Chem. J. Chinese Universities ›› 2020, Vol. 41 ›› Issue (11): 2435.doi: 10.7503/cjcu20190652
Previous Articles Next Articles
ZHOU Jinlong, LIU Xiaolong, FU Yao()
Received:
2020-05-11
Online:
2020-11-10
Published:
2020-11-06
Contact:
FU Yao
E-mail:fuyao@ustc.edu.cn
Supported by:
CLC Number:
TrendMD:
ZHOU Jinlong, LIU Xiaolong, FU Yao. Visible-light-induced Selective Oxidation of Alcohols[J]. Chem. J. Chinese Universities, 2020, 41(11): 2435.
Compd. | 1H NMR(400 MHz, CDCl3), δ | 13C NMR(101 MHz, CDCl3), δ |
---|---|---|
2a | 10.02(s, 1H), 7.89(ddd, J=7.0, 2.9, 1.6 Hz, 2H), 7.66—7.59(m, 1H), 7.56—7.50(m, 2H) | 192.38, 136.33, 134.52, 129.63, 128.47 |
2b | 7.76(d, J=8.1 Hz, 2H), 7.32(d, J=7.8 Hz, 2H), 2.41(s, 3H) | 191.91, 145.61, 134.26, 129.85, 129.71, 21.83 |
2c | 9.89(s, 1H), 7.95—7.52(m, 2H), 7.14—6.69(m, 2H), 3.89(s, 3H) | 190.79, 164.63, 131.99, 130.01, 114.33, 55.59 |
2d | 10.02(s, 1H), 7.89(ddd, J=7.0, 2.9, 1.6 Hz, 2H), 7.66—7.59(m, 1H), 7.56—7.50(m, 2H) | 190.29, 154.32, 131.97, 125.29, 111.09, 40.12 |
2e | 10.02(s, 1H), 7.89(ddd, J=7.0, 2.9, 1.6 Hz, 2H), 7.66—7.59(m, 1H), 7.56—7.50(m, 2H) | 190.79, 140.95, 134.75, 130.89, 129.45 |
2f | 10.14(s, 2H), 8.04(m, 4H) | 191.58, 140.18, 130.27 |
2g | 9.81(s, 1H), 7.41(dd, J=1.9 Hz, 2H), 7.36(d, J=1.9 Hz, 1H), 6.94(d, J=8.2 Hz, 1H), 3.92(s, 3H), 3.90(s, 3H) | 190.86, 154.50, 149.64,130.16, 126.83, 110.44, 108.99, 56.18, 56.01 |
2h | 10.02(s, 1H), 7.89(ddd, J=7.0, 2.9, 1.6 Hz, 2H), 7.66—7.59(m, 1H), 7.56—7.50(m, 2H) | 189.76, 137.94, 135.08, 132.52, 130.61, 129.39, 127.28 |
2i | 10.78(s, 1H), 9.41(d, J=9.4 Hz, 1H), 8.43(d, J=7.9 Hz, 1H), 8.27(ddd, J=18.1, 9.6, 5.6 Hz, 5H), 8.14—7.99(m, 2H) | 193.06, 135.55, 131.38, 131.10, 130.97, 130.84, 130.72, 130.45, 127.44, 127.21, 127.06, 126.85, 126.58, 124.69, 124.56, 124.09, 123.04 |
2j | 10.10(s, 1H), 9.07(d, J=2.0 Hz, 1H), 8.82—8.84(q, 1H), 8.15—8.18(m, 1H),7.46—7.50(q, 1H) | 190.64, 154.63, 151.91,135.72, 131.44, 124.02 |
Compd. | 1H NMR(400 MHz, CDCl3), δ | 13C NMR(101 MHz, CDCl3), δ |
2k | 9.87(s, 2H), 7.35(s, 2H) | 179.19, 154.23, 119.26 |
2l | 9.91(d, J=1.3 Hz, 1H), 7.85—7.64(m, 2H), 7.19(dd, J=4.9, 3.8 Hz, 1H) | 183.04, 144.10, 136.39, 135.18, 128.40 |
2m | 7.80(ddd, J=7.3, 2.9, 1.6 Hz, 4H), 7.61—7.53(m, 2H), 7.50—7.40(m, 4H) | 196.73, 137.64, 132.43, 130.07, 128.30 |
2n | 7.91(d, J=8.5 Hz, 2H), 7.45(d, J=8.5 Hz, 2H),2.60(s, 3H) | 196.71, 139.52, 135.45, 129.72, 128.86, 26.54 |
2o | 7.54(dd, J=1.5, 2.0 Hz, 1H), 7.36—7.42(m, 2H),7.31(td, J=7.5, 1.5 Hz, 1H), 2.64(s, 3H) | 200.43, 139.16, 131.93, 131.20, 130.60, 129.31, 126.92, 30.57 |
2p | 7.91(t, J=1.8 Hz, 1H),7.81—7.84(m, 1H),7.52—7.55(m, 1H),7.41(t, J=7.7 Hz, 1H), 2.59(s, 3H) | 196.58, 138.61, 134.91, 132.91, 129.86, 128.34, 126.31, 26.53 |
2q | 7.96(dt, J=8.6, 1.7 Hz, 2H), 7.59—7.51(m, 1H), 7.49—7.39(m, 2H), 2.60(s, 3H) | 198.13, 137.17, 133.10, 128.58, 128.31, 26.60 |
2r | 8.74(d, J=8.6 Hz, 1H), 7.92(ddd, J=25.7, 23.8, 8.2 Hz, 3H), 7.69—7.41(m, 3H), 2.74(s, 3H) | 201.84, 135.51, 134.01, 133.04, 130.18, 128.67, 128.43, 128.07, 126.46, 126.04, 124.35, 30.00 |
2s | 8.69(ddd, J=4.8, 1.6, 0.9 Hz, 1H), 8.05(dt, J=7.9, 1.1 Hz, 1H), 7.83(td, J=7.7, 1.7 Hz, 1H), 7.47(ddd, J=7.6, 4.8, 1.3 Hz, 1H), 2.73(s, 3H) | 200.10, 153.62, 148.98, 136.82, 127.06, 121.63, 25.76 |
2t | 7.77(d, J=7.7 Hz, 1H), 7.58(dd, J=7.4, 1.1 Hz, 1H), 7.50—7.44(m, 1H), 7.38(dd, J=10.9, 3.9 Hz, 1H), 3.23—3.06(m, 2H), 2.78—2.60(m, 2H) | 207.05, 155.16, 137.13, 134.60, 127.30, 126.71, 123.76, 36.24, 25.82 |
2u | 7.70(dd, J=3.8, 1.1 Hz, 1H), 7.64(dd, J=5.0, 1.1 Hz, 1H), 7.13(dd, J=5.0, 3.8 Hz, 1H), 2.62—2.49(m, 3H) | 190.71, 144.61, 133.76, 132.45, 128.11, 26.93 |
Compd. | 1H NMR(400 MHz, CDCl3), δ | 13C NMR(101 MHz, CDCl3), δ |
---|---|---|
2a | 10.02(s, 1H), 7.89(ddd, J=7.0, 2.9, 1.6 Hz, 2H), 7.66—7.59(m, 1H), 7.56—7.50(m, 2H) | 192.38, 136.33, 134.52, 129.63, 128.47 |
2b | 7.76(d, J=8.1 Hz, 2H), 7.32(d, J=7.8 Hz, 2H), 2.41(s, 3H) | 191.91, 145.61, 134.26, 129.85, 129.71, 21.83 |
2c | 9.89(s, 1H), 7.95—7.52(m, 2H), 7.14—6.69(m, 2H), 3.89(s, 3H) | 190.79, 164.63, 131.99, 130.01, 114.33, 55.59 |
2d | 10.02(s, 1H), 7.89(ddd, J=7.0, 2.9, 1.6 Hz, 2H), 7.66—7.59(m, 1H), 7.56—7.50(m, 2H) | 190.29, 154.32, 131.97, 125.29, 111.09, 40.12 |
2e | 10.02(s, 1H), 7.89(ddd, J=7.0, 2.9, 1.6 Hz, 2H), 7.66—7.59(m, 1H), 7.56—7.50(m, 2H) | 190.79, 140.95, 134.75, 130.89, 129.45 |
2f | 10.14(s, 2H), 8.04(m, 4H) | 191.58, 140.18, 130.27 |
2g | 9.81(s, 1H), 7.41(dd, J=1.9 Hz, 2H), 7.36(d, J=1.9 Hz, 1H), 6.94(d, J=8.2 Hz, 1H), 3.92(s, 3H), 3.90(s, 3H) | 190.86, 154.50, 149.64,130.16, 126.83, 110.44, 108.99, 56.18, 56.01 |
2h | 10.02(s, 1H), 7.89(ddd, J=7.0, 2.9, 1.6 Hz, 2H), 7.66—7.59(m, 1H), 7.56—7.50(m, 2H) | 189.76, 137.94, 135.08, 132.52, 130.61, 129.39, 127.28 |
2i | 10.78(s, 1H), 9.41(d, J=9.4 Hz, 1H), 8.43(d, J=7.9 Hz, 1H), 8.27(ddd, J=18.1, 9.6, 5.6 Hz, 5H), 8.14—7.99(m, 2H) | 193.06, 135.55, 131.38, 131.10, 130.97, 130.84, 130.72, 130.45, 127.44, 127.21, 127.06, 126.85, 126.58, 124.69, 124.56, 124.09, 123.04 |
2j | 10.10(s, 1H), 9.07(d, J=2.0 Hz, 1H), 8.82—8.84(q, 1H), 8.15—8.18(m, 1H),7.46—7.50(q, 1H) | 190.64, 154.63, 151.91,135.72, 131.44, 124.02 |
Compd. | 1H NMR(400 MHz, CDCl3), δ | 13C NMR(101 MHz, CDCl3), δ |
2k | 9.87(s, 2H), 7.35(s, 2H) | 179.19, 154.23, 119.26 |
2l | 9.91(d, J=1.3 Hz, 1H), 7.85—7.64(m, 2H), 7.19(dd, J=4.9, 3.8 Hz, 1H) | 183.04, 144.10, 136.39, 135.18, 128.40 |
2m | 7.80(ddd, J=7.3, 2.9, 1.6 Hz, 4H), 7.61—7.53(m, 2H), 7.50—7.40(m, 4H) | 196.73, 137.64, 132.43, 130.07, 128.30 |
2n | 7.91(d, J=8.5 Hz, 2H), 7.45(d, J=8.5 Hz, 2H),2.60(s, 3H) | 196.71, 139.52, 135.45, 129.72, 128.86, 26.54 |
2o | 7.54(dd, J=1.5, 2.0 Hz, 1H), 7.36—7.42(m, 2H),7.31(td, J=7.5, 1.5 Hz, 1H), 2.64(s, 3H) | 200.43, 139.16, 131.93, 131.20, 130.60, 129.31, 126.92, 30.57 |
2p | 7.91(t, J=1.8 Hz, 1H),7.81—7.84(m, 1H),7.52—7.55(m, 1H),7.41(t, J=7.7 Hz, 1H), 2.59(s, 3H) | 196.58, 138.61, 134.91, 132.91, 129.86, 128.34, 126.31, 26.53 |
2q | 7.96(dt, J=8.6, 1.7 Hz, 2H), 7.59—7.51(m, 1H), 7.49—7.39(m, 2H), 2.60(s, 3H) | 198.13, 137.17, 133.10, 128.58, 128.31, 26.60 |
2r | 8.74(d, J=8.6 Hz, 1H), 7.92(ddd, J=25.7, 23.8, 8.2 Hz, 3H), 7.69—7.41(m, 3H), 2.74(s, 3H) | 201.84, 135.51, 134.01, 133.04, 130.18, 128.67, 128.43, 128.07, 126.46, 126.04, 124.35, 30.00 |
2s | 8.69(ddd, J=4.8, 1.6, 0.9 Hz, 1H), 8.05(dt, J=7.9, 1.1 Hz, 1H), 7.83(td, J=7.7, 1.7 Hz, 1H), 7.47(ddd, J=7.6, 4.8, 1.3 Hz, 1H), 2.73(s, 3H) | 200.10, 153.62, 148.98, 136.82, 127.06, 121.63, 25.76 |
2t | 7.77(d, J=7.7 Hz, 1H), 7.58(dd, J=7.4, 1.1 Hz, 1H), 7.50—7.44(m, 1H), 7.38(dd, J=10.9, 3.9 Hz, 1H), 3.23—3.06(m, 2H), 2.78—2.60(m, 2H) | 207.05, 155.16, 137.13, 134.60, 127.30, 126.71, 123.76, 36.24, 25.82 |
2u | 7.70(dd, J=3.8, 1.1 Hz, 1H), 7.64(dd, J=5.0, 1.1 Hz, 1H), 7.13(dd, J=5.0, 3.8 Hz, 1H), 2.62—2.49(m, 3H) | 190.71, 144.61, 133.76, 132.45, 128.11, 26.93 |
1 | Sood A., Panchagnula R., Chem. Rev., 2001, 101(11), 3275—3304 |
2 | Leeson P. D., Springthorpe B., Nat. Rev. Drug Disco., 2007, 6(11), 881—890 |
3 | Castral T. C., Matos A. P., Monteiro J. L., Araujo F. M., Bondancia T. M., Batista-Pereira L. G., Fernandes J. B., Vieira P. C., Da Silva M. F. G. F., Corrêa A. G., J. Agric. Food Chem., 2011, 59(9), 4822—4827 |
4 | Legacy C. J., Wang A., O’day B. J., Emmert M. H., Angew. Chem. Int. Ed., 2015, 54(49), 14907—14910 |
5 | Wu X. F., Bheeter C. B., Neumann H., Dixneuf P. H., Beller M., Chem. Commun., 2012, 48(100), 12237—12239 |
6 | Alfonsi K., Colberg J., Dunn P. J., Fevig T., Jennings S., Johnson T. A., Kleine H. P., Knight C., Nagy M. A., Perry D. A., Stefaniak M., Green Chem., 2008, 10(1), 31—36 |
7 | Wu X. F., Sharif M., Feng J. B., Neumann H., Pews⁃Davtyan A., Langer P., Beller M., Green Chem., 2013, 15(7), 1956—961 |
8 | Albright J. D., Goldman L., J. Am. Chem. Soc., 1965, 87(18), 4214—4216 |
9 | Huang W., Ma B. C., Lu H., Li R., Wang L., Landfester K., Zhang K. A., ACS Catal., 2017, 7(8), 5438—5442 |
10 | Xu X., Liu R., Cui Y., Liang X., Lei C., Meng S., Ma Y., Lei Z., Yang Z., Appl. Catal. B, 2017, 210, 484—494 |
11 | Gaster E., Kozuch S., Pappo D., Angew. Chem. Int. Ed., 2017, 56(21), 5912—5915 |
12 | Zhang M., Chen C., Ma W., Zhao J., Angew. Chem. Int. Ed., 2008, 47(50), 9730—9733 |
13 | Tsang A. S. K., Kapat A., Schoenebeck F., J. Am. Chem. Soc., 2016, 138(2), 518—526 |
14 | Tebben L., Studer A., Angew. Chem. Int. Ed., 2011, 50(22), 5034—5068 |
15 | Gogoi N., Borah G., Gogoi P. K., Chetia T. R., Chem. Phys. Lett., 2018, 692, 224—231 |
16 | Zhang X., Rakesh K., Ravindar L., Qin H. L., Green Chem., 2018, 20(21), 4790—4833 |
17 | Schilling W., Riemer D., Zhang Y., Hatami N., Das S., ACS Catal., 2018, 8(6), 5425—5430 |
18 | Lechner R., Kümmel S., König B., Photoch. Photobio. Sci., 2010, 9(10), 1367—1377 |
19 | Ohkubo K., Mizushima K., Iwata R., Souma K., Suzuki N., Fukuzumi S., Chem. Commun., 2010, 46(4), 601—603 |
[1] | GONG Yanxi, WANG Jianbing, CHAI Buyu, HAN Yuanchun, MA Yunfei, JIA Chaomin. Preparation of Potassium Doped g-C3N4 Thin Film Photoanode and Its Application in Photoelectrocatalytic Oxidation of Diclofenac Sodium in Water [J]. Chem. J. Chinese Universities, 2022, 43(6): 20220005. |
[2] | JIANG Shan, SHEN Qianqian, LI Qi, JIA Husheng, XUE Jinbo. Pd-loaded Defective TiO2 Nanotube Arrays for Enhanced Photocatalytic Hydrogen Production Performance [J]. Chem. J. Chinese Universities, 2022, 43(10): 20220206. |
[3] | TIAN Xiaokang, ZHANG Qingsong, YANG Shulin, BAI Jie, CHEN Bingjie, PAN Jie, CHEN Li, WEI Yen. Porous Materials Inspired by Microbial Fermentation: Preparation Method and Application [J]. Chem. J. Chinese Universities, 2022, 43(10): 20220216. |
[4] | SHAO Wenhui, HU Xin, SHANG Jing, LIN Feng, JIN Liming, QUAN Chunshan, ZHANG Yanmei, LI Jun. Design, Synthesis and Photocatalytic Antibacterial Mechanism of Ag-AgVO3/BiVO4 Composite as a High-efficient and Broad-spectral Antibacterial Agent [J]. Chem. J. Chinese Universities, 2022, 43(10): 20220132. |
[5] | MA Jianxin, LIU Xiaodong, XU Na, LIU Guocheng, WANG Xiuli. A Multi-functional Zn(II) Coordination Polymer with Luminescence Sensing, Amperometric Sensing, and Dye Adsorption Performance [J]. Chem. J. Chinese Universities, 2022, 43(1): 20210585. |
[6] | CHANG Shuqing, XIN Xu, HUANG Yaqi, ZHANG Xincong, FU Yanghe, ZHU Weidong, ZHANG Fumin, LI Xiaona. Pyroelectrically-induced Catalytic Performance of Zr-based MOF Under Cold-hot Alternation [J]. Chem. J. Chinese Universities, 2021, 42(8): 2558. |
[7] | SU Yingli, REN Haisheng, LI Xiangyuan. Application of New Nonequilibrium Solvation Theory in Electronic Spectra of Organic Dyes [J]. Chem. J. Chinese Universities, 2021, 42(7): 2254. |
[8] | XU Anqi, LI Bin, DU Fanglin. Synthesis of Ordered Mesoporous TiO2 and Their Application for Hydrogen Production from Photocatalytic Water-splitting [J]. Chem. J. Chinese Universities, 2021, 42(4): 978. |
[9] | YAN Yanhong, WU Simin, YAN Yilun, TANG Xihao, CAI Songliang, ZHENG Shengrun, ZHANG Weiguang, GU Fenglong. Sulfonic Acid-functionalized Spherical Covalent Organic Framework with Ultrahigh Capacity for the Removal of Cationic Dyes [J]. Chem. J. Chinese Universities, 2021, 42(3): 956. |
[10] | GUI Chen, WANG Haolin, SHAO Baixuan, YANG Yujing, XU Guangqing. Molten-salt-assistance Synthesis and Photocatalytic Hydrogen Evolution Performances of g-C3N4 Nanostructures [J]. Chem. J. Chinese Universities, 2021, 42(3): 827. |
[11] | PAN Jing, XU Minmin, YUAN Yaxian, YAO Jianlin. Rapid Detection of Banned Dyes in Textiles Based on Surface-enhanced Raman Spectroscopy [J]. Chem. J. Chinese Universities, 2021, 42(12): 3716. |
[12] | SUN Yaguang, ZHANG Hanyan, MING Tao, XU Baotong, GAO Yu, DING Fu, XU Zhenhe. Synthesis of ZnIn2S4/g-C3N4 Nanocomposites with Efficient Photocatalytic H2 Generation Activity by a Simple Hydrothermal Method [J]. Chem. J. Chinese Universities, 2021, 42(10): 3160. |
[13] | LI Xiaoqian, ZHANG Hua, LU Haijian, LIU Chang, LIU Qinglong, MA Xiayu, FANG Yuanping, LIANG Dapeng. Mechanism of Photocatalytic Degradation of Rhodamine B by TiO2 Nanowire Array with Internal Extraction Electrospray Ionization Mass Spectrometry [J]. Chem. J. Chinese Universities, 2020, 41(9): 2003. |
[14] | LI Li, LI Pengfei, WANG Bo. Photocatalytic Application of Covalent Organic Frameworks [J]. Chem. J. Chinese Universities, 2020, 41(9): 1917. |
[15] | XU Wenyi,FENG Yisi. Oxidative Trifluoromethylation of CF3SO2Na with Olefins Mediated by Diacetyl† [J]. Chem. J. Chinese Universities, 2020, 41(7): 1567. |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||