Surface modification of ferrite nanoparticles with dicarboxylic acids for the synthesis of 5-hydroxymethylfurfural: a novel and green protocol

RSC Advances ◽  
2016 ◽  
Vol 6 (80) ◽  
pp. 76795-76801 ◽  
Author(s):  
Melad Shaikh ◽  
Mahendra Sahu ◽  
Kiran Kumar Atyam ◽  
Kalluri V. S. Ranganath

5-Hydroxymethylfurfural (5-HMF) has been synthesized under solvent free conditions using surface modified ferrite nanoparticles. The flexible ligand modified ferrites showed higher activity than rigid modified ferrites.

2021 ◽  
Vol 76 (2) ◽  
pp. 85-90
Author(s):  
Abdolkarim Zare ◽  
Manije Dianat

Abstract A highly efficient and green protocol for the synthesis of pyrimido[4,5-b]quinolines has been described. The one-pot multicomponent reaction of dimedone with arylaldehydes and 6-amino-1,3-dimethyluracil in the presence of N,N-diethyl-N-sulfoethanaminium chloride ([Et3N–SO3H][Cl]) as an ionic liquid (IL) catalyst under solvent-free conditions afforded the mentioned compounds in high yields and short reaction times. Our protocol is superior to many of the reported protocols in terms of two or more of these factors: the reaction times, yields, conditions (solvent-free versus usage of organic solvents), temperature and catalyst amount.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Ehsan Valiey ◽  
Mohammad G. Dekamin ◽  
Zahra Alirezvani

AbstractThis study introduces a practical approach to fabricate a novel hybrid acidic catalyst, namely sulfamic acid pyromellitic diamide-functionalized MCM-41 (MCM-41-APS-PMDA-NHSO3H). Various techniques such as FTIR, TGA, XRD, BET, FESEM, and EDX were used to confirm its structural characteristics. The efficiency of the new MCM-41-APS-PMDA-NHSO3H organosilica nanomaterials, as a heterogenous nanocatalyst, was examined in the synthesis of biologically active 3,4-dihydropyrimidin-2-(1H)-one derivatives under solvent-free conditions. It was found that the nanoporous MCM-41-APS-PMDA-NHSO3H, demonstrating acidic nature and high surface area, can activate all the Biginelli reaction components to afford desired 3,4-dihydropyrimidin-2-(1H)-ones under solvent-free conditions in short reaction time. Furthermore, easy and quick isolation of the new introduced hybrid organosilica from the reaction mixture as well as its reusability with negligible loss of activity in at least five consecutive runs are another advantages of this green protocol.


RSC Advances ◽  
2016 ◽  
Vol 6 (59) ◽  
pp. 54236-54240 ◽  
Author(s):  
Seyed Mohsen Sadeghzadeh

A green and efficient method for the synthesis of various triazolo[1,2-a]indazoletrione under mild conditions is reported, that making it a genuinely green protocol.


RSC Advances ◽  
2018 ◽  
Vol 8 (1) ◽  
pp. 38-43 ◽  
Author(s):  
Souvanik Talukdar ◽  
Rupali Rakshit ◽  
André Krämer ◽  
Frank A. Müller ◽  
Kalyan Mandal

We have developed bio-compatible magneto-fluorescent NiFe2O4 nanoparticles (NPs) by modifying the surface of the NPs with Na-tartrate. The surface modified NiFe2O4 NPs are beneficial for cell imaging, wastewater treatment and therapeutics.


RSC Advances ◽  
2021 ◽  
Vol 11 (35) ◽  
pp. 21291-21300
Author(s):  
Nitin Tandon ◽  
Shripad M. Patil ◽  
Runjhun Tandon ◽  
Pushpendra Kumar

Novel silica-coated ferrite nanoparticles supported with montmorillonite (K10) have been prepared and explored for their catalytic activity for the O, N, and S-acylation reactions under solvent-free conditions.


2020 ◽  
Vol 07 ◽  
Author(s):  
Abid H. Banday ◽  
Victor J. Hruby

Background: Unprecedented, one-pot regioselective synthesis of 1,4-disubstituted 1,2,3-triazoles through azide- aldehyde (3+2) organo-click cycloaddition under metal and solvent-free conditions, is described. Objective: Solvent and metal free synthesis of biologically and industrially important triazoles. Methods: Efficient and high yielding synthesis of products avoiding the tedious high solvent workups and chromatographic separations. The synthesis doesn’t involve the routine acetylenes which are very costly but instead cheaper starting materials like aldehydes and organic azides are used. Results: Green protocol based on the catalysis through Ionic Liquids which simultaneously act as solvents. The products are obtained in good to excellent yields in hassle free synthesis. Conclusion: Efficient and green synthesis of structurally and biologically important triazoles.


RSC Advances ◽  
2015 ◽  
Vol 5 (15) ◽  
pp. 10869-10877 ◽  
Author(s):  
R. Tayebee ◽  
M. Jarrahi ◽  
B. Maleki ◽  
M. Kargar Razi ◽  
Z. B. Mokhtari ◽  
...  

An efficient method for the preparation of 1,3,5-triarylbenzenes. Natural surface-modified NCP as a new and reusable catalyst. Using solvent-free conditions.


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