Catalytic synthesis of dialkyl sulfides from dialkyl disulfides
- 作者: Mashkina A.V.1, Khairulina L.N.1
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隶属关系:
- Boreskov Institute of Catalysis, Siberian Branch
- 期: 卷 58, 编号 4 (2017)
- 页面: 402-408
- 栏目: Article
- URL: https://journal-vniispk.ru/0023-1584/article/view/163113
- DOI: https://doi.org/10.1134/S0023158417040115
- ID: 163113
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详细
Dialkyl disulfides R2S2 where R = Me, Et, or Pr, both as individual compounds and as their mixtures, isolated from petroleum products can turn into alkanethiols and dialkyl sulfides under the action of catalysts having strong acid sites and medium-strength basic sites on their surface. In a helium atmosphere, the main conversion products are alkanethiols, while dialkyl sulfides form in low yield at a selectivity of no higher than 20%. A much higher dialkyl sulfide selectivity is attained in the reaction involving methanol. The most efficient catalyst for this reaction is alumina, with which the dialkyl sulfide selectivity is up to 99%.
作者简介
A. Mashkina
Boreskov Institute of Catalysis, Siberian Branch
编辑信件的主要联系方式.
Email: amash@catalysis.ru
俄罗斯联邦, Novosibirsk, 630090
L. Khairulina
Boreskov Institute of Catalysis, Siberian Branch
Email: amash@catalysis.ru
俄罗斯联邦, Novosibirsk, 630090
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