eng
Sami Publishing Company
Asian Journal of Green Chemistry
2588-5839
2588-4328
2018-01-01
2
1
1
10
10.22631/ajgc.2017.95751.1018
50891
One-pot, clean and energy efficient synthesis of dibenzo[b,f][1,4]oxazepine derivatives promoted by ultrasound
Hossein Paghandeh
h_porkaleh@gmail.com
1
Hamid Saeidian
saeidian1980@gmail.com
2
Ebrahim Saeedian Moghadam
saeidian@pnu.ac.ir
3
Zohreh Mirjafary
zmirjafary@srbiau.ac.ir
4
Mohammad Ghaffarzadeh
saeidian1980@pnu.ac.ir
5
Department of Science, Payame Noor University (PNU), PO Box.,19395-4697, Tehran, Iran
Department of Science, Payame Noor University (PNU), PO Box.,19395-4697, Tehran, Iran
Chemistry and Chemical Engineering Research Center of Iran, PO Box 14335-186, Tehran, Iran
Department of Chemistry, Tehran Science and Research Branch, Islamic Azad University, Tehran, Iran
Chemistry and Chemical Engineering Research Center of Iran, PO Box 14335-186, Tehran, Iran
In the present study, a variety of dibenzo [b,f][1,4] oxazepine derivatives was successfully synthesized in good yields under ultrasonic irradiation as an environmental friendly technique. This one-pot method is practically reliable, mild, catalyst-free, and inexpensive. Ultrasonic irradiation on the reaction mixture leads to fine emulsion between the reactants and violent collapses of a lot of cavitation bubbles in less than a microsecond releases extreme heat, leading to cross the activation energy barrier. In the absence of ultrasonic irradiation, a trace amount of the product was formed after 50 min. The superiority of the ultrasound irradiation over other methods in the synthesis of dibenzo [b,f][1,4] oxazepine derivatives is its low reaction temperature and operational simplicity in approximately same yields.
https://www.ajgreenchem.com/article_50891_c6e33f6ec171422ee5586590327a3c6a.pdf
Dibenzo[b
f][1
4]oxazepine Ultrasonic irradiation Sonocatalytic ability Catalyst-free reaction
eng
Sami Publishing Company
Asian Journal of Green Chemistry
2588-5839
2588-4328
2018-01-01
2
1
11
24
10.22631/ajgc.2017.95985.1019
51780
Synergy of binary ionic liquids in a three component one-pot synthesis of 3,4,6-triarylpyridazine at ambient temperature
Pranab Jyoti Das
pranabjdas52@gmail.com
1
Dimpee Das
dimpeedas16@gmail.com
2
Department of Chemistry, Gauhati University, Guwahati -781014, India
Department of Chemistry, Gauhati University, Guwahati -781014, India
A mixture of two ionic liquids have been used for a green synthesis of 3,4,6-triarylpyridazine in high yield and at room temperature. The two ionic liquids acts in tandem. The advantage of this method is a room temperature synthesis of the target compounds using green methodology. Product recovery is simple and the mixture of ionic liquids can be recovered and recycled.
https://www.ajgreenchem.com/article_51780_b3df78157789763299539d6171b2f180.pdf
Pyridazine
Pyridinium based ionic liquid
Hydrazine
Tetra-n-butyl ammonium hydroxide
Acetophenones
eng
Sami Publishing Company
Asian Journal of Green Chemistry
2588-5839
2588-4328
2018-01-01
2
1
25
40
10.22631/ajgc.2017.94356.1009
51917
Enhanced adsorption of anionic diazo dye by magnetic layered double hydroxide (Zn0.5Cu0.5Fe2O4@SiO2@Ni-CrLDH) from aqueous solution
Fatemeh Arab
fat_arab@yahoo.com
1
Nahid Rasouli
n.rasooli55@yahoo.com
2
Maryam Movahedi
maria_movahedi@yahoo.com
3
Department of Chemistry, Payame Noor University, PO Box 19395-3697, Tehran, Iran
Department of Chemistry, Payame Noor University, PO Box 19395-3697, Tehran, Iran
Department of Chemistry, Payame Noor University, PO Box 19395-3697, Tehran, Iran
A novel magnetic layered double hydroxide known as Zn0.5Cu0.5 Fe2O4@SiO2@Ni−Cr layered double hydroxide was synthesized with Zn0.5 Cu0.5Fe2O4, SiO2 and Ni−CrLDH by using coprecipitation method. In order to compare the adsorption efficiency, the Ni−CrLDH sample also was synthesized. The synthesized samples were characterized by X−ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FTIR). The adsorption of Congo red (CR) by magnetic layered double hydroxide depended upon the contact time, initial dye concentration and pH. The adsorption of the Congo red (CR) reached equilibrium at 180 min and followed the pseudo−second−order kinetic equation. The adsorption capacity of the magnetic layered double hydroxide changed significantly between pH 4−10 and the maximum dye removal were 88% for CR. Moreover, the magnetic layered double hydroxide can be quickly separated from the aqueous solution by an external magnet before and after adsorption process. This indicated that the Zn0.5Cu0.5Fe2O4@SiO2@Ni−CrLDH composite was an effective adsorbent for CR dye removal with quick separation. The adsorption performance of the synthesized Zn0.5 Cu0.5Fe2O4, SiO2 and Ni−CrLDH and comparing with Ni−CrLDH show that the Zn0.5Cu0.5Fe2O4@SiO2@Ni−CrLDH can be more efficient than Ni−CrLDH for removal of CR dye.
https://www.ajgreenchem.com/article_51917_4a226249e2995d1fd17187cc5a3509b2.pdf
Layered double hydroxide
Magnetic separation
Adsorption kinetics
Anionic diazo dye
eng
Sami Publishing Company
Asian Journal of Green Chemistry
2588-5839
2588-4328
2018-01-01
2
1
41
50
10.22631/ajgc.2017.96293.1020
53163
Green synthesis and characterization of silver nanoparticles using fructose
Elham Arshadi
arshadi.chemist@gmail.com
1
Sajjad Sedaghat
2
Omid Moradi
3
Department of Chemistry, College of Science, Shahr–e–Qods Branch, Islamic Azad University, Shahr–e–Qods, Iran
Department of Chemistry, College of Science, Shahr–e–Qods Branch, Islamic Azad University, Shahr–e–Qods, Iran
Department of Chemistry, College of Science, Shahr–e–Qods Branch, Islamic Azad University, Shahr–e–Qods, Iran
The green synthesis of nanoparticles is an important branch and a relatively new emerging field in nanotechnology which is easy, environmentally friendly, cost effective, and economically efficient in comparison with the chemical and physical methods. In the present work, for the first time, green synthesis of silver nanoparticles (AgNPs) was carried out by using fructose solution as a reducing agent at room temperature. The silver nanoparticles were characterized by UV-Vis, FTIR, XRD, and TEM analysis. The UV-Vis spectral studies confirmed the surface plasmon resonance of the green synthesized silver nanoparticles. The role of different functional groups in formation of the AgNps was shown by FTIR. X-ray diffraction results confirmed the formation of the the AgNPs and TEM results indicated that the average particle size of the silver nanoparticles was 13.24±8.591 nm.
https://www.ajgreenchem.com/article_53163_4f76a437de8a2eccea955c7298bdec5c.pdf
Green synthesis
Silver nanoparticles
Fructose
Transmission electron microscopy
eng
Sami Publishing Company
Asian Journal of Green Chemistry
2588-5839
2588-4328
1999-11-30
2
1
51
58
10.22631/ajgc.2017.101962.1033
53527
Synthesis of 3-amino-5-methyl-[1,1'-biaryl]-2,4-dicarbonitriles using ZnFe2O4 magnetic nanoparticles
Bagher Mohammadi
bzsa.mohammadi@gmail.com
1
Laleh Salmani
lalesalmani242@yahoo.com
2
Department of Chemistry, Payame Noor university, P. O. BOX 19395-3697, Tehran, Iran
Department of Chemistry, Payame Noor university, P. O. BOX 19395-3697, Tehran, Iran
This work studies an efficient, one-pot pseudo multi-component synthesis of 3-amino-5-methyl-[1, 1'-biaryl]-2, 4-dicarbonitriles. This reaction performed under solvent free conditions in the presence of ZnFe2O4 magnetic nanoparticles. The ZnFe2O4 nanoparticles were prepared by an eco-friendly hydrothermal method
https://www.ajgreenchem.com/article_53527_4ff2b1586b100d8c542e1ccebf68fad9.pdf
Biaryl Multi
component reaction Nano ZnFe2O4 Malononitrile Aloe vera
eng
Sami Publishing Company
Asian Journal of Green Chemistry
2588-5839
2588-4328
2018-01-01
2
1
59
69
10.22631/ajgc.2017.101572.1032
53824
Sulfonic acid supported on Fe2O3/VO2 nanocatalyst: A highly efficient and reusable nanocatalyst for synthesis of spirooxindole derivatives
Hassan Hassani
hassaniir@yahoo.com
1
Batol Zakerinasab
2
Azadeh Nozarie
nozariazadeh@gmail.com
3
Department of Chemistry, Payam Noor University, Birjand, Iran
Department of Chemistry, Payam Noor University, Birjand, Iran
Department of Chemistry, Payam Noor University, Birjand, Iran
Fe2O3/VO2/SO3H nanocatalyst is reported for simple, and three-component reaction for the synthesis of spirooxindole derivatives by the reaction of isatin, 1,3-cyclohexadiene and malonitrile in solvent-free condition. The method allows easy construction of a library of spirooxindoles in moderate to good yields. The prepared nanocomposite was characterized using fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), x-ray diffraction (XRD) analysis, and energy dispersive x-ray spectroscopy (EDX). The nanocomposite was easily recovered using an external magnet and reused several times without a significant loss of the efficiency.
https://www.ajgreenchem.com/article_53824_384beb8477cf9e67e60dff21d5793c33.pdf
Fe2O3/VO2/SO3H Spirooxindole Isatin 1
3-Cyclohexadiene Malonitrile
eng
Sami Publishing Company
Asian Journal of Green Chemistry
2588-5839
2588-4328
2018-01-01
2
1
70
84
10.22631/ajgc.2017.101557.1031
53947
Quinolinium bound chromium(VI) reagents for efficient electrophilic aromatic nitration and thiocyanation reactions using sodium nitrate and ammonium thiocyanate
Satish Babu Kodali
1
Narendar Reddy Jakku
2
Chinna Rajanna Kamatala
kcrajannaou@yahoo.com
3
Rajeshwar Rao Yerraguntla
4
Ivon Chakravarthi Elisha
5
Department of Chemistry, Rayalaseema University, Kurnool-518 007 (A.P.) India
Department of Chemistry, Rayalaseema University, Kurnool-518 007 (A.P.) India
Department of Chemistry,
Osmania University,
Hyderabad (T.S)-500007
India
Department of Chemistry, Govt. City College, Hyderabad-500002 (T.S.) India
Department of Chemistry, Rayalaseema University, Kurnool-518 007 (A.P.) India
Quinolinium dichromate (QDC) and quinolinium chlorochromate (QCC) were studied as efficient reagents for electrophilic aromatic nitration using sodium nitrite and thiocyanation by using ammonium thiocyanate under conventional, ultrasonic and solvent-free microwave assisted conditions. The microwave-assisted protocols exhibited remarkable rate acceleration and offered selective thiocyanation of the aromatic and heteroaromatic compounds with good yields. Addition of anionic (SDS) micelle to the reaction medium afforded considerable rate enhancements, while cationic (CTAB) and nonionic (Tx-100) micelles did not affect the rate noticeably. These protocols have were extended to regioselective thiocyanation of various aromatic compounds. Results were are completely similar to the nitration protocols. However, the reactions revealed comparatively shorter reaction times, and better yields in nitration reactions than in thiocyanation protocols. Catalytic effect of the SDS was attributed to the electrostatic stabilization of the cationic electrophile (NO2+ in nitration, and SCN+ in thiocyanation).
https://www.ajgreenchem.com/article_53947_fafa764c3e31e4ce28ada80161d91cf9.pdf
Quinolinium chlorochromate
Quinolinium dichromate
NaNO2/KHSO4
Nitration
NH4SCN/KHSO4