Citation: Luo Liang, Cao Xiaomei, Lai Guowei, Liu Jinxiang, Luo Haiqing, Lu Dongliang, Zhang Yong. "On Water" Nucleophilic Addition of Pyrazolones to Trifluoromethyl Ketones[J]. Chinese Journal of Organic Chemistry, ;2020, 40(5): 1323-1330. doi: 10.6023/cjoc201910038 shu

"On Water" Nucleophilic Addition of Pyrazolones to Trifluoromethyl Ketones

Key Laboratory of Organo-pharmaceutical Chemistry, Gannan Normal University, Ganzhou, Jiangxi 341000

Corresponding author: Zhang Yong, yong_zhanggnnu@126.com
Received Date: 29 October 2019
Revised Date: 14 January 2020
Available Online: 14 February 2020
Fund Project: the Education Department of Jiangxi Province GJJ170835the Jiangxi Provincial Department of Science and Technology Fund 20144BAB2130003Project supported by the National Natural Science Foundation of China (No. 21562003), the Jiangxi Provincial Department of Science and Technology Fund (20192BAB213007 and 20144BAB2130003), and the Education Department of Jiangxi Province (No. GJJ170835)the Jiangxi Provincial Department of Science and Technology Fund 20192BAB213007the National Natural Science Foundation of China 21562003

Figures(2)

A green and efficient nucleophilic addition reaction of trifluoromethyl ketone with pyrazolone was developed under "on water" conditions, affording pyrazolone substituted tertiary trifluoromethyl alcohols in high yields. The advantages of being catalyst-free, column chromatography-free, environmentally benign and easy workup make it a promising method for preparation of a variety of pyrazolone substituted tertiary trifluoromethyl alcohols.
- "on water" reaction,
- nucleophilic addition,
- pyrazolone,
- trifluoromethyl ketone
1. [1]
  (a) Trost, B. M. Angew. Chem. Int. Ed. 1995, 34, 259.
  (b) Anastas, P. T.; Williamson, T. C. Green Chemistry: Frontiers in Chemical Synthesis and Processes, Oxford University Press, Oxford, 1998.
  (c) Li, C. J. Chem. Rev. 2005, 105, 3095.
  (d) Sheldon, R. A. Green Chem. 2005, 7, 267.
  (e) Gawande, M. B.; Bonifacio, V. D.; Luque, R.; Branco, P. S.; Varma, R. S. Chem. Soc. Rev. 2013, 42, 5522.
2. [2]
  (a) Lindstrom, U. M. Chem. Rev. 2002, 102, 2751.
  (b) Kobayashi, S.; Manabe, K. Acc. Chem. Res. 2002, 35, 209.
  (c) Horvath, I. T.; Anastas, P. T. Chem. Rev. 2007, 107, 2167.
  (d) Niu, R.; Xiao, J.; Liang, T.; Li, X. Org. Lett. 2012, 14, 676.
  (e) Shen, Z. L.; Wang, S. Y.; Chok, Y. K.; Xu, Y. H.; Loh, T. P. Chem. Rev. 2013, 113, 271.
  (f) Butler, R. N.; Coyne, A. G. Org. Biomol. Chem. 2016, 14, 9945.
  (g) Xiao, J.; Wen, H.; Wang, L.; Xu, L.; Hao, Z.; Shao, C.-L.; Wang, C.-Y. Green Chem. 2016, 18, 1032.
  (h) Guo, W.; Liu, X.; Liu, Y.; Li, C. ACS Catal. 2017, 8, 328.
  (i) Kitanosono, T.; Masuda, K.; Xu, P.; Kobayashi, S. Chem. Rev. 2018, 118, 679.
  (j) Xie, P.; Wang, J.; Liu, Y.; Fan, J.; Wo, X.; Fu, W.; Sun, Z.; Loh, T. P. Nat. Commun. 2018, 9, 1321.
  (k) Han, J.; Zhang, J.-L.; Zhang, W.-Q.; Gao, Z.; Xu, L.-W.; Jian, Y. J. Org. Chem. 2019, 84, 7642.
  (l) Wang, W.; Wang, S. X.; Qin, X. Y.; Li, J. T. Synth. Commun. 2005, 35, 1263.
  (m) Wang, A.-Q.; Jin, T.-S.; Cheng, Z.-L.; Li, T.-S. Asian J. Chem. 2010, 22, 1973.
  (n) Thakur, P. B.; Meshram, H. M. RSC Adv. 2014, 4, 6019.
  (o) Zhou, Z.; Duan, J. F.; Mu, X. J.; Xiao, X. Y. Chin. J. Org. Chem. 2018, 38, 585(in Chinese).
  (周曌, 段建凤, 穆小静, 肖尚友, 有机化学, 2018, 38, 585.)
  (p) Hu, X. Y.; Yu, H. F.; Wang, W. J.; Jiang, S. Q.; Liu, Q.; He, J. Chin. J. Org. Chem. 2019, 39, 3183(in Chinese).
  (胡小宇, 于海丰, 王文举, 姜思傲, 刘奇, 何洁, 有机化学, 2019, 39, 3183.)
3. [3]
  (a) Narayan, S.; Muldoon, J.; Finn, M. G.; Fokin, V. V.; Kolb, H. C.; Sharpless, K. B. Angew. Chem., Int. Ed. 2005, 44, 3275.
  (b) Paladhi, S.; Chauhan, A.; Dhara, K.; Tiwari, A. K.; Dash, J. Green Chem. 2012, 14, 2990.
  (c) Paladhi, S.; Bhati, M.; Panda, D.; Dash, J. J. Org. Chem. 2014, 79, 1473.
  (d) Yu, J. S.; Liu, Y. L.; Tang, J.; Wang, X.; Zhou, J. Angew. Chem., Int. Ed. 2014, 53, 9512.
  (e) Zhang, Y.; Wei, B. W.; Lin, H.; Zhang, L.; Liu, J. X.; Luo, H. Q.; Fan, X. L. Green Chem. 2015, 17, 3266.
  (f) SaiPrathima, P.; Srinivas, K.; Rao, M. M. Green Chem. 2015, 17, 2339.
  (g) Luque-Agudo, V.; Gil, M. V.; Roman, E.; Serrano, J. A. Green Chem. 2016, 18, 3844.
  (h) Balaraman, K.; Ding, R.; Wolf, C. Adv. Synth. Catal. 2017, 359, 4165.
  (i) Dilauro, G.; Dell'Aera, M.; Vitale, P.; Capriati, V.; Perna, F. M. Angew. Chem., Int. Ed. 2017, 56, 10200.
  (j) Zhu, S.; Chen, C. Q.; Xiao, M. Y.; Yu, L. P.; Wang, L.; Xiao, J. Green Chem. 2017, 19, 5653.
  (k) Hajra, S.; Singha Roy, S.; Aziz, S. M.; Das, D. Org. Lett. 2017, 19, 4082.
  (l) Hikawa, H.; Ichinose, R.; Kikkawa, S.; Azumaya, I. Green Chem. 2018, 20, 1297.
  (m) Hikawa, H.; Ichinose, R.; Kikkawa, S.; Azumaya, I. A. J. Org. Chem. 2018, 7, 416.
  (n) Wang, Z.; Cui, Y.-T.; Xu, Z.-B.; Qu, J. J. Org. Chem. 2008, 73, 2270.
4. [4]
  (a) Rideout, D. C.; Breslow, R. J. Am. Chem. Soc. 1980, 102, 7816.
  (b) Narayan, S.; Muldoon, J.; Finn, M. G.; Fokin, V. V.; Kolb, H. C.; Sharpless, K. B. Angew. Chem., Int. Ed. 2005, 44, 3275.
5. [5]
  (a) Gouverneur, V.; Müller, K. In Fluorine in Pharmaceutical and Medicinal Chemistry: From Biophysical Aspects to Clinical Applications, Imperial College Press, London, 2012.
  (b) Jeschke, P. Pest Manage. Sci. 2010, 66, 10.
  (c) Lectard, S.; Hamashima, Y.; Sodeoka, M. Adv. Synth. Catal. 2010, 352, 2708.
  (d) Ni, C.; Hu, J. Chem. Soc. Rev. 2016, 45, 5441.
  (e) Politanskaya, L. V.; Selivanova, G. A.; Panteleeva, E. V.; Tretyakov, E. V.; Platonov, V. E.; Nikul'shin, P. V.; Vinogradov, A. S.; Zonov, Y. V.; Karpov, V. M.; Mezhenkova, T. V.; Vasilyev, A. V.; Koldobskii, A. B.; Shilova, O. S.; Morozova, S. M.; Burgart, Y. V.; Shchegolkov, E. V.; Saloutin, V. I.; Sokolov, V. B.; Aksinenko, A. Y.; Nenajdenko, V. G.; Moskalik, M. Y.; Astakhova, V. V.; Shainyan, B. A.; Tabolin, A. A.; Ioffe, S. L.; Muzalevskiy, V. M.; Balenkova, E. S.; Shastin, A. V.; Tyutyunov, A. A.; Boiko, V. E.; Igumnov, S. M.; Dilman, A. D.; Adonin, N. Y.; Bardin, V. V.; Masoud, S. M.; Vorobyeva, D. V.; Osipov, S. N.; Nosova, E. V.; Lipunova, G. N.; Charushin, V. N.; Prima, D. O.; Makarov, A. G.; Zibarev, A. V.; Trofimov, B. A.; Sobenina, L. N.; Belyaeva, K. V.; Sosnovskikh, V. Y.; Obydennov, D. L.; Usachev, S. A. Russ. Chem. Rev. 2019, 88, 425.
  (f) Ren, Z. W.; Ren, N.; Zhang, F. G.; Ma, J. A. Acta Chim. Sin. 2018, 76, 940(in Chinese).
  (任智雯, 任楠, 张发光, 马军安, 化学学报, 2018, 76, 940.)
  (g) Hu, J. J.; Huang, Y. G.; Xu, X. H.; Qin, F. L. Chin. J. Org. Chem. 2019, 39, 177(in Chinese).
  (胡娟娟, 黄焰根, 徐修华, 卿凤翎, 有机化学, 2019, 39, 177.)
6. [6]
  (a) Müller, K.; Faeh, C.; Diederich, F. Science 2007, 317, 1881.
  (b) Purser, S.; Moore, P. R.; Swallow, S.; Gouverneur, V. Chem. Soc. Rev. 2008, 37, 320.
  (c) Zhou, Y.; Wang, J.; Gu, Z.; Wang, S.; Zhu, W.; Aceña, J. L.; Soloshonok, V. A.; Izawa, K.; Liu, H. Chem. Rev. 2016, 116, 422.
7. [7]
  (a) Kawai, H.; Okusu, S.; Tokunaga, E.; Sato, H.; Shiro, M.; Shibata, N. Angew. Chem., Int. Ed. 2012, 51, 4959.
  (b) Merino, E.; Nevado, C. Chem. Soc. Rev. 2014, 43, 6598.
  (c) Feng, Z.; Min, Q.-Q.; Xiao. Y.-L.; Zhang, B.; Zhang, X. Angew. Chem., Int. Ed. 2014, 53, 1669.
  (d) Zhou, D.; Huang, Z.; Yu, X.; Wang, Y.; Li, J.; Wang, W.; Xie, H. Org. Lett. 2015, 17, 5554.
  (e) Xu, X.-H.; Matsuzaki, K.; Shibata, N. Chem. Rev. 2015, 115, 731.
  (f) Wang, L.; Chen, J.; Huang, Y. Angew. Chem., Int. Ed. 2015, 54, 15414.
  (g) Huang, Y.-Y.; Yang, X.; Chen, Z.; Verpoort, F.; Shibata, N. Chem.-Eur. J. 2015, 21, 8664.
  (h) Montesinos-Magraner, M.; Vila, C.; Blay, G.; Fernández, I.; Muñoz, M. C.; Pedro, J. R. Adv. Synth. Catal. 2015, 357, 3047.
  (i) Feng, Z.; Min, Q.-Q.; Zhao, H.-Y.; Gu, J.-W.; Zhang, X. Angew. Chem., Int. Ed. 2015, 54, 1270.
  (j) Lou, H. Q.; Wang, Y.; Jin, E.; Lin, X. J. Org. Chem. 2016, 81, 2019.
  (k) Cook, A. M.; Wolf, C. Angew. Chem., Int. Ed. 2016, 55, 2929.
  (l) Zhang, Z. M.; Xu, B.; Xu, S.; Wu, H. H.; Zhang, J. Angew. Chem., Int. Ed. 2016, 55, 6324.
  (m) Feng, Z.; Min, Q.-Q.; Zhang, X. Org. Lett. 2016, 18, 44.
  (n) Duan, J.; Cheng, Y.; Cheng, J.; Li, R.; Li, P. Chem.-Eur. J. 2017, 23, 519.
  (o) Holmes, M.; Nguyen, K. D.; Schwartz, L. A.; Luong, T.; Krische, M. J. J. Am. Chem. Soc. 2017, 139, 8114.
  (p) Xie, E.; Rahman, A.; Lin, X. Org. Chem. Front. 2017, 4, 1407.
  (q) Xu, B.; Zhang, Z.-M.; Xu, S.; Liu, B.; Xiao, Y.; Zhang, J. ACS Catal. 2017, 7, 210.
  (r) Feng, Z.; Min, Q.-Q.; Fu, X.-P.; An, L.; Zhang, X. Nat. Chem. 2017, 9, 918.
  (s) Feng, Z.; Xiao, Y.-L.; Zhang, X. Acc. Chem. Res. 2018, 51, 2264.
  (t) Qing, F.-L. Chin. J. Org. Chem. 2012, 32, 815(in Chinese).
  (卿凤翎, 有机化学, 2012, 32, 815.)
  (u) Zhang, F. G.; Peng, X.; Ma, J. A. Chin. J. Org. Chem. 2019, 39, 109(in Chinese).
  (张发光, 彭星, 马军安, 有机化学, 2019, 39, 109.)
8. [8]
  (a) Gursoy, A.; Demirayak, S.; Capan, G.; Erol, K.; Vural, K. Eur. J. Med. Chem. 2000, 35, 359.
  (b) Rubtsov, A. E.; Makhmudov, R. R.; Kovylyaeva, N. V.; Prosyanik, N. I.; Bobrov, A. V.; Zalesov, V. V. Pharm. Chem. J. 2002, 36, 608.
  (c) Nishio, M.; Matsuda, M.; Ohyanagi, F.; Sato, Y.; Okumura, S.; Tabata, D.; Morikawa, A.; Nakagawa, K.; Horai, T. Lung Cancer 2005, 49, 245.
  (d) Bondock, S.; Rabie, R.; Etman, H. A.; Fadda, A. A. Eur. J. Med. Chem. 2008, 43, 2122.
  (e) Rostom, S. A.; el-Ashmawy, I. M.; Abd el Razik, H. A.; Badr, M. H.; Ashour, H. M. Bioorg. Med. Chem. 2009, 17, 882.
  (f) Bayrak, H.; Demirbas, A.; Demirbas, N.; Karaoglu, S. A. Eur. J. Med. Chem. 2010, 45, 4726.
  (g) Fustero, S.; Sanchez-Rosello, M.; Barrio, P.; Simon-Fuentes, A. Chem Rev. 2011, 111, 6984.
  (h) Li, J.-H.; Du, D.-M. Org. Biomol. Chem. 2013, 11, 6215.
  (i) Ansari, A.; Ali, A.; Asif, M.; Shamsuzzaman. New J. Chem. 2017, 41, 16.
  (j) Liu, S.; Bao, X.; Wang, B. Chem. Commun. 2018, 54, 11515.
9. [9]
  (a) Jung, Y. S.; Marcus, R. A. J. Am. Chem. Soc. 2007, 129, 5492.
  (b) Thomas, L. L.; Tirado-Rives, J.; Jorgensen, W. L. J. Am. Chem. Soc. 2010, 132, 3097.
  (c) Manna, A.; Kumar, A. J. Phys. Chem. A 2013, 117, 2446.
  (d) Sela, T.; Vigalok, A. Org. Lett. 2014, 16, 1964.
10. [10]
  (a) Kelly, C. B.; Mercadante, M. A.; Hamlin, T. A.; Fletcher, M. H.; Leadbeater, N. E. J. Org. Chem. 2012, 77, 8131.
  (b) Martinelli, E.; Vicini, A. C.; Mancinelli, M.; Mazzanti, A.; Zani, P.; Bernardi, L.; Fochi, M. Chem. Commun. 2015, 51, 658.
11. [11]
  (a) Rassu, G.; Zambrano, V.; Pinna, L.; Curti, C.; Battistini, L.; Sartori, A.; Pelosi, G.; Casiraghi, G.; Zanardi, F. Adv. Synth. Catal. 2014, 356, 2330.
  (b) Zhu, Y.-F.; Wei, B.-L.; Wei, J.-J.; Wang, W.-Q.; Song, W.-B.; Xuan, L.-J. Tetrahedron Lett. 2019, 60, 1202.
  (c) Stefane B.; Polanc S. Tetrahedron 2007, 63, 10902.
  (d) MacLean, M. A.; Diez-Cecilia, E.; Lavery, C. B.; Reed, M. A.; Wang, Y. F.; Weaver, D. F.; Stradiotto, M. Bioorg. Med. Chem. Lett. 2016, 26, 100.
  (e) Nishi, H.; Watanabe, T.; Yuki, S.; Morinaka, Y.; Iseki, K.; Sakurai, H. EP 208874, 1987.
1. [1]
  Yi Zhang , Biao Wang , Chao Hu , Muhammad Humayun , Yaping Huang , Yulin Cao , Mosaad Negem , Yigang Ding , Chundong Wang . Fe–Ni–F electrocatalyst for enhancing reaction kinetics of water oxidation. Chinese Journal of Structural Chemistry, 2024, 43(2): 100243-100243. doi: 10.1016/j.cjsc.2024.100243
2. [2]
  Jiawei Ge , Xian Wang , Heyuan Tian , Hao Wan , Wei Ma , Jiangying Qu , Junjie Ge . Iridium-based catalysts for oxygen evolution reaction in proton exchange membrane water electrolysis. Chinese Chemical Letters, 2025, 36(5): 109906-. doi: 10.1016/j.cclet.2024.109906
3. [3]
  Zhenguo Zhang , Lanyang Li , Xinlong Zong , Yongheng Lv , Shuanglei Liu , Liang Ji , Xuefei Zhao , Zhenhua Jia , Teck-Peng Loh . "Water" accelerated B(C₆F₅)₃-catalyzed Mukaiyama-aldol reaction: Outer-sphere activation model. Chinese Chemical Letters, 2025, 36(7): 110504-. doi: 10.1016/j.cclet.2024.110504
4. [4]
  Guihuang Fang , Wei Chen , Hongwei Yang , Haisheng Fang , Chuang Yu , Maoxiang Wu . Improved performance of LiMn_0.8Fe_0.2PO₄ by addition of fluoroethylene carbonate electrolyte additive. Chinese Chemical Letters, 2024, 35(6): 108799-. doi: 10.1016/j.cclet.2023.108799
5. [5]
  Yan-Li Li , Zhi-Ming Li , Kai-Kai Wang , Xiao-Long He . Beyond 1,4-addition of in-situ generated (aza-)quinone methides and indole imine methides. Chinese Chemical Letters, 2024, 35(7): 109322-. doi: 10.1016/j.cclet.2023.109322
6. [6]
  Chonglong He , Yulong Wang , Quan-Xin Li , Zichen Yan , Keyuan Zhang , Shao-Fei Ni , Xin-Hua Duan , Le Liu . Alkylarylation of alkenes with arylsulfonylacetate as bifunctional reagent via photoredox radical addition/Smiles rearrangement cascade. Chinese Chemical Letters, 2025, 36(5): 110253-. doi: 10.1016/j.cclet.2024.110253
7. [7]
  Ya-Ling Li , Jia-Wei Ke , Yue Liu , Dong-Mei Yao , Jing-Dong Zhang , You-Cai Xiao , Fen-Er Chen . Asymmetric conjugated addition of aryl Grignard reagents for the construction of chromanones bearing quaternary stereogenic centers in batch and flow. Chinese Chemical Letters, 2025, 36(6): 110377-. doi: 10.1016/j.cclet.2024.110377
8. [8]
  Cong-Bin Ji , Ding-Xiong Xie , Mei Chen , Ye-Ying Lan , Bao-Hua Zhang , Ji-Ying Yang , Zheng-Hui Kang , Shu-Jie Chen , Yu-Wei Zhang , Yun-Lin Liu . Green synthesis of 2-trifluoromethylquinoline skeletons via organocatalytic N-[(α-trifluoromethyl)vinyl]isatins CN bond activation. Chinese Chemical Letters, 2025, 36(7): 110598-. doi: 10.1016/j.cclet.2024.110598
9. [9]
  Xiangan Song , Shaogang Shen , Mengyao Lu , Ying Wang , Yong Zhang . Trifluoromethyl enable high-performance single-emitter white organic light-emitting devices based on quinazoline acceptor. Chinese Chemical Letters, 2024, 35(4): 109118-. doi: 10.1016/j.cclet.2023.109118
10. [10]
  Yi Luo , Lin Dong . Multicomponent remote C(sp²)-H bond addition by Ru catalysis: An efficient access to the alkylarylation of 2H-imidazoles. Chinese Chemical Letters, 2024, 35(10): 109648-. doi: 10.1016/j.cclet.2024.109648
11. [11]
  Lei Shen , Hongmei Liu , Ming Jin , Jinchao Zhang , Caixia Yin , Shuxiang Wang , Yutao Yang . “Three-in-one” strategy of trifluoromethyl regulated blood-brain barrier permeable fluorescent probe for peroxynitrite and antiepileptic evaluation of edaravone. Chinese Chemical Letters, 2024, 35(10): 109572-. doi: 10.1016/j.cclet.2024.109572
12. [12]
  Yuexiang Liu , Xiangqiao Yang , Tong Lin , Guantian Yang , Xiaoyong Xu , Bubing Zeng , Zhong Li , Weiping Zhu , Xuhong Qian . Efficient continuous synthesis of 2-[3-(trifluoromethyl)phenyl]malonic acid, a key intermediate of Triflumezopyrim, coupling with esterification-condensation-hydrolysis. Chinese Chemical Letters, 2025, 36(1): 109747-. doi: 10.1016/j.cclet.2024.109747
13. [13]
  Han Yuan , Fengcai Zhang , Hongzhe Huang , Jiafei Wu , Yi Yang , Wanyi Huang , Dongjing Yang , Zhuoming Li , Zhe Li , Ling Huang , Yi-You Huang , Hai-Bin Luo , Lei Guo . Discovery of 3-trifluoromethyl-substituted pyrazoles as selective phosphodiesterase 10A inhibitors for orally attenuating isoprenaline-induced cardiac hypertrophy. Chinese Chemical Letters, 2025, 36(4): 109965-. doi: 10.1016/j.cclet.2024.109965
14. [14]
  Fang-Yuan Chen , Wen-Chao Geng , Kang Cai , Dong-Sheng Guo . Molecular recognition of cyclophanes in water. Chinese Chemical Letters, 2024, 35(5): 109161-. doi: 10.1016/j.cclet.2023.109161
15. [15]
  Yu-Chen Fang , Jia-He Chen , Mi-Zhuan Li , Hui-Min Li , Mei Bai , Yong-Zheng Chen , Zi-Wei Gao , Wen-Yong Han . Forging of silaoxycarbocyclics by interrupted Catellani reaction. Chinese Chemical Letters, 2025, 36(7): 110474-. doi: 10.1016/j.cclet.2024.110474
16. [16]
  Kun Tang , Yu-Wu Zhong . Water reduction by an organic single-chromophore photocatalyst. Chinese Journal of Structural Chemistry, 2024, 43(8): 100376-100376. doi: 10.1016/j.cjsc.2024.100376
17. [17]
  Rui Wang , Yang Liang , Julius Rebek Jr. , Yang Yu . Stabilization and detection of labile reaction intermediates in supramolecular containers. Chinese Chemical Letters, 2024, 35(6): 109228-. doi: 10.1016/j.cclet.2023.109228
18. [18]
  Xin Li , Zhen Xu , Donglei Bu , Jinming Cai , Huamei Chen , Qi Chen , Ting Chen , Fang Cheng , Lifeng Chi , Wenjie Dong , Zhenchao Dong , Shixuan Du , Qitang Fan , Xing Fan , Qiang Fu , Song Gao , Jing Guo , Weijun Guo , Yang He , Shimin Hou , Ying Jiang , Huihui Kong , Baojun Li , Dengyuan Li , Jie Li , Qing Li , Ruoning Li , Shuying Li , Yuxuan Lin , Mengxi Liu , Peinian Liu , Yanyan Liu , Jingtao Lü , Chuanxu Ma , Haoyang Pan , JinLiang Pan , Minghu Pan , Xiaohui Qiu , Ziyong Shen , Shijing Tan , Bing Wang , Dong Wang , Li Wang , Lili Wang , Tao Wang , Xiang Wang , Xingyue Wang , Xueyan Wang , Yansong Wang , Yu Wang , Kai Wu , Wei Xu , Na Xue , Linghao Yan , Fan Yang , Zhiyong Yang , Chi Zhang , Xue Zhang , Yang Zhang , Yao Zhang , Xiong Zhou , Junfa Zhu , Yajie Zhang , Feixue Gao , Yongfeng Wang . Recent progress on surface chemistry Ⅰ: Assembly and reaction. Chinese Chemical Letters, 2024, 35(12): 110055-. doi: 10.1016/j.cclet.2024.110055
19. [19]
  Tiantian Long , Hongmei Luo , Jingbo Sun , Fengniu Lu , Yi Chen , Dong Xu , Zhiqin Yuan . Carbonization-engineered ultrafast chemical reaction on nanointerface. Chinese Chemical Letters, 2025, 36(3): 109728-. doi: 10.1016/j.cclet.2024.109728
20. [20]
  Yang Yang , Jing-Li Luo , Xian-Zhu Fu . Water-oxidation intermediates enabling electrochemical propylene epoxidation. Chinese Journal of Structural Chemistry, 2024, 43(5): 100269-100269. doi: 10.1016/j.cjsc.2024.100269

Get Citation

PDF

XML

Metrics

PDF Downloads(10)
Abstract views(1187)
HTML views(145)

通讯作者: 陈斌, bchen63@163.com

1.
沈阳化工大学材料科学与工程学院沈阳 110142