Related Experiment Video
Updated: Jun 11, 2026

Protocol for the Synthesis of Ortho-trifluoromethoxylated Aniline Derivatives
Published on: January 19, 2016
Ti(IV)-amino triphenolate complexes as effective catalysts for sulfoxidation
Miriam Mba1, Leonard J Prins, Cristiano Zonta
1Dipartimento di Scienze Chimiche, Università di Padova, via Marzolo 1, 35131, Padova, Italy.
C(3)-symmetric Titanium(IV) catalysts efficiently oxidize sulfides at room temperature using hydrogen peroxide. These novel catalysts offer high yields and low loadings, making them effective for green chemistry applications.
Area of Science:
- Organometallic Chemistry
- Catalysis
- Green Chemistry
Background:
- Sulfides are important industrial intermediates.
- Oxidation of sulfides often requires harsh conditions or toxic reagents.
- Development of efficient and environmentally friendly oxidation catalysts is crucial.
Purpose of the Study:
- To develop novel C(3)-symmetric Titanium(IV) amino triphenolate complexes.
- To investigate the catalytic efficiency of these complexes in sulfide oxidation.
- To explore the use of environmentally friendly oxidants like aqueous hydrogen peroxide.
Main Methods:
- Synthesis and characterization of C(3)-symmetric Ti(IV) amino triphenolate complexes.
- Catalytic oxidation of sulfides using cumene hydroperoxide (CHP) and aqueous hydrogen peroxide.
- Reaction monitoring and product analysis.
- Characterization of catalysts and intermediates using (1)H NMR and ESI-MS.
- Density functional theory (DFT) studies.
Main Results:
- The Ti(IV) complexes efficiently catalyze sulfide oxidation at room temperature.
- Excellent yields were achieved using both CHP and aqueous hydrogen peroxide.
- Catalyst loadings as low as 0.01% were effective.
- Intermediate Ti(IV)-peroxo species were identified.
Conclusions:
- C(3)-symmetric Ti(IV) amino triphenolate complexes are highly effective catalysts for sulfide oxidation.
- The catalytic system operates under mild conditions and utilizes green oxidants.
- These findings present a promising advancement in sustainable oxidation catalysis.
Related Concept Videos
Preparation and Reactions of Thiols
Preparation and Reactions of Sulfides
Phase II Reactions: Sulfation and Conjugation with α-Amino Acids
Phase II Reactions: Glutathione Conjugation and Mercapturic Acid Formation
Several distinctive characteristics distinguish glutathione conjugation from other phase II...
Electrophilic Aromatic Substitution: Sulfonation of Benzene
Amines to Sulfonamides: The Hinsberg Test
Generally, a primary amine reacts with the Hinsberg reagent to produce an N-substituted benzenesulfonamide. The electron-withdrawing sulfonyl...
