵, 陈元元, 刘萍, 付海燕, 马梦林. 1,8-萘酰亚胺衍生物的设计、合成及其对半胱氨酸的识别研究[J]. 有机化学, 2024, 44(1): 180-194.
[5]	徐利军, 李宗军, 韩福社, 高翔. N,N-二甲基甲酰胺促进的富勒烯稠合噁唑啉衍生物的合成[J]. 有机化学, 2024, 44(1): 242-250.
[6]	马翠云, 罗海澜, 张福华, 郭丹, 陈树兴, 王飞. 3-Pyrrolyl BODIPY的绿色生物合成、光物理性质及应用研究[J]. 有机化学, 2024, 44(1): 216-223.
[7]	王兢睿, 冯永奎, 王能中, 黄年玉, 姚辉. 钯催化立体选择性合成硝基烷类β-碳糖苷[J]. 有机化学, 2023, 43(9): 3216-3225.
[8]	李焕清, 陈兆华, 陈祖佳, 邱琪雯, 张又才, 陈思鸿, 汪朝阳. 基于有机小分子的汞离子荧光探针研究进展[J]. 有机化学, 2023, 43(9): 3067-3077.
[9]	朱传涛, 王松, 赵一凡, Herdewijn Piet, 刘丰五. 新型2,2'-缩水-L-苏糖嘧啶膦酸核苷的合成[J]. 有机化学, 2023, 43(9): 3167-3173.
[10]	岁丹丹, 岑南楠, 龚若蕖, 陈阳, 陈文博. 无支持电解质条件下连续流电化学合成三氟甲基化氧化吲哚[J]. 有机化学, 2023, 43(9): 3239-3245.
[11]	钟赟哲, 陈颖, 俞磊, 周宏伟. 电化学介导羧酸与醇的酯化反应[J]. 有机化学, 2023, 43(8): 2855-2863.
[12]	丁炳辉, 韩少辉, 熊海青, 王本花, 左伯军, 宋相志. 高选择性比率型荧光探针用于急性肺损伤中次氯酸的检测[J]. 有机化学, 2023, 43(8): 2878-2884.
[13]	张周, 郭钰, 羊静, 吴丹, 王佳昕, 洪欣玥, 蔡佩君, 荣良策. 电化学促进咪唑并[1,2-a]吡啶与二氯(溴)乙烷及碘仿的卤化反应[J]. 有机化学, 2023, 43(6): 2104-2109.
[14]	李宜芳, 王耀, 牛华伟, 陈秀金, 李兆周, 王永国. 线粒体靶向的二氧化硫荧光探针研究进展[J]. 有机化学, 2023, 43(6): 1952-1962.
[15]	刘飞冉, 敬静, 张小玲. 细胞器靶向型半胱氨酸荧光探针研究进展[J]. 有机化学, 2023, 43(6): 2053-2067.