TEMPO and its derivatives mediated reactions under transition-metal-free conditions
* Corresponding author.
E-mail addresses: fenghan@sdau.edu.cn (F. Han), chxmiao@sdau.edu.cn (C. Miao).
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
O.L. Lebedev, S.N. Kazarnovsky, Tr. Khim, Khim. Tekhnol. 3(1959) 649-653.
J.A. Cella, J.A. Kelly, E.F. Kenehan, J. Org. Chem. 40(1975) 1860-1862.
doi: 10.1021/jo00900a049
A. Rahimi, A. Azarpira, H. Kim, J. Ralph, S.S. Stahl, J. Am. Chem. Soc.135(2013) 6415-6418.
doi: 10.1021/ja401793n
(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.
R. Shinoda, T. Saito, Y. Okita, A. Isogai, Biomacromolecules13(2012) 842-849.
doi: 10.1021/bm2017542
A. Badalyan, S.S. Stahl, Nature 535(2016) 406-410.
doi: 10.1038/nature18008
(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.
B.L. Ryland, S.S. Stahl, Angew. Chem. Int. Ed. 53(2014) 8824-8838.
doi: 10.1002/anie.201403110
K. Mitsudo, T. Shiraga, H. Tanaka, Tetrahedron Lett. 49(2008) 6593-6595.
doi: 10.1016/j.tetlet.2008.09.022
S. Maity, S. Manna, S. Rana, et al., J. Am. Chem. Soc. 135(2013) 3355-3358.
doi: 10.1021/ja311942e
(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.
(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.
M.F. Sloan, A.S. Matlack, D.S. Breslow, J. Am. Chem. Soc. 85(1963) 4014-4018.
doi: 10.1021/ja00907a023
Y. Zhu, Q. Wang, R.G. Cornwall, Y. Shi, Chem. Rev. 114(2014) 8199-8256.
doi: 10.1021/cr500064w
C.J.R. Bataille, T.J. Donohoe, Chem. Soc. Rev. 40(2011) 114-128.
doi: 10.1039/B923880H
C.X. Miao, B. Yu, L.N. He, Green Chem. 13(2011) 541-544.
doi: 10.1039/c0gc00676a
M.J.S. Dewar, R.C. Fahey, J. Am. Chem. Soc. 85(1963) 3645-3648.
doi: 10.1021/ja00905a025
F. Minisci, Acc. Chem. Res. 8(1975) 165-171.
doi: 10.1021/ar50089a004
X. Wang, A. Studer, Acc. Chem. Res. 50(2017) 1712-1724.
doi: 10.1021/acs.accounts.7b00148
B. Zhang, A. Studer, Org. Lett. 15(2013) 4548-4551.
doi: 10.1021/ol402106x
M. Hartmann, Y. Li, C. Mück-Lichtenfeld, A. Studer, Chem. -Eur. J. 22(2016) 3485-3490.
doi: 10.1002/chem.201504852
M. Hartmann, Y. Li, A. Studer, J. Am. Chem. Soc. 134(2012) 16516-16519.
doi: 10.1021/ja307638u
Y. Li, M. Hartmann, C.G. Daniliuc, A. Studer, Chem. Commun. 51(2015) 5706-5709.
doi: 10.1039/C5CC00591D
Y. Li, A. Studer, Angew. Chem. Int. Ed. 51(2012) 8221-8224.
doi: 10.1002/anie.201202623
I. Colomer, R.C. Barcelos, K.E. Christensen, T.J. Donohoe, Org. Lett. 18(2016) 5880-5883.
doi: 10.1021/acs.orglett.6b02959
J.L. Liu, S.W. Wu, Q.Y. Wu, F. Liu, J. Org. Chem. 83(2018) 8183-8192.
doi: 10.1021/acs.joc.8b00954
J.E. Nutting, M. Rafiee, S.S. Stahl, Chem. Rev. 118(2018) 4834-4885.
doi: 10.1021/acs.chemrev.7b00763
J.C. Siu, G.S. Sauer, A. Saha, et al., J. Am. Chem. Soc. 140(2018) 12511-12520.
doi: 10.1021/jacs.8b06744
J.C. Siu, J.B. Parry, S. Lin, J. Am. Chem. Soc. 141(2019) 2825-2831.
doi: 10.1021/jacs.8b13192
C. Wan, R.J. Song, J.H. Li, Org. Lett. 21(2019) 2800-2803.
doi: 10.1021/acs.orglett.9b00771
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
D. Gangaprasad, J.P. Raj, T. Kiranmye, K. Karthikeyan, J. Elangovan, Eur. J. Org. Chem. 2016(2016) 5642-5646.
doi: 10.1002/ejoc.201601121
(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.
T. Wang, N. Jiao, J. Am. Chem. Soc. 135(2013) 11692-11695.
doi: 10.1021/ja403824y
(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.
G.K. Kole, G.K. Tan, J.J. Vittal, Org. Lett. 12(2010) 128-131.
doi: 10.1021/ol9025233
(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.
M.L. Conner, Y. Xu, M.K. Brown, J. Am. Chem. Soc. 137(2015) 3482-3485.
doi: 10.1021/jacs.5b00563
S. Kyokane, Y. Tanaka, Y. Sei, M. Shiotsuki, Tetrahedron Lett. 58(2017) 4755-4758.
doi: 10.1016/j.tetlet.2017.10.072
(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.
Y. Dong, X. Zhao, R. Liu, Chin. J. Chem. 33(2015) 1019-1023.
doi: 10.1002/cjoc.201500357
M.S. Laeini, A. Shaabani, ChemistrySelect 2(2017) 9084-9087.
doi: 10.1002/slct.201701428
(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.
M. Rafiee, K.C. Miles, S.S. Stahl, J. Am. Chem. Soc. 137(2015) 14751-14757.
doi: 10.1021/jacs.5b09672
A. Das, S.S. Stahl, Angew. Chem. Int. Ed. 56(2017) 8892-8897.
doi: 10.1002/anie.201704921
H. Shiigi, H. Mori, T. Tanaka, Y. Demizu, O. Onomura, Tetrahedron Lett. 49(2008) 5247-5251.
doi: 10.1016/j.tetlet.2008.06.112
M. Tomizawa, M. Shibuya, Y. Iwabuchi, Org. Lett. 11(2009) 1829-1831.
doi: 10.1021/ol900441f
M. Shibuya, M. Tomizawa, I. Suzuki, Y. Iwabuchi, J. Am. Chem. Soc.128(2006) 8412-8413.
doi: 10.1021/ja0620336
M. Shibuya, T. Shibuta, H. Fukuda, Y. Iwabuchi, Org. Lett.14(2012) 5010-5013.
doi: 10.1021/ol3021435
S. Zhang, C. Miao, C. Xia, W. Sun, ChemCatChem 7(2015) 1865-1870.
doi: 10.1002/cctc.201500214
Y. Jing, C.G. Daniliuc, A. Studer, Org. Lett. 16(2014) 4932-4935.
doi: 10.1021/ol5024568
R. Ray, R.D. Jana, M. Bhadra, D. Maiti, G.K. Lahiri, Chem. -Eur. J. 20(2014) 15618-15624.
doi: 10.1002/chem.201403786
(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.
J.M. Vatèle, Synlett 26(2015) 2280-2284.
doi: 10.1055/s-0034-1381056
(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.
J.M. Vatèle, Synlett 25(2014) 1275-1278.
doi: 10.1055/s-0033-1341124
T. Chinnusamy, Catal. Commun. 119(2019) 51-56.
doi: 10.1016/j.catcom.2018.08.021
(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.
(a) Y. Bansal, O. Silakari, Bioorg. Med. Chem. 20 (2012) 6208-6236;
(b) J.P. Michael, Nat. Prod. Rep. 25 (2008) 166-187.
D. Xue, Y.Q. Long, J. Org. Chem. 79(2014) 4727-4734.
doi: 10.1021/jo5005179
J. Hu, H. Xu, P. Nie, et al., Chem. -Eur. J. 20(2014) 3932-3938.
doi: 10.1002/chem.201304923
J.P. Lin, F.H. Zhang, Y.Q. Long, Org. Lett. 16(2014) 2822-2825.
doi: 10.1021/ol500864r
B. Han, X.L. Yang, R. Fang, et al., Angew. Chem. Int. Ed. 51(2012) 8816-8820.
doi: 10.1002/anie.201203799
X.Y. Duan, X.L. Yang, R. Fang, et al., J. Org. Chem. 78(2013) 10692-10704.
doi: 10.1021/jo4016908
X.Y. Duan, N.N. Zhou, R. Fang, et al., Angew. Chem. Int. Ed. 53(2014) 3158-3162.
doi: 10.1002/anie.201309918
F. Chen, X.L. Yang, Z.W. Wu, B. Han, J. Org. Chem. 81(2016) 3042-3050.
doi: 10.1021/acs.joc.6b00180
X. Zhu, Y.F. Wang, W. Ren, F.L. Zhang, S. Chiba, Org. Lett.15(2013) 3214-3217.
doi: 10.1021/ol4014969
X. Zhu, S. Chiba, Org. Biomol. Chem. 12(2014) 4567-4570.
doi: 10.1039/C4OB00839A
J.L. Zhan, M.W. Wu, D. Wei, et al., ACS Catal. 9(2019) 4179-4188.
doi: 10.1021/acscatal.9b00832
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
K.M. Lambert, J.M. Bobbitt, S.A. Eldirany, et al., Chem. -Eur. J. 22(2016) 5156-5159.
doi: 10.1002/chem.201600549
P. Galletti, G. Martelli, G. Prandini, C. Colucci, D. Giacomini, RSC Adv. 8(2018) 9723-9730.
doi: 10.1039/C8RA01365A
A.H. Bansode, G. Suryavanshi, RSC Adv. 8(2018) 32055-32062.
doi: 10.1039/C8RA07451H
Y. Chen, L. Qian, W. Zhang, B. Han, Angew. Chem. Int. Ed. 47(2008) 9330-9333.
doi: 10.1002/anie.200803381
H. Huo, X.Y. Tang, Y. Gong, Synthesis 50(2018) 2727-2740.
doi: 10.1055/s-0037-1610131
B. Han, C. Wang, R.F. Han, et al., Chem. Commun. 47(2011) 7818-7820.
doi: 10.1039/c1cc12308d
T. Kano, F. Shirozu, K. Maruoka, J. Am. Chem. Soc. 135(2013) 18036-18039.
doi: 10.1021/ja4099627
X. Zhao, T.X. Liu, N. Ma, G. Zhang, J. Org. Chem. 82(2017) 6125-6132.
doi: 10.1021/acs.joc.7b00686
S.E. Baillie, V.L. Blair, T.D. Bradley, et al., Chem. Sci. 4(2013) 1895-1905.
doi: 10.1039/c3sc22326d
X.L. Yang, X.X. Peng, F. Chen, B. Han, Org. Lett. 18(2016) 2070-2073.
doi: 10.1021/acs.orglett.6b00702
W.B. Qin, J.Y. Zhu, Y.B. Kong, et al., Org. Biomol. Chem.12(2014) 4252-4259.
doi: 10.1039/C4OB00356J
(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.
X. Jia, P. Li, Y. Shao, et al., Green Chem. 19(2017) 5568-5574.
doi: 10.1039/C7GC02775C
H. Liu, Y. Fang, S.Y. Wang, S.J. Ji, Org. Lett. 20(2018) 930-933.
doi: 10.1021/acs.orglett.7b03783
X.Y. Qian, S.Q. Li, J. Song, H.C. Xu, ACS Catal. 7(2017) 2730-2734.
doi: 10.1021/acscatal.7b00426
B. Dong, S. Lu, J. Jiang, et al., J. Chem. Technol. Biotechnol. 87(2012) 341-345.
doi: 10.1002/jctb.2719
L. Yang, S. Li, Y. Dou, et al., Asian J. Org. Chem. 6(2017) 265-268.
doi: 10.1002/ajoc.201600588
(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.
U. Dutta, S. Maity, R. Kancherla, D. Maiti, Org. Lett. 16(2014) 6302-6305.
doi: 10.1021/ol503025n
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
X.H. Hao, P. Gao, X.R. Song, et al., Chem. Commun. 51(2015) 6839-6842.
doi: 10.1039/C5CC00872G
B. Gou, D. Li, C. Yang, et al., J. Photochem. Photobiol. A 233(2012) 46-49.
doi: 10.1016/j.jphotochem.2012.02.008
Z. Shen, M. Chen, T. Fang, et al., Tetrahedron Lett. 56(2015) 2768-2772.
doi: 10.1016/j.tetlet.2015.04.033
A. Chennaiah, A.K. Verma, Y.D. Vankar, J. Org. Chem. 83(2018) 10535-10540.
doi: 10.1021/acs.joc.8b01191
X. Tian, Y.L. Ren, F. Ren, et al., Synlett 29(2018) 2444-2448.
doi: 10.1055/s-0037-1611062
J.H. Noh, J. Kim, J. Org. Chem. 80(2015) 11624-11628.
doi: 10.1021/acs.joc.5b02333
C. Fang, M. Li, X. Hu, et al., Adv. Synth. Catal. 358(2016) 1157-1163.
doi: 10.1002/adsc.201501130
S. Chiba, H. Chen, Org. Biomol. Chem. 12(2014) 4051-4060.
doi: 10.1039/C4OB00469H
P. Novák, A. Correa, J. Gallardo-Donaire, R. Martin, Angew. Chem. Int. Ed. 50(2011) 12236-12239.
doi: 10.1002/anie.201105894
G. Zhang, Y. Zhang, R. Wang, Angew. Chem. Int. Ed. 50(2011) 10429-10432.
doi: 10.1002/anie.201105123
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
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
Z.L. Wang, X.L. An, L.S. Ge, et al., Tetrahedron 70(2014) 3788-3792.
doi: 10.1016/j.tet.2014.04.021
C. Li, C.C. Zeng, L.M. Hu, et al., Electrochim. Acta 114(2013) 560-566.
doi: 10.1016/j.electacta.2013.10.093
Z. Zhang, Y. Gao, Y. Liu, et al., Org. Lett. 17(2015) 5492-5495.
doi: 10.1021/acs.orglett.5b02877
B. Zhang, Y. Cui, N. Jiao, Chem. Commun. 48(2012) 4498-4500.
doi: 10.1039/c2cc30684k
W. Hu, J.P. Lin, L.R. Song, Y.Q. Long, Org. Lett. 17(2015) 1268-1271.
doi: 10.1021/acs.orglett.5b00248
J. Peng, G. Huang, H.J. Wang, et al., J. Org. Chem. 83(2018) 85-95.
doi: 10.1021/acs.joc.7b02378
C. Ganachaud, V. Garfagnoli, T. Tron, G. Iacazio, Tetrahedron Lett. 49(2008) 2476-2478.
doi: 10.1016/j.tetlet.2008.02.021
W.B. Qin, Q. Chang, Y.H. Bao, et al., Org. Biomol. Chem. 10(2012) 8814-8821.
doi: 10.1039/c2ob26390d
Chunxiu Yu , Zelin Wu , Hongle Shi , Lingyun Gu , Kexin Chen , Chuan-Shu He , Yang Liu , Heng Zhang , Peng Zhou , Zhaokun Xiong , Bo Lai . Insights into the electron transfer mechanisms of peroxydisulfate activation by modified metal-free acetylene black for degradation of sulfisoxazole. Chinese Chemical Letters, 2024, 35(8): 109334-. doi: 10.1016/j.cclet.2023.109334
Zhengzhong Zhu , Shaojun Hu , Zhi Liu , Lipeng Zhou , Chongbin Tian , Qingfu Sun . A cationic radical lanthanide organic tetrahedron with remarkable coordination enhanced radical stability. Chinese Chemical Letters, 2025, 36(2): 109641-. doi: 10.1016/j.cclet.2024.109641
Xiao-Bo Liu , Ren-Ming Liu , Xiao-Di Bao , Hua-Jian Xu , Qi Zhang , Yu-Feng Liang . Nickel-catalyzed reductive formylation of aryl halides via formyl radical. Chinese Chemical Letters, 2024, 35(12): 109783-. doi: 10.1016/j.cclet.2024.109783
Xiaoxue Li , Hongwei Zhou , Rongrong Qian , Xu Zhang , Lei Yu . A concise synthesis of Se/Fe materials for catalytic oxidation reactions of anthracene and polyene. Chinese Chemical Letters, 2025, 36(3): 110036-. doi: 10.1016/j.cclet.2024.110036
Zuyou Song , Yong Jiang , Qiao Gou , Yini Mao , Yimin Jiang , Wei Shen , Ming Li , Rongxing He . Promoting the generation of active sites through "Co-O-Ru" electron transport bridges for efficient water splitting. Chinese Chemical Letters, 2025, 36(4): 109793-. doi: 10.1016/j.cclet.2024.109793
Zhikang Wu , Guoyong Dai , Qi Li , Zheyu Wei , Shi Ru , Jianda Li , Hongli Jia , Dejin Zang , Mirjana Čolović , Yongge Wei . POV-based molecular catalysts for highly efficient esterification of alcohols with aldehydes as acylating agents. Chinese Chemical Letters, 2024, 35(8): 109061-. doi: 10.1016/j.cclet.2023.109061
Chen Lian , Si-Han Zhao , Hai-Lou Li , Xinhua Cao . A giant Ce-containing poly(tungstobismuthate): Synthesis, structure and catalytic performance for the decontamination of a sulfur mustard simulant. Chinese Chemical Letters, 2024, 35(10): 109343-. doi: 10.1016/j.cclet.2023.109343
Le Zhang , Hui-Yu Xie , Xin Li , Li-Ying Sun , Ying-Feng Han . SOMO-HOMO level conversion in triarylmethyl-cored N-heterocyclic carbene-Au(I) complexes triggered by selecting coordination halogens. Chinese Chemical Letters, 2024, 35(11): 109465-. doi: 10.1016/j.cclet.2023.109465
Supphachok Chanmungkalakul , Syed Ali Abbas Abedi , Federico J. Hernández , Jianwei Xu , Xiaogang Liu . The dark side of cyclooctatetraene (COT): Photophysics in the singlet states of “self-healing” dyes. Chinese Chemical Letters, 2024, 35(8): 109227-. doi: 10.1016/j.cclet.2023.109227
Cunjun Li , Wencong Liu , Xianlei Chen , Liang Li , Shenyu Lan , Mingshan Zhu . Adsorption and activation of peroxymonosulfate on BiOCl for carbamazepine degradation: The role of piezoelectric effect. Chinese Chemical Letters, 2024, 35(10): 109652-. doi: 10.1016/j.cclet.2024.109652
Huaixiang Yang , Miao-Miao Li , Aijun Zhang , Jiefei Guo , Yongqi Yu , Wei Ding . Visible-light-induced photocatalyst- and metal-free radical phosphinoyloximation of alkenes with tert-butyl nitrite as bifunctional reagent. Chinese Chemical Letters, 2025, 36(3): 110425-. doi: 10.1016/j.cclet.2024.110425
Yu-Yu Tan , Lin-Heng He , Wei-Min He . Copper-mediated assembly of SO2F group via radical fluorine-atom transfer strategy. Chinese Chemical Letters, 2024, 35(9): 109986-. doi: 10.1016/j.cclet.2024.109986
Lei Shi . Nucleophilicity and Electrophilicity of Radicals. University Chemistry, 2024, 39(11): 131-135. doi: 10.3866/PKU.DXHX202402018
Kexin Yin , Jingren Yang , Yanwei Li , Qian Li , Xing Xu . Metal-free diatomaceous carbon-based catalyst for ultrafast and anti-interference Fenton-like oxidation. Chinese Chemical Letters, 2024, 35(12): 109847-. doi: 10.1016/j.cclet.2024.109847
Weixu Li , Yuexin Wang , Lin Li , Xinyi Huang , Mengdi Liu , Bo Gui , Xianjun Lang , Cheng Wang . Promoting energy transfer pathway in porphyrin-based sp2 carbon-conjugated covalent organic frameworks for selective photocatalytic oxidation of sulfide. Chinese Journal of Structural Chemistry, 2024, 43(7): 100299-100299. doi: 10.1016/j.cjsc.2024.100299
Shuo Li , Xinran Liu , Yongjie Zheng , Jun Ma , Shijie You , Heshan Zheng . Effective peroxydisulfate activation by CQDs-MnFe2O4@ZIF-8 catalyst for complementary degradation of bisphenol A by free radicals and non-radical pathways. Chinese Chemical Letters, 2024, 35(5): 108971-. doi: 10.1016/j.cclet.2023.108971
Yuchen Wang , Zhenhao Xu , Kai Yan . Rational design of metal-metal hydroxide interface for efficient electrocatalytic oxidation of biomass-derived platform molecules. Chinese Journal of Structural Chemistry, 2025, 44(1): 100418-100418. doi: 10.1016/j.cjsc.2024.100418
Shili Wang , Mamitiana Roger Razanajatovo , Xuedong Du , Shunli Wan , Xin He , Qiuming Peng , Qingrui Zhang . Recent advances on decomplexation mechanisms of heavy metal complexes in persulfate-based advanced oxidation processes. Chinese Chemical Letters, 2024, 35(6): 109140-. doi: 10.1016/j.cclet.2023.109140
Jia-Cheng Hou , Hong-Tao Ji , Yu-Han Lu , Jia-Sheng Wang , Yao-Dan Xu , Yan-Yan Zeng , Wei-Min He . Sustainable and practical semi-heterogeneous photosynthesis of 5-amino-1,2,4-thiadiazoles over WS2/TEMPO. Chinese Chemical Letters, 2024, 35(8): 109514-. doi: 10.1016/j.cclet.2024.109514
Boqiang Wang , Yongzhuo Xu , Jiajia Wang , Muyang Yang , Guo-Jun Deng , Wen Shao . Transition-metal free trifluoromethylimination of alkenes enabled by direct activation of N-unprotected ketimines. Chinese Chemical Letters, 2024, 35(9): 109502-. doi: 10.1016/j.cclet.2024.109502