Synthesis of sulfides via reaction of aryl/alkyl halides with S8 as a sulfur-transfer reagent catalyzed by Fe3O4-magnetic-nanoparticles-supported L-Histidine-Ni(II)

被引：19

作者：

Azadi, Gouhar ^{[1
]}

Taherinia, Zahra ^{[1
]}

Naghipour, Ali ^{[1
]}

Ghorbani-Choghamarani, Arash ^{[1
]}

机构：

[1] Ilam Univ, Dept Chem, Fac Sci, POB 69315516, Ilam, Iran

来源：

JOURNAL OF SULFUR CHEMISTRY | 2017年 / 38卷 / 03期

关键词：

Fe3O4@SiO2@His@Ni(II); symmetrical sulfides; reusable; magnetic nanoparticles; sulfur-transfer reagent; EFFICIENT THIOL EQUIVALENTS; MICHAEL ADDITION-REACTIONS; S-S BOND; ORGANIC SEMICONDUCTORS; ARYL HALIDES; FE3O4; NANOPARTICLES; DISULFIDE; IODIDE; NANOCATALYSTS; CLEAVAGE;

D O I：

10.1080/17415993.2017.1287265

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

One-pot synthesis of symmetrical diaryl/alkyl sulfides in high yields from the reaction between aryl/alkyl halides and S-8 can be carried out in a short period, using Fe3O4@SiO2@His@Ni(II) as a reusable catalyst. The present approach offers the advantages of a clean reaction, simple methodology and high efficiency, and avoids the use of a toxic catalyst.

引用

页码：303 / 313

页数：11

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