苯并咪唑基荧光化学传感器的合成与应用研究进展

doi:10.6023/cjoc201507022

有机化学 ›› 2015, Vol. 35 ›› Issue (12): 2465-2486.DOI: 10.6023/cjoc201507022 上一篇下一篇

综述与进展

苯并咪唑基荧光化学传感器的合成与应用研究进展

吴彦城^a, 尤嘉宜^b, 关丽涛^c, 石杰^a, 曹梁^a, 汪朝阳^a

a 华南师范大学化学与环境学院教育部环境理论化学重点实验室广州 510006;
b 广东药学院医药化工学院中山 528458;
c 华南农业大学材料与能源学院广州 510642

收稿日期:2015-07-20 修回日期:2015-08-21 发布日期:2015-08-31
通讯作者: 汪朝阳 E-mail:wangzy@scnu.edu.cn
基金资助:
广东省自然科学基金(No. 2014A030313429)、广东省高等学校人才引进专项资金(No. 粤财教[2011]431号)、国家自然科学基金(No. 31200439)资助项目.

Progress in the Synthesis and Application of Benzimidazole-Based Fluorescent Chemosensors

Wu Yancheng^a, You Jiayi^b, Guan Litao^c, Shi Jie^a, Cao Liang^a, Wang Zhaoyang^a

a Key Laboratory of Theoretical Chemistry of Environment, Ministry of Education, School of Chemistry and Environment, South China Normal University, Guangzhou 510006;
b School of Chemistry and Chemical Engineering, Guangdong Pharmaceutical University, Zhongshan 548528;
c College of Materials and Energy, South China Agricultural University, Guangzhou 510642

Received:2015-07-20 Revised:2015-08-21 Published:2015-08-31
Supported by:
Project supported by the Natural Science Foundation of Guangdong Province (No. 2014A030313429), the 3rd Talents Special Funds of Guangdong Higher Education (No. Guangdong-Finance-Education [2011]431) and the National Natural Science Foundation of China (No. 31200439).

文章分享

摘要/Abstract

苯并咪唑类化合物在多种有机溶剂和水溶液中能够发出特征荧光, 而且在一定条件下荧光性质会因多种因素而发生改变, 因此其在荧光检测领域的应用受到了广泛的关注. 综述了苯并咪唑类传感器的合成及其在各种金属离子、阴离子、无机物小分子、金属氧化物纳米粒子和有机小分子等物质检测中应用的新进展, 并展望了苯并咪唑基荧光化学传感器的发展趋势.

关键词: 苯并咪唑, 传感器, 合成, 荧光检测, 进展

Many benzimidazole compounds can emit characteristic fluorescence in various organic solvents and aqueous solutions, and their fluorescence properties can be influenced by some factors under certain conditions, which make them used in the field of fluorescence detection. Recently, more and more attention has been attached to the benzimidazole-based fluorescent chemosensors. Their synthesis and the extensive application in the detection of metal ions, anions, inorganic small molecules, metal oxide nanoparticles, organic small molecules, and so on are reviewed. The development trend of benzimidazole-based fluorescent chemosensors is prospected.

Key words: benzimidazole, sensor, synthesis, fluorescence detection, progress

引用此文

吴彦城, 尤嘉宜, 关丽涛, 石杰, 曹梁, 汪朝阳. 苯并咪唑基荧光化学传感器的合成与应用研究进展[J]. 有机化学, 2015, 35(12): 2465-2486.

Wu Yancheng, You Jiayi, Guan Litao, Shi Jie, Cao Liang, Wang Zhaoyang. Progress in the Synthesis and Application of Benzimidazole-Based Fluorescent Chemosensors[J]. Chin. J. Org. Chem., 2015, 35(12): 2465-2486.

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

分享此文

参考文献

[1] Singh, S.; Bharti, N.; Mohapatra, P. P. Chem. Rev. 2009, 109, 1900.
[2] Marson, C. M. Chem. Rev. 2011, 111, 7121.
[3] Mao, Z.-Z.; Wang, Z.-Y.; Hou, X.-N.; Song, X.-M.; Luo, Y.-F. Chin. J. Org. Chem. 2008, 28, 542 (in Chinese). (毛郑州, 汪朝阳, 侯晓娜, 宋秀美, 罗玉芬, 有机化学, 2008, 28, 542.)
[4] Zhu, G.-M.; Yang, L.-Y.; Cui, D.-M. Chin. J. Org. Chem. 2014, 34, 495 (in Chinese.) (朱观明, 杨柳阳, 崔冬梅. 有机化学, 2014, 34, 495.)
[5] Peng, P.; Xiong, J.-F.; Li, B.; Mo, G.-Z.; Chen, R.-H.; Wang, Z.-Y. Chin. J. Org. Chem. 2013, 33, 1891 (in Chinese). (彭湃, 熊金锋, 李豹, 莫广珍, 陈任宏, 汪朝阳, 有机化学, 2013, 33, 1891.)
[6] Li, Y.; Ma, H.-Q.; Wang, Y.-L. Chin. J. Org. Chem. 2008, 28, 210 (in Chinese). (李焱, 马会强, 王玉炉, 有机化学, 2008, 28, 210.)
[7] Mao, Z.-Z.; Li, J.-X.; Xue, F.-L.; Chen, R.-H.; Wang, Z.-Y. Chem. Res. Appl. 2012, 24, 497 (in Chinese). (毛郑州, 李建晓, 薛福玲, 陈任宏, 汪朝阳, 化学研究与应用, 2012, 24, 497.)
[8] Xiong, J.-F.; Luo, S.-H.; Wang, Q.-F.; Wang, Z.-Y.; Qi, J. Des. Monomers Polym. 2013, 16, 389.
[9] Xiong, J.-F.; Wang,Q.-F.; Peng, P.; Shi, J.; Wang, Z.-Y.; Yang, C.-L. J. Appl. Polym. Sci. 2014, 131, 40275.
[10] Xiong, J.-F.; Luo, S.-H.; Huo, J.-P.; Liu, J.-Y.; Chen, S.-X.; Wang, Z.-Y. J. Org. Chem. 2014, 79, 8366.
[11] Tzeng, B. C.; Chen, B. S.; Chen, C. K.; Chang, Y. P.; Tzeng, W. C.; Lin, T. Y.; Lee, G. H.; Chou, P. T.; Fu, Y. J.; Chang, A. H. H. Inorg. Chem. 2011, 50, 5379.
[12] Yu, H.; Wang, S.; Son, Y. A. Mol. Cryst. Liq. Cryst. 2012, 568, 117.
[13] Zhong, K.-L.; Zhou, X.; Hou, R.-B.; Zhou, P.; Hou, S.-H.; Bian, Y.-J.; Zhang, G.; Tang, L.-J.; Shang, X.-H. RSC Adv. 2014, 4, 16612.
[14] Hu, J.-H.; Li, J.-B.; Qi, J.; Chen, J.-J. New J. Chem. 2015, 39, 843.
[15] Yang, Y.; Li, B.; Zhang, L.-M.; Guan, Y.-L. J. Lumin. 2014, 145, 895.
[16] Peng, P.; Xiong, J.-F.; Mo, G.-Z.; Zheng, J.-L.; Chen, R.-H.; Chen, X.-Y.; Wang, Z.-Y. Amino Acids 2014, 46, 2427.
[17] Chen, R.-H.; Xiong, J.-F.; Peng, P.; Mo, G.-Z.; Tang, X.-S.; Wang, Z.-Y.; Wang X.-F. Asian J. Chem. 2014, 26, 926.
[18] Ghosh, K.; Sarkar, T. Supramol. Chem. 2012, 24, 748.
[19] Madhu, S.; Sharma, D. K.; Basu, S. K.; Jadhav, S.; Chowdhury, A.; Ravikanth, M. Inorg. Chem. 2013, 52, 11136.
[20] Wang, Q.-M.; Tan, C.-L. Anal. Chim. Acta 2011, 708, 111.
[21] Kim, S. J.; Kool, E. T. J. Am. Chem. Soc. 2006, 128, 6164.
[22] Jayabharathi, J.; Thanikachalam, V.; Jayamoorthy, K.; Sathishkumar, R. Spectrochim. Acta, Part A 2012, 97, 384.
[23] Cimen, O. Z; Dincalp, H.; Varlikli, C. Sens. Actuators B 2015, 209, 853.
[24] Li, J.-B.; Hu, Q.-H.; Yu, X.-L.; Zeng, Y.; Cao, C.-C.; Liu, X.-W.; Guo, J.; Pan, Z.-Q. J. Fluoresc. 2011, 21, 2005.
[25] Zhang, Y.; Wang, J.-M.; Shu, W.-H.; Chen, Q.; Ma, Z.-G.; Chen, X.-M. Chin. J. Inorg. Chem. 2013, 29, 150 (in Chinese). (张勇, 王继猛, 舒威虎, 陈其, 马志刚, 陈雪梅. 无机化学学报, 2013, 29, 150.)
[26] Liu, J.; Lin, Q.; Zhang, Y.-M.; Wei, T.-B. Sci. China Chem. 2014, 57, 1257.
[27] Wang, M.; Wang, J.-G.; Xue, W.-J.; Wu, A.-X. Dyes Pigm. 2013, 97, 475.
[28] Jung, H. J.; Singh, N.; Jang, D. O. Tetrahedron Lett. 2008, 49, 2960.
[29] Lee, D. Y.; Singh, N.; Jang, D. O. Tetrahedron Lett. 2010, 51, 1103.
[30] Lu, L.-J.; Yin, M.-C.; Fan, Y-T.; Hou, H.-W.; Wu, Y.-J. Chin. J. Inorg. Chem. 2001, 17, 478 (in Chinese). (卢会杰, 尹明彩, 樊耀亭, 侯红卫, 吴养洁, 无机化学学报, 2001, 17, 478.)
[31] Lee, D. Y.; Singh, N.; Jang, D. O. Tetrahedron Lett. 2011, 52, 1368.
[32] Lee, D. Y.; Singh, N.; Jang, D. O. Tetrahedron Lett. 2011, 52, 3886.
[33] Tang, L. J.; Zhou, P.; Zhong, K. L.; Hou, S. H. Sens. Actuators, B 2013, 182, 439.
[34] Tang, L. J.; Wang, N. N.; Zhang, Q.; Guo, J. J.; Nandhakumar, R. Tetrahedron Lett. 2013, 54, 536.
[35] Saluja, P.; Kaur, N.; Singh, N.; Jang, D. O. Tetrahedron Lett. 2012, 53, 3292.
[36] Tang, L.-J.; Cai, M.-J. Sens. Actuators B 2012, 173, 862.
[37] Wang, X.-J.; Xu, T.; Duan, H.-D. Sens. Actuators B 2015, 214, 138.
[38] Tang, L.-J.; Dai, X.; Cai, M.-J.; Zhao, J.; Zhou, P.; Huang, Z.-L. Spectrochim. Acta, Part A 2014, 122, 656.
[39] Mahiya, K.; Mathur, P. J. Fluoresc. 2013, 23, 767.
[40] Mahiya, K.; Mathur, P. Spectrochim. Acta, Part A 2013, 113, 386.
[41] Ghosh, K.; Sarkar, T. Supramol. Chem. 2011, 23, 435.
[42] Tang, L.-J.; Li, F.-F.; Liu, M.-H.; Nandhakumar, R. Bull. Korean Chem. Soc. 2010, 31, 3212.
[43] Chipem, F. A. S.; Behera, S. K.; Krishnamoorthy, G. Sens. Actuators B 2014, 191, 727.
[44] Pandey, A. D.; Pissurlenkar, R. R. S.; Karnik, A. V. J. Inclusion Phenom. Macrocycl. Chem. 2015, 81,251.
[45] Pathak, R. K.; Hinge, V. K.; Mondal, P.; Rao, C. P. Dalton Trans. 2012, 41, 10652.
[46] Goswami, S.; Maity, S.; Maity, A. C.; Maity, A. K.; Das, A. K.; Saha, P. RSC Adv. 2014, 4, 6300.
[47] Lal, A. K.; Milton, M. D. Sens. Actuators B 2014, 202, 257.
[48] Jayabharathi, J.; Thanikachalam, V.; Jayamoorthy, K. Spectrochim. Acta, Part A 2012, 95, 143.
[49] El Majzoub, A.; Cadiou, C.; Dechamps-Olivier, I.; Chuburu, F.; Aplincourt, M. Eur. J. Inorg. Chem. 2007, 5087.
[50] El Majzoub, A.; Cadiou, C.; Dechamps-Olivier, I.; Chuburu, F.; Aplincourt, M.; Tinant, B. Inorg. Chim. Acta 2009, 362, 1169.
[51] El Majzoub, A.; Cadiou, C.; Dechamps-Olivier, I.; Tinant, B.; Chuburu, F. Inorg. Chem. 2011, 50, 4029.
[52] Zhong, K.-L.; Cai, M.-J.; Hou, S.-H.; Bian, Y.-J.; Tang, L.-J. Bull. Korean Chem. Soc. 2014, 35, 489.
[53] Tang, L.-J.; Cai, M.-J.; Zhou, P.; Zhao, J.; Zhong, K.-L.; Hou, S.-H.; Bian, Y.-J. RSC Adv. 2013, 3, 16802.
[54] Tang, L.-J.; Cai, M.-J.; Zhou, P.; Zhao, J. ; Huang, Z.-L.; Zhong, K.-L.; Hou, S.-H.; Bian, Y.-J. J. Lumin. 2014, 147, 179.
[55] Martin, D.; Rouffet, M.; Cohen, S. M.. Inorg. Chem. 2010, 49, 10226.
[56] Henary, M. M.; Wu, Y.; Fahrni, C. J. Chem. Eur. J. 2004, 10, 3015.
[57] Henary, M. M.; Fahrni, C. J. J. Phys. Chem. A 2002, 106, 5210.
[58] Kim, M. J.; Kaur, K.; Singh, N.; Jang, D. O. Tetrahedron 2012, 68, 5429.
[59] Mashraqui, S. H.; Sundaram, S.; Khan, T. Chem. Lett. 2006, 135, 786.
[60] Lohar, S.; Karak, D.; Guha, S.; Banerjee, A.; Sahana, A.; Das, D. Spectrosc. Lett. 2013, 46, 28.
[61] Kumar, A.; Singh, A. K.; Gupta, T. Analyst 2013, 138, 3356.
[62] Velmurugan, K.; Raman, A;. Don, D.; Tang, L.-J.; Easwaramoorthi, S.; Nandhakuma, R. RSC Adv. 2015, 5, 44463.
[63] Cao, W.; Zheng, X.-J.; Sun, J.-P.; Wong, W.-T.; Fang, D.-C; Zhang, J.-X.; Jin, L.-P. Inorg. Chem. 2014, 53, 3012.
[64] Jeyanthi, D.; Iniya, M.; Krishnaveni, K.; Chellappa, D. RSC Adv. 2013, 3, 20984.
[65] Iniya, M.; Jeyanthi, D.; Krishnaveni, K.; Chellappa, D. J. Lumin. 2014, 157, 383.
[66] Ma, T.; Zhang, J.; Liu, L.-Z. He, Y.; Zhang, Z.-T. Chin. J. Org. Chem. 2014, 34, 1780 (in Chinese). (马拓, 张瑾, 刘龙珠, 贺云, 张尊听, 有机化学, 2014, 34, 1780.)
[67] Alvaro, M.; Garcia, H.; Palomares, E.; Achour, R.; Moussaif, A.; Zniber, R. Chem. Phys. Lett. 2001, 350, 240.
[68] Saluja, P.; Sharma, H.; Kaur, N.; Singh, N.; Jang, D. O. Tetrahedron 2012, 68, 2289.
[69] Saluja, P.; Kaur, N.; Singh, N.; Jang, D. O. Tetrahedron 2012, 68, 8551.
[70] Alizadeh, A.; Khodaei, M. M.; Hamidi, Z. Sens. Actuators, B 2014, 190, 782.
[71] Firooz, A. R.; Ensafi, A. A.; Kazemifard, N.; Sharghi, H. Talanta 2012, 101, 171.
[72] Dessingou, J.; Mitra, A.; Tabbasum, K.; Baghel, G. S.; Rao, C. P. J. Org. Chem. 2012, 77, 371.
[73] Li, G.; Gong, W.-T.; Ye, J.-W.; Lin, Y.-A.; Ning, G.-L. Tetrahedron Lett. 2011, 52, 1313.
[74] Pang, S.-T.; Zheng, Y.-H.; Zhou, Z.; Tan, C.-L.; Wang, Q.-M.; Li, X.-D. Opt. Mater. 2013, 35, 1157.
[75] Wang, J.-A.; Bai, F.-Q.; Xia, B.-H.; Sun, L.; Zhang, H.-X. J. Phys. Chem. A 2011, 115, 1985.
[76] Khanmohammadi, H.; Rezaeian, K. New J. Chem. 2014, 38, 5536.
[77] Chetia, B.; Iyer, P. K. Sens. Actuators, B 2014, 201, 191.
[78] Gupta, A. S.; Paul, K.; Luxami, V. Spectrochim. Acta, Part A 2015, 138, 67.
[79] Madhu, S.; Ravikanth, M. Inorg. Chem. 2014, 53, 1646.
[80] Bren, V. A.; Tolpygin, I. E.; Tikhomirova, K. S.; Popova, O. S.; Bren, Z. V.; Revinskii, Y. V.; Dubonosov, A. D.; Minkin, V. I. Chem. Heterocycl. Compd. 2014, 50, 1665.
[81] Moon, K. S.; Singh, N.; Lee, G. W.; Jang, D. O. Tetrahedron 2007, 63, 9106.
[82] Shao, J.; Qiao, Y.-H.; Lin, H.; Lin, H.-K. J. Fluoresc. 2009, 19, 183.
[83] Yang, X.-F.; Qi, H.-P.; Wang, L.-P.; Su, Z.; Wang, G. Talanta 2009, 80, 92.
[84] Kaur, N.; Dhaka, G.; Singh, J. Tetrahedron Lett. 2015, 56, 1162.
[85] Sharma, H.; Guadalupe, H. J.; Narayanan, J.; Hofeld, H.; Pandiyan, T. Singh, N. Anal. Methods 2013, 5, 3880.
[86] Sharma, H.; Bhardwaj, V. K.; Kaur, N.; Singh, N.; Jang, D. O. Tetrahedron Lett. 2013, 54, 5967.
[87] Lee, D. Y.; Singh, N.; Kim, M. J.; Jang, D. O. Org. Lett. 2011, 13, 3024.
[88] Mahapatra, A. K.; Maiti, K.; Manna, S. K.; Maji, R.; Das M. C.; Pakhira, B.; Sarkar, S. Chem. Asian J. 2014, 9, 3623.
[89] Zelder, F. H. Inorg. Chem. 2008, 47, 1264.
[90] Li, J.-B.; Hu, J.-H.; Chen, J.-J.; Qi, J. Spectrochim. Acta, Part A 2014, 133, 773.
[91] Guo, Y.-Y.; Tang, X.-L.; Hou, F.-P.; Wu, J.; Dou, W.; Qin, W.-W.; Ru, J.-X.; Zhang, G.-L.; Liu, W.-S.; Yao, X.-J. Sens. Actuators B 2013, 181, 202.
[92] Chetia, B.; Iyer, P. K. Spectrochim. Acta, Part A 2011, 81, 313.
[93] Mukherjee, M.; Pal, S.; Sen, B.; Lohar, S.; Banerjee, S.; Banerjee, S.; Chattopadhyay, P. RSC Adv. 2014, 4, 27665.
[94] Wang, G.; Qi, H.-P.; Yang, X.-F. Luminescence 2013, 28, 97.
[95] Das, S.; Banerjee, A.; Lohar, S.; Sarkar, B.; Mukhopadhyay, S. K.; Matalobos, J. S.; Sahana, A.; Das, D. New J. Chem. 2014, 38, 2744.
[96] Kar, C.; Das, G. J. Photochem. Photobiol., A 2013, 251, 128.
[97] Sun, M.-T.; Yu, H.; Li, H.-H.; Xu, H.-D.; Huang, D.-J.; Wang, S.-H. Inorg. Chem. 2015, 54, 3766.
[98] Choi, H. W.; Kim, Y. S.; Yang, N. C.; Suh, D. H. J. Appl. Polym. Sci. 2004, 91, 90.
[99] Saikia, G.; Iyer, P. K. Macromolecules 2011, 44, 3753.
[100] Lirag, R. C.; Le, H. T. M.; Miljanic, O. S. Chem. Commun. 2013, 49, 4304.
[101] Zhao, Y; Gao, F.-B; Wu, K; Shen, C; Hong, H; Wang, X.-Y; Chen, J.-N; Mang, J.-F. Chin. J. Inorg. Chem. 2009, 25, 1513 (in Chinese). (赵勇, 高凤博, 吴可, 沈超, 洪浩, 王晓勇, 洪浩, 陈江宁, 张峻峰, 无机化学学报, 2009, 25, 1513.)
[102] Ishida, M.; Kim, P.; Choi, J.; Yoon, J.; Kim, D.; Sessler, J. L. Chem. Commun. 2013, 49, 6950.
[103] Karunakaran, C.; Jayabharathi, J.; Jayamoorthy, K.; Vinayagamoorthy, P. J. Photochem. Photobiol., A 2012, 247, 16.
[104] Karunakaran, C.; Jayabharathi, J.; Jayamoorthy, K. Sens. Actuators B 2013, 188, 207.
[105] Karunakaran, C.; Jayabharathi, J.; Jayamoorthy, K. Sens. Actuators B 2013, 182, 514.
[106] Han, Y.; Cao, H.-T.; Sun, H.-Z.; Shan, G.-G.; Wu, Y.; Su, Z.-M.; Liao, Y. J. Mater. Chem. C 2015, 3, 2341.
[107] Kandpal, M.; Bandela, A. K.; Hinge, V. K.; Rao, V. R.; Rao, C. P. ACS Appl. Mater. Interfaces 2013, 5, 13448.
[108] Xiong, J.-F.; Luo, S.-H.; Huo, J.-P.; Liu, J.-Y.; Chen, S.-X.; Wang, Z.-Y. J. Org. Chem. 2014, 79, 11619.
[109] Arici, M.; Yesilel, O. Z.; Tas, M. Dalton Trans. 2015, 44, 1627.
[110] Ghosh, K.; Sen, T.; Patra, A. New J. Chem. 2010, 34, 1387.
[111] Saluja, P.; Kaur, N.; Kang, J.; Singh, N.; Jang, D. O. Tetrahedron 2013, 69, 9001.
[112] Dai, M.; Zhu, W.-P.; Xu, Y.-F.; Qian, X.-H.; Liu, Y.; Xiao, Y.; You, Y. J Fluoresc. 2008, 18, 591.
[113] Khattar, R.; Mathur, P. Inorg. Chem. Commun. 2013, 31, 37.
[114] Ghosh, K.; Tarafdar, D.; Samadder, A.; Khuda-Bukhsh, A. R. RSC Adv. 2014, 4, 58530.
[115] Saeed, M. A.; Le, H. T. M.; Miljanic, O. S. Acc. Chem. Res. 2014, 47, 2074.
[116] Tolpygin, I. E.; Revinskii, Y. V.; Starikov, A. G.; Dubonosov, A. D.; Bren, V. A.; Minkin, V. I. Chem. Heterocycl. Compd. 2013, 47, 1230.
[117] You, Q.-H.; Fan, L.; Chan, W.-H.; Lee, A. W. M.; Shuang, S.-M. RSC Adv. 2013, 3, 15762.
[118] Kim, H. J.; Heo, C. H.; Kim, H. M. J. Am. Chem. Soc. 2013, 135, 17969.
[119] Ashton T. D.; Jolliffe K. A.; Pfeffer F. M. Chem. Soc. Rev. 2015, 44, 4547.
[120] Vendrell, M.; Zhai, D. T.; Er, J. C.; Chang, Y. T. Chem. Rev. 2012, 112, 4391.
[121] Daly, B.; Ling, J.; de Silva, A. P. C Chem. Soc. Rev. 2015, 44, 4203.
[122] Guo, X.-X.; Gu, D.-W.; Wu, Z.-X.; Zhang, W.-B. Chem. Rev. 2015, 115, 1622.

苯并咪唑基荧光化学传感器的合成与应用研究进展

Progress in the Synthesis and Application of Benzimidazole-Based Fluorescent Chemosensors

PDF

可视化

被引次数

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]	李路瑶, 贺忠文, 张振国, 贾振华, 罗德平. 三芳基碳正离子在有机合成中的应用[J]. 有机化学, 2024, 44(2): 421-437.
[3]	梅青刚, 李清寒. 可见光促进C(3)(杂)芳硫基吲哚化合物的合成研究进展[J]. 有机化学, 2024, 44(2): 398-408.
[4]	冯康博, 陈炯, 古双喜, 王海峰, 陈芬儿. 全连续流反应技术在药物合成中的新进展(2019~2022)[J]. 有机化学, 2024, 44(2): 378-397.
[5]	李鹏辉, 谢青洋, 万福贤, 张元红, 姜林. 含环丙基的新型取代嘧啶-5-甲酰胺的合成及杀菌活性研究[J]. 有机化学, 2024, 44(2): 650-656.
[6]	佘春艳, 王安静, 刘珊, 舒文明, 余维初. 芳乙酰叠氮的制备及其在有机合成中的应用进展[J]. 有机化学, 2024, 44(2): 481-507.
[7]	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.
[8]	赵茜帆, 陈永正, 张世明. 碳基非金属催化剂在有机合成领域的应用及机理研究[J]. 有机化学, 2024, 44(1): 137-147.
[9]	陈珊, 陈志林, 胡琼, 蒙艳双, 黄悦, 陶萍芳, 卢丽如, 黄国保. 含双硫脲基团分子钳在非极性溶剂中识别中性分子[J]. 有机化学, 2024, 44(1): 277-281.
[10]	王化坤, 任晓龙, 宣宜宁. 卤盐催化的α,β-环氧羧酸酯与异氰酸酯[3＋2]环加成反应研究[J]. 有机化学, 2024, 44(1): 251-258.
[11]	金玉坤, 任保轶, 梁福顺. 可见光介导的三氟甲基的选择性C－F键断裂及其在偕二氟类化合物合成中的应用[J]. 有机化学, 2024, 44(1): 85-110.
[12]	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.
[13]	王博珍, 张婕, 粘春惠, 金茗茗, 孔苗苗, 李物兰, 何文斐, 吴建章. 含有3,4-二氯苯基的酰胺类化合物的合成及抗肿瘤活性研究[J]. 有机化学, 2024, 44(1): 232-241.
[14]	于士航, 刘嘉威, 安碧玉, 边庆花, 王敏, 钟江春. 黑腹尼虎天牛接触性信息素的不对称合成[J]. 有机化学, 2024, 44(1): 301-308.
[15]	贾小英, 普佳霞, 韩丽荣, 李清寒. 含双杂原子苯并[d]五元杂环硫醚类化合物的合成研究进展[J]. 有机化学, 2024, 44(1): 18-40.