Citation: Zhuang Hongfeng, Li Heng, Zhang Shuai, Yin Yanbin, Han Feng, Sun Chao, Miao Chengxia. TEMPO and its derivatives mediated reactions under transition-metal-free conditions[J]. Chinese Chemical Letters, ;2020, 31(1): 39-48. doi: 10.1016/j.cclet.2019.06.027 shu

TEMPO and its derivatives mediated reactions under transition-metal-free conditions

College of Chemistry and Material Science, Shandong Agricultural University, Tai'an 271018, China

Author Bio: Hongfeng Zhuang was born in Shandong province in 1996, and entered College of Chemistry and Material Science, Shandong Agricultural University in 2015. At present, she is carrying out scientific research under the guidance of Prof. Chengxia Miao, developing the green catalytic oxidation

Feng Han received his PhD in physical chemistry from Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences in 2012 under the guidance of Prof. Chungu Xia. And he worked in Lanzhou Institute of Chemical Physics until 2017. Then he moved to Shandong Agricultural University. At present, his primary research interest is homogeneous catalysis, especially designing and synthesizing novel functionalized ionic liquids for exploiting new reactions for building a series of C-X bonds

Chengxia Miao obtained her PhD in organic chemistry from Nankai University in 2010 under the guidance of Prof. Liang-Nian He. Then she joined the group of Prof. Wei Sun in Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences. In 2017 she moved to her present position as professor in Shandong Agricultural University. Her current research interests focus on oxidation reactions catalyzed by organic small molecules or biomimetic catalysts
Received Date: 18 April 2019
Accepted Date: 10 June 2019
Available Online: 22 January 2020

Figures(30)

2, 2, 6, 6-Tetramethyl-1-piperidinyl-N-oxyl (TEMPO) and its derivatives as stable radicals can participate in many reactions. During the process, TEMPO and its derivatives could act not only as the substrates to capture or initiate new radical intermediates to provide new compounds but also as organic catalysts or oxidants for transformations of alkenes, alcohols, aldehydes and so on to synthesize various high valueadded compounds. In this review, we would introduce recent advances of the transformations of different substrates mediated by TEMPO and its derivatives under transition-metal-free conditions.
- TEMPO,
- Transition-metal-free,
- Oxidation,
- Radical,
- Electron transfer
1. [1]
  O.L. Lebedev, S.N. Kazarnovsky, Tr. Khim, Khim. Tekhnol. 3(1959) 649-653.
2. [2]
  J.A. Cella, J.A. Kelly, E.F. Kenehan, J. Org. Chem. 40(1975) 1860-1862. doi: 10.1021/jo00900a049
3. [3]
  A. Rahimi, A. Azarpira, H. Kim, J. Ralph, S.S. Stahl, J. Am. Chem. Soc.135(2013) 6415-6418. doi: 10.1021/ja401793n
4. [4]
  (a) X.Q. Hu, X. Qi, J.R. Chen, et al., Nat. Commun. 7 (2016) 11188;
  (b) C.F. Harris, C.S. Kuehner, J. Bacsa, J.D. Soper, Angew. Chem. Int. Ed. 57 (2018) 1311-1315.
5. [5]
  R. Shinoda, T. Saito, Y. Okita, A. Isogai, Biomacromolecules13(2012) 842-849. doi: 10.1021/bm2017542
6. [6]
  A. Badalyan, S.S. Stahl, Nature 535(2016) 406-410. doi: 10.1038/nature18008
7. [7]
  (a) J.M. Hoover, B.L. Ryland, S.S. Stahl, J. Am. Chem. Soc. 135 (2013) 2357-2367;
  (b) Y. Jing, J. Jiang, B. Yan, et al., Adv. Synth. Catal. 353 (2011) 1146-1152.
8. [8]
  B.L. Ryland, S.S. Stahl, Angew. Chem. Int. Ed. 53(2014) 8824-8838. doi: 10.1002/anie.201403110
9. [9]
  K. Mitsudo, T. Shiraga, H. Tanaka, Tetrahedron Lett. 49(2008) 6593-6595. doi: 10.1016/j.tetlet.2008.09.022
10. [10]
  S. Maity, S. Manna, S. Rana, et al., J. Am. Chem. Soc. 135(2013) 3355-3358. doi: 10.1021/ja311942e
11. [11]
  (a) M.C. Baldovi, N. Mohtat, J.C. Scaiano, Macromolecules 29 (1996) 5497-5499;
  (b) L. Tebben, A. Studer, Angew. Chem. Int. Ed. 50 (2011) 5034-5068.
12. [12]
  (a) R.C. Larock, Pure Appl. Chem. 71 (1999) 1435-1442;
  (b) C.M. Che, J.S. Huang, Coord. Chem. Rev. 231 (2002) 151-164;
  (c) S. Tang, K. Liu, C. Liu, A. Lei, Chem. Soc. Rev. 44 (2015) 1070-1082;
  (d) G. Yin, X. Mu, G. Liu, Acc. Chem. Res. 49 (2016) 2413-2423.
13. [13]
  M.F. Sloan, A.S. Matlack, D.S. Breslow, J. Am. Chem. Soc. 85(1963) 4014-4018. doi: 10.1021/ja00907a023
14. [14]
  Y. Zhu, Q. Wang, R.G. Cornwall, Y. Shi, Chem. Rev. 114(2014) 8199-8256. doi: 10.1021/cr500064w
15. [15]
  C.J.R. Bataille, T.J. Donohoe, Chem. Soc. Rev. 40(2011) 114-128. doi: 10.1039/B923880H
16. [16]
  C.X. Miao, B. Yu, L.N. He, Green Chem. 13(2011) 541-544. doi: 10.1039/c0gc00676a
17. [17]
  M.J.S. Dewar, R.C. Fahey, J. Am. Chem. Soc. 85(1963) 3645-3648. doi: 10.1021/ja00905a025
18. [18]
  F. Minisci, Acc. Chem. Res. 8(1975) 165-171. doi: 10.1021/ar50089a004
19. [19]
  X. Wang, A. Studer, Acc. Chem. Res. 50(2017) 1712-1724. doi: 10.1021/acs.accounts.7b00148
20. [20]
  B. Zhang, A. Studer, Org. Lett. 15(2013) 4548-4551. doi: 10.1021/ol402106x
21. [21]
  M. Hartmann, Y. Li, C. Mück-Lichtenfeld, A. Studer, Chem. -Eur. J. 22(2016) 3485-3490. doi: 10.1002/chem.201504852
22. [22]
  M. Hartmann, Y. Li, A. Studer, J. Am. Chem. Soc. 134(2012) 16516-16519. doi: 10.1021/ja307638u
23. [23]
  Y. Li, M. Hartmann, C.G. Daniliuc, A. Studer, Chem. Commun. 51(2015) 5706-5709. doi: 10.1039/C5CC00591D
24. [24]
  Y. Li, A. Studer, Angew. Chem. Int. Ed. 51(2012) 8221-8224. doi: 10.1002/anie.201202623
25. [25]
  I. Colomer, R.C. Barcelos, K.E. Christensen, T.J. Donohoe, Org. Lett. 18(2016) 5880-5883. doi: 10.1021/acs.orglett.6b02959
26. [26]
  J.L. Liu, S.W. Wu, Q.Y. Wu, F. Liu, J. Org. Chem. 83(2018) 8183-8192. doi: 10.1021/acs.joc.8b00954
27. [27]
  J.E. Nutting, M. Rafiee, S.S. Stahl, Chem. Rev. 118(2018) 4834-4885. doi: 10.1021/acs.chemrev.7b00763
28. [28]
  J.C. Siu, G.S. Sauer, A. Saha, et al., J. Am. Chem. Soc. 140(2018) 12511-12520. doi: 10.1021/jacs.8b06744
29. [29]
  J.C. Siu, J.B. Parry, S. Lin, J. Am. Chem. Soc. 141(2019) 2825-2831. doi: 10.1021/jacs.8b13192
30. [30]
  C. Wan, R.J. Song, J.H. Li, Org. Lett. 21(2019) 2800-2803. doi: 10.1021/acs.orglett.9b00771
31. [31]
  X.Q. Hu, J. Chen, J.R. Chen, D.M. Yan, W.J. Xiao, Chem. Eur. J. 22(2016) 14141-14146. doi: 10.1002/chem.201602597
32. [32]
  D. Gangaprasad, J.P. Raj, T. Kiranmye, K. Karthikeyan, J. Elangovan, Eur. J. Org. Chem. 2016(2016) 5642-5646. doi: 10.1002/ejoc.201601121
33. [33]
  (a) Y. Liu, H. Hu, J. Zhou, et al., Org. Biomol. Chem. 15 (2017) 5016-5024;
  (b) F. Shi, Y. Zhang, Z. Lu, et al., Synthesis 48 (2016) 413-420.
34. [34]
  T. Wang, N. Jiao, J. Am. Chem. Soc. 135(2013) 11692-11695. doi: 10.1021/ja403824y
35. [35]
  (a) S. Manna, S. Jana, T. Saboo, A. Maji, D. Maiti, Chem. Commun. 49 (2013) 5286-5288;
  (b) S. Maity, T. Naveen, U. Sharma, D. Maiti, Org. Lett. 15 (2013) 3384-3387.
36. [36]
  G.K. Kole, G.K. Tan, J.J. Vittal, Org. Lett. 12(2010) 128-131. doi: 10.1021/ol9025233
37. [37]
  (a) T. Mitsudo, H. Naruse, T. Kondo, Y. Ozaki, Y. Watanabe, Angew. Chem. Int. Ed. 33 (1994) 580-581;
  (b) N.N. Noucti, E.J. Alexanian, Angew. Chem. Int. Ed. 54 (2015) 5447-5450.
38. [38]
  M.L. Conner, Y. Xu, M.K. Brown, J. Am. Chem. Soc. 137(2015) 3482-3485. doi: 10.1021/jacs.5b00563
39. [39]
  S. Kyokane, Y. Tanaka, Y. Sei, M. Shiotsuki, Tetrahedron Lett. 58(2017) 4755-4758. doi: 10.1016/j.tetlet.2017.10.072
40. [40]
  (a) R. Liu, X. Liang, C. Dong, X. Hu, J. Am. Chem. Soc. 126 (2004) 4112-4113;
  (b) X. Wang, R. Liu, Y. Jin, X. Liang, Chem. -Eur. J. 14 (2008) 2679-2685;
  (c) Y. Xie, W. Mo, D. Xu, et al., J. Org. Chem. 72 (2007) 4288-4291.
41. [41]
  Y. Dong, X. Zhao, R. Liu, Chin. J. Chem. 33(2015) 1019-1023. doi: 10.1002/cjoc.201500357
42. [42]
  M.S. Laeini, A. Shaabani, ChemistrySelect 2(2017) 9084-9087. doi: 10.1002/slct.201701428
43. [43]
  (a) G.E. Dwulet, D.L. Gin, Chem. Commun. 54 (2018) 12053-12056;
  (b) M. Liu, B. Zhou, L. Zhou, et al., J. Mater. Chem. A 6 (2018) 9860-9865;
  (c) B. Karimi, S. Vahdati, H. Vali, RSC Adv. 6 (2016) 63717-63723;
  (d) H. Zhang, L. Fu, H. Zhong, Chin. J. Catal. 34 (2013) 1848-1854.
44. [44]
  M. Rafiee, K.C. Miles, S.S. Stahl, J. Am. Chem. Soc. 137(2015) 14751-14757. doi: 10.1021/jacs.5b09672
45. [45]
  A. Das, S.S. Stahl, Angew. Chem. Int. Ed. 56(2017) 8892-8897. doi: 10.1002/anie.201704921
46. [46]
  H. Shiigi, H. Mori, T. Tanaka, Y. Demizu, O. Onomura, Tetrahedron Lett. 49(2008) 5247-5251. doi: 10.1016/j.tetlet.2008.06.112
47. [47]
  M. Tomizawa, M. Shibuya, Y. Iwabuchi, Org. Lett. 11(2009) 1829-1831. doi: 10.1021/ol900441f
48. [48]
  M. Shibuya, M. Tomizawa, I. Suzuki, Y. Iwabuchi, J. Am. Chem. Soc.128(2006) 8412-8413. doi: 10.1021/ja0620336
49. [49]
  M. Shibuya, T. Shibuta, H. Fukuda, Y. Iwabuchi, Org. Lett.14(2012) 5010-5013. doi: 10.1021/ol3021435
50. [50]
  S. Zhang, C. Miao, C. Xia, W. Sun, ChemCatChem 7(2015) 1865-1870. doi: 10.1002/cctc.201500214
51. [51]
  Y. Jing, C.G. Daniliuc, A. Studer, Org. Lett. 16(2014) 4932-4935. doi: 10.1021/ol5024568
52. [52]
  R. Ray, R.D. Jana, M. Bhadra, D. Maiti, G.K. Lahiri, Chem. -Eur. J. 20(2014) 15618-15624. doi: 10.1002/chem.201403786
53. [53]
  (a) M. Ji, X. Wang, Y.N. Lim, Y.W. Kang, H.Y. Jang, Eur. J. Org. Chem. 2013 (2013) 7881-7885;
  (b) Y.W. Kang, H.Y. Jang, RSC Adv. 4 (2014) 44486-44490.
54. [54]
  J.M. Vatèle, Synlett 26(2015) 2280-2284. doi: 10.1055/s-0034-1381056
55. [55]
  (a) L.M. Dornan, Q. Cao, J.C.A. Flanagan, et al., Chem. Commun. 49 (2013) 6030-6032;
  (b) S.U. Dighe, D. Chowdhury, S. Batra, Adv. Synth. Catal. 356 (2014) 3892-3896.
56. [56]
  J.M. Vatèle, Synlett 25(2014) 1275-1278. doi: 10.1055/s-0033-1341124
57. [57]
  T. Chinnusamy, Catal. Commun. 119(2019) 51-56. doi: 10.1016/j.catcom.2018.08.021
58. [58]
  (a) J.J. Mousseau, A.B. Charette, Acc. Chem. Res. 46 (2013) 412-424;
  (b) C. Zhang, C. Tang, N. Jiao, Chem. Soc. Rev. 41 (2012) 3464-3484.
59. [59]
  (a) Y. Bansal, O. Silakari, Bioorg. Med. Chem. 20 (2012) 6208-6236;
  (b) J.P. Michael, Nat. Prod. Rep. 25 (2008) 166-187.
60. [60]
  D. Xue, Y.Q. Long, J. Org. Chem. 79(2014) 4727-4734. doi: 10.1021/jo5005179
61. [61]
  J. Hu, H. Xu, P. Nie, et al., Chem. -Eur. J. 20(2014) 3932-3938. doi: 10.1002/chem.201304923
62. [62]
  J.P. Lin, F.H. Zhang, Y.Q. Long, Org. Lett. 16(2014) 2822-2825. doi: 10.1021/ol500864r
63. [63]
  B. Han, X.L. Yang, R. Fang, et al., Angew. Chem. Int. Ed. 51(2012) 8816-8820. doi: 10.1002/anie.201203799
64. [64]
  X.Y. Duan, X.L. Yang, R. Fang, et al., J. Org. Chem. 78(2013) 10692-10704. doi: 10.1021/jo4016908
65. [65]
  X.Y. Duan, N.N. Zhou, R. Fang, et al., Angew. Chem. Int. Ed. 53(2014) 3158-3162. doi: 10.1002/anie.201309918
66. [66]
  F. Chen, X.L. Yang, Z.W. Wu, B. Han, J. Org. Chem. 81(2016) 3042-3050. doi: 10.1021/acs.joc.6b00180
67. [67]
  X. Zhu, Y.F. Wang, W. Ren, F.L. Zhang, S. Chiba, Org. Lett.15(2013) 3214-3217. doi: 10.1021/ol4014969
68. [68]
  X. Zhu, S. Chiba, Org. Biomol. Chem. 12(2014) 4567-4570. doi: 10.1039/C4OB00839A
69. [69]
  J.L. Zhan, M.W. Wu, D. Wei, et al., ACS Catal. 9(2019) 4179-4188. doi: 10.1021/acscatal.9b00832
70. [70]
  K.M. Lambert, J.M. Bobbitt, S.A. Eldirany, K.B. Wiberg, W.F. Bailey, Org. Lett.16(2014) 6484-6487. doi: 10.1021/ol503345h
71. [71]
  K.M. Lambert, J.M. Bobbitt, S.A. Eldirany, et al., Chem. -Eur. J. 22(2016) 5156-5159. doi: 10.1002/chem.201600549
72. [72]
  P. Galletti, G. Martelli, G. Prandini, C. Colucci, D. Giacomini, RSC Adv. 8(2018) 9723-9730. doi: 10.1039/C8RA01365A
73. [73]
  A.H. Bansode, G. Suryavanshi, RSC Adv. 8(2018) 32055-32062. doi: 10.1039/C8RA07451H
74. [74]
  Y. Chen, L. Qian, W. Zhang, B. Han, Angew. Chem. Int. Ed. 47(2008) 9330-9333. doi: 10.1002/anie.200803381
75. [75]
  H. Huo, X.Y. Tang, Y. Gong, Synthesis 50(2018) 2727-2740. doi: 10.1055/s-0037-1610131
76. [76]
  B. Han, C. Wang, R.F. Han, et al., Chem. Commun. 47(2011) 7818-7820. doi: 10.1039/c1cc12308d
77. [77]
  T. Kano, F. Shirozu, K. Maruoka, J. Am. Chem. Soc. 135(2013) 18036-18039. doi: 10.1021/ja4099627
78. [78]
  X. Zhao, T.X. Liu, N. Ma, G. Zhang, J. Org. Chem. 82(2017) 6125-6132. doi: 10.1021/acs.joc.7b00686
79. [79]
  S.E. Baillie, V.L. Blair, T.D. Bradley, et al., Chem. Sci. 4(2013) 1895-1905. doi: 10.1039/c3sc22326d
80. [80]
  X.L. Yang, X.X. Peng, F. Chen, B. Han, Org. Lett. 18(2016) 2070-2073. doi: 10.1021/acs.orglett.6b00702
81. [81]
  W.B. Qin, J.Y. Zhu, Y.B. Kong, et al., Org. Biomol. Chem.12(2014) 4252-4259. doi: 10.1039/C4OB00356J
82. [82]
  (a) B.M. Trost, E. Keinan, J. Org. Chem. 45 (1980) 2741-2746;
  (b) R. Shi, L. Lu, H. Zhang, et al., Angew. Chem. Int. Ed. 52 (2013) 10582-10585.
83. [83]
  X. Jia, P. Li, Y. Shao, et al., Green Chem. 19(2017) 5568-5574. doi: 10.1039/C7GC02775C
84. [84]
  H. Liu, Y. Fang, S.Y. Wang, S.J. Ji, Org. Lett. 20(2018) 930-933. doi: 10.1021/acs.orglett.7b03783
85. [85]
  X.Y. Qian, S.Q. Li, J. Song, H.C. Xu, ACS Catal. 7(2017) 2730-2734. doi: 10.1021/acscatal.7b00426
86. [86]
  B. Dong, S. Lu, J. Jiang, et al., J. Chem. Technol. Biotechnol. 87(2012) 341-345. doi: 10.1002/jctb.2719
87. [87]
  L. Yang, S. Li, Y. Dou, et al., Asian J. Org. Chem. 6(2017) 265-268. doi: 10.1002/ajoc.201600588
88. [88]
  (a) S. Manna, S. Jana, T. Saboo, A. Majia, D. Maiti, Chem. Commun. 49 (2013) 5286-5288;
  (b) A. Zhao, Q. Jiang, J. Jia, et al., Tetrahedron Lett. 57 (2016) 80-84.
89. [89]
  U. Dutta, S. Maity, R. Kancherla, D. Maiti, Org. Lett. 16(2014) 6302-6305. doi: 10.1021/ol503025n
90. [90]
  X.H. Yang, X.H. Ouyang, W.T. Wei, R.J. Song, J.H. Li, Adv. Synth. Catal. 357(2015) 1161-1166. doi: 10.1002/adsc.201400895
91. [91]
  X.H. Hao, P. Gao, X.R. Song, et al., Chem. Commun. 51(2015) 6839-6842. doi: 10.1039/C5CC00872G
92. [92]
  B. Gou, D. Li, C. Yang, et al., J. Photochem. Photobiol. A 233(2012) 46-49. doi: 10.1016/j.jphotochem.2012.02.008
93. [93]
  Z. Shen, M. Chen, T. Fang, et al., Tetrahedron Lett. 56(2015) 2768-2772. doi: 10.1016/j.tetlet.2015.04.033
94. [94]
  A. Chennaiah, A.K. Verma, Y.D. Vankar, J. Org. Chem. 83(2018) 10535-10540. doi: 10.1021/acs.joc.8b01191
95. [95]
  X. Tian, Y.L. Ren, F. Ren, et al., Synlett 29(2018) 2444-2448. doi: 10.1055/s-0037-1611062
96. [96]
  J.H. Noh, J. Kim, J. Org. Chem. 80(2015) 11624-11628. doi: 10.1021/acs.joc.5b02333
97. [97]
  C. Fang, M. Li, X. Hu, et al., Adv. Synth. Catal. 358(2016) 1157-1163. doi: 10.1002/adsc.201501130
98. [98]
  S. Chiba, H. Chen, Org. Biomol. Chem. 12(2014) 4051-4060. doi: 10.1039/C4OB00469H
99. [99]
  P. Novák, A. Correa, J. Gallardo-Donaire, R. Martin, Angew. Chem. Int. Ed. 50(2011) 12236-12239. doi: 10.1002/anie.201105894
100. [100]
  G. Zhang, Y. Zhang, R. Wang, Angew. Chem. Int. Ed. 50(2011) 10429-10432. doi: 10.1002/anie.201105123
101. [101]
  U. Osorio-Nieto, D. Chamorro-Arenas, L. Quintero, H. Höpfl, F. Sartillo-Piscil, J. Org. Chem. 81(2016) 8625-8632. doi: 10.1021/acs.joc.6b01566
102. [102]
  D. Chamorro-Arenas, U. Osorio-Nieto, L. Quintero, L. Hernández-García, F. Sartillo-Piscil, J. Org. Chem. 83(2018) 15333-15346. doi: 10.1021/acs.joc.8b02564
103. [103]
  Z.L. Wang, X.L. An, L.S. Ge, et al., Tetrahedron 70(2014) 3788-3792. doi: 10.1016/j.tet.2014.04.021
104. [104]
  C. Li, C.C. Zeng, L.M. Hu, et al., Electrochim. Acta 114(2013) 560-566. doi: 10.1016/j.electacta.2013.10.093
105. [105]
  Z. Zhang, Y. Gao, Y. Liu, et al., Org. Lett. 17(2015) 5492-5495. doi: 10.1021/acs.orglett.5b02877
106. [106]
  B. Zhang, Y. Cui, N. Jiao, Chem. Commun. 48(2012) 4498-4500. doi: 10.1039/c2cc30684k
107. [107]
  W. Hu, J.P. Lin, L.R. Song, Y.Q. Long, Org. Lett. 17(2015) 1268-1271. doi: 10.1021/acs.orglett.5b00248
108. [108]
  J. Peng, G. Huang, H.J. Wang, et al., J. Org. Chem. 83(2018) 85-95. doi: 10.1021/acs.joc.7b02378
109. [109]
  C. Ganachaud, V. Garfagnoli, T. Tron, G. Iacazio, Tetrahedron Lett. 49(2008) 2476-2478. doi: 10.1016/j.tetlet.2008.02.021
110. [110]
  W.B. Qin, Q. Chang, Y.H. Bao, et al., Org. Biomol. Chem. 10(2012) 8814-8821. doi: 10.1039/c2ob26390d
1. [1]
  Yang Xiaojiang , Mao Jincheng , Zhang Heng , Zhang Yang , Mao Jinhua . Copper-Catalyzed Aerobic Oxidation Reaction of Benzyl Alcohol in Water under Base-Free Condition. Chinese Journal of Organic Chemistry, 2018, 38(10): 2780-2783. doi: 10.6023/cjoc201802018
2. [2]
  Arash Ghorbani-Choghamarani , Mina Abbasi . Poly(4-vinylpyridinium tribromide) as metal-free,green and recoverable oxidizing polymer for the chemoselective oxidation of sulfides into sulfoxides. Chinese Chemical Letters, 2011, 22(1): 114-118. doi: 10.1016/j.cclet.2010.09.011
3. [3]
  Yang Xiao , Xiao Yan Zhang , Qin Bo Wang , Ze Tan , Can Cheng Guo , Wei Deng , Zhi Gang Liu , He Fei Zhang . The preparation of terephthalic acid by solvent-free oxidation of p-xylene with air over T(pCl)PPMnCl and Co(OAc)₂. Chinese Chemical Letters, 2011, 22(2): 135-138. doi: 10.1016/j.cclet.2010.09.027
4. [4]
  Xiao Quan Lu , De Fang Dong , Xiu Hui Liu , Dong Na Yao , Wen Ting Wang , Yu Mei Xu . Investigation of the oxidation of hydroquinone at the liquid/liquid interface. Chinese Chemical Letters, 2010, 21(2): 225-228. doi: 10.1016/j.cclet.2009.09.004
5. [5]
  Xu-Wei Wu , Bin-Dong Li . Preparation of high purity 1,2-diols by catalytic oxidation of linear terminal alkenes with H₂O₂ in the presence of carboxylic acids under solvent-free conditions. Chinese Chemical Letters, 2014, 25(3): 459-462. doi: 10.1016/j.cclet.2013.11.049
6. [6]
  Xiao-Jun Dai , Xiao-Liang Xu , Dong-Ping Cheng , Xiao-Nian Li . Visible-light photoredox-mediated oxidation of N-methyl tertiaryamines under catalyst free conditions：Direct synthesis of methylene-bridged bis-1,3-dicarbonyl compounds. Chinese Chemical Letters, 2014, 25(4): 545-548. doi: 10.1016/j.cclet.2014.01.021
7. [7]
  Warangkana Kanjina , Wimonrat Trakarnpruk . Mixed metal oxide catalysts for the selective oxidation of ethylbenzene to acetophenone. Chinese Chemical Letters, 2011, 22(4): 401-404. doi: 10.1016/j.cclet.2010.10.035
8. [8]
  Xiu Hui Liu , Cun Wu Dong , Kai Zhang , Fu Peng Zhi , Zhen Ding , Xiao Quan Lu . Effect of SDBS on interfacial electron transfer at the　liquid/liquid interface by thin layer metho. Chinese Chemical Letters, 2009, 20(9): 1115-1118. doi: 10.1016/j.cclet.2009.04.035
9. [9]
  Yong Hui WANG , Man Zhou ZHU , Tao LIU , Qing Xiang GUO . The Electron Transfer Reaction between p-Nitrobenzoates and β-N, N-Dimethylaminonaphthalene. Chinese Chemical Letters, 2003, 14(2): 159-162.
10. [10]
  Yu Mei XING , Zheng Yu ZHOU , Ben Ni DU . DFT Calculations for Electron Transfer Bond-breaking Reaction of CH₃-X. Chinese Chemical Letters, 2001, 12(4): 347-350.
11. [11]
  Hua JIANG , Hui Jun XU . Synthesis and Cation-Mediated Electron Transfer in Fluorescence Quenching of Donor-Acceptor Podands. Chinese Chemical Letters, 2000, 11(9): 767-770.
12. [12]
  Bing Xia , Qiang Miao , Jie Chao , Shou Jun Xiao , Hai Tao Wang , Zhong Dang Xiao . Charge transfer on porous silicon membranes studied by current-sensing atomic force microscopy. Chinese Chemical Letters, 2008, 19(2): 199-202. doi: 10.1016/j.cclet.2007.12.003
13. [13]
  Bao Kun ZHU , Hong Bin ZHANG , Yu Shun ZHANG , Hui Min ZHONG , Jian Ping LIU . Oxidation of Hecogenin and Diosgenin Derivatives with Dimethyldioxirane. Chinese Chemical Letters, 2005, 16(2): 143-146.
14. [14]
  Chuan Zhi XU , Lin CHEN , Zhen LI , Wei SUN , Chun Gu XIA . A Mild and Efficient Oxidation of Alcohols in Water. Chinese Chemical Letters, 2004, 15(10): 1149-1152.
15. [15]
  Dong Po Shi , Hong Bing Ji . β-Cyclodextrin promoted oxidation of aldehydes to carboxylic acids in water. Chinese Chemical Letters, 2009, 20(2): 139-142. doi: 10.1016/j.cclet.2008.10.037
16. [16]
  Hui Ming Jin , Lin Nan Zhang . High temperature oxidation of chromium with nanometric ceria sol-gel coating. Chinese Chemical Letters, 2008, 19(12): 1504-1508. doi: 10.1016/j.cclet.2008.09.038
17. [17]
  Xiao Gang Li , Jing Wang , Ren He . Selective oxidation of ethylbenzene catalyzed by fluorinated metalloporphyrins with molecular oxygen. Chinese Chemical Letters, 2007, 18(9): 1053-1056. doi: 10.1016/j.cclet.2007.06.019
18. [18]
  Jun LIU , Rui ZHANG , Liang GAO , Tao JIANG , Zhi Min LIU , Jun HE , Bu Xing HAN , Guan Ying YANG . The Oxidation of Cyclohexene with Polymer Supported Co(II) in Supercritical Carbon Dioxide. Chinese Chemical Letters, 2002, 13(12): 1162-1163.
19. [19]
  Nor Aqilah Mohd Fadzil , Mohd Hasbi Ab. Rahim , Gaanty Pragas Maniam . A brief review of para-xylene oxidation to terephthalic acid as a model of primary C-H bond activation. Chinese Journal of Catalysis, 2014, 35(10): 1641-1652. doi: 10.1016/S1872-2067(14)60193-5
20. [20]
  Ali Reza Pourali , Mehrosadat Tabaean , S. Mohamad Reza Nazifi . A novel and selective oxidation of benzylic alcohols with polymer-supported periodic acid under mild aprotic conditions. Chinese Chemical Letters, 2012, 23(1): 21-24. doi: 10.1016/j.cclet.2011.07.022

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沈阳化工大学材料科学与工程学院沈阳 110142