Visible Light-Catalyzed Reactions of Polysulfide (DBSPS) with Aryldiazonium

被引:1
|
作者
Tang, Ling-Juan [1 ]
Zhu, Wei-Chen [2 ]
Deng, Hong-He [2 ]
Jiang, Yi-Fan [2 ]
Liu, Xin-Yu [2 ]
Rao, Weidong [3 ]
Shen, Shu-Su [4 ]
Song, Ping [5 ]
Wang, Shun-Yi [2 ]
机构
[1] Nantong Univ, Anal & Testing Ctr, 1 Nanhai Rd, Nantong 226019, Peoples R China
[2] Soochow Univ, Key Lab Organ Synth Jiangsu Prov, Coll Chem Chem Engn & Mat Sci, 199 Renai Rd, Suzhou 215000, Peoples R China
[3] Nanjing Forestry Univ, Coll Chem Engn, Key Lab Biomass Based Green Fuels & Chem, 159 Longpan Rd, Nanjing 210000, Peoples R China
[4] Suzhou Univ Sci & Technol, Sch Environm Sci & Engn, 1 Kerui Rd, Suzhou 215009, Peoples R China
[5] Soochow Univ, Anal & Testing Ctr, 199 Renai Rd, Suzhou 215000, Peoples R China
基金
中国国家自然科学基金;
关键词
C-S/Se bond; Photocatalysis; Sulfur Reagent; Radicals; METAL-FREE; SULFONYL HYDRAZIDES; SULFINYL RADICALS; FREE PROTOCOL; THIOSULFONATES; DISULFIDES; SALTS; OXIDATION; THIOLS;
D O I
10.1002/asia.202400086
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A visible light-catalyzed radical coupling reaction of polysulfide reagents with aryldiazonium was developed, which gave thiosulfonates under mild conditions. In this reaction, the thiosulfonates were isolated in good yields with a broad tolerance to functional groups. And the synthesis of diaryl monosulfides were achieved through a step-by-step reaction of two molecular aryldiazonium with DBSPS, where the sulfur source was provided by DBSPS. It was worth noting that the reaction of this monosulfides could also be achieved by a one pot two-step process. The described polysulfide reagents were able to produce three new radicals: sulfonyl radicals, sulfur-sulfonyl radicals and sulfur-sulfur-sulfonyl radicals.
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页数:5
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