Related Experiment Video
Updated: Apr 21, 2026

Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyltroponeiron
Published on: August 12, 2019
Sulfonamide-substituted iron phthalocyanine: design, solubility range, stability and oxidation of olefins
Umit Işci1, Celal Caner, Yunus Zorlu
1Department of Chemistry, Gebze Institute of Technology, PO Box 141, Gebze, 41400 Kocaeli, Turkey. u.isci@gyte.edu.tr ahsen@gyte.edu.tr.
Abstract:
4-tert-Butylbenzenesulfonamide was used as a substituent of tetra peripherally substituted Fe(ii) phthalocyanine, taking into account several parameters crucial for the design of potential oxidation catalysts such as solubility and stability. The resulting phthalocyanine exhibits a remarkable stability under oxidative conditions. The main product of the oxidation of cyclohexene using H2O2 as the oxidant is the allylic ketone, 2-cyclohexen-1-one. Styrene oxidation led mainly to the formation of benzaldehyde.
More Related Videos
12:07Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Published on: April 1, 2013
09:34Synthesis and Characterization of Fe-doped Aluminosilicate Nanotubes with Enhanced Electron Conductive Properties
Published on: November 15, 2016
Related Concept Videos
Preparation and Reactions of Sulfides
Extraction: Advanced Methods
Electrophilic Aromatic Substitution: Sulfonation of Benzene
Preparation and Reactions of Thiols
Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate
Phase I Oxidative Reactions: Overview