An efficient clean methodology for the C–S coupling to aryl thioethers and S–S homocoupling to aromatic disulfides catalyzed over a Ce(iv)-leucine complex immobilized on mesoporous MCM-4. (13th June 2019)

• Record Type: Journal Article
• Authors: Veisi, Hojat; Tamoradi, Taibeh; Karmakar, Bikash
• Is Part Of: New journal of chemistry. Volume 43:Number 26(2019)
• Page Start: 10343
• Page End: 10351
• Publication Date: 2019-06-13
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/c9nj02270h
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : Anchored Ce(iv ) on the surface of MCM-41 mesoporous silica was used for the synthesis of aryl thioethers and aromatic disulfides. Abstract : A novel Ce(iv )-anchoredl -leucine covalently bonded to mesoporous MCM-41 has been synthesized by a non-hydrothermal post-functionalization approach. It has been thoroughly characterized by sophisticated physicochemical techniques. The material was applied in the efficient green synthesis of aromatic sulfides by C–S coupling using molecular sulfur and haloarenes. Another catalytic application was in the synthesis of symmetric disulfides by the homocoupling of aromatic thiols in the presence of H2 O2 as an oxidant. The ligand-free protocol is simple, clean and free from hazardous chemicals. Moreover, the catalyst is reusable for several times, thus making the methodology sustainably viable.