Citation: Xiao Liwei, Dai Fucai, Li Zheng, Jing Xuemin, Kong Jie, Liu Guangxian. Polyethylene Glycol: A New Medium for Green Organic Synthesis[J]. Chinese Journal of Organic Chemistry, ;2019, 39(3): 648-660. doi: 10.6023/cjoc201807056 shu

Polyethylene Glycol: A New Medium for Green Organic Synthesis

Faculty of Chemistry and Material Science, Langfang Normal University, Langfang 065000

Corresponding author: Xiao Liwei, xiaoliwei2000@sina.com
Received Date: 31 July 2018
Revised Date: 15 October 2018
Available Online: 11 March 2018
Fund Project: Project supported by the Educational Commission of Hebei Province (No. ZD2016046)the Educational Commission of Hebei Province ZD2016046

Figures(11)

Polyethylene glycols (PEG) can dissolve a lot of organic compounds and metallic complexes. Moreover, they are thermally stable, nonvolatile, non-toxic, biodegradable, inexpensive and recyclable. Thus, PEG as green medium has been successfully employed in many organic reactions, such as carbon-carbon coupling reaction, carbon-hetero coupling reaction, multicomponent reaction, condensation reaction, addition reaction, substitution reaction, oxidation reaction, reductive reaction, and so on. The recent advances of PEG applied in orgainc synthesis are reviewed.
- polyethylene glycol (PEG),
- green solvent,
- catalyst carrier,
- organic synthesis
1. [1]
  Zhang, M.; Liu, Y.-H.; Shang, Z.-R.; Hu, H.-C.; Zhang, Z.-H. Catal. Commun. 2017, 88, 39. doi: 10.1016/j.catcom.2016.09.028
2. [2]
  Zhang, M.; Fu, Q.-Y.; Gao, G.; He, H.-Y.; Zhang, Y.; Wu, Y.-S.; Zhang, Z.-H. ACS Sustainable Chem. Eng. 2017, 5, 6175. doi: 10.1021/acssuschemeng.7b01102
3. [3]
  Gu, Y. Green Chem. 2012, 14, 2091. doi: 10.1039/c2gc35635j
4. [4]
  Liu, P.; Hao, J.-W.; Mo, L.-P.; Zhang. Z.-H. RSC Adv. 2015, 5, 48675. doi: 10.1039/C5RA05746A
5. [5]
  Gao, G.; Wang, P.; Liu, P.; Zhang, W.; Mo, L.; Zhang, Z. Chin. J. Org. Chem. 2018, 38, 846(in Chinese).
6. [6]
  Chen, J.; Spear, S. K.; Huddleston, J. G.; Rogers, R. D. Green Chem. 2005, 7, 64. doi: 10.1039/b413546f
7. [7]
  Zhou, H.; Fan, Q.; He, Y.; Gu, L.; Chan, A. S. C. Prog. Chem. 2007, 19, 1517(in Chinese). doi: 10.6023/cjoc201711014
8. [8]
  Yin, L.; Zhang, Z.-H.; Wang, Y.-M. Tetrahedron 2006, 62, 9359. doi: 10.1016/j.tet.2006.07.067
9. [9]
  Li, J.; Liu, W.; Xie, Y. J. Org. Chem. 2005, 70, 5409. doi: 10.1021/jo050353m
10. [10]
  Li, J.; Hu, X.; Liang, Y.; Xie, Y. Tetrahedron 2006, 62, 3. doi: 10.1016/S0040-4020(06)00445-5
11. [11]
  Liu, L.; Zhang, Y.; Wang, Y. J. Org. Chem. 2005, 70, 6122. doi: 10.1021/jo050724z
12. [12]
  Silva, A.; Senra, J.; Aguiar, L. Tetrahedron Lett. 2010, 51, 3883. doi: 10.1016/j.tetlet.2010.04.092
13. [13]
  Han, W.; Liu, C.; Jin, Z. Org. Lett. 2007, 9, 4005. doi: 10.1021/ol701709q
14. [14]
  Razler, T. M.; Hsiao, Y.; Qian, F.; Fu, R.; Khan, R. K.; Doubleday, W. J. Org. Chem. 2009, 74, 1381. doi: 10.1021/jo802277z
15. [15]
  Mao, J.; Guo, J.; Fang, F.; Ji, S.-J. Tetrahedron 2008, 64, 3905. doi: 10.1016/j.tet.2008.02.068
16. [16]
  Chandrasekhar, S.; Narsihmulu, C.; Sultana, S. S.; Reddy, N. R. Org. Lett. 2002, 4, 4399. doi: 10.1021/ol0266976
17. [17]
  Nowrouzi, N.; Zarei, M. Tetrahedron 2015, 71, 7847. doi: 10.1016/j.tet.2015.08.023
18. [18]
  Declerck, V.; Lamaty, F. Eur. J. Org. Chem. 2007, 1, 201.
19. [19]
  Luo, C.; Zhang, Y.; Wang, Y. J. Mol. Catal. A:Chem. 2005, 229, 7 doi: 10.1016/j.molcata.2004.10.039
20. [20]
  Datta, G. K.; Schenck, H.; Hallberg, A.; Larhed, M. J. Org. Chem. 2006, 71, 3896. doi: 10.1021/jo0602367
21. [21]
  Zhou, W; Wang, K.; Wang, J. J. Org. Chem. 2009, 74, 5599. doi: 10.1021/jo9005206
22. [22]
  Xin, B.; Zhang, Y.; Cheng, K. J. Org. Chem. 2006, 71, 5725. doi: 10.1021/jo060749d
23. [23]
  Close, A. J.; Kemmitt, P.; Emmerson, M. K.; Spence, J. Tetrahedron 2014, 70, 9125. doi: 10.1016/j.tet.2014.09.044
24. [24]
  Ackermann, L.; Vicénte, R. Org. Lett. 2009, 11, 4922. doi: 10.1021/ol9020354
25. [25]
  Kabalka, G. W.; Dong, G.; Venkataiah, B.; Chen, C. J. Org. Chem. 2005, 70, 9207. doi: 10.1021/jo051177k
26. [26]
  Li, J.-H.; Zhu, Q.-M.; Liang, Y.; Yang, D. J. Org. Chem. 2005, 70, 5347. doi: 10.1021/jo0506635
27. [27]
  Shi, S.; Zhang, Y. J. Org. Chem. 2007, 72, 5927. doi: 10.1021/jo070855v
28. [28]
  Srimani, D.; Sawoo, S.; Sarkar, A. Org. Lett. 2007, 9, 3639. doi: 10.1021/ol7015143
29. [29]
  Bortolini, O.; Fantin, G.; Fogagnolo, M.; Giovannini, P. P.; Venturi, V.; Pacifico, S.; Massi, A. Tetrahedron 2011, 67, 8110. doi: 10.1016/j.tet.2011.08.056
30. [30]
  Mao, J.; Hua, Q.; Xie, G.; Yao, Z.; Shi, D. Eur. J. Org. Chem. 2009, 2262.
31. [31]
  Wang, L.; Zhang, Y.; Liu, L.; Wang, Y. J. Org. Chem. 2006, 71, 1284. doi: 10.1021/jo052300a
32. [32]
  Li, X.; Yuan, T.; Yang, Y.; Chen, J. Tetrahedron 2004, 70, 9652
33. [33]
  Chen, J.; Zhang, Y.; Hao, W.; Zhang, R.; Yi, F. Tetrahedron 2013, 69, 613. doi: 10.1016/j.tet.2012.11.014
34. [34]
  Colacino, E.; Villebrun, L.; Martinez, J.; Lamaty, F. Tetrahedron 2010, 66, 3730. doi: 10.1016/j.tet.2010.03.065
35. [35]
  Burley, G. A.; Davies, D. L.; Griffith, G. A.; Lee, M.; Singh, K. J. Org. Chem. 2010, 75, 980. doi: 10.1021/jo902466f
36. [36]
  Spina, R.; Colacino, E.; Gabriele, B.; Salerno, G.; Martinez, J.; Lamaty, F. J. Org. Chem. 2013, 78, 2698. doi: 10.1021/jo302474r
37. [37]
  Lara, R. G.; Rosa, P. C.; Soares, L. K.; Silva, M. S.; Jacob, R. G.; Perin, G. Tetrahedron 2012, 68, 10414. doi: 10.1016/j.tet.2012.08.055
38. [38]
  Chatterjee, T.; Ranu, B. C. J. Org. Chem. 2013, 78, 7145. doi: 10.1021/jo401062k
39. [39]
  Firouzabadi, H.; Iranpoor, N.; Abbasi, M. Tetrahedron 2009, 65, 5293. doi: 10.1016/j.tet.2009.04.079
40. [40]
  She, J.; Jiang, Z.; Wang, Y. G. Tetrahedron Lett. 2009, 50, 593. doi: 10.1016/j.tetlet.2008.11.082
41. [41]
  Lu, J.; Guan, Z.-Z.; Gao, J.-W.; Zhang, Z.-H. Appl. Organomet. Chem. 2011, 25, 537. doi: 10.1002/aoc.v25.7
42. [42]
  Wang, P.; Lu, J.; Zhang, Z.-H. J. Chem. Res. 2013, 359 doi: 10.3184/174751913X13686082295417
43. [43]
  Xiao, L.; Gao, H.; Ren, L.; Kang, J. Chin. J. Appl. Chem. 2015, 32, 304(in Chinese). doi: 10.11944/j.issn.1000-0518.2015.03.140228
44. [44]
  Yang, X.; Li, C.; Ma, J.; Wang, C.; Zhang, L. Chem. Res. Appl. 2010, 22, 1004(in Chinese). doi: 10.3969/j.issn.1004-1656.2010.08.008
45. [45]
  Modugu, N. R.; Pittala, P. K. New J. Chem. 2017, 41, 14062. doi: 10.1039/C7NJ03515B
46. [46]
  Zhang, X.-N.; Li, Y.-X.; Zhang, Z-H. Tetrahedron 2011, 67, 7426. doi: 10.1016/j.tet.2011.07.002
47. [47]
  Zareai, Z.; Khoobi, M.; Ramazani, A.; Foroumadi, A.; Souldozi, A.; Slepokura, K.; Lis, T.; Shafiee, A. Tetrahedron 2012, 68, 6721. doi: 10.1016/j.tet.2012.05.112
48. [48]
  Balwe, S. G.; Lim, K. T.; Cho, B. G.; Jeong, Y. T. Tetrahedron 2017, 73, 3564. doi: 10.1016/j.tet.2017.05.047
49. [49]
  Jain, S. L.; Singhal, S.; Sain, B. Green Chem. 2007, 9, 740. doi: 10.1039/b702311a
50. [50]
  Kidwai, M.; Bhatnagar, D. Tetrahedron Lett. 2010, 51, 2700. doi: 10.1016/j.tetlet.2010.03.033
51. [51]
  Kidwai, M.; Bhatnagar, D.; Mishra, N. K. Catal. Commun. 2008, 9, 2547. doi: 10.1016/j.catcom.2008.07.010
52. [52]
  Hasaninejad, A.; Beyrati, M. RSC Adv. 2018, 8, 1934. doi: 10.1039/C7RA13133J
53. [53]
  Survase, D.; Bandgar, B.; Helavi, V. Synth. Commun. 2017, 47, 680. doi: 10.1080/00397911.2017.1278774
54. [54]
  Reddy, M. V.; Kim, J. S.; Lim, K. T.; Jeong, Y. T Tetrahedron Lett. 2014, 55, 6459. doi: 10.1016/j.tetlet.2014.09.135
55. [55]
  Chandrasekhar, S.; Prakash, S. J.; Rao, C. L. J. Org. Chem. 2006, 71, 2196. doi: 10.1021/jo052604x
56. [56]
  Xu, C.; Huang, B.; Yan, T.; Cai, M. Green Chem. 2018, 20, 391. doi: 10.1039/C7GC02823G
57. [57]
  Wang, X.; Quan, Z.; Zhang, Z. Tetrahedron 2007, 63, 8227. doi: 10.1016/j.tet.2007.05.108
58. [58]
  Kumar, D.; Patel, G.; Mishra, B. G.; Varma, R. S. Tetrahedron Lett. 2008, 49, 6974. doi: 10.1016/j.tetlet.2008.09.116
59. [59]
  Billault, I.; Pessel, F.; Petit, A.; Turgis, R.; Scherrmann, M.-C. New J. Chem. 2015, 39, 1986. doi: 10.1039/C4NJ01784F
60. [60]
  Kumaraswamy, G.; Ankamma, K.; Pitchaiah, A. J. Org. Chem. 2007, 72, 9822. doi: 10.1021/jo701724f
61. [61]
  Chandrasekhar, S.; Reddy, N. R.; Sultana, S. S.; Narsihmulu, C.; Reddy, K. V. Tetrahedron 2006, 62, 338. doi: 10.1016/j.tet.2005.09.122
62. [62]
  Dawane, B. S.; Konda, S. G.; Shaikh, B. M.; Bhosale, R. B. Acta Pharm. 2009, 59, 473. doi: 10.2478/v10007-009-0034-7
63. [63]
  Liu, Y.; Liang, J.; Liu, X. H.; Fan, J. C.; Shang, Z. C. Chin. Chem. Lett. 2008, 19, 1043. doi: 10.1016/j.cclet.2008.06.016
64. [64]
  Wang, X.; Ye, H.; Quan, Z. J. Northwest Normal Univ. (Nat. Sci.) 2009, 45, 79(in Chinese). doi: 10.3969/j.issn.1001-988X.2009.03.021
65. [65]
  Ballini, R.; Barboni, L.; Alessandro, P. Green Chem. 2008, 10, 1004. doi: 10.1039/b805985c
66. [66]
  Yadav, G. D.; Motirale, B. G. Org. Process Res. Dev. 2009, 13, 341. doi: 10.1021/op800206c
67. [67]
  Guravaiah, N.; Rao, V. R. J. Chem. Res. 2009, 237. doi: 10.3184/030823410X12652994990526
68. [68]
  Jawale, D. V.; Lingampalle, D. L.; Pratap, U. R.; Mane, R. A. Chin. Chem. Lett. 2010, 21, 412. doi: 10.1016/j.cclet.2009.11.035
69. [69]
  Zhu, D.; Chen, J.; Xiao, H.; Liu, M.; Ding, J.; Wu, H. Synth. Commun. 2009, 39, 2895, doi: 10.1080/00397910802691874
70. [70]
  Lin, P.; Hou, R.; Wang, H.; Kang, I.; Chen, L. J. Chin. Chem. Soc. 2009, 56, 455. doi: 10.1002/jccs.v56.3
71. [71]
  Mukhopadhyay, C.; Tapaswi, P. K. Tetrahedron Lett. 2008, 49, 6237. doi: 10.1016/j.tetlet.2008.08.041
72. [72]
  Deligeorgiev, T. G.; Kaloyanova, S.; Vasilev, A.; Vaquero, J. J. Phosphorus, Sulfur Silicon Relat. Elem. 2010, 185, 2292. doi: 10.1080/10426501003598648
73. [73]
  Liu, L.; Zhang, F.; Wang, H.; Zhu, N.; Liu, B.; Hong, H.; Han, L. Phosphorus, Sulfur Silicon Relat. Elem. 2017, 192, 464. doi: 10.1080/10426507.2016.1259227
74. [74]
  Wang, X.; Gong, H.; Quan, Z.; Li, L.; Ye, H. Chin. Chem. Let. 2009, 20, 44. doi: 10.1016/j.cclet.2008.10.005
75. [75]
  Wang, J.; Song, X. J. Northwest Normal Univ. (Nat. Sci.) 2010, 46, 78(in Chinese). doi: 10.3969/j.issn.1001-988X.2010.02.018
76. [76]
  Nalage, S. V.; Kalyankar, M. B.; Patil, V. S.; Bhosale, S. V.; Deshmukh, S. U.; Pawar, R. P. Open Catal. J. 2010, 3, 58. doi: 10.2174/1876214X01003010058
77. [77]
  Xiao, L.; Gao, H.; Kong, J.; Liu, G.; Li, L.; Duan, J. Chin. J. Org. Chem. 2014, 34, 2511(in Chinese).
78. [78]
  Rao, H. S. P.; Jothilingama, S.; Scheerenb, H. W. Tetrahedron 2004, 60, 1625. doi: 10.1016/j.tet.2003.11.087
79. [79]
  Zhao, H.; Zhang, T.; Yan, T.; Cai, M. J. Org. Chem. 2015, 80, 8849. doi: 10.1021/acs.joc.5b01388
80. [80]
  Mukhopadhyay, C.; Tapaswi, P. K.; Butcher, R. J. Org. Biomol. Chem. 2010, 8, 4720. doi: 10.1039/c0ob00177e
81. [81]
  Nakka, M.; Tadikonda, R.; Rayavarapu, S.; Sarakula, P.; Vidavalur, S. Synthesis 2015, 47, 517. doi: 10.1055/s-0034-1378909
82. [82]
  Cho, C. S.; Ren, W. X.; Yoon, N. S. J. Mol. Catal. A:Chem. 2009, 299, 117. doi: 10.1016/j.molcata.2008.10.024
83. [83]
  Zhang, X. Z.; Wang, J. X.; Sun, Y. J.; Zhan, H. W. Chin. Chem. Lett. 2010, 21, 395. doi: 10.1016/j.cclet.2009.12.015
84. [84]
  He, Q.; Wang, J.; Feng, R. Lett. Org. Chem. 2010, 7, 172. doi: 10.2174/157017810790796228
85. [85]
  Jorapur, Y.; Rajagopal, G.; Saikia, P.; Pal, R. R. Tetrahedron Lett. 2008, 49, 1495. doi: 10.1016/j.tetlet.2007.12.115
86. [86]
  Liang, J.; Lv, J.; Shang, Z. C. Tetrahedron 2011, 67, 8532. doi: 10.1016/j.tet.2011.08.091
87. [87]
  Liao, Y.; Wei, T.; Yan, T.; Cai, M. Tetrahedron 2017, 73, 1238. doi: 10.1016/j.tet.2017.01.023
88. [88]
  Wang, J.-Q.; Cai, F.; Wang, E.; He, L.-N. Green Chem. 2007, 9, 882. doi: 10.1039/b701875d
89. [89]
  Chandrasekhar, S.; Reddy, N. K.; Kumar, V. P. Tetrahedron Lett. 2010, 51, 3623. doi: 10.1016/j.tetlet.2010.05.006
90. [90]
  Guo, W.; Liu, Y.; Li, C. Org. Lett. 2017, 19, 1044 doi: 10.1021/acs.orglett.7b00032
91. [91]
  Martirosyan, A.; Tamazyan, R.; Gasparyan, S.; Alexanyan, M.; Panosyan, H.; Martirosyan, V.; Schinazi, R. Tetrahedron Lett. 2010, 51, 231. doi: 10.1016/j.tetlet.2009.11.010
92. [92]
  Zhou, H. F.; Fan, Q. H.; Huang, Y. Y.; Wu, L.; He, Y. M.; Tang, W. J.; Gu, L. Q.; Chan, A. S. C. J. Mol. Catal. A:Chem. 2007, 275, 47. doi: 10.1016/j.molcata.2007.05.029
93. [93]
  Liu, W.; Wang, F. Tetrahedron Lett. 2017, 58, 1673. doi: 10.1016/j.tetlet.2017.03.016
94. [94]
  Ding, M.; Jiang, X.; Peng, J.; Zhang, L.; Cheng, Z.; Zhu, X. Green Chem. 2015, 17, 271. doi: 10.1039/C4GC01169D
95. [95]
  Huang, X.; Liu, J.; Sheng, J.; Song, X.; Du, Z.; Li, M.; Zhang, X.; Zou, Y. Green Chem. 2018, 20, 804. doi: 10.1039/C7GC02994B
96. [96]
  Zhang, Z.-H. Monatsh. Chem. 2005, 136, 1191. doi: 10.1007/s00706-005-0298-7
1. [1]
  Shuhui Li , Rongxiuyuan Huang , Yingming Pan . Electrochemical Synthesis of 2,5-Diphenyl-1,3,4-Oxadiazole: A Recommended Comprehensive Organic Chemistry Experiment. University Chemistry, 2025, 40(5): 357-365. doi: 10.12461/PKU.DXHX202407028
2. [2]
  Xinhao Yan , Guoliang Hu , Ruixi Chen , Hongyu Liu , Qizhi Yao , Jiao Li , Lingling Li . Polyethylene Glycol-Ammonium Sulfate-Nitroso R Salt System for the Separation of Cobalt (II). University Chemistry, 2024, 39(6): 287-294. doi: 10.3866/PKU.DXHX202310073
3. [3]
  Nengmin ZHU , Wenhao ZHU , Xiaoyao YIN , Songzhi ZHENG , Hao LI , Zeyuan WANG , Wenhao WEI , Xuanheng CHEN , Weihai SUN . Preparation of high-performance CsPbBr₃ perovskite solar cells by the aqueous solution solvent method. Chinese Journal of Inorganic Chemistry, 2025, 41(6): 1131-1140. doi: 10.11862/CJIC.20240419
4. [4]
  Fengxiao Wang , Zhiwei Miao , Yaofeng Yuan . 有机磷化学与化学教学. University Chemistry, 2025, 40(8): 158-168. doi: 10.12461/PKU.DXHX202410077
5. [5]
  Yongjian Zhang , Fangling Gao , Hong Yan , Keyin Ye . Electrochemical Transformation of Organosulfur Compounds. University Chemistry, 2025, 40(5): 311-317. doi: 10.12461/PKU.DXHX202407035
6. [6]
  Aidang Lu , Yunting Liu , Yanjun Jiang . Comprehensive Organic Chemistry Experiment: Synthesis and Characterization of Triazolopyrimidine Compounds. University Chemistry, 2024, 39(8): 241-246. doi: 10.3866/PKU.DXHX202401029
7. [7]
  Yinuo Wang , Ziyu Liu , Hongxia Tan , Jun Tong , Dazhen Xu . Synthesis of Bromobenzoxazine: Introduce a Comprehensive Organic Chemistry Experiment Transformed from Undergraduate Research Innovation. University Chemistry, 2025, 40(10): 208-216. doi: 10.12461/PKU.DXHX202411077
8. [8]
  Yingtong Shi , Guotong Xu , Guizeng Liang , Di Lan , Siyuan Zhang , Yanru Wang , Daohao Li , Guanglei Wu . PEG-VN改性PP隔膜用于高稳定性高效率锂硫电池. Acta Physico-Chimica Sinica, 2025, 41(7): 100082-0. doi: 10.1016/j.actphy.2025.100082
9. [9]
  Shiyan Cheng , Yonghong Ruan , Lei Gong , Yumei Lin . Research Advances in Friedel-Crafts Alkylation Reaction. University Chemistry, 2024, 39(10): 408-415. doi: 10.12461/PKU.DXHX202403024
10. [10]
  Lewang Yuan , Yaoyao Peng , Zong-Jie Guan , Yu Fang . Insights into the development of 2D covalent organic frameworks as photocatalysts in organic synthesis. Acta Physico-Chimica Sinica, 2025, 41(8): 100086-0. doi: 10.1016/j.actphy.2025.100086
11. [11]
  Xuejie Wang , Guoqing Cui , Congkai Wang , Yang Yang , Guiyuan Jiang , Chunming Xu . Research Progress on Carbon-based Catalysts for Catalytic Dehydrogenation of Liquid Organic Hydrogen Carriers. Acta Physico-Chimica Sinica, 2025, 41(5): 100044-0. doi: 10.1016/j.actphy.2024.100044
12. [12]
  Yuanyuan Ping , Wangqing Kong . 光催化碳氢键官能团化合成1-苯基-1,2-乙二醇. University Chemistry, 2025, 40(6): 238-247. doi: 10.12461/PKU.DXHX202408092
13. [13]
  Yinwu Su , Xuanwen Zheng , Jianghui Du , Boda Li , Tao Wang , Zhiyan Huang . Green Synthesis of 1,3-Dibromoacetone Using Halogen Exchange Method: Recommending a Basic Organic Synthesis Teaching Experiment. University Chemistry, 2024, 39(5): 307-314. doi: 10.3866/PKU.DXHX202311092
14. [14]
  Ping LI , Geng TAN , Xin HUANG , Fuxing SUN , Jiangtao JIA , Guangshan ZHU , Jia LIU , Jiyang LI . Green synthesis of metal-organic frameworks with open metal sites for efficient ammonia capture. Chinese Journal of Inorganic Chemistry, 2025, 41(10): 2063-2068. doi: 10.11862/CJIC.20250020
15. [15]
  Yan Kong , Wei Wei , Lekai Xu , Chen Chen . Electrochemical Synthesis of Organonitrogen Compounds from N-integrated CO₂ Reduction Reaction. Acta Physico-Chimica Sinica, 2024, 40(8): 2307049-0. doi: 10.3866/PKU.WHXB202307049
16. [16]
  Zelong LIANG , Shijia QIN , Pengfei GUO , Hang XU , Bin ZHAO . Synthesis and electrocatalytic CO₂ reduction performance of metal-organic framework catalysts loaded with silver particles. Chinese Journal of Inorganic Chemistry, 2025, 41(1): 165-173. doi: 10.11862/CJIC.20240409
17. [17]
  .
  CCS Chemistry 综述推荐│绿色氧化新思路：光/电催化助力有机物高效升级
  . CCS Chemistry, 2025, 7(10.31635/ccschem.024.202405369): -.
18. [18]
  Hailian Tang , Siyuan Chen , Qiaoyun Liu , Guoyi Bai , Botao Qiao , Liu Fei . Stabilized Rh/hydroxyapatite Catalyst for Furfuryl Alcohol Hydrogenation: Application of Oxidative Strong Metal-Support Interactions in Reducing Conditions. Acta Physico-Chimica Sinica, 2025, 41(4): 2408004-0. doi: 10.3866/PKU.WHXB202408004
19. [19]
  Mian Wei , Chang Cheng , Bowen He , Bei Cheng , Kezhen Qi , Chuanbiao Bie . Inorganic-organic CdS/YBTPy S-scheme photocatalyst for efficient hydrogen production and its mechanism. Acta Physico-Chimica Sinica, 2025, 41(12): 100158-0. doi: 10.1016/j.actphy.2025.100158
20. [20]
  Jingjing QING , Fan HE , Zhihui LIU , Shuaipeng HOU , Ya LIU , Yifan JIANG , Mengting TAN , Lifang HE , Fuxing ZHANG , Xiaoming ZHU . Synthesis, structure, and anticancer activity of two complexes of dimethylglyoxime organotin. Chinese Journal of Inorganic Chemistry, 2024, 40(7): 1301-1308. doi: 10.11862/CJIC.20240003

Get Citation

PDF

XML

Metrics

PDF Downloads(29)
Abstract views(6672)
HTML views(396)

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