A non-heme cationic Fe(iii)-complex intercalated in montmorillonite K-10: synthesis, characterization and catalytic alkane hydroxylation with H2O2 at room temperature

2014 ◽  
Vol 4 (9) ◽  
pp. 3180-3185 ◽  
Author(s):  
Anand Pariyar ◽  
Suranjana Bose ◽  
Achintesh Narayan Biswas ◽  
Sudip Barman ◽  
Pinaki Bandyopadhyay

An efficient catalyst for highly selective hydroxylation of alkanes with environmentally benign H2O2 at room temperature has been designed by the intercalation of a non-heme iron(iii) complex into smectite montmorillonite K-10.

2020 ◽  
Vol 17 (4) ◽  
pp. 321-326
Author(s):  
Pradeep M. Mhaldar ◽  
Dattaprasad M. Pore

A simple and environmentally benign room temperature synthesis of 1,2,4-triazolidine-3- thiones is described using Envirocat EPZ-10R as a solid acid catalyst in the aqueous medium. The use of Envirocat EPZ-10R as a green catalyst, reusability of the catalyst, water as a universal solvent and good yields of the product are the attractive features of the present method.


2015 ◽  
Vol 51 (77) ◽  
pp. 14469-14472 ◽  
Author(s):  
Sujoy Rana ◽  
Aniruddha Dey ◽  
Debabrata Maiti

Non-heme iron(iv)–oxo species form iron(iii) intermediates during hydrogen atom abstraction (HAA) from the C–H bond.


2013 ◽  
Vol 27 (S1) ◽  
Author(s):  
Wen‐I Luo ◽  
Chun‐Wei Chang ◽  
Ravirala Ramu ◽  
Yi‐Fang Tsai ◽  
Kok Yaoh Ng ◽  
...  

2020 ◽  
Vol 17 (9) ◽  
pp. 694-703
Author(s):  
Sonatai Patil ◽  
Ananda Mane ◽  
Savita Dhongade-Desai

We have successfully explored the potential MoO3 nanoparticles as a heterogeneous catalyst for the cyclocondensation of hydrazines/hydrazides with 1,3-dicarbonyl compound in aqueousalcoholic medium at room temperature. The present method has been developed using green chemistry measures and offers a range of N-substituted pyrazoles with moderate to excellent yields. Utilization of non-toxic catalyst, wide substrate scope and environmentally benign reaction medium are the important features of the developed protocol. Interestingly, MoO3 nanocatalyst can easily be recovered from the reaction mixture and showed excellent reusability with a modest change in product yield. We have reported herein the synthetic pathway with less disastrous effect in the atmosphere.


2020 ◽  
Vol 07 ◽  
Author(s):  
Naoures Jamel Eddine ◽  
Fayçal Jennen ◽  
Yakdhane Kacem ◽  
Jamil Kraiem

Background: Acetylation of protic nucleophiles is used to protect these functional groups. Most of the methods described in the literature use solvents, one equivalent or more of toxic bases or expensive and toxic catalysts. Therefore, new methodologies are still in demand, above all, greener and more economical procedures. Objective: An eco-efficient method developed for acetylation of alcohols, phenols, thiols, amines and carbohydrates, using acetic anhydride and a catalytic amount of the environmentally benign and inexpensive FeCl3.6H2O under solvent free conditions. Methods: Acetylation of a variety of protic nucleophiles was performed using 0.2 mol % of FeCl3.6H2O as the catalyst, and 1.2 equiv. as the acetylating agent at room temperature and under solvent free conditions. Results: Our procedure appears to be highly efficient and promoted rapid and quantitative acetylation under simple and minimum manipulation. Chromatography or recrystallization were generally not necessary for the purification of products. Conclusion: This eco-friendly protocol appears to be potentially universally applicable in organic design to protect protic nucleophiles and potentially scalable for industrial fields.


2006 ◽  
Vol 128 (26) ◽  
pp. 8590-8606 ◽  
Author(s):  
Hajime Hirao ◽  
Devesh Kumar ◽  
Lawrence Que ◽  
Sason Shaik

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